Ionic Liquids in Analytical Chemistry: Fundamentals, Advances, and

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Ionic Liquids in Analytical Chemistry: Fundamentals, Advances, and Perspectives Tien D. Ho, Cheng Zhang, Leandro W. Hantao, and Jared L. Anderson Anal. Chem., Just Accepted Manuscript • Publication Date (Web): 08 Nov 2013 Downloaded from http://pubs.acs.org on November 26, 2013

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Analytical Chemistry

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Ionic Liquids in Analytical Chemistry: Fundamentals, Advances, and Perspectives

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Tien D. Ho, Cheng Zhang, Leandro W. Hantao, and Jared L. Anderson*

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a

b

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Department of Chemistry, The University of Toledo, Toledo, OH 43606 USA

School of Green Chemistry and Engineering, The University of Toledo, Toledo OH

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43606 USA

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*

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E-mail addresses: [email protected] (J.L. Anderson).

Corresponding author. Tel.:+1 4195301508; fax: +1 4195304033.

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1. Introduction Since their initial discovery in 1914, ionic liquids (ILs) have been widely studied

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in a multiple of chemistry disciplines. Applications of ILs in analytical chemistry have

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enjoyed much success and contributed to the rapid evolution of this field. ILs are

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collectively known as organic salts which possess melting points at or below 100 ºC. In

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most cases, ILs are comprised of an organic cation and an organic or inorganic anion. It

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has been estimated there can be up to 1018 possible combinations of ILs, due to the ability

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to interchange their corresponding cationic/anionic moieties.1

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A number of ILs exhibit beneficial characteristics, such as high thermal stability,

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negligible vapor pressure, non-flammability, in addition to varying viscosities,

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conductivity, and miscibility in different solvents. This is due to the electrostatic

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interactions associated with the cation and anion moieties comprised within the ILs, as

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well as their ability to undergo unique intermolecular interactions with one another.

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These characteristics can also be finely tuned to meet specific requirements by imparting

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different functional groups and/or varying the combinations of cations and anions in the

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ILs. In light of these attributes, ILs are practical for many analytical applications and can

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be an indispensable alternative to traditional organic solvents in many sample preparation

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techniques. Although the properties of ILs will not be discussed within this review, the

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audience is referred to a number of publications which describes the structural

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relationship of ILs to their physicochemical properties.2-6

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Aside from the aforementioned properties, ILs can also be engineered to exhibit

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exceptional selectivity towards specific groups of compounds. For example, imparting

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polar substituents to an IL can promote dipolar interactions between the IL and polar

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solutes. Analogously, tailoring long aliphatic alkyl chains to an IL can enhance its ability

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to undergo dispersion interactions with non-polar analytes. Overall, the ability to tune the

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selectivity of ILs can enable high preconcentration of analytes in various sample

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preparation and detection techniques. On the other hand, when applied as

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chromatographic stationary phases, ILs can produce to excellent separation efficiency

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and peak capacities.

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This review aims to provide an update to novel applications of ILs in analytical

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chemistry. Due to the increasing popularity of ILs and the large volume of scientific

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literature that currently exists, it is not possible to exhaustively cover all previous studies.

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Therefore, significant advances pertaining to the applications of ILs in sample

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preparation and extraction, chromatography, capillary electrophoresis, mass

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spectrometry, and electrochemical sensing within the past two years will be discussed.

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2. Ionic Liquids in Solvent-based Microextractions

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2.1 Single drop microextraction

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Single drop microextraction (SDME) is a micro-scale preconcentration technique developed by Dasgupta and co-workers in the 1990s.7 Cantwell and co-workers expanded

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the applicability of SDME by coupling the technique to chromatographic systems.8 In

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SDME, a single microdroplet of extraction solvent is exposed to a sample matrix by use

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of a chromatographic syringe. Extraction can typically be performed in the sample

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headspace or by direct immersion in the sample solution. Following the extraction step,

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the microdroplet can be withdrawn back into the syringe and injected to a

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chromatographic system for analysis. This method is rapid, easy to operate, and provides

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good sensitivity due to the preconcentration of analytes. The application of ILs as

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extraction solvents, initially reported by Liu and co-workers 9, provides multiple

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advantages compared to employing traditional organic solvents as the extraction phase.

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For convenience, common IL cations and anions previously employed in a number of

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analytical chemistry fields are shown in Figure 1. Due to their high viscosity and low

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vapor pressure, ILs enable the formation of large, stable microdroplets that are not prone

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to evaporation during extraction. This can provide superior analyte extraction capabilities

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as well as improved analytical precision compared to organic solvents. Additionally, the

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tunable characteristics of ILs can further increase method sensitivity, leading to better

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limits of detection (LODs) for trace and ultra-trace level analysis.8-10 The following

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studies provide a brief update on the recent progress of IL-based SDME in environmental

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and biological analysis.

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2.1.1 IL-SDME in environmental applications

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IL-SDME has recently been applied in the extraction of analytes in various

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environmental water samples. For instance, the 1-butyl-3-methylimidazolium

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hexafluorophosphate ([C4MIM][PF6]) IL and diethyldithiocarbamate (DDTC) was

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employed as the extraction solvent and chelating reagent, respectively, in the analysis of

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copper ions (Cu).11 The method demonstrated good Cu recovery in both food and water

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matrixes. Applying an IL-based extraction solvent also significantly improved the overall

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analytical performance of the technique, compared to using no ILs. Rahmani and co-

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workers also successfully employed the same IL in the extraction of

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methylcyclopentadienyl-manganese tricarbonyl in gasoline and water, while Wen et al.

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recently applied this IL in the analysis of cadmium in rice and waters samples.12,13

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Márquez-Sillero and co-workers reported the analysis of 2,4,6-trichloroanisole in water

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and wine samples using IL-SDME coupled to ion mobility mass spectrometry (IMS). The

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1-hexyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide ([C6MIM][NTf2 ]) IL

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was used as an extraction microdroplet in headspace mode, wherein high analyte

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selectivity and method sensitivity was achieved.14,15 Four extraction solvents, namely,

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toluene, n-heptane, [C6MIM][PF6], and 1-octyl-3-methylimidazolium [PF6]

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([C8MIM][PF6]) were compared in the automated extraction of musk fragrances in

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environmental water samples.16 The [C8MIM][PF6] IL and toluene provided the highest

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extraction peak areas; however, the [C8MIM][PF6] IL was chosen as a superior solvent

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since this IL microdroplet exhibited improved stability and yielded significantly better

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method precision.

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2.1.2 IL-SDME in Bioanalytical Applications

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IL-SDME was also demonstrated to be highly useful for bioanalytical

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applications. Pathogenic bacteria were extracted by the [C4MIM][PF6] IL impregnated

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with platinum nanoparticles and characterized by matrix-assisted laser desorption

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ionization time-of-flight mass spectrometry (MALDI-TOF MS).17 This method showed

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promising results for the potential analysis of pathogenic organisms in biological

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samples. IL microdroplets were modified with CdSe/ZnS quantum dots (QDs) for the

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analysis of trimethylamine (TMA) in fish.18 The QD-[C6MIM][PF6] IL mixture was used

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to extract volatile TMA from fish samples followed by QD-based fluorimetric detection.

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Quantification was achieved by observing signal enhancements from pure QD-IL relative

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to QD-IL containing TMA.

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2.2 Hollow fiber membrane liquid phase microextraction

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Hollow fiber membrane liquid phase microextraction (HF-LPME) is a solvent

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preconcentration technique developed by Pedersen-Bjergaard and Rasmussen in the late

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1990s.19 This method employs a porous polymer membrane that enables the permeation

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of analytes from an aqueous sample solution (donor phase) to an extraction solvent

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(acceptor phase). Extraction in HF-LPME can be categorized into two different modes,

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namely, two-phase and three-phase mode. In two-phase mode, the lumen of the hollow

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fiber is filled with the same organic acceptor phase as those impregnated within its

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porous walls. On the other hand, the three-phase mode involves the fiber lumen being

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filled with an aqueous solution while its porous walls are impregnated with a water-

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immiscible organic solvent. During the extraction step, a solvent-impregnated hollow

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fiber containing an acceptor phase is immersed into the aqueous sample solution.

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Analytes can permeate through the porous structure of the membrane wall and

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subsequently partition in the acceptor phase. Afterwards, a syringe can be used to

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withdraw and inject the acceptor phase to a chromatographic system for analysis. The

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primary advantages of employing HF-LPME in various analytical procedures include its

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cost-effectiveness, high throughput, low solvent consumption, and high applicability in

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complex sample analyses.

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Similar to other extraction techniques, a potential drawback to using traditional

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organic acceptor phases in HF-LPME stems from the volatility, toxicity, and low

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selectivity of these solvents. To address this issue, Peng and co-workers initially reported

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the application of ILs in three-phase HF-LPME.20 The [C8MIM][PF6] IL was

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impregnated in the hollow fiber membrane, while aqueous sodium hydroxide was

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employed as an acceptor phase, for the HF-LPME of chlorophenols in environmental

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water samples. The high stability, hydrophobicity, and negligible volatility of the IL

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contributed to the good extraction efficiency and precision of the method.

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2.2.1 ILs as acceptor phases in HF-LPME

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Ma and co-workers exploited the [C4MIM][PF6] IL as an acceptor phase in the

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IL-HF-LPME of benzene, toluene, ethylbenzene, xylene (BTEX).21 After extraction, the

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IL was directly injected to a GC-FID for analysis with no manipulation. Good analytical

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performance was obtained; however, the GC injector required frequent maintenance due

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to IL contamination within the GC liner. Ge and co-workers investigated four different

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ILs, namely, [C6MIM] tris(pentafluoroethyl)trifluorophosphate) ([C6MIM][FAP]), 1-

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butyl-1-methylpyrrolidinium [FAP] ([C4MPL][FAP]), [C4MIM] phosphate

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([C4MIM][PO4]) and [C4MIM][PF6], as acceptor phases in IL-HF-LPME coupled to

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HPLC-UV for the analysis of UV filters.22 High enrichment factors were obtained by

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using the [C6MIM][FAP] IL compared to other ILs. Furthermore, the enrichment factors

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obtained using this method were superior to other microextraction techniques, such as

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DLLME and SDME.

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2.2.2 ILs as additives in HF-LPME

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The water-miscible [C4MIM][Cl] IL was utilized as an acceptor phase additive in

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the three-phase HF-LPME of alkaline, acidic, and neutral organic compounds.23 As

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shown in Figure 2A, the water-miscible IL was dissolved in the aqueous acceptor phase.

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As analytes partition from the donor to the acceptor phase, the IL can interact with the

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analytes and mitigate their back-extraction to the organic phase of the membrane. Using

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this approach resulted in slightly better extraction performance for alkaline and acidic

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compounds. On the other hand, as shown in Figure 2B, significant enhancements in

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extraction efficiency were obtained for neutral organic compounds compared to

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analogous three-phase HF-LPME systems containing no IL additives. Zeng and co-

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workers explored a variety of ILs as donor phase additives for the extraction of Cr (VI)

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and Cr (III).24 After a preliminary screening, it was determined that the addition of the

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[C4MIM][BF4] IL, alongside a metal chelating agent (diethyldithiocarbamate (DDTC)),

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to the donor phase significantly enhanced the extraction of the chromium complexes by

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up to 3.5 fold. It should be noted that the addition of DDTC to sample could promote the

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formation of a hydrophobic metal complex, which can easily be extracted by an organic

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acceptor phase. However, the mechanism describing the extraction enhancements

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obtained from adding an IL to the donor phase is still unknown. Recently, an automated

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technique using IL-impregnated HF membranes was also successfully employed for the

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determination of Cr (VI).25

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2.3 Dispersive liquid-liquid microextraction

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Although ILs have been extensively applied in various sample preparation and/or

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preconcentration techniques, the utilization of ILs as extraction solvents in dispersive

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liquid-liquid microextraction (DLLME) have generated the most interest and publications

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within the past two years. Introduced by Rezaee and co-workers in 2006, DLLME is a

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solvent extraction technique that preconcentrates analytes from an aqueous sample matrix

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to a water-immiscible extraction phase in the presence of a disperser solvent.26 During the

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extraction step, microliter volumes of a hydrophobic organic solvent and a disperser

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solvent are injected to an aqueous sample solution. The hydrophobic solvent functions as

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the analyte extraction phase, while the disperser solvent (an organic modifier that is

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miscible with both the aqueous matrix and the extraction solvent) is used to facilitate the

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formation of fine microdroplets of the extraction phase in solution. Subsequently, the

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extraction phase can be recovered by centrifugation and injected to a chromatographic

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system for analysis. The primary advantages of employing DLLME over traditional

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liquid-liquid extraction (LLE) techniques are its low solvent consumption, high

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extraction throughput, and excellent extraction efficiency, which is primarily achieved by

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the large surface area of the microdroplets formed during extraction.

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Zhou and co-workers initially applied hydrophobic ILs as extraction phases in

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DLLME.27 Instead of utilizing organic disperser solvents, the formation of IL

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microdroplets was achieved by the manipulation of the solution temperature. This

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approach, noted as temperature-controlled IL-DLLME (TC-IL-DLLME), demonstrated

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high method sensitivity as a result of the selectivity attained from employing ILs as

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extraction solvents. Additionally, the use of toxic organic solvents during extraction was

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minimized. Anderson and co-workers developed an in situ IL-DLLME method, wherein

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a hydrophilic IL is injected to a sample solution as the extraction solvent instead of a

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hydrophobic IL.28 Subsequent to the complete dissolution of the hydrophilic IL, an ion-

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exchange reagent, such as LiNTf2, was added to the solution to promote the metathesis

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reaction and the subsequent formation of a hydrophobic IL extraction phase. Overall, the

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in situ IL-DLLME method demonstrated better enrichment factors compared to

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conventional DLLME due to the formation of smaller microdroplets during extraction.

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Furthermore, no organic disperser solvents were needed during the extraction step.

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The following studies will explore the recent applications of ILs in DLLME.

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Emphasis will be placed on the applicability of this technique for the analysis of

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pharmaceutical products, metal ions, and organic environmental pollutants.

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2.3.1 Application of IL-DLLME in the analysis of pharmaceutical entities

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The TC-IL-DLLME of various isoquinoline alkaloids, namely, berberine,

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palmatine, jatrorrhizine, and coptisine, were investigated by Wu and co-workers.29 The

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[C8MIM][PF6] IL was shown to exhibit high selectivity for the alkaloids in the presence

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of various metals and organic species. Additionally, coupling this extraction method to

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fluorescence detection provided good method sensitivity and LODs in the sub-ppb range.

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The same IL was later successfully applied in the ultrasonic-assisted IL-DLLME (UA-IL-

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DLLME) of various pharmaceutical entities in wastewaters,30 and the conventional IL-

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DLLME of antichagasic drugs in human plasma, using an organic disperser solvent.31 A

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rapid IL-DLLME sampling procedure was developed in the analysis of salmeterol in

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dried blood spot (DBS).32 After adding the DBS to a micro-centrifugation tube, a

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conventional IL-DLLME approach, using methanol as a disperser solvent, was employed

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to extract the salmeterol. The method was proven to be effective for monitoring

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salmeterol in DBS samples obtained from asthmatic patients. In another example,

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aminoglycosides in milk samples were quantified using IL-DLLME coupled to

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HPLC/fluorescence.33 Dispersion of the extraction phase, namely, the [C6MIM][PF6] IL,

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was achieved by using a nonionic surfactant, Triton X-100. Additionally, derivatization

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of the analyte via fluorescent labeling was accomplished simultaneously during the

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extraction step. This method provided competitive performance compared to previous

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analytical procedures, such as biosensor immunoassays and solid phase extraction (SPE)

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coupled to HPLC-ESI-MS/MS.

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The analysis of anti-hypertensives in rat serum was demonstrated by conventional

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IL-DLLME coupled to HPLC-UV. Excellent method precision and recovery was

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achieved by using the [C4MIM][PF6] IL as the extraction solvent in this study.34 Recently

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Ge and co-workers coupled IL-DLLME to micro-solid phase extraction (µ-SPE) for the

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determination of tricyclic antidepressants from water samples.35 The [C6MIM][FAP] IL

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was employed as an extraction phase and methanol was used as a disperser solvent in this

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method. During emulsion formation by IL-DLLME, a µ-SPE device, containing zeolite

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imidazolate frameworks (ZIF), was exposed to the sample solution to back-extract

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analytes preconcentrated in the IL. Subsequently, the analytes are desorbed from the µ-

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SPE device and analyzed by HPLC. This technique provided high analyte extraction

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efficiency since the µ-SPE device is exposed to a large surface area of the IL during the

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extraction step. In relation to genetic engineering in biopharmaceuticals, Anderson and

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co-workers recently applied in situ IL-DLLME for the preconcentration of

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deoxyribonucleic acid (DNA).36 After screening a number of ILs, it was determined that

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DNA was best-extracted using the 1-(1,2-dihydroxypropyl)- 3-hexadecylimidazolium

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bromide ([C16POHIM][Br]) and N,N-didecyl-N-methyl-D-glucaminium bromide

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([(C10)2NMDG][Br]) ILs, which provided extraction efficiencies above 97 %. Based on

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ILs interact favorably through electrostatic and π-π interactions.

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2.3.2 IL-DLLME in the analysis of metal ions

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P nuclear magnetic resonance (NMR) spectroscopy, it was observed that the DNA and

As ILs are not highly suitable for extracting charged metal ions, a metal chelating

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agent can be injected to the sample solution during extraction to enhance the affinity of

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the ILs towards the metal species.37 A schematic representation of this method for the

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speciation of arsenite and arsenate by electrothermal atomic absorption spectrometry

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(ETAAS) is shown in Figure 3.38 Similar approaches using various IL extraction phases

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and metal complexing agents were successfully employed for the analysis of Cr (III) and

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(IV),39, 40 Au (III) and Ag (I),41 As (III) and As (V),38,42 Pb (II),43,44 Cd (II),44 Co (II),45

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and Hg (II).46 The DLLME of Tl (III) involved utilizing tetradecyl(trihexyl)phosphonium

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chloride ([P66614][Cl]) as an ion-pairing reagent rather than an extraction phase.47

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Subsequent to forming a [TlCl4]-chlorocomplex by reaction with HCl, the anionic

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thalium species were ion-paired with the phosphonium IL in solution and were extracted

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using chloroform. Compared to traditional ion-pairing reagents such as

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cetyltrimethylammonium bromide (CTAB), trimethyltetradecylammonium bromide

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(TTAB), and tetrabutylammonium bisulfate, the [P66614][Cl] IL contributed to higher

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extraction efficiency of the Tl complex. Pressure-assisted IL-DLLME was recently

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developed for the determination of a vanadium complex in real water samples.48 The

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[C4MIM][PF6] IL was applied as an extraction phase while pressurized argon was

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exploited as a dispersive medium during the extraction step. The use of pressurized argon

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enabled highly efficient dispersion of the selective IL phase and provided superior

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analytical performance compared to other preconcentration techniques.

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2.3.3 Application of IL-DLLME in the analysis of organic environmental pollutants Zhang et al. compared various IL dispersion strategies for the IL-DLLME of

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pyrethroid pesticides in honey/water samples.49 The [C8MIM][PF6] IL was dispersed in a

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honey/water matrix by either using a methanol disperser solvent (conventional IL-

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DLLME), controlling the extraction temperature (TC-IL-DLLME), or applying ultrasonic

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treatment (UA-IL-DLLME). Based on the superior extraction efficiency and good

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recoveries obtained for all pesticides, UA-IL-DLLME was selected as the optimal IL

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dispersion strategy in this study. The extraction of pyrethroids was also performed by

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coupling UA-IL-DLLME with dispersive µ-SPE, wherein magnetic barium ferrite

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nanoparticles were dispersed into the sample solution to retrieve the IL after extraction.50

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Similarly, magnetic Fe3O4 nanoparticles were used to recover the [C6MIM][PF6] IL in the

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IL-DLLME of benzoylurea insecticides.51

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A hydrophobic IL and a hydrophilic IL was selected as the extraction solvent and

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disperser solvent, respectively, in the IL/IL-DLLME of triclosan and triclocarban in

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environmental water.52 Following a preliminary screening of various hydrophilic and

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hydrophobic ILs, the [C8MIM][PF6] IL was chosen as the extraction phase while the

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[C4MIM][BF4] IL was selected as the disperser solvent. The synergistic effects of both

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ILs provided wide linear ranges, good method precision, and LODs in the sub-ppb levels.

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A similar IL/IL-DLLME method was applied for the extraction of sulfonamides in milk

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powder.53

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In situ IL-DLLME was compared with conventional IL-DLLME in the extraction

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of emerging contaminants in water samples.54 Overall, the in situ IL-DLLME method

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demonstrated better enrichment factors for all contaminants compared to the conventional

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IL-DLLME technique employing the same IL. In regards to analyte selectivity, the 1-(6-

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amino-hexyl)-1-methylpyrrolidinium [FAP] ([C6NH2MPL][FAP]) IL used in this study

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exhibited higher enrichment factors in the extraction of tertiary amines compared to other

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FAP-based ILs. Boron species were extracted from water by in situ IL-DLLME.55,56 The

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cis diol functionality, comprised within the carbohydrate moiety of the cation, enabled

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the selective complexation of boron to the IL. Additionally, the IL was regenerated after

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extraction by displacing the boron-IL complex using hydrochloric acid. In situ IL-

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DLLME was also successfully applied in the extraction of phenols, phenylurea

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pesticides, triazine herbicides, and acaricides.57-60

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3. Ionic Liquids in Sorption-based Extractions

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3.1 Solid-Phase Extraction

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Solid-phase extraction is a technique used to extract sample analytes from liquid

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matrixes. Very simply, this sorbent-type extraction method functions by exposing liquid

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samples to solid supports containing suitable materials that can retain analytes of interest.

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Subsequently, analytes can be desorbed from the sorbent materials and further analyzed.

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Similar to other extraction techniques, continuous development in SPE materials revolves

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around improving the sorbent-to-analyte selectivity and capacity. The exploitation of ILs

293

as sorbents in SPE was first explored by Tian and co-workers in 2009, wherein silica

294

substrates were modified by N-methylimidazolium chloride for the extraction of

295

tanshinones.61 Since then, there have been numerous studies that investigate the potential

296

of ILs as selective sorbents in SPE. A couple recent reviews provide additional insight

297

into the applications and development of ILs in SPE.62,63 The following sections highlight

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298

the recent advancements in IL-SPE and are broadly categorized based on analyte classes

299

and matrix composition.

300

3.1.1 IL-SPE of metal ions in aqueous matrixes

301

Within the past two years, there have been a number of investigations involving

302

the application of ILs in SPE for the analysis of transition metals. The analysis of Pb (II)

303

ions from various environmental water sources has been reported. Within these studies,

304

ILs comprised of varying hydrophobicity and polarities were physically adsorbed to silica

305

substrates and applied as selective sorbent phases. The IL-modified SPE silica substrates

306

were demonstrated to provide good recovery of Pb (II).64-68 Two ILs comprised of either

307

imidazolium [Cl] or imidazolium [PF6] were covalently linked to Merrifield resin and

308

successfully applied as solid substrates for the analysis of Sc (III).69 The IL-Merrifield

309

resin was further impregnated with Cyanex 923 and the [C8MIM][PF6] IL to promote the

310

extraction of Sc (III) via cation exchange. The extraction of trivalent Eu (III) and Am

311

(III) was achieved by impregnating the [C8MIM][NTf2] IL extraction phase in

312

Chromosorb-W.70 Compared to an analogous Chromosorb-W resin impregnated with n-

313

dodecane, the IL-impregnated resin exhibited up to one order of magnitude higher metal-

314

to-resin weight distribution coefficients for Am (III). Amjadi and co-workers recently

315

reported the application of titanium dioxide (TiO2) nanoparticles physically coated with

316

1-hexadecyl-3-methylimidazolium [Br] ([C16MIM][Br]) in the extraction of Ni (II).71 The

317

IL-modified nanoparticles provided a Ni (II) adsorption capacity of 630 mg g-1, which

318

was superior to nanoparticles immobilized with CTAB. IL-modified magnetic

319

nanoparticles were also reported for the extraction of various heavy metals in human hair

320

and urine.72 The magnetic nanoparticles were exploited as a robust solid substrate that

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321

can easily be separated from the sample solution by an external magnetic field. On the

322

other hand, the methyltrioctylammonium [Cl] IL was employed as a chelate-free

323

extraction phase capable of providing good method sensitivity.

324

3.1.2 IL-SPE of organic compounds in aqueous matrixes

325

A large number of organic compounds can be extracted from aqueous samples by

326

using IL-modified SPE materials. The 1-vinyl-3-butylimidazolium [Cl] ([VC4IM][Cl]) IL

327

was applied as a functional monomer to produce a molecularly imprinted polymer (MIP)

328

that can selectively extract chlorosulfuron from water samples.73 Rapid

329

adsorption/desorption kinetics of chlorosulfuron, in addition to low ppb-level detection

330

limits was obtained using the chloride-based IL as the MIP. Similarly, imidazolium [Cl]

331

IL-modified MIPs were applied as SPE sorbents in the extraction of tanshinones from

332

Salvia miltiorrhiza Bunge extract and functional drinks.74 Analyte-to-sorbent hydrogen-

333

bonding interactions played a crucial role in enhancing adsorption selectivity and

334

capacity. This observation was justified by the high selectivity obtained by employing IL-

335

modified MIPs functionalized with a carboxylic acid moiety. Magnetic microspheres

336

covalently bounded with an imidazolium [Cl] IL was successfully applied in the

337

extraction of chlorophenols from environmental water samples.75 A similar approach

338

using imidazolium [PF6] bound magnetic nanoparticles was fruitfully employed for the

339

extraction of PAHs in water.76 Due to their high analyte adsorption capabilities, soft

340

materials such as IL-modified carbon nanotubes (IL-CNTs) can also be used as extraction

341

materials for PAHs.77 In a similar manner, IL-CNTs was exploited in conjunction with

342

in-line capillary electrophoresis (CE) to analyze nitrophenols at ultra-trace levels.78

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343

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Vidal and co-workers reported the SPE of a variety of organic acids, amines, and

344

aldehydes using silica materials modified with three different imidazolium-based ILs.79 A

345

side-by-side screening of the analyte-to-sorbent extraction efficiencies revealed the

346

unique selectivity achieved by functionalizing each IL with diverse substituents.

347

Organophosphate pesticides were successfully analyzed using methylimidazolium [PF6]

348

functionalized silica as the extraction phase in dispersive µ-solid phase extraction

349

coupled to ultra performance liquid chromatography (UPLC).80 Compared to an

350

analogous IL-functionalized silica comprising of [Cl] anions, IL-modified silica

351

containing the [PF6] anion provided superior analyte interactions due its enhanced

352

hydrophobicity. The enrichment factors of all organophosphates ranged from 74 to 111

353

using the proposed method. Methylimidazolium [PF6] IL-modified gold nanoparticles

354

(GNPs) were exploited as extraction sorbents in the preconcentration and analysis of

355

sulfonylurea herbicides in water.81 Superior method LODs, LOQs, and recoveries were

356

obtained by using the IL-modified GNPs compared to analogous unmodified

357

nanoparticles and conventional C18 sorbents.

358

3.1.3 IL-SPE of organic compounds in biological matrixes

359

There have been increasing reports on the use of IL-modified materials as

360

selective sorbents enabling the analysis of various organic compounds in biological

361

samples. Microspheres comprised of IL-based MIPs were applied in the analysis of

362

clenbuterol and clorprenaline from urine samples.82 The IL-based MIP microspheres

363

provided high selectivity for the two compounds which resulted in low chromatographic

364

background when analyzing the biological samples. An IL-mediated MIP containing the

365

[C4MIM][PF6] IL was produced by precipitation polymerization and applied in the SPE

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Analytical Chemistry

366

of dicofol from different vegetable samples.83 The IL-mediated MIPs exhibited superior

367

adsorption capacity and selectivity compared to non-modified MIPs, C18-functionalized

368

sorbents, NH2-functionalized sorbents, and silica sorbents. Precipitation polymerization,

369

using the [C4MIM][PF6] IL as a functional monomer, was also recently applied for the

370

analysis of four Sudan dyes in foodstuff.84 It was observed that the [C4MIM][PF6] IL

371

provided significantly better recovery of all Sudan dyes compared to commercial alumina

372

and C18 sorbents. A number of ILs, each possessing different functionalities, were

373

covalently bonded to silica particles for the extraction of oxymatrine from Sophora

374

flavescens Ait.85 Aside from the higher extraction efficiencies obtained compared to

375

conventional sorbents, the IL-modified silica was also capable of separating matrine from

376

oxymatrine as a result of competitive adsorption.

377

3.2 Ionic liquids and Polymeric Ionic Liquids in Solid-Phase Microextraction

378

Solid-phase microextraction (SPME) is a popular sorbent-type extraction

379

technique developed by Pawliszyn in the early 1990’s.86 The preconcentration of analytes

380

in SPME is achieved by exposing a solid substrate coated with a thin sorbent layer to a

381

sample solution, either by headspace or direct immersion mode. Subsequently, the

382

sorbent layer is exposed to high temperatures in the GC injector or different organic

383

solvents in HPLC to rapidly desorb the analytes from the coating for analysis. Unlike

384

SPE, SPME is an equilibrium-based extraction technique. In other words, extractions by

385

SPME are non-exhaustive, thereby allowing for multiple analyses of a single sample and

386

preventing analyte-to-sorbent breakthrough. Additionally, this technique enables the

387

consolidation of sample preparation and sampling into one simple step which can

388

significantly reduce the cost and increase the throughput of an analysis. Owing to their

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389

unique characteristics and tunable selectivity, ILs were firstly applied as SPME sorbent

390

coatings for the analysis of BTEX in paints.87 Another major advancement was the

391

application of polymeric ionic liquids (PILs) as sorbent coatings, wherein the robustness

392

and reusability of the sorbent phase was significantly enhanced without sacrificing

393

analyte selectivity.88 Recent reviews provide detailed overviews on the development of

394

IL and PIL sorbent phases in SPME.89, 90 The following sections are arranged based on

395

different IL/PIL sorbent loading strategies developed within the past two years.

396

3.2.1 IL/PIL Sorbent Coatings Prepared by Physical Dip-Coating

397

Physical dip coating is a quick and simple strategy for loading a sorbent coating

398

onto a SPME support. To showcase the tunable selectivity and applicability of PIL-based

399

SPME in the analysis of important pharmaceutical impurities, Anderson and co-workers

400

screened a number of dip-coated PIL sorbents comprised of different functionalities for

401

the analysis of genotoxic impurities (GTIs) in water.91 PIL-based sorbent coatings

402

comprised of the [Cl] anion provided the highest selectivity for anilines while a

403

glucaminium-based PIL containing alkyl substituents and a benzyl-functionalized PIL,

404

poly(1-4-vinylbenzyl-3-hexadecylimidazolium) [NTf2] (poly([VBC16IM][NTf2]),

405

exhibited the highest sensitivities for large aliphatic alkyl halides and aromatics,

406

respectively. The selectivity of various PIL-based coatings was evaluated in coffee

407

aromas, wherein the poly([VBC16IM][NTf2]) coating was highly selective towards

408

aldehydes and acids, and the poly(1-vinyl-3-hexylimidazolium) chloride

409

(poly([VC6IM][Cl]) sorbent exhibited good selectivity for aromatic alcohols.92 Recently,

410

two vinylimidazolium-based PIL sorbent coatings containing of a cyclohexanol moiety

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Analytical Chemistry

411

were synthesized and successfully employed in the analysis of various volatile organic

412

compounds in beer.93

413

PILs-based sorbent coatings can also assist in the extraction of chiral organic

414

compounds. Anderson and co-workers successfully applied a physically-coated

415

poly([VC6IM][NTf2]) PIL SPME sorbent to investigate the enantiomeric purity of chiral

416

molecules in crude synthetic batches.94 The PIL-based sorbent coating was used to

417

extract the chiral compounds, while GC (containing a chiral stationary phase) was used to

418

separate and quantify each enantiomer.

419

3.2.2 IL/PIL Sorbents Prepared by Chemical Bonding to Fiber Support

420

Even though PIL-based sorbent coatings provided superior robustness, reusability,

421

and stability for SPME compared to ILs, physically-coated PILs lacked the mechanical

422

stability needed for extractions in harsh matrix conditions. As a result, various PIL

423

sorbent loading techniques were employed to overcome this drawback. Pang and co-

424

workers developed a chemical bonding technique to immobilize 1-vinyl-3-(3-

425

triethoxysilylpropyl)-4,5-dihydroimidazolium [Cl] to a silica-modified steel support.95

426

The covalently bound fiber demonstrated good thermal and mechanical stability in

427

addition to providing comparable extraction performance to a commercial polydimethyl

428

siloxane (PDMS) coating. In another study, Zhang and co-workers covalently linked 1-

429

vinyl-3-hexadecylimidazolium [PF6] to a substrate derivatized with by γ-

430

methacryloxypropyltrimethoxysilane via copolymerization.96 The PIL-bound sorbent

431

coating provided higher extraction efficiency of pyrethroids in vegetables compared to a

432

commercial PDMS coating. Electrochemical deposition was employed to load a

433

[C4MIM][PF6] IL-polyaniline composite sorbent on a steel wire.97 This technique was

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434

then applied in the extraction of organochlorine pesticides in various water samples.

435

Aside from providing better analytical performance compared to a commercial PDMS

436

coating and an analgous polyaniline coating, the composite coating exhibited high

437

robustness with thermal stabilities up to 350 ºC.

438

Page 20 of 79

Feng and co-workers covalently bound and polymerized 1-vinyl-3-

439

octylimidazolium [PF6] ([VC8IM][PF6]) to a steel substrate via in situ surface radical

440

chain-transfer polymerization for the analysis of BTEX, phenols, and PAHs in water and

441

soil.98 The method provided good analytical performance and acceptable precision values

442

after 56 extraction/desorption steps. A PIL-based SPME sorbent comprised of a

443

naphthalene sulfonate anion was also fabricated using this technique and applied for the

444

extraction of PAHs in hair spray and nail polish.99 The sensitivity of the novel aromatic

445

functionalized PIL was superior compared to an anolgous PIL containing a [PF6] anion.

446

Surface radical chain-transfer polymerization was also employed to covalently link a PIL

447

containing both polymerizable cations and anions, namely, [VC8IM] p-styrenesulfonate,

448

to a stainless steel substrate for the analysis of anilines, phenols, and PAEs in water

449

samples.100 The double-confined PIL sorbent coating exhibited better resistance to high

450

ionic strength aqueous samples compared to a PIL containing no polymerizable anions.

451

Sol-gel chemistry has also been employed in multiple occasions to produce

452

thermally stable and covalently linked PIL sorbent coatings that are applicable in both

453

headspace and direct-immersion SPME. An organic/inorganic hybrid IL-silica composite

454

consisting of a benzo-crown ether moiety was developed as a sorbent coating in the

455

extraction of a variety of organic compounds.101 Enhanced π-π and hydrogen bonding

456

interactions were achieved by tailoring this substituent to the IL-silica composite. The

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Analytical Chemistry

457

role of anions in IL-sol gel composites for the extraction of a variety of polar and non-

458

polar compounds was investigated by Shu and co-workers.102 The 1-(3-triethoxysilyl

459

propyl)-3-methyl imidazolium [PF6] ([TESPMIM][PF6]), [TESPMIM][BF4],

460

[TESPMIM][NTf2]) IL-sol gel composites showed high resistance to various organic

461

solvents and aqueous solutions with extreme pH conditions. Additionally, the [BF4]-,

462

[PF6], and [NTf2]-based IL composites were thermally stable up to 285 ºC, 300 ºC, and

463

454 ºC, respectively. An ultra-thermally stable IL-sol gel composite, namely, 1-allyl-3-

464

methylimidazolium [NTf2]–hydroxy-terminated silicone oil ([AMIM][NTf2]–OH-TSO),

465

was developed for the extraction of phthalate esters (PAEs) in agricultural plastic

466

films.103 The high thermal stability of this IL-sol gel composite enabled a thermal

467

desorption temperature of 360 ºC (8 min desorption time), which increased method

468

precision and mitigated analyte carryover effects. The same sorbent loading methodology

469

was recently applied in the analysis organophosphate esters in water samples by Gao and

470

co-workers.104 ILs can not only be applied as a selective copolymeric sorbent in sol-gel

471

chemistry, but they can also be used to mediate the production of molecular sol-gel

472

sorbents in hollow fiber SPME (HF-SPME), as demonstrated by Ebrahimi and co-

473

workers.105,106

474

3.3.3 Crosslinked Copolymeric PIL-based SPME Sorbent Coatings

475

IL/PIL composite materials have been shown to provide significant improvements

476

in thermal stability, resistance to matrix composition, and overall robustness for a SPME

477

fiber. Nevertheless, using these materials may alter the unique selectivity gained by using

478

pure IL/PIL sorbent phases. Crosslinked PIL sorbent coatings have recently been

479

developed to address this potential drawback. Feng and co-workers reported the

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Page 22 of 79

480

exploitation of covalently bound polar crosslinked PIL sorbent coatings for the headspace

481

extraction of polar compounds.107 An IL monomer and IL crosslinker comprised of

482

bromide anions were copolymerized in situ by AIBN-initiated free radical polymerization

483

while covalent bonding to a derivatized stainless steel support. The crosslinked PIL

484

coating exhibited superior thermal stability and longer fiber lifetimes compared to non-

485

crosslinked PIL fibers. Anderson and co-workers further expanded the development and

486

application of polar crosslinked PILs in the analysis of multiple organic compounds from

487

water samples using both headspace and direct immersion SPME.108 Using UV-initiated

488

photopolymerization, two IL crosslinkers, 1,8-di (3- vinylimidazolium) octane dibromide

489

([(VIM)2C8] 2[Br]) or 1,12-di (3-vinylimidazolium) dodecane dibromide ([(VIM)2C12]

490

2[Br]), were copolymerized with an IL monomer, [VC6IM][Cl], to produce polar

491

crosslinked PIL-based sorbent coatings. A schematic representing the fabrication of the

492

crosslinked copolymeric PIL coating is shown in Figure 4. This coating approach

493

eliminated the need for organic dispersive solvents and increased production throughput

494

since neat IL monomer and crosslinkers were copolymerized on-fiber, while also being

495

chemically-linked to an etched and derivatized silica support. The crosslinked PIL-based

496

sorbent coatings also possessed high robustness and fiber lifetimes, even when applied

497

for direct immersion experiments in complex water samples. Recently, the extraction

498

mechanism of both crosslinked and non-crosslinked PIL coatings was also

499

investigated.109 The linearity, sensitivity, and linear range obtained for a model analyte,

500

1-octanol, were largely unaffected when a high concentration of an interfering species,

501

naphthalene, was added to the sample. This indicated that non-competitive analyte

502

partitioning was the primary mechanism of extraction for all PIL coatings studied. In a

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Analytical Chemistry

503

subsequent study, benzyl functionality was imparted to a dicationic IL crosslinker and

504

applied in the analysis of PCBs in milk and seawater.110 The crosslinker exhibited higher

505

method sensitivity for most polychlorinated biphenyls (PCBs) compared to a non-

506

functionalized IL counterpart and a PDMS coating, which may be due to enhanced π-π

507

interactions.

508

4. Gas chromatography

509

Over the past decades, gas chromatography (GC) has become the most popular

510

technique for the separation, detection and identification of volatile and semi-volatile

511

analytes in complex samples. Two paramount requirements to obtain separation of

512

analytes involve enhancing the migration rate differences between a pair of

513

chromatographic bands and decreasing the effect of zone spreading.111, 112 Even though

514

there have been major instrumental advances, zone spreading can only be diminished to a

515

certain extent. Hence, in order to effectively enhance peak capacity, the development of

516

new stationary phases for conventional and multidimensional gas chromatographic

517

(MDGC) separations has been extensively reported. ILs have drawn considerable

518

attention as GC stationary phases, due to their unique and tunable selectivity and thermal

519

stability.113 Unlike conventional PDMS and poly(ethylene glycol) (PEG) stationary

520

phases, ILs are capable of undergoing multiple solvation interactions, thereby imparting

521

unique selectivities towards a wide range of analytes with different functional groups.114

522

As a result, the possibilities for engineering new ILs for specific applications are

523

endless.1 While this section is largely confined to the latest contributions to the field,

524

several excellent reviews describing the most important developments and applications

525

over the last decade are available for the interested reader 115-123. A broad compendium of

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Page 24 of 79

526

studies describing the chromatographic selectivity of several ILs and PILs and their

527

application in GC and MDGC has also been reported.117,124

528

The main limitations of early molten salt-based stationary phases was based on

529

their limited thermal stability, narrow liquid range and poor chromatographic

530

efficiency.113 The operating temperatures for most of the ammonium-based molten salts

531

were between 120 and 170˚C with selected salts capable of reaching 200˚C.124 Hence,

532

over the past decade, ILs have been rigorously engineered to possess different

533

physicochemical properties from the initial molten salts.

534

The ILs employed today as stationary phases in GC consists mainly of cations

535

such as phosphonium, imidazolium, pyridinium and pyrrolidinium paired with several

536

inorganic and, more frequently, organic anions. In addition, several monocationic and

537

polycationic ILs, as well as PILs, have been exploited in GC and MDGC. Furthermore,

538

these ILs have been used to disperse different selectors to modify the overall selectivity

539

of stationary phases.

540

The solvation parameter model, proposed by Abraham and co-workers, has been

541

used to evaluate the strength of the stationary phase solvation capabilities, namely, the

542

ability of the stationary phase to interact with the analytes through - or n-

543

interactions (e), polarizability/dipolarity (s), hydrogen bond basicity and acidity of the

544

stationary phase (a and b, respectively), and through dispersion forces (l).125 The system

545

constants are determined by the multiple linear regression analysis of the numerous solute

546

descriptors and the retention factor of the probes. For convenience, the system constants

547

of all IL stationary phases discussed within this review are reported in Table 1.

548

4.1. Phosphonium, sulfonium, and guanidinium ionic liquid stationary phases

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Analytical Chemistry

549

Phosphonium-based ILs typically exhibit superior chemical and/or thermal

550

stability compared to those ILs possessing nitrogen-containing cations.124 A number of

551

studies which display the applications of phosphonium-based ILs as GC stationary phases

552

has been published recently.126,127 An interesting application of phosphonium-based ILs

553

is the analysis of the residual water in high purity organic solvents. Two of the main

554

challenges that stationary phases face are: (1) water should not degrade or alter the

555

stationary phase and (2) the chromatographic peaks should show good separation

556

efficiency and symmetry.127,128 Thus, three ILs, namely trigonal tripropylphosphonium

557

triflate

558

dimethylimidazolium)-PEG [TfO] were designed and evaluated.127 The analytical

559

performance of these columns was compared to that of a commercially available PEG

560

stationary phase. The phosphonium-based IL, [TTP][TfO] IL, provided the best results

561

and displayed unique selectivity towards water. This IL also provided increased

562

resolution, allowing the use of internal standards and enabling quantitation of trace

563

amounts of water in several organic solvents.127-129 Sulfonium and guanidinium-based ILs

564

were evaluated as stationary phases and the retention behavior of various molecules were

565

examined.126,130-132. The guanidinium-based ILs were shown to operate up to 250˚C

566

without significant loss in efficiency and separation of probe analytes;132 the sulfonium-

567

based IL, however, exhibited poor thermal stability.126

568

4.2. Morpholinium, piperidinium, pyrrolidinium, pyridinium, and imidazolium

569

ionic liquid stationary phases

([TTP][TfO]),

bis(3-hydroxyalkylimidazolium)-PEG

[TfO]

and

bis(2,3-

570

A series of morpholinium, piperidinium, pyrrolidinium, and pyridinium-based ILs

571

have been evaluated as GC stationary phases and characterized by the Abraham

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572

parameter solvation model.114,126,133 In general, the hydrogen bond acidity of non-

573

functionalized ILs largely depends on the nature of the cation, which can be regulated by

574

the anion.114,134,135 Recently, the hydrogen bond basicity of [C4MPL] paired with

575

thiocyanate, tricyanomethide, tetracyanoborate and [FAP] anions has been reported.114

576

Interestingly, ILs paired with cyano-containing anions exhibited enhanced dipolarity and

577

hydrogen bond basicity, compared to the FAP-based ILs. These solvation characteristics

578

were enhanced with an increase in the number of cyano-moieties.

579

Twu et al. observed superior hydrogen bond basicity for the N-hexyl-4-(N’,N’-

580

dimethylamino)pyridinium [FAP] IL compared to N-hexyl-pyridinium [FAP].114 This

581

may be due to the enhanced interaction between the tertiary amine moiety of the IL and

582

the hydrogen bond acidic solute. Similarly, introducing hydroxyl functionality to the IL

583

can

584

hydroxypropylpyridinium [FAP]- compared to N-hexyl-pyrridinium [FAP] IL.

585

lead

to

a

two-fold

increase

in

the

hydrogen

bond

acidity

of

N-

The solvation properties of a number of FAP-based ILs, namely, 1-methoxyethyl-

586

3-methylimidazolium

587

methoxyethyl-1-methylmorpholinium

588

[FAP] and 1-methoxypropyl-1-methylpiperidinium [FAP] were also evaluated.114 The

589

dispersive interaction capability of these ILs did not appear to be significantly affected by

590

the cation type. Additionally, the hydrogen bond acidities and basicities of ILs containing

591

imidazolium, ammonium, and morpholinium cations were similar to one another, with

592

the exception of the 1-methoxyethyl-1-methyl-piperidinium [FAP] IL.

[FAP],

methoxyethyl-dimethyl-ethylammonium [FAP],

[FAP],

1-

1-methoxyethyl-1-methyl-piperidinium

593

Several imidazolium-based ILs, with thermal stabilities ranging from 280 to

594

320˚C, have been previously studied.114,126,136 One advantage of imidazolium-based ILs

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Analytical Chemistry

595

over pyridinium and pyrrolidinium-based ILs is that the latter ILs normally exhibit higher

596

melting points compared to imidazolium-based ILs, thereby decreasing their usefulness

597

as GC stationary phases.124 It was observed that introducing ether functionality to the IL

598

increased the hydrogen bond basicity of the IL.114

599

4.3. Polycationic ionic liquid stationary phases

600

One way to increase the liquid range and thermal stability of ILs is by exploiting

601

polycationic ILs.124 González-Álvarez and co-workers reported the synthesis of seven

602

hexacationic imidazolium-based ILs,137 most of which exhibited thermal stabilities

603

ranging from 260 to 365˚C. The thermal stability of these polycationic ILs was superior

604

to analogous monocationic ILs and commercially available PEG-based stationary

605

phases.136,137 In addition, these hexacationic ILs possess similar thermal stabilities

606

compared to other families of dicationic and tricationic ILs.138,139 As a result, these

607

stationary phases may be an interesting alternative for the characterization of complex

608

samples such as those currently found in aroma and fragrance, metabolomics, lipidomics,

609

and petrochemical-derivatives.

610

4.4. Polymeric ionic liquid stationary phases

611

Unfortunately, a number of IL-based stationary phases may have a tendency to

612

agglomerate or pool at high temperatures. Consequently, maintaining the homogeneity of

613

the IL coated film throughout the capillary can often be problematic.124 PIL-based

614

stationary phases have been developed in an effort to circumvent this limitation.

615

Recently, a series of imidazolium-based PILs has been explored as GC stationary

616

phases.140 These stationary phases exhibited thermal stabilities ranging from 240˚C to

617

300˚C. They also displayed high selectivities toward polar analytes, allowing for the

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Page 28 of 79

618

separation of fragrances, alcohols, and amines. Good chromatographic resolution of

619

xylene isomers was achieved by employing the poly[3-allyl-1-(2-cyclohexanol)-

620

imidazolium] [NTf2] as a PIL-based stationary phase.141,142 Interestingly, poly([VC8IM])

621

paired with [NTf2] and bis[(pentafluoroethyl)sulfonyl]imide also displayed unique

622

selectivities for xylene isomers.

623

4.5. Hybrid ionic liquid-based stationary phases

624

Sun and co-workers and Wei and co-workers reported separately the

625

functionalization of polysiloxane with IL-based moieties.143,144 Although the authors

626

employed different synthetic routes, they successfully modified the selectivity of these

627

hybrid materials compared to conventional PDMS stationary phases. The reported

628

thermal stabilities for the hybrid [VC6IM] stationary phase paired with [NTf2] and [PF6]

629

anions were approximately 225˚C and 250˚C, respectively.144 Methylimidazolium-based

630

hybrids paired with [Cl] and [NTf2] resulted in phases exhibiting thermal stabilities

631

ranging from 220˚C to 380˚C, respectively.143 The latter were successfully used for the

632

resolution of fatty acid methyl esters (FAME) and several PCBs.

633

ILs have also been applied as a medium for the dispersion of macromolecules,

634

such as cyclodextrins145, and calixarenes146, and CNTs147 to yield stationary phases with

635

unique selectivities and thermal stabilities. For chiral separations, the stationary phases

636

consists of chiral ILs or dispersions of the chiral selectors in the bulk IL.145,148 Recently,

637

Zhao and co-workers reported the dispersion of CNTs in a chiral IL as a GC stationary

638

phase.147 Introducing CNTs to the bulk of the IL improved the resolution of enantiomers

639

when compared to a neat IL phase.

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Analytical Chemistry

640

4.6. Applications of commercial ionic liquid stationary phases in 1D-GC and MDGC

641

Multidimensional separation techniques are powerful methods in which two or

642

more independent separative steps are linked together for separation.149 A typical MDGC

643

separation employs two or more gas chromatographic separations in a sequential

644

fashion.150 To achieve a significant increment in resolution power, the stationary phases

645

employed often possess different selectivities. Additionally, separation produced in each

646

stage/dimension is maintained, at least in part, so that the resolving power of the

647

composite separation exceeds that of the individual stages.150 Recently Marriott and co-

648

workers

649

chromatography,151 while Seeley and co-workers reported the advances of comprehensive

650

two-dimensional gas chromatography (GC×GC).150

described

the

fundamentals

of

heart-cutting

multidimensional

gas

651

At the current time, commercially available IL-based GC stationary phases are

652

commonly rated by their polarity number, determined by the normalized sum of the

653

Kovats retention indices, with respect to the polarity number of poly[1,9-di(3-

654

vinylimidazolium)nonane] [NTf2] (SBL-IL100).152,153 A number of commercially

655

available ILs, namely 1,12-di(tripropylphosphonium)dodecane [NTf2] (SBL-IL59), 1,12-

656

di(tripropylphosphonium)dodecane

657

di(tripropylphosphonium)dodecane paired with [NTf2] and trifluoromethylsulfonate

658

(SBL-IL61), tri(tripropylphosphoniumhexanamido)triethylamine [NTf2] (SBL-IL76),

659

1,12-di(2,3-dimethylimidazolium)dodecane [NTf2] (SBL-IL82), SBL-IL100, 1,5-di(2,3-

660

dimethyllimidazolium)pentane [NTf2] (SBL-IL111), have been used for the analysis of

661

essential oils,152-154 biological fluids,155 fuel and petrochemical samples,156-159

662

environmental contaminants,160-163 lipids,164-169 and other applications.170

[NTF2]

(SBL-IL60),

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1,12-

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Page 30 of 79

663

Mondello and co-workers compared the thermal stability of SBL-IL59 with

664

respect to a standard SupelcoWax 10 [100% PEG] stationary phase by monitoring the

665

first dimension bleed profile by a GC×GC-quadropole mass spectrometry (QMS) system

666

fitted with a loop-modulator.152 At 280 and 300˚C, the signal intensities from the 1D

667

bleed profile of the IL-based stationary phase were consistently two orders of magnitude

668

lower. Subsequently, this stationary phase was successfully employed in the analysis of

669

lemon essential oil by GC-QMS. Compared to SBL-5 [5% phenyl poly(silphenylene-

670

siloxane)] and SupelcoWax 10 phases, the SBL-IL59 significantly improved the

671

resolution of several critical pairs of analytes, namely, neryl acetate/geranial and

672

limonene/-phellandrene/1,8-cineole, trans-sabinene hydrate/linalool and neral/carvone.

673

A preparative three-dimensional heart-cutting gas chromatographic system for the

674

isolation and characterization of a novel compound found in wampee essential oil was

675

recently reported.154 Separation was performed by employing a combination of Equity-5

676

[poly(5% diphenyl/ 95% dimethylsiloxane)], SupelcoWax 10 and SBL-IL59 in the 1D, 2D

677

and 3D, respectively.

678

Cagliero and co-workers reported a systematic evaluation of several IL stationary

679

phases, namely, SBL-IL59, SBL-IL60, SBL-IL61, SBL-IL76, SBL-IL82, SBL-IL100,

680

and SBL-IL111 for the analysis of flavor, fragrances and essential oils by GC.153 The

681

overall chromatographic performance of the SBL-IL76 stationary phase was the lowest

682

among the evaluated phases, which was in agreement with previous results.162 Both SBL-

683

IL100 and SBL-IL111 stationary phases displayed the lowest retention factors for non-

684

polar solutes, such as monoterpene hydrocarbons. Using the SBL-IL61 followed by the

685

SBL-IL60 stationary phase seemed to provide the best chromatographic performance in

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Analytical Chemistry

686

the analysis of allergens by GC-FID, comparable to the performance of the 14%

687

cyanopropylphenyl/ 86% dimethylpolysiloxane (OV-1701) phase. The SBL-IL59, SBL-

688

IL60 and SBL-IL61 were the most promising stationary phases in the 1D-GC analysis of

689

essential oils. On the other hand, SBL-IL 60 was the most effective stationary phase for

690

the analysis of low-volatility analytes, such as pesticides.153 SBL-IL61 and SBL-IL111

691

were also successfully applied as stationary phases for the analysis of 136 tetra- to octa-

692

polychlorinated dibenzo-p-dioxins and dibenzofurans by GC-MS.162 Additionally, the

693

separation of 196 polychlorinated biphenyls congeners by GC×GC-TOFMS employing

694

SBL-IL59 in the second dimension was also reported.160

695

Augusto and co-workers successfully established a source-independent method

696

for the quantitation of biodiesel in mineral diesel blends by GC×GC-FID employing

697

SBL-IL61 in the 2D.158 Unique selectivities toward FAMEs in mineral diesel were

698

obtained using this technique. SBL-IL82, SBL-IL100, and SBL-IL111 stationary phases

699

were employed in the separation of FAME in complex matrices, such as marine algae and

700

milk fat, by 1D-GC and GC×GC.164,166,167 Marriott and co-workers examined

701

simultaneously the chromatographic efficiency of two IL-based stationary phases in

702

GC×GC for the analysis of FAMEs from Safflower oil.169 The combination of SBL-

703

IL111 in the 1D and SBL-IL59 in the 2D provided excellent separation of the FAMEs,

704

when compared to several other stationary phases, as illustrated in Figure 5. A hybrid

705

MDGC system was developed for the analysis of FAMEs in fish oil and milk fat.171 This

706

integrated instrument can operate as either a heart-cut MDGC-FID or a GC×GC-FID.

707

The nitroterephthalic acid-modified PEG (DB-FFAP) stationary phase and three IL-based

708

stationary phases, namely, SBL-IL76, SBL-IL100 and SBL-IL111, were evaluated in

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Page 32 of 79

709

heart-cut MDGC analysis. Enhanced resolution of the C18 FAMEs, including their

710

monounsaturated geometric isomers, was obtained by the IL phases while the same

711

isomers were unresolved by a DB-FFAP phase. The peak capacity for the 2D IL phases

712

was 34, 41 and 42 for SBL-IL76, 100 and 111, respectively. These capacities were

713

superior to the DB-FFAP stationary phase, which showed a peak capacity of 30.

714

A series of fundamental studies evaluating the retention behavior of several ILs

715

toward specific groups of analytes, such as alkyl phosphates, and FAMEs were

716

reported.168,172 Schmarr and co-workers studied the retention behavior of deuterated and

717

non-deuterated probe molecules in liquid IL-based and conventional silicone stationary

718

phases.173 Heavier deuterated isotopic compounds elute earlier than corresponding non-

719

deuterated solutes (inverse isotope effect) in conventional PDMS phase. On the other

720

hand, normal isotope effects, where deuterated solutes are more retained with respect to

721

analogous non-deuterated molecules, were observed in polar IL-based stationary phases,

722

such as SBL-IL100 and SBL-IL111. As for the intermediate polarity IL stationary phases,

723

such as SBL-IL59 and SBL-61, both deuterated and non-deuterated molecules co-elute.

724

It is apparent that IL-based stationary phases exhibiting intermediate polarity,

725

similar to conventional PEG phases, namely, SBL-IL59, SBL-IL60 and SBL-IL61, are

726

suitable for the analysis of volatile and semi-volatile analytes possessing a wide range of

727

polarities. These stationary phases can be highly applicable to food chemistry,

728

metabolomics and fragrance and aroma-related fields. Highly polar phases, such as SBL-

729

IL100 and SBL-IL111, are most effective for the analysis of high-boiling point analytes

730

commonly encountered in complex lipid samples, fuels, and petrochemical-derivatives.

731

The performance of most IL-based stationary phases is now comparable to the traditional

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Analytical Chemistry

732

polar phases, such as DB-FFAP, OV-1701, and SupelcoWax10. Additionally, the IL

733

phases are also capable of providing higher peak capacity, thereby reducing peak overlap

734

in the analysis of complex samples.

735

4.2 High performance liquid chromatography (HPLC)

736

4.2.1 Utilization of ILs as HPLC stationary phases

737

The development of new IL-modified LC stationary phases have received much

738

success since their introduction in 2004.174 The main advantages of employing IL-

739

modified stationary phases stem from the tunability of the ILs, which can consequently

740

change the properties of the stationary phases. Recent studies of IL-modified stationary

741

phases have been summarized by Qiu and co-workers.175 The development of IL-

742

modified LC stationary phases reported within the past two years will be summarized in

743

this section.

744

The 1-allyl-3-butylimidazolium bromide ([AC4IM][Br]) IL was applied for the

745

modification of 3-mercaptopropyltrimethoxysilane-functionalized silica through the

746

surface radical chain-transfer addition reaction.176 The IL-modified silica stationary phase

747

enabled multiple solvation interactions, including dispersion, π–π, and ion–dipole

748

interactions for the separation of polycyclic aromatic hydrocarbons (PAHs) and dipolar

749

compounds. Superior selectivity was obtained using this stationary phase compared to a

750

conventional octadecylsilica (ODS) stationary phase. The same procedure was also

751

employed to prepare a 1-(2-acryloyloxyundecyl)-3-methylimidazolium bromide

752

([mC11MIM][Br]) modified silica stationary phase.177 The synthesis scheme and

753

separation results are shown in Figure 6. The column was successfully applied for

754

multiple chromatographic modes, including ion-exchange, reversed-phase, and

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Page 34 of 79

755

hydrophilic interaction chromatography. Additionally, the [mC11MIM][Br] modified

756

column demonstrated better selectivity for the separation of PAHs compared to an ODS

757

phase.

758

4.2.2 Applications of ILs as HPLC mobile phase additives

759

The addition of ILs into conventional mobile phases may result in decreasing the

760

zone broadening and improving chromatographic resolution. This is due to the masking

761

of residual free-silanol groups on the surface of the silica-based stationary phases.

762

Additionally, IL-based additives exhibit minimal influence on the pH of the mobile

763

phase.

764

Han and co-workers applied a number of 1-alkyl-3-methylimidazolium-based ILs as

765

mobile phase additives for the separation of β-Lactam antibiotics. The best resolution was

766

obtained when adding 1.0 mM [C4MIM][BF4] to the mobile phase.178 Additionally, the

767

retention factors for the antibiotics were enhanced by increasing the alkyl chain length of

768

the IL. A mobile phase consisting 0.4 % (v/v) [C4IM][Cl], 0.4 % (v/v) [C4MIM][BF4] and

769

99.2 % (v/v) water was used for the separation of selenium species.179 Good efficiency

770

and shorter separation times were achieved using the ILs compared to common ion-pair

771

reagents. A similar strategy has also been applied for the separation of alkaloids,180,181

772

antiretroviral drugs,182 nitroaromatic explosives,183 fangchinoline and tetrandrine,184 and

773

β-blockers185 on different stationary phases. An achaotropic salt, NaPF6, and the

774

[C2MIM][PF6] IL were compared as mobile phase additives for the separation of biogenic

775

amines.186 Excellent separation resolution was achieved when 40 mM of IL was added.

776

However, the LODs of the eluent system modified with NaPF6 was 10 times better

777

compared to systems modified with the IL. The ([C8MIM][BF4]) IL was utilized as a

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Analytical Chemistry

778

cationic surfactant reagent in the separation urea derivatives.187 It was observed that

779

analytes could hydrogen bond with the imidazolium cation of the IL modifier, resulting in

780

improved peak symmetry factors. The formation of IL-based micelles also improved the

781

separation selectivity of chloro and methoxy substituted derivatives.

782

A HPLC electrochemical detector was developed by Jia and co-workers in the

783

analysis of phenolic acids.188 The [C4MIM][Br] IL, in addition to gold nanoparticles

784

(GNP), were utilized as additives to enhance the efficiency of the separation. Compared

785

to analogous separations using no IL modifications, the separation times of all analytes

786

were decreased while the separation efficiency and method sensitivity were significantly

787

increased.

788

Both achiral and chiral ILs have also been employed as mobile phase additives for

789

the separation of ofloxacin enantiomers by ligand-exchange HPLC.189 The chiral amino

790

acid IL, namely, [C4MIM][L-leucine], demonstrated superior enantioseparation

791

efficiency compared to the achiral ILs. Baseline separation of the enantiomers was

792

achieved within 14 min, while the enantioseparation factor was observed to be 1.34. Zhou

793

and co-workers applied isopropylammonium formate (IPAF) as a mobile phase modifier

794

for the separation of native proteins.190 A significant enhancement in protein stability was

795

observed when using IPAF as a mobile phase modifier compared to acetonitrile. All

796

proteins, except for lactate dehydrogenase, maintained their native structures within up to

797

50% IPAF. On the other hand, the proteins were denatured when using only 10%

798

acetonitrile in the mobile phase. The superior stability of proteins in IPAF can be a result

799

of the strong interaction between the IL and their native structures.

800

5. Capillary electrophoresis (CE)

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Analytical Chemistry

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801

Page 36 of 79

Due to their high conductivity and tunable miscibility in aqueous solutions, ILs

802

have been used as supporting electrolytes and/or additives to running buffers in CE. The

803

recent application of IL-assisted CE in the analysis of phenols, aromatic acids, metal ions,

804

medicines, enantiomers, and biological materials such as amino acids and proteins has

805

been reviewed by Xu and co-workers.191 In this section, the recent development of

806

ILs/PILs in capillary electrophoresis will be summarized.

807

The poly(1-vinyl-3-butylimidazoliumbromide) PIL was physically deposited to a

808

silica capillary for applications in CE.192 The coating enabled the reversal of the

809

electroosmotic flow (EOF) at pH 3.0 to 9.0 while exhibiting high tolerance to organic

810

solvent. In another study, an IL-bonded organic-silica hybrid monolithic column was

811

prepared for capillary electrochromatography (CEC).193 EOF reversal and better

812

separation efficiency was observed for the IL-bonded column compared to an analogous

813

column without IL modification.

814

The EOF modulation capability of several ILs comprised of phosphonium,

815

sulfonium, cysteinium, ammonium, and guanidinium cations were evaluated by Mendes

816

and co-workers.194 Phosphonium-based ILs and the tri-octyl methylammonium chloride

817

IL demonstrated the strongest ability to reverse the EOF under both acidic and basic

818

conditions. ILs were exploited as background electrolyte (BGE) additives for the CE of

819

neutral carbohydrates.195 The ILs functioned as both a chromophore for indirect UV

820

detection and as a selector to improve analyte separation. Under optimized conditions,

821

sucrose, glucose, and fructose were fully separated within 7 min. The utilization of PILs

822

as BGE additives was also reported by Zhou and co-workers.196

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823

Analytical Chemistry

Achiral and chiral additives have also attracted significant attention in chiral

824

separations by CE. A series of achiral ILs were employed as modifiers to cooperate with

825

β-cyclodextrin derivatives for the enantioseparation of three β-blockers.197 The

826

glycidyltrimethylammonium chloride ([GTMA][Cl]) IL was most effective for improving

827

the enantioseparation of the β-blockers. This indicated a synergistic effect that exists

828

between the IL and β-cyclodextrin derivatives. Two chiral amino acid derivatized ILs

829

were applied in conjunction with β-cyclodextrin derivatives for the separation of

830

naproxen, pranoprofen, and warfarin enantiomers.198 Significant improvements in

831

enantioseparation, which can be attributed to the participation of the IL in chiral

832

recognition, was obtained for all compounds. A similar synergistic system, using

833

glycogen as a chiral selector, was also recently studied.199 As shown in Figure 7,

834

significant improvement in the enantioseparation can be observed in the chiral

835

ILs/glycogen synergistic system when compared to the single glycogen separation system.

836

Amino acid derivatized ILs have also been applied as a chiral ligand to coordinate with

837

Zn( II ) in the enantioseparation of dansyl amino acids (Dns-D,L-AAs) by chiral ligand

838

exchange capillary electrophoresis (CLE-CE).200,201 Baseline separation of multiple Dns-

839

D,L-AA pairs was achieved using this method. Yu and co-workers reported the synthesis

840

and application of a chiral IL-functionalized β-cyclodextrin selector, namely, 6-O-2-

841

hydroxpropyltrimethylammonium-β-cyclodextrintetrafluoroborate ([HPTMA-β-

842

CD][BF4]) in CE.202 Tailoring the IL chiral selector significantly enhanced the solubility

843

of β-cyclodextrin in the aqueous buffer. Additionally, the [HPTMA-β-CD][BF4]

844

exhibited better enantioresolution compared to an analogous β-CD selector possessing no

845

IL functionality.

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Analytical Chemistry

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Page 38 of 79

846

6. Mass spectrometry

847

6.1 Ionic liquids in matrix-assisted laser desorption ionization

848

Since its introduction in 1988, MALDI has become a widespread and powerful

849

source for the production of intact gas-phase ions for a broad range of large, non-volatile,

850

and/or thermally labile compounds. The matrices employed in MALDI should adhere to

851

specific requirements, such as possessing a strong absorbance at the laser wavelength,

852

low molecular mass, stability under vacuum, ability to promote analyte ionization, and

853

adequate solubility of the analyte.113,118 Since a number of ILs can accommodate these

854

requirements, they have been successfully employed as MALDI matrices.203-209

855

Many IL-based matrices are comprised of cations paired with -cyano-4-

856

hydroxycinnamate

857

hydroxypicolinate (3-HPA). Recently, the IL/[4-CHCA] matrices were employed in

858

various forensic investigations,210,211 polymer analysis,212 and melamine screening in

859

milk.213 Novel IL matrices were proposed for the study of intact pathogenic bacterial

860

cells.214 Tetraalkyl phosphonium-based ILs were prepared and used for a single-step

861

extraction of dyes and analysis by MALDI-TOFMS,215 while two new ammonium-based

862

ILs paired with 3-oxocoumarate and dihydroxymonooxoacetophenoate were explored as

863

MALDI matrices for the analysis of biodegradable photoluminescent polymers.216 The

864

dihydroxymonooxoacetophenoate IL provided similar signal intensities and shot-to-shot

865

reproducibility when compared to the analogous [4-CHCA]-based IL matrix.

(4-CHCA),

2,5-dihydroxybenzoate

(2,5-DHBA),

or

3-

866

It is known that IL-based MALDI matrices should possess labile protons to

867

promote ionization, although there appears to be no correlation between the matrix pKa

868

and the analyte signal.203 Lately, a method devised to measure the ion yield in MALDI

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Analytical Chemistry

869

experiments was reported. This metric was applied in an attempt to understand the gas-

870

phase ion formation of preformed ions, such as those formed in ILs versus pure CHCA

871

acid matrices.217 In another study, Dertinger and co-workers explored the structural role

872

of ILs and their effects on analyte signal enhancements.218,219

873

Matrix-assisted laser desorption ionization in-source decay (MALDI-ISD) can be

874

an alternative approach to determine the sequence of a protein, without the need for

875

enzymatic digestion.220 It was observed that 2,5-DHBA acid and 1,5-diaminonaphtalene

876

(1,5-DAN) matrices efficiently induced MALDI-ISD fragments, separately. However, the

877

ISD-fragments were suppressed when the RTIL, 1,5-diammoniumnaphtalene [2,5-

878

DHBA], was employed as matrix. Consequently, the use of IL matrices for MALDI–ISD

879

experiments will require additional fundamental studies to improve the induction of ISD

880

fragments.

881

6.2 Ionic liquids in atmospheric pressure ionization techniques

882

The analysis of various organometallic complexes by electrospray ionization mass

883

spectrometry (ESI-MS) is often problematic due to their solubility in protic organic

884

solvents.221

885

bis(triphenylphosphine)palladium II, was successfully analyzed by employing [C4MIM]-

886

based ILs. The best sensitivities were obtained when employing more hydrophobic

887

anions such as [BF4], trifluoromethylsulfonate, and heptafluorobutanoate. The analysis of

888

polysaccharides by ESI-MS was recently reported by Chang and co-workers.222 These

889

analyses were carried out with the use of ILs dissolved in the sample solution. The

890

addition of butylammonium paired with [2,5DHBA] or [4-CHCA] significantly increased

Nevertheless,

a

neutral

organometallic

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Page 40 of 79

891

the sensitivity of the method. Additionally, the mass spectra obtained using this approach

892

were also greatly simplified, due to a narrower charge distribution window.

893

ILs have also been applied for enzyme kinetic and inhibition studies. Typical

894

assays used to visualize enzymatic activity depend on the direct measurement of

895

radioactive or fluorescent substrates. Galan and co-workers proposed a task-specific IL

896

that easily attaches and detaches to target-substrates.223 This facilitated both substrate

897

purification and allowed enzymatic reaction monitoring. The proposed method was

898

demonstrated to be more rapid and sensitive compared to conventional methods. In

899

subsequent reports, the chemical stability of the IL-based probes was enhanced and

900

successfully employed for the measurement of apparent kinetic parameters for enzyme

901

catalyzed transformations with glycosyltransferases.224,225

902

The [C4MIM][Br] IL was applied as a solvent for the detection of dimethoate in

903

fruit juices by thermal dissociation atmospheric chemical ionization ion trap mass

904

spectrometry.226 The [C4MIM][BF4] IL was also employed as a matrix in the analysis of

905

pharmaceuticals and pesticides by matrix-assisted corona beam ionization.227 This

906

allowed the successful and reproducible quantitation of pharmaceuticals and pesticides in

907

synthetic samples.

908

7. ILs in electrochemical sensing systems

909

Many ILs exhibits wide electrochemical potential windows and good conductivity

910

making them highly useful for various electrochemical applications.228-230 Since their

911

initial application for electrode modification in 1997,231 ILs have received much attention

912

as alternative electrolytes in many electrochemical devices. The application of ILs in

913

electrode modification has been reviewed by Opallo and co-workers.228 A number of IL-

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914

modified electrode fabrication techniques, including direct mixing, casting and rubbing,

915

physical adsorption, electro deposition, layer-by-layer approach, sol-gel encapsulation,

916

and sandwich-type assays were recently described.229 The application of ILs in

917

electrochemical sensing systems was also summarized by Silvester.230 The following

918

sections provide a brief update on the application of ILs in electrode modifications within

919

the past two years.

920

7.1 ILs as surface modifiers for electrodes

921

Electrochemical sensors can be modified by directly applying ILs as droplets or

922

films on the surface of an electrode. Zevenbergen and co-workers employed a gold

923

working electrode covered by a thin layer of the [C4MIM][NTf2] IL for the detection of

924

ethylene.232 An LOD of 760 ppb and a linear response up to 10 ppm was achieved using

925

this IL-modified system. Hu and co-workers exploited the [C4MIM][PF6] IL as an

926

electrolyte on paper-based gold electrode arrays (PGEAs) for oxygen sensing.233 The

927

fabrication of the IL-modified PGEA is illustrated in Figure 8. The resulting sensor

928

exhibited several unique properties including good conductivity, excellent flexibility, and

929

high electrochemical performance. The PGEAs also possessed high method sensitivity in

930

the determination of trace oxygen in a nitrogen atmosphere, wherein a LOD of 0.0075

931

v/v % (O2/N2) was obtained.

932

The electro-deposition of ILs to the surface of an electrode has also become a

933

popular method for the fabrication of IL-modified electrodes. For example,

934

Pandurangachar and co-workers deposited the1-butyl-4-methyl-pyridinium [BF4]

935

([BMPY][BF4]) IL to the surface of a carbon paste electrode (CPE) by cyclic

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936

voltammetry (CV).234 Excellent electrocatalytic activity for the selective detection of

937

dopamine in the presence of ascorbic acid and uric acid was obtained using this electrode.

938

7.2 IL-composite electrochemical sensing systems

939

ILs can also be incorporated into different matrixes, such as graphite, graphene,

940

carbonnanotubes, metal nanoparticles, and polymers to form stable composite materials.

941

The mechanical and electrical properties of the IL-based composites can be significantly

942

enhanced by synergistically exploiting and combining the unique physicochemical

943

properties found within each component.

944

7.2.1 Incorporation of ILs in carbon-based composites in electrochemical sensing

945

systems

946

Recently, ILs have been applied as an alternative to the non-conducting organic

947

binder, such as paraffin, in carbon paste electrodes.228 The IL carbon paste composite

948

electrodes (ILCPEs) were prepared by mixing or grinding graphite powder/or carbon

949

nanotubes with ILs to form a uniformly wetted paste. The resulting paste can then be

950

packed firmly into the cavity of an electrode. An n-octylpyridinium [PF6] ([C8PY][PF6])

951

modified carbon paste electrode was developed by Ping and co-workers for the evaluation

952

of trace amounts of cadmium and lead in soil samples.235 Superior electrochemical

953

activity and low ppb-level LODs were obtained using the ILCPE compared to a

954

traditional carbon paste electrode, which employs paraffin oil as a binder. The same

955

ILCPE was applied in the determination of (−)-Epigallocatechin Gallate in tea infusion

956

samples.236 Various ILCPEs and IL-based carbon nanotube paste electrodes were also

957

utilized for the determination of adenosine-5'-triphosphate (ATP),237 carbidopa,238

958

epinephrine,239 ascorbic acid,240 morphine,241 nitric oxide,242 and norepinephrine243 in

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Analytical Chemistry

959

different sample matrixes. The electrochemical performance of IL-based, graphene-

960

based, and IL-graphene modified carbon electrodes was evaluated by Du and co-

961

workers.244 Faster redox chemistry and favorable electron transfer kinetics were observed

962

using the IL-graphene modified carbon electrode compared to the IL-based and

963

graphene-based carbon paste electrode.

964

Imidazolium-based ILs can form a physical gel when ground with single-walled

965

carbon nanotubes (SWCNTs).245 The CNT/IL composites typically possess the

966

mechanical, electrical, and thermal properties of the CNT, in addition to the conductivity

967

inherent to the ILs. Direct rubbing is a common method for the preparation of a CNT/IL

968

composite sensor. The nanocomposite gel can be fabricated by mixing specific amounts

969

of CNTs (typically lower than 5 % w/w) with ILs. After grounding and/or sonication, the

970

gel can be directly applied to the surface of an electrode.229 Bu and co-workers developed

971

a multiwalled carbon nanotubes (MWCNTs)/IL glassy carbon electrode (GCE) for the

972

simultaneous determination of hydroquinone and catechol.246 The IL-modified GCE

973

showed well-defined redox waves for both analytes in both CV and DPV. In other

974

studies, an IL-graphene hybrid nanosheet was applied for the rapid detection of

975

trinitrotoluene, wherein sub-ppb level LODs were obtained.247 In addition, the application

976

of IL-graphene modified electrode in the analysis of metronidazole in pharmaceutical

977

dosage forms has also been reported.248 Recently, carboxylated-SWNTs (SWCNTs-

978

COO) comprised of 3-butyl-1-[3-(N-pyrrolyl)propyl]imidazolium cations was

979

synthesized and coated on a GCE.249 Polymerization of the IL was performed by cyclic

980

voltammetric scanning to produce a PIL/SWCNTs-COO hybrid. The PIL/SWCNTs-COO

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981

GCE was applied for the determination of bisphenol A, wherein LODs in the nM range

982

were obtained.

983

7.2.2 Application of metal nanomaterials/IL-modified electrodes

984

Due to their large surface-to-volume ratios and high thermal stability, several metal

985

nanoparticles have been applied in conjunction with ILs as electrodes. Bo and co-workers

986

employed PIL-coated mesoporous carbons (OMCs) as support materials for the

987

deposition and formation of Pt nanoparticles.250 The PIL provided sufficient binding sites

988

to anchor the metal ion precursors and facilitated the homogenous formation of ultrafine

989

nanoparticles. The novel electrode also exhibited higher electrocatalytic activity towards

990

hydrogen peroxide (H2O2) compared to an analogous Pt/OMCs nanocomposite

991

containing no PIL. Similar methods have also been applied for the electrodeposition of

992

gold nanoparticle251 and gold-platinum alloy nanoparticles252 on various substrates.

993

7.2.3 Application of IL-based multi-component electrochemical sensors

994

Recently, the incorporation of ILs to multi-component electrochemical sensor

995

systems has enjoyed increasing attention in the analytical community. An IL/CNT

996

modified glassy carbon (GCA) was used to facilitate the electro deposition of Prussian

997

blue (PB) nanoparticles.253 Incorporating an IL to the system improved the deposition

998

efficiency of PB by 1.8 fold and provided a 2.35 fold enhancement in the electron

999

transfer rate compared to a non-IL modified PB/CNTs/GCA electrode. Similarly, the

1000

production and application of different electrodes, including chitosan/copper/IL,254

1001

nickel/IL/MWCNTs,255 stacked graphene platelet nanofibers/IL/chitosan256 and

1002

manganese oxide nanoparticles/IL/chitosan257 have been reported. Different ILs were

1003

homogenized with GNPs and CNTs and applied as non-enzymatic glucose sensors.258

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Analytical Chemistry

1004

The imidazolium-based IL exhibited better stability and detection sensitivity to glucose

1005

compared to tetrabutylammonium, pyrrolidinium, and piperdinium-based ILs.

1006

Additionally, the oxidation of glucose was enhanced by appending hydrophilic moieties,

1007

such as a sulfonate substituent, to the IL.

1008

7.3 Application of IL-modified biosensors

1009

Various electrodes including GCA, metal, CPE, and screen-printed electrodes

1010

have been applied for the deposition of biological recognition elements. However,

1011

conventional electrodes usually suffer from poor production reproducibility and

1012

compatibility to biological samples.229 Due to their biocompatibility, ILs and IL-based

1013

composites have been shown to be ideal matrixes for the immobilization and/or

1014

encapsulation of biological components in biosensors. Recent development of IL-based

1015

electrochemical biosensing systems have been summarized in a number of review

1016

articles.229,259

1017

A novel PIL-functionalized graphene material, namely, poly([VC4IM][Br])-

1018

graphene was synthesized and applied for the detection of glucose.260 The PIL-based

1019

nanocomposite can easily be dispersed in aqueous solution to form a homogenous

1020

colloidal suspension. The surface of the PIL-modified material is also positively charged,

1021

which enables the immobilization of negatively charged glucose oxidase (GOD) to the

1022

electrode under mild conditions, as shown in Figure 9A. Well-defined redox peaks can be

1023

observed after the assembly of GOD to the PIL-modified electrode, as shown in Figure

1024

9B. Additionally, the electrode exhibited excellent sensitivity, stability and a wide linear

1025

range for the detection of glucose. Similar strategies were used to immobilize

1026

hemoglobin,260,261 glucose dehydrogenase,262 GOD,263 nicotinamide adenine

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1027

dinucleotide,264 single-stranded DNA (ssDNA),265,266 bovine serum albumin (BSA),267

1028

horseradish peroxidase (HRP),268,269 carcinoembryonic antigen antibody,270 laccase and

1029

polyphenol oxidase,271,272 HRP and GOD,273 antigoat immunoglobulin Gamma and

1030

human dihydrofolate reductase274 to the surface of IL-modified electrode. The

1031

encapsulation of biomolecules, including HRP275,276 and myoglobin277 in IL-modified

1032

biochemical sensors has also been reported. An electrochemical DNA biosensor was

1033

developed by Gao and coworkers by assembling ssDNA with a Au/IL-CPE.278 The

1034

sensor demonstrated high selectivity for one-base and three-base mismatched ssDNA

1035

sequences. Cholesterol oxidase, was immobilized onto modified electrodes using a

1036

similar approach.252

1037

A graphene/IL/Nafion-modified pyrolytic graphite electrode was developed by

1038

Qiu and co-workers to investigate DNA damage by acrylamide (AA) and its

1039

metabolites.279 A layer-by-layer fabrication method was applied by alternately coating

1040

HRP and natural double-stranded DNA on the graphene/IL/Nafion-modified electrode.

1041

The co-existence of HRP, H2O2, and AA catalyzed the transformation of AA to

1042

glycidamide. It was determined that in the presence of H2O2, AA could be transformed to

1043

glycidamide and induce more severe damage to DNA than AA. Yang and co-workers

1044

designed a sandwich-type immunosensor comprised of an IL-doped chitosan

1045

immobilization matrix.280 Subsequent to applying the matrix to a GCE, various sensing

1046

components were successfully immobilized to the IL-doped matrix. The synergistic

1047

effects of all components, in addition to the suitable electrochemical properties of the IL,

1048

allowed for the determination of immunoglobulin G at ppt-levels. A similar sandwich-

1049

type immunosensor, comprised of Pd nanoparticles in functionalized SBA-15 (Pd@SBA-

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Analytical Chemistry

1050

15) and the [C4MIM][Br] IL, has also been developed for the detection of salbutamol.281

1051

The sensitivity obtained for the IL-modified sandwich-type immunosensor was

1052

significantly better than analogous immunosensors containing no ILs.

1053

8. Conclusions and Perspectives

1054

Owing to their unique physicochemical properties, ILs have been successfully

1055

utilized in all major fields within analytical chemistry. In the fields of sample preparation

1056

and extraction, ILs were shown to be highly effective extraction phases that can provide

1057

superior analyte selectivity and exceptional analytical performance. Furthermore, these

1058

contemporary ionic solvents were demonstrated to be powerful alternatives to traditional

1059

molecular solvents, which often possess high toxicity and volatility. The versatility of ILs

1060

has made them an interesting class of new stationary phases or additives in GC, HPLC,

1061

and CEC. In many cases, exploiting task-specific ILs provides unique analyte selectivity

1062

and improved chromatographic separation for a number of analyte classes. This is

1063

especially true for heart-cutting MDGC and GC×GC, where the selectivity of the second

1064

dimension stationary phase is crucial. Select IL stationary phases also exhibited superior

1065

thermal stability and high polarity numbers compared to conventional polar stationary

1066

phases. ILs have played an important role as buffer additives in CE to improve the

1067

separation of numerous pharmaceutical drugs, organic compounds, and biomolecules.

1068

Modulation of the EOF can also be achieved by choosing the appropriate IL. With

1069

respect to mass spectrometry, ILs are applicable as matrices for MALDI-based

1070

techniques. IL-based matrices can be useful alternatives to traditional matrices, providing

1071

better shot-to-shot reproducibility and matrix homogeneity, while exhibiting broader

1072

solubility windows for many analytes. Novel applications of ILs in electrochemical

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1073

sensing systems have shown promising results for the detection of various analytes.

1074

Additionally, ILs can also be combined with a number of organic/inorganic compounds

1075

to yield materials that exhibit enhanced electrocatalytic activity, thermal stability,

1076

mechanical stability, and selectivity.

1077

Although ILs have been utilized to enhance numerous analytical processes,

1078

further characterization and synthetic optimization is critical for the applicability of these

1079

materials. For example, the synthesis of highly pure ILs is vital for many analytical

1080

procedures. Impurities often introduce significant background noise in various detection

1081

methods and alter the unique selectivity exhibited by the IL in

1082

chromatographic/electrophoretic techniques. Similarly, impurities also influence the

1083

physicochemical properties of an IL and can detrimentally affect their analytical

1084

performance in sample preparation. As a result, effort should be focused on improving

1085

synthetic and/or purification methods to produce pure ILs in high yields. Although ILs

1086

exhibits negligible vapor pressures at room temperature, which results in virtually no air

1087

pollution, improper disposal of these compounds may adversely affect the ecosystem.

1088

Therefore, it is important to continue to investigate and monitor the toxicity of ILs and

1089

their effects on the surrounding environment.

1090

A promising trend of ILs in analytical chemistry resides on the ability to combine

1091

these compounds with other organic/inorganic materials. As demonstrated in current

1092

literature, the union between ILs with other materials, such as CNTs, silica, metals, and

1093

organic polymers can significantly alter the physicochemical properties of such materials.

1094

Many IL-based composites exhibit high thermal and chemical stability, good mechanical

1095

strength, suitable electrochemical properties, and enhanced robustness. Therefore,

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Analytical Chemistry

1096

combining ILs with different materials, in addition to synthesizing novel task-specific

1097

ILs, can ultimately broaden the usefulness of these compounds within the many

1098

interdisciplinary subfields of analytical chemistry.

1099

Acknowledgements

1100 1101 1102 1103 1104 1105 1106 1107 1108 1109 1110 1111 1112 1113 1114 1115 1116 1117 1118 1119 1120 1121 1122 1123 1124 1125 1126 1127 1128 1129 1130 1131 1132 1133 1134 1135 1136 1137

The table of contents image was created using four figures obtained with permission from the following sources: (Sample Preparation) Reproduced from Ho, T.D.; Yu, H.; Cole, W.T.; Anderson, J.L. Anal. Chem. 2012, 84, 9520, Copyright 2012 American Chemical Society; (Sensors) Reproduced from Hu, C.; Bai, X.; Wang, Y.; Jin, W.; Zhang, X.; Hu, S. Anal. Chem. 2012, 84, 3745, Copyright 2012 American Chemical Society; (Separations) Reprinted from Nosheen, A.; Mitrevski, B.; Bano, A.; Marriott, P.J. J. Chromatogr. A 2013, 1312, 118, Copyright 2013, with permission from Elsevier; (Mass Spectrometry) Reprinted from Abdelhamid, H. N.; Gopal, J.; Wu, H. F. Anal. Chim. Acta. 2013, 767, 104, Copyright 2013, with permission from Elsevier.

AUTHOR BIOGRAPHIES Jared L. Anderson obtained his Bachelor of Science degree in chemistry at South Dakota State University in 2000 and his Ph.D. in Analytical Chemistry at Iowa State University in 2005. He joined The University of Toledo in 2005 as an Assistant Professor of Chemistry and was promoted to Associate Professor of Chemistry with tenure in 2009. In 2011, he was promoted to the rank of Full Professor of Chemistry. His research interests include the synthesis of new classes of ionic liquids and materials derived from polymeric ionic liquids, the use of ionic liquids as catalytic solvents, and all aspects of separation science including sample preparation and chromatography. Tien D. Ho received his Bachelor of Science degree from Aquinas College (Michigan) in 2009. He is currently a Ph.D student at The University of Toledo under the supervision of Prof. Jared Anderson. His research explores the fundamentals of polymeric ionic liquid-based sorbent materials in SPME as well as the use of ionic liquids in the separation and analysis of impurities within active pharmaceutical ingredients. Cheng Zhang received his Bachelor of Science degree in Chemistry from Shanxi University in 2007 and his M.S. degree in Environmental Science from Zhejiang University of Technology in 2010. He is currently a Ph.D. student in Prof. Anderson’s group where his research involves the synthesis and design of polymeric ionic liquidbased materials and their use in sample preparation and chromatography.

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AUTHOR BIOGRAPHIES (continued) Leandro W. Hantao received his Bachelor of Science degree in Chemistry and M.S. degree in Analytical Chemistry from the University of Campinas (São Paulo, Brazil) in 2009 and 2011, respectively. Since 2011, he attends the University of Campinas as a Ph.D. student in Prof. Fabio Augusto’s group. He is currently a visiting graduate student in Prof. Anderson’s group at The University of Toledo. His research involves the study of plant metabolomics by GC×GC-MS and LC-MS.

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(233) Hu, C.; Bai, X.; Wang, Y.; Jin, W.; Zhang, X.; Hu, S. Anal. Chem. 2012, 84, 3745. (234) Pandurangachar, M.; Kumara Swamy, B. E.; Chandrashekar, B. N.; Gilbert, O.; Sherigara, B. S. J. Mol. Liq. 2011, 158, 13. (235) Ping, J.; Wu, J.; Ying, Y.; Wang, M.; Liu, G.; Zhang, M. J. Agric. Food. Chem. 2011, 59, 4418. (236) Fan, K.; Luo, X.; Ping, J.; Tang, W.; Wu, J.; Ying, Y.; Zhou, Q. J. Agric. Food. Chem. 2012, 60, 6333. (237) Gao, H.; Xi, M.; Xu, L.; Sun, W. Microchim. Acta 2011, 174, 115. (238) Beitollah, H.; Goodarzian, M.; Khalilzadeh, M. A.; Karimi-Maleh, H.; Hassanzadeh, M.; Tajbakhsh, M. J. Mol. Liq. 2012, 173, 137. (239) Tavana, T.; Khalilzadeh, M. A.; Karimi-Maleh, H.; Ensafi, A. A.; Beitollahi, H.; Zareyee, D. J. Mol. Liq. 2012, 168, 69. (240) Ping, J.; Wang, Y.; Wu, J.; Ying, Y.; Ji, F. Food Chem. 2012, 135, 362. (241) Ensafi, A. A.; Rezaei, B.; Krimi-Maleh, H. Ionics 2011, 17, 659. (242) Ng, S. R.; Guo, C. X.; Li, C. M. Electroanal. 2011, 23, 442. (243) Salmanpour, S.; Tavana, T.; Pahlavan, A.; Khalilzadeh, M. A.; Ensafi, A. A.; Karimi-Maleh, H.; Beitollahi, H.; Kowsari, E.; Zareyee, D. Mater. Sci. Eng. C 2012, 32, 1912. (244) Du, M.; Yang, T.; Ma, S.; Zhao, C.; Jiao, K. Anal. Chim. Acta 2011, 690, 169. (245) Fukushima, T.; Kosaka, A.; Ishimura, Y.; Yamamoto, T.; Takigawa, T.; Ishii, N.; Aida, T. Science 2003, 300, 2072. (246) Bu, C.; Liu, X.; Zhang, Y.; Li, L.; Zhou, X.; Lu, X. Colloid. Surface. B 2011, 88, 292. (247) Guo, S.; Wen, D.; Zhai, Y.; Dong, S.; Wang, E. Biosens. Bioelectron. 2011, 26, 3475. (248) Peng, J.; Hou, C.; Hu, X. Sensor. Actuat. B-Chem. 2012, 169, 81. (249) Chen, X.; Ren, T.; Ma, M.; Wang, Z.; Zhan, G.; Li, C. Electrochim. Acta 2013, 111, 49. (250) Bo, X.; Bai, J.; Qi, B.; Guo, L. Biosens. Bioelectron. 2011, 28, 77. (251) Hu, S.; Wang, Y.; Wang, X.; Xu, L.; Xiang, J.; Sun, W. Sensor. Actuat. B-Chem. 2012, 168, 27. (252) Safavi, A.; Farjami, F. Biosens. Bioelectron. 2011, 26, 2547. (253) Keihan, A.; Sajjadi, S. Electrochim. Acta 2013, In Press. (254) Yu, Q.; Shi, Z.; Liu, X.; Luo, S.; Wei, W. J. Electroanal. Chem. 2011, 655, 92. (255) Sun, A.; Zheng, J.; Sheng, Q. Electrochim. Acta 2012, 65, 64. (256) Niu, X.; Yang, W.; Guo, H.; Ren, J.; Yang, F.; Gao, J. Talanta 2012, 99, 984. (257) MansouriMajd, S.; Teymourian, H.; Salimi, A.; Hallaj, R. Electrochim. Acta 2013, 108, 707. (258) Zhu, H.; Liang, X.; Chen, J.; Li, M.; Zhu, Z. Talanta 2011, 85, 1592. (259) Wei, D.; Ivaska, A. Anal. Chim. Acta 2008, 607, 126. (260) Zhang, Q.; Wu, S.; Zhang, L.; Lu, J.; Verproot, F.; Liu, Y.; Xing, Z.; Li, J.; Song, X.-M. Biosens. Bioelectron. 2011, 26, 2632. (261) Zhang, Y.; Cao, H.; Fei, W.; Cui, D.; Jia, N. Sensor. Actuat. B-Chem. 2012, 162, 143. (262) Bai, L.; Wen, D.; Yin, J.; Deng, L.; Zhu, C.; Dong, S. Talanta 2012, 91, 110.

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(263) Jiang, Y.; Zhang, Q.; Li, F.; Niu, L. Sensor. Actuat. B-Chem. 2012, 161, 728. (264) Teymourian, H.; Salimi, A.; Hallaj, R. Talanta 2012, 90, 91. (265) Sun, W.; Qi, X.; Chen, Y.; Liu, S.; Gao, H. Talanta 2011, 87, 106. (266) Zhang, W.; Zheng, X.; Jiao, K. Sensor. Actuat. B-Chem. 2012, 162, 396. (267) Ping, J.; Wang, Y.; Fan, K.; Wu, J.; Ying, Y. Biosens. Bioelectron. 2011, 28, 204. (268) Cao, A.; Ai, H.; Ding, Y.; Dai, C.; Fei, J. Sensor. Actuat. B-Chem. 2011, 155, 632. (269) Liu, X.; Feng, H.; Zhang, J.; Zhao, R.; Liu, X.; Wong, D. K. Biosens. Bioelectron. 2012, 32, 188. (270) Yu, S.; Cao, X.; Yu, M. Microchem. J. 2012, 103, 125. (271) Zapp, E.; Brondani, D.; Vieira, I. C.; Dupont, J.; Scheeren, C. W. Electroanal. 2011, 23, 764. (272) Zapp, E.; Brondani, D.; Vieira, I. C.; Scheeren, C. W.; Dupont, J.; Barbosa, A. M.; Ferreira, V. S. Sensor. Actuat. B-Chem. 2011, 155, 331. (273) Chen, X.; Zhu, J.; Tian, R.; Yao, C. Sensor. Actuat. B-Chem. 2012, 163, 272. (274) Ratel, M.; Provencher-Girard, A.; Zhao, S. S.; Breault-Turcot, J.; LabrecqueCarbonneau, J.; Branca, M.; Pelletier, J. N.; Schmitzer, A. R.; Masson, J.-F. Anal. Chem. 2013, 85, 5770. (275) Liu, X.; Feng, H.; Zhao, R.; Wang, Y.; Liu, X. Biosens. Bioelectron. 2012, 31, 101. (276) Gurban, A.-M.; Rotariu, L.; Baibarac, M.; Baltog, I.; Bala, C. Talanta 2011, 85, 2007. (277) Ruan, C.; Li, T.; Niu, Q.; Lu, M.; Lou, J.; Gao, W.; Sun, W. Electrochim. Acta 2012, 64, 183. (278) Gao, H.; Qi, X.; Chen, Y.; Sun, W. Anal. Chim. Acta 2011, 704, 133. (279) Qiu, Y.; Qu, X.; Dong, J.; Ai, S.; Han, R. J. Hazard. Mater. 2011, 190, 480. (280) Yang, Y.-C.; Dong, S.-W.; Shen, T.; Jian, C.-X.; Chang, H.-J.; Li, Y.; Zhou, J.-X. Electrochim. Acta 2011, 56, 6021. (281) Cui, Z.; Cai, Y.; Wu, D.; Yu, H.; Li, Y.; Mao, K.; Wang, H.; Fan, H.; Wei, Q.; Du, B. Electrochim. Acta 2012, 69, 79.

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Analytical Chemistry

1631 1632 1633 1634 1635

Figure Captions.

1636

employed in techniques and methods within analytical chemistry.

1637

Figure 2. Application of ILs as acceptor phase additives in HF-LPME A) Schematic of

1638

HF-LPME employing ILs as additives in the acceptor phase. ipd : analyte in the aqueous

1639

donor phase; ipo: analyte in the immobilized organic phase; ipa: analyte in the IL-modifed

1640

acceptor phase; K1: ratio of the concentration of analyte i in the organic phase with

1641

respect to the donor phase under equilibrium; K2: ratio of the concentration of analyte i in

1642

the acceptor phase with respect to the organic phase under equilibrium. B) Extraction

1643

comparison of 0.4 µg mL-1 neutral analytes, wherein (a) is a direct injection of a 10 µg

1644

mL-1 standard solution, (b) HF-LPME using no IL additives, and (c) HF-LPME using 4.5

1645

MIL in the acceptor phase. Reprinted from Liu, W.; Wei, Z.; Zhang, Q.; Wu, F.; Lin, Z.;

1646

Lu, Q.; Lin, F.; Chen, G.; Zhang, L. Talanta 2012, 88, 43, Copyright 2012, with

1647

permission from Elsevier.

1648

Figure 3. Schematic illustrating the extraction steps involved in the speciation of arsenite

1649

and arsenate species by IL-DLLME coupled to ETAAS. Reprinted from Rabieh, S.;

1650

Bagheri, M.; Planer-Friedrich, B. Microchim. Acta 2013, 180, 415, with kind permission

1651

from Springer Science and Business Media.

1652

Figure 4. Schematic showing the fabrication procedure of polar crosslinked PIL-based

1653

sorbent coatings by “on-fiber” photoinitiated polymerization. Reproduced from Ho, T.D.;

1654

Yu, H.; Cole, W.T.; Anderson, J.L. Anal. Chem. 2012, 84, 9520, Copyright 2012

1655

American Chemical Society.

Figure 1. Chemical structures of selected IL and PIL cation/anion pairs commonly

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1656

Figure 5. Chromatograms of a fatty acid methyl esters mixture obtained on several

1657

combinations of capillary columns by GC×GC-FID. BPX5: 5% phenyl polysilphenylene-

1658

siloxane; BPX35: 35% phenyl polysilphenylene-siloxane; BPX50: 50% phenyl

1659

polysilphenylene-siloxane; BPX70: 70% cyanopropyl polysilphenylene-siloxane;

1660

INNOWax: poly(ethylene glycol); SBL-IL59: 1,12-di(tripropylphosphonium)dodecane

1661

[NTf2]-; SBL-IL61: mixture of 1,12-di(tripropylphosphonium)dodecane paired with

1662

[NTf2]- and trifluoromethylsulfonate; SBL-IL76:

1663

tri(tripropylphosphoniumhexanamido)triethylamine [NTf2]-; SBL-IL82: 1,12-di(2,3-

1664

dimethylimidazolium)dodecane [NTf2]-; SBL-IL100: poly[1,9-di(3-

1665

vinylimidazolium)nonane] [NTf2]- and SBL-IL111: 1,5-di(2,3-

1666

dimethylimidazolium)pentane [NTf2]-. Reprinted from Nosheen, A.; Mitrevski, B.; Bano,

1667

A.; Marriott, P.J. J. Chromatogr. A 2013, 1312, 118, Copyright 2013, with permission

1668

from Elsevier.

1669

Figure 6. Illustration of the (A) synthesis procedure for fabricating a novel multi-mode

1670

stationary phase (Sil-pC11MIm). (B) Chromatogram showing the separation of inorganic

1671

anions including nitrite, nitrate and iodide. Reproduced from Qiu, H.; Mallik, A.K.;

1672

Takafuji, M.; Jiang, S.; Ihara, H. Analyst 2012, 137, 2553, with permission of The Royal

1673

Society of Chemistry.

1674

Figure 7. Illustration of the (A) chemical structures of the synthesized chiral additives.

1675

(B) Electropherograms of the chiral separations of nefopam hydrochloride (NEF),

1676

citalopram hydrobromide (CIT), and duloxetine hydrochloride (DUL). Conditions: (a)

1677

2.5% glycogen; (b) 2.5% glycogen + 60 mM TMA-OH; (c) 2.5% glycogen + 60 mM

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Analytical Chemistry

1678

TMA-L-Asp; (d) 2.5% glycogen +60 mM TMA-l-Arg. Reprinted from Zhang, Q.; Du, Y.

1679

J. Chromatogr. A 2013, 1306, 97, Copyright 2013, with permission from Elsevier.

1680

Figure 8. Schematic showing (A) the fabrication of paper-based solid-state

1681

electrochemical oxygen sensors. (1) Inkjet printing of GNP patterns on cellulose

1682

membranes, (2) growth of GNP patterns into gold electrode arrays, (3) cutting single

1683

PGEA, (4) electric connection of a PGEA, (5) fabrication of oxygen sensor by applying

1684

[BMIM][PF6] onto the PGEA. (B) Illustration of a homemade gas mixing setup for the

1685

electrochemical sensing of oxygen. (C) Amperometric responses of oxygen at different

1686

concentrations. Reproduced from Hu, C.; Bai, X.; Wang, Y.; Jin, W.; Zhang, X.; Hu, S.

1687

Anal. Chem. 2012, 84, 3745, Copyright 2012 American Chemical Society.

1688

Figure 9. Schematic showing the (A) preparation of GOD/poly([VBIM][Br])-

1689

graphene/GC electrode and the direct electron transfer between GOD and GC electrode.

1690

(B) Cyclic voltammograms of the poly([VC4IM][Br])-graphene/GC electrode (a) and

1691

GOD/poly([VC4IM][Br])-graphene/GC electrode (b). Reprinted from Zhang, Q.; Wu, S.;

1692

Zhang, L.; Lu, J.; Verproot, F.; Liu, Y.; Xing, Z.; Li, J.; Song, X.-M. Biosens.

1693

Bioelectron. 2011, 26, 2632, Copyright 2011, with permission from Elsevier.

1694 1695 1696 1697 1698 1699 1700 1701 1702 1703 1704

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1727 1728

Analytical Chemistry

Table 1. Structure, physicochemical and chromatographic properties of selected ionic liquids.

Ionic liquid

bis(3-hydroxyalkylimidazolium)poly(ethylene glycol) [TfO] trigonal tripropylphosphonium [TfO] bis(2,3-dimethylimidazolium)poly(ethylene glycol) [TfO]

e

Solvation parameter model Temperature s a b l (˚C) Phosphonium-based ILs

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-

-0.18

1.96

1.97

-0.27

0.63

70˚C

X'=234, Y'=392, Z'=353, U'=538, S'=426 (120˚C)

Separation of alcohols and fatty acid methyl esters.

[132]

-

Analysis of n-alkanes, esters and alcohols.

[126]

Analysis of n-alkanes, xylenes, ketones, alcohols, amines and esters.

[140]

N,N,N’,N’-tetramethyl-N”,N”dioctylguanidinium [PF6]

250˚C (a)

tetradecyltrihexylphosphonium bis(2,4,4trimethylpentyl)phosphinate

300˚C

poly(1-(3-butenyl)-3-(2cyclohexanol)-imidazolium) [Br]

System/phase constants

Maximum temperature (˚C)

-

poly(1-(3-butenyl)-3-(2cyclohexanol)-imidazolium) [NTf2]

250˚C

poly(1-(3-butenyl)-3-(2cyclohexanol)-imidazolium) [SCN]

200˚C

-0.11

1.83

1.73

-0.22

0.54

100˚C

-

-

-

-

-

-

0.11 -0.10 -0.28 0.24 -0.08 -0.03 -0.13 0.13 0.11

1.18 0.70 0.42 1.40 1.45 1.21 1.37 1.37 0.90

Imidazolium-based ILs 3.11 1.34 0.55 3.00 0.17 0.46 1.67 0.08 0.42 2.62 0.90 0.57 1.33 1.64 0.51 0.99 1.42 0.50 3.70 0.90 0.69 2.41 0.77 0.53 2.11 0.43 0.38

ACS Paragon Plus Environment

50˚C 70˚C 100˚C 50˚C 70˚C 100˚C 50˚C 70˚C 100˚C

McReynolds constants

Application

Referen

Trace analysis of water.

[127-12

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1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48

-0.18 -0.45 -0.54 0.09 -0.28 -0.31 0.11 -0.14 -0.23 0.11 -0.21 -0.23

1.24 1.19 1.14 1.57 1.22 1.07 1.48 1.56 1.49 1.48 0.66 0.32

1.27 3.34 1.95 2.14 1.20 1.10 1.41 2.06 1.39 1.41 1.02 0.99

1.39 0.54 0.20 1.12 0.95 0.50 1.58 1.00 0.84 1.58 0.89 0.73

0.74 0.58 0.27 0.62 0.63 0.56 0.64 0.58 0.55 0.64 0.56 0.50

50˚C 70˚C 100˚C 50˚C 70˚C 100˚C 50˚C 70˚C 100˚C 50˚C 70˚C 100˚C

320˚C

-

-

-

-

-

-

-

320˚C

-

-

-

-

-

-

-

poly(1-(3-butenyl)-3-(2cyclohexanol)-imidazolium) [BF4]

220˚C

poly(1-allyl-3-(2-cyclohexanol)imidazolium) [NTf2]

250˚C

poly(1-(2-cyclohexanol)-3-(1octenyl)-imidazolium) [NTf2]

320˚C

poly(1-(2-cyclohexanol)-3-(4vinylbenzyl)-imidazolium) [NTf2]

270˚C

1-(1,2-dimethyl)-3propylimidazolium [NTf2] 1-(1,2-dimethyl)-3propylimidazolium [NTf2] 1-butyl-1-methylpyrrolidinium [NTf2] 3-methyl-1-propylpyridinium [NTf2] 1-butyl-3-methylimidazolium [BF4] 1,2-dimethyl-3-propylimidazolium [NTf2] 1,2,-dimethyl-3-propylimidazolium [NTf2] 1,2-dimethyl-3-(3cyanopropyl)imidazolium [NTf2] 1,2-dimethyl-3-(3hydroxypropyl)imidazolium [NTf2] 1-methoxyethyl-3methylimidazolium [FAP]

Page 66 of 79

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300˚C

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300˚C

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280˚C

-

-

-

-

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250˚C (a)

-

-

-

-

-

-

-

250˚C (a)

0.08

1.59

1.15

0.15

0.36

120˚C

-

250˚C (a)

0.01

1.67

1.21

0.12

0.31

120˚C

-

250˚C (a)

0.21

1.50

1.25

0.66

0.34

120˚C

-

-

0.05 0.06

1.96 1.78

0.09 0.86

0.89 0.73

0.53 0.43

50˚C 80˚C

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ACS Paragon Plus Environment

Analysis of n-alkanes, esters and alcohols.

[126]

Analysis of n-alkanes, alcohols, esters, phenols and organic acids.

[133]

Comparison of several IL-based GC columns.

[114]

66

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1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48

1-ethyl-3-methylimidazolium [FAP] 1,9-bis(2,3dimethylimidazolium)nonane [NTf2] 1,9-bis[3-(3-cyanopropyl)-2methylimidazolium]nonane [NTf2] 3,3’,3’’,3’’’,3’’’’,3’’’’’-[benzene1,2,3,4,5,6hexaylhexakis(methylene)]hexakis[1 -(trans-2-hydroxycyclopentyl)-1Himidazol-3-ium [NTf2] 3,3’,3’’,3’’’,3’’’’,3’’’’’-[benzene1,2,3,4,5,6hexaylhexakis(methylene)]hexakis[1 -(trans-2-hydroxycyclohexyl)-1Himidazol-3-ium [NTf2] 3,3’,3’’,3’’’,3’’’’,3’’’’’-[benzene1,2,3,4,5,6hexaylhexakis(methylene)]hexakis[1 -(trans-2-hydroxycyclopentyl)-1Himidazol-3-ium [NTf2]

Analytical Chemistry

0.06 0.17 0.15 0.11

1.61 1.91 1.74 1.74

0.68 0.89 0.70 0.64

0.65 0.89 0.72 0.66

0.37 0.51 0.42 0.41

110˚C 50˚C 80˚C 110˚C

250˚C (a)

0.37

1.62

0.00

1.13

0.14

120˚C

-

250˚C (a)

0.37

1.62

0.00

1.22

0.29

120˚C

-

-0.31

1.15

0.91

1.88

0.41

70˚C

-0.16

1.10

0.5

1.28

0.38

100˚C

1.05

1.78

1.71

2.36

0.41

70˚C

0.84

0.56

1.15

1.01

0.34

100˚C

-0.61

1.31

2.45

1.06

0.51

70˚C

-0.05

0.29

2.13

0.59

0.22

100˚C

120˚C

-

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-

[133]

Analysis of alcohols and aromatic compounds.

[137]

Analysis of n-alkanes, alcohols, esters, phenols and organic acids.

[133]

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2-methyl-1-propylpyridinium [NTf2]

250˚C (a)

0.06

1.62

Pyridinium-based ILs 1.19 0.17 0.31

3-methyl-1-propylpyridinium [NTf2]

250˚C (a)

0.07

1.6

1.15

0.15

0.31

120˚C

-

4-methyl-1-propylpyridinium [NTf2] 2,6-dimethyl-1-propylpyridinium [NTf2] 3,5-dimethyl-1-propylpyridinium [NTf2]

250˚C (a)

0.10

1.57

1.13

0.10

0.32

120˚C

-

250˚C (a)

0.18

1.70

1.35

0.30

0.37

120˚C

-

250˚C (a)

0.16

1.55

1.11

0.28

0.37

120˚C

-

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Analysis of n-alkanes, alcohols, esters, phenols and organic acids.

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Analytical Chemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48

1-propyl-2,4,6-trimethylpyridinium [NTf2] 1,9-bis(4-methylpyridinium)nonane [NTf2] 1,9-bis(2-methylpyridinium)nonane [NTf2]

250˚C (a)

0.28

1.61

1.40

0.59

0.42

120˚C

-

250˚C (a)

0.35

1.66

1.25

0.11

0.35

120˚C

-

250˚C (a)

0.33

1.74

1.29

0.13

0.35

120˚C

-

0.12 0.24 0.21 0.24 0.30 0.26 0.28 0.23 0.13

1.71 1.47 1.39 1.61 1.44 1.32 1.76 1.71 1.66

0.09 0.13 0.10 0.00 0.00 0.00

1.97 1.68 1.62 1.90 1.73 1.66

0.16 0.16 0.17 0.16 0.16 0.17

1.82 1.65 1.52 1.82 1.65 1.52

0.73 0.82 0.60 0.55 0.79 0.50 0.47 0.66 0.42 0.86 0.57 0.63 0.65 0.50 0.54 0.50 0.41 0.46 1.01 1.78 0.50 0.84 1.44 0.43 0.66 1.20 0.37 Ammonium-based ILs 0.91 0.85 0.53 0.67 0.76 0.44 0.62 0.64 0.37 2.00 0.45 0.59 1.68 0.37 0.48 1.49 0.31 0.41 Piperidinium-based ILs 0.95 0.58 0.56 0.74 0.46 0.46 0.58 0.43 0.40 0.95 0.58 0.56 0.74 0.46 0.46 0.58 0.43 0.40

N-hexylpyridinium [FAP]

-

N-hexyl-4-(N′ ,N′ dimethylamino)pyridinium [FAP]

-

N-hydroxypropylpyridinium [FAP]

-

methoxyethyl-dimethylethylammonium [FAP]

Hexyl-trimethylammonium [NTf2]

1-methoxyethyl-1methylpiperidinium [FAP] 1-methoxypropyl-1methylpiperidinium [FAP]

Page 68 of 79

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50˚C 80˚C 110˚C 50˚C 80˚C 110˚C 50˚C 80˚C 110˚C 50˚C 80˚C 110˚C 50˚C 80˚C 110˚C 50˚C 80˚C 110˚C 50˚C 80˚C 110˚C

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Comparison of several IL-based GC columns.

[114]

Comparison of several IL-based GC columns.

[114]

Comparison of several IL-based GC columns.

[114]

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Analytical Chemistry

1-butyl-1-methylpyrrolidinium [SCN]

-

1- butyl-1-methylpyrrolidinium tricyanomethide

-

1-butyl-1-methylpyrrolidinium tetracyanoborate

-

1-butyl-1-methylpyrrolidinium bis[oxalate(2-)]borate

-

1-propyl-1-methylpiperidinium [NTf2]

-

N,N,N’,N’-tetramethyl-N”,N”dioctylguanidinium [NTf2]

N,N,N’,N’-tetraoctyl-N”,N”dimethylguanidinium [NTf2]

250˚C (a)

250˚C (a)

0.44 0.41 0.51 0.18 0.28 0.28 0.11 0.22 0.21 0.11 0.16 0.17 0.28 0.30 0.27

2.21 2.14 1.98 2.07 1.99 1.82 1.97 1.76 1.67 2.46 2.16 1.97 1.87 1.77 1.63

-0.23

1.81

Pyrrolidinium-based ILs 4.40 0.15 0.54 4.10 0.00 0.42 3.60 0.10 0.31 3.17 0.16 0.56 2.81 0.24 0.47 2.43 0.20 0.39 2.25 0.29 0.57 1.95 0.34 0.47 1.76 0.26 0.40 2.45 0.16 0.55 2.04 0.18 0.45 1.80 0.14 0.38 2.11 0.35 0.55 1.86 0.26 0.45 1.60 0.21 0.39 Guanidinium-based ILs 1.81 0.00 0.67

-0.18

1.66

1.54

0.00

0.59

100˚C

-0.18

1.16

1.50

0.42

0.66

70˚C

0.09

0.98

1.09

0.35

0.55

100˚C

50˚C 80˚C 110˚C 50˚C 80˚C 110˚C 50˚C 80˚C 110˚C 50˚C 80˚C 110˚C 50˚C 80˚C 110˚C 70˚C

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Comparison of several IL-based GC columns.

[114]

X'=283,Y'=395 , Z'=367, U'=506, S'=397 (120˚C) X'=209, Y'=302, Z'=275, U'=354, S'=327 (120˚C)

Separation of alcohols and fatty acid methyl esters.

[132]

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Analysis of n-alkanes, esters and alcohols.

[126]

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Sulfonium-based ILs triethylsulfonium [NTf2]

200˚C

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Morpholinium-based ILs

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Analytical Chemistry

1 2 3 4 5 0.10 2.05 1.02 0.86 0.51 50˚C 6 1- methoxyethyl-10.10 1.87 0.81 0.70 0.42 80˚C 7 methylmorpholinium [FAP] 0.10 1.71 0.68 0.63 0.35 110˚C 8 (a) No bleed profile was reported. 9 1729 10 11 1730 Abbreviations – [NTf2]: bis[(trifluoromethyl)sulfonyl]imide, [Br]: bromide, [PF6]: hexafluorophosphate, [BF4]: 12 1731 [SCN]: thiocyanate, [TfO]: triflate, [FAP]: tris(pentafluoroethyl)trifluorophate 13 1732 14 15 1733 16 1734 17 1735 18 1736 19 1737 20 21 1738 22 1739 23 1740 24 1741 25 1742 26 1743 27 28 1744 29 1745 30 1746 31 1747 32 1748 33 34 1749 35 1750 36 1751 37 1752 38 1753 39 40 1754 41 1755 42 43 44 45 46 ACS Paragon Plus Environment 47 48

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Comparison of several IL-based GC columns.

tetrafluoroborate,

70

[114]

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1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48

1756 1757 1758

Analytical Chemistry

Figures Figure 1.

1759 1760

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Analytical Chemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48

1761 1762 1763 1764

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Figure 2.

1765 1766 1767 1768 1769 1770 1771 1772 1773 1774 1775 1776

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1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48

1777 1778 1779

Analytical Chemistry

Figure 3.

1780 1781

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Analytical Chemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

1782 1783 1784 1785 1786 1787

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Figure 4.

1788 1789 1790 1791 1792 1793 1794 1795 1796 1797 1798 1799 1800

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1801 1802

Analytical Chemistry

Figure 5.

1803 1804 1805

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Analytical Chemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

1806 1807 1808 1809 1810

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Figure 6.

1811 1812 1813 1814 1815 1816 1817 1818 1819 1820 1821

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1822 1823 1824 1825

Analytical Chemistry

Figure 7.

1826 1827 1828 1829 1830 1831 1832 1833 1834 1835 1836 1837 1838 1839 1840 1841 1842 1843 1844 1845 1846 1847 1848 1849

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Analytical Chemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

1850 1851 1852

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Figure 8.

1853 1854 1855 1856 1857 1858 1859 1860 1861 1862 1863 1864 1865 1866 1867 1868 1869 1870 1871 1872 1873 1874 1875 1876 1877 1878 1879 1880

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1881 1882 1883

Analytical Chemistry

Figure 9.

1884 1885 1886 1887 1888 1889 1890 1891 1892 1893 1894 1895 1896 1897 1898 1899 1900 1901 1902 1903

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