Nanocage-confined synthesis of fluorescent polycyclic aromatic

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Nanocage-confined synthesis of fluorescent polycyclic aromatic hydrocarbons in zeolite Seung Hyeon Ko, Taekyoung Lee, Hongjun Park, Doo-Sik Ahn, Kyoungsoo Kim, Yonghyun Kwon, Sung June Cho, and Ryong Ryoo J. Am. Chem. Soc., Just Accepted Manuscript • DOI: 10.1021/jacs.8b00900 • Publication Date (Web): 26 Apr 2018 Downloaded from http://pubs.acs.org on April 26, 2018

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Journal of the American Chemical Society

Nanocage-confined synthesis of fluorescent polycyclic aromatic hydrocarbons in zeolite Seung Hyeon Ko, *,† Taekyoung Lee,†, ‡ Hongjun Park,†, ‡ Doo-Sik Ahn,† Kyoungsoo Kim,† Yonghyun Kwon,†, ‡ Sung June Cho§ & Ryong Ryoo*,†, ‡ †

Center for Nanomaterials and Chemical Reactions, Institute for Basic Science, Daejeon 34141, Korea. ‡ Department of Chemistry, Korea Advanced Institute of Science and Technology, Daejeon 34141, Korea. § Clean Energy Technology Laboratory and Department of Chemical Engineering, Chonnam National University, Gwangju 61186, Korea.

ABSTRACT: Polycyclic aromatic hydrocarbons (PAHs) attract much attention for applications to organic lightemitting diodes, field-effect transistors, and photovoltaic cells. The current synthetic approaches to PAHs involve high-temperature flash pyrolysis or complicated step-by-step organic reactions, which lead to low yields of PAHs. Herein, we report a facile and scalable synthesis of PAHs, which is carried out simply by flowing acetylene gas into zeolite under mild heating, typically at 400 °C, and generates the products of 0.30 g g-1 zeolite. PAHs are synthesized via acetylene polymerization inside Ca2+-ion exchanged LTA zeolite, of which α-cage puts a limit to the product molecular size as a confined-space nanoreactor. The resultant product after the removal of the zeolite framework exhibit brilliant white fluorescence emission in N-methylpyrrolidone solution. The product is separated into four different color emitters (violet, blue, green, and orange) by column chromatography. Detailed characterizations of the products by means of various spectroscopic methods and mainly mass spectrometric analyses indicate that coronene (C24H12) is the main component of the blue emitter, while the green emitter is a mixture of planar and curved PAHs. The orange can be attributed to curved PAHs larger than ovalene, and the violet to smaller molecules. The PAH growth mechanism inside Ca2+-exchanged LTA zeolite is proposed on a basis of mass spectral analyses and density functional theory calculations.

INTRODUCTION Polycyclic aromatic hydrocarbons (PAHs) have a narrow HOMO–LUMO gap due to π-extended backbone. Depending on the orbital gap, PAH molecules exhibit characteristic fluorescence emissions. Often, the orbital gap can be modulated by strong π–π interactions between adjacent PAH molecules.1-5 In some cases, the delocalized electrons over the πbackbone system can exhibit plasmonic characteristics in the visible region.6, 7 These optoelectronic properties attract great interest for potential applications of the PAHs to advanced organic devices, such as lightemitting diodes (LEDs), field-effect transistors, and photovoltaic cells.1-5 In adition, they have attracted

much attention because they can serve as synthetic precursors for rational synthesis of fullerenes, carbon nanotubes, nanographene, and so on.8 PAHs can be synthesized through various organic reactions, such as the Diels–Alder reaction,9-11 ringclosing olefin metathesis,12-13 benzannulation and electrophilic cyclization,15-17 and oxidative cyclodehydrogenation.18-22 In general, the laboratory-scale organic syntheses of PAHs involve multi-step reactions with low product yields. On the other hand, practical production of PAHs depends on flash vacuum pyrolysis in a furnace at high temperature, around 1000 °C.23-26 In addition, the thermal pyrolysis route generates a very

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wide range of carbonaceous products with various molecular sizes, including soots and carbon nanotubes. Here we report a catalyst-assisted ship-in-bottle-type approach to the synthesis of PAH molecules, which is simply to feed acetylene gas into Ca2+ ion-exchanged Linde type A (LTA) zeolite (Figure 1) under mild heating. The Ca2+ ions were embedded into LTA zeolite (i.e., CaA zeolite) to promote polymerization of acetylene, based on our recent work which showed the catalytic effect of Ca2+ ions to achieve selective carbon deposition inside the zeolite.27 The LTA zeolite has αcages with a wide cage diameter of 1.1 nm and narrow apertures of only 0.5 nm. Thus, an acetylene molecule can enter the cage aperture, but once it is polymerized even to a trimer (benzene), the product cannot escape. In addition, we expected that the nanocage diameter would impose a proper restriction onto the growth of molecules, so that the resulting products should have a narrow distribution of molecular sizes.

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exhibited dark brown color, indicating that the polymerization product was not carbonaceous materials, but likely to be organic compounds. The product was not directly extracted from the zeolite into organic solvents, but could be released from the zeolite framework by dissolving the zeolite in HF/HCl solution. The obtained product after the zeolite removal was soluble in several organic solvents, such as N-methyl-2pyrrolidone (NMP), toluene, and 1-chloronaphthalene. These observations indicated that the polymerization of acetylene occurred selectively inside the zeolite cages in a ship-in-bottle-like manner, as we expected. We attempted the polymerization of acetylene using CaA at higher temperatures than 400 °C, to investigate the temperature effect on the reaction. Above 520 °C, the nanocage-confined polymerization of acetylene was not possible.: the product was deposited not only inside the zeolite but also on external surfaces of the zeolite. The product layer on the zeolite surface blocked the zeolite pores, preventing the diffusion of the acetylene into internal pores. The color of composite obtained at >520 °C was not dark brown any more, but black. The products synthesized at 400 °C and 520 °C exhibited fluorescence of different colors in NMP solution (after removal of the zeolite), such as brilliant white and green, respectively, upon exposure to a single ultraviolet-light excitation (Figure 2). Nevertheless, their fluorescence emission spectra had generally similar features with the multiple peaks in a broad range of wavelength (350–600 nm).

Figure 1. Schematic representation of formation of PAHs in α-cages of Ca2+-exchanged LTA zeolite.

For the synthesis, acetylene gas was supplied into the CaA nanoreactor and the final products were collected after dissolving the zeolite in an acid solution. Detailed characterizations of the products were performed by means of solid state 13C NMR spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, elemental analysis and mainly mass spectrometry, with the support of density functional theory (DFT) calculations. On basis of the obtained results, we propose the PAH growth mechanism inside the LTA nanocage reactor containing Ca2+-ion catalysts. RESULTS AND DISCUSSION Polymerization of acetylene in CaA zeolite. The polymerization of acetylene was carried out using CaA zeolite as nanoreactors, which was prepared by Ca2+ ion-exchange of a Na+ form of LTA zeolite.27 The CaA zeolite was heated under acetylene gas (N2/C2H2/H2O) flow at 400 °C (See SI for the experimental details). The saturated weight increase of the product/zeolite composite was 0.30 g g-1 zeolite. The composite

Figure 2. (a) Photographs of NMP solutions, illuminated under white light (left) and UV light (right, 365 nm) and (b) Fluorescence spectra of the products synthesized at 400 °C and 520 °C.

We characterized the products synthesized at two different temperatures, 400 °C and 520 °C, using solidstate 13C NMR spectroscopy, FT-IR spectroscopy (Figure S1 & S2) and elemental analysis. 13C NMR spectrum of the product synthesized at 520 °C exhibited a broad peak covering from 100 to 140 ppm, corresponding to sp2-carbon, whereas the product formed at 400 °C showed an additional sp3-carbon peak at 19.4 ppm, besides the sp2-carbon peak.

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Figure 3. Different mass distributions of the products depending on the reaction temperature. (a) Mass spectra of the products formed at different temperatures, 400 °C and 520 °C were obtained. Additionally, mass spectrum of the product, which was produced at 400 °C and further thermally treated at 520 °C, was analyzed. (b) Upper colored panels show calculated relative abundance of each hydrogenated species. Three following panels are the expanded view of the mass spectra for the selected peak regions including m/z 300, 398 and 470 for the products at each reaction temperature. Orange arrows point out strong peaks at +2 and +4 mass larger than the main masses.

Consistent with the NMR results, FT-IR spectrum for the product synthesized at 520 °C indicated the presence of sp2 C-H (3010 cm-1) and sp2 C=C (1580 cm-1), while the product obtained at 400 °C showed additional sp3 CH (2920 cm-1) as well. Elemental analyses revealed that the products contained only carbon and hydrogen atoms and the carbon to hydrogen molar ratios were also temperature-dependent; ~2.0 to 1 and ~2.8 to 1 for 400 °C and 520 °C, respectively. These experimental results showed that the products were aromatic hydrocarbons, composed of sp2-carbons, and they might have additional alkyl groups at lower reaction temperature (400 °C). Mass spectrum analyses. The products synthesized at 400 °C and 520 °C were further analyzed with their mass spectra, which were obtained by using matrix assisted laser desorption/ionization time-of-flight mass

spectrometer. The measurement conditions were kept as soft as possible to avoid fragmentation of the molecules. As shown in Figure 3a, the mass spectra of the products indicated that size distribution of the products was strongly dependent on the reaction temperature. Mass spectrum of the product synthesized at 520 °C displayed a simplified pattern of mass peaks, indicating preferential formation of the molecules centering at specific mass-to-charge ratios, m/z = 300, 374, 398 and 422. The aromatic hydrocarbons with these molecular weights and the obtained C/H ratios should be PAH molecules. Thus, we assigned these mass peaks with corresponding PAH molecules, C24H12 (m/z = 300), C30H14 (374), C32H14 (398) and C34H14 (422) (Figure S3). In comparison, the mass spectrum of the products obtained at 400 °C exhibits two distinct series of mass

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peaks around m/z = 300 (C24H12) and 398 (C32H14), with a group of small peaks extending into a wide range of high m/z region. Each group consists of a series of peaks at regular intervals of 24 amu with additional peaks of 14 amu larger than them (Figure S4 and a comb-like indicator in Figure 3a). This spectral feature in mass spectrum is quite similar to that of PAH products in aromatization of acetylene pyrolysis, which also has distinct 24 amu progression of peaks.28-33 This regular sequence of 24 amu is explained by a specific mechanism, which implies consecutive reactions of hydrogen abstraction from the aromatic hydrocarbon followed by acetylene addition to the radical site, so called hydrogen abstraction-acetylene addition (HACA. See SI for the details Figure S5). 28-33 In addition, the peaks of +14 mass number from the adjacent 24 amu interval-series of peaks are assigned as methylated species of the 24 mass interval-series of peaks, which have been frequently observed in acetylene pyrolysis as well.33 The presence of methyl groups was previously confirmed by 13C NMR spectrum of the products formed at 400 °C, as aforementioned. The absence of additional peaks of +14 amu for the products obtained at 520 °C strongly suggests that these additional methyl groups, which do not belong to the extended benzene ring system, are eliminated at high temperature. To assess the assumption, the product, synthesized at 400 °C, was additionally heat-treated at 520 °C without the supply of feedstock C2H2. Its mass spectrum was very similar to that of the product synthesized at 520 °C (Figure 3a), indicating the assumption was reasonable. To obtain in-depth insights into the temperature effect on PAH formation, we analyzed the enlarged view of the mass spectra for the selected peak regions, including m/z = 300, 398 and 470 (Figure 3b). It was apparent that a substantial amount of hydrogenated species existed during the PAH growth and their relative amounts were much high for the products of high mass or the products synthesized at 400 °C. Considering the natural isotopic abundance of 13C, isotopic patterns of mass peak were theoretically calculated and displayed as blue filledcircles in the spectra. In the spectrum of the products formed at 400 °C, there are strong peaks at +2 and +4 mass larger than the main masses with much higher intensity (pointed out by orange arrows) than the theoretical isotopic values. We assigned these peaks as hydrogenated PAHs with different degrees of hydrogenation. The degree of hydrogenation becomes more significant in the region of ~470 amu (C38H14). By comparison of the peak intensities, we derived the relative abundance of each hydrogenated species (Figure 3b, upper colored panel). In particular, the presence of a substantial amount of even-numbered hydrogenated species (+2 and +4) suggests that the Ca2+-promoted condition induces the addition of acetylene without following hydrogen abstraction, which generates sp3-carbons in polycyclic network formed at 400 °C. These observations imply that the

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sp3-carbon peak in 13C NMR spectrum of the product synthesized at 400 °C would be corresponding to both the methyl groups and the sp3-carbons in polycyclic network.

Figure 4. (a) Representative reaction pathway of acetylene addition/hydrogen abstraction under the Ca2+-catalytic condition. (b) DFT calculated structures of hydrogenated coronenes. The number indicates the position of hydrogen atoms and the out-of-plane angle by hydrogenation at each position is shown as well.

In contrast, the mass peak intensities in the same regions of the products obtained at 520 °C spectrum are very similar to the theoretical isotopic values except high mass region (for example, m/z = 470). It indicates that hydrogen abstraction has occurred after acetylene addition, to produce aromatic compounds with only sp2carbons. Furthermore, the expanded mass spectra of the product, which was formed at 400 °C and thermally post-treated at 520 °C, show that the amount of evennumbered hydrogenated species significantly decreases. It clearly demonstrates that sufficient thermal treatment can promote the hydrogen abstraction process after the acetylene addition. In light of these experimental observations, we suggest that the confined Ca2+promoted condition induces the addition of an acetylene molecule first, followed by hydrogen abstraction (Figure S6 & Figure 4a), which is the reverse order of the HACA mechanism, a key route to acetylene pyrolysis. 28-33 DFT calculations suggest that sp3-carbon inside the polycyclic network system, where hydrogen atoms remain, promotes the polycyclic network to adopt nonplanar geometries around the sp3-carbon (Figure 4b). The calculations show that the growth of PAH thermodynamically prefers the formation of extended planar benzene family to curved aromatics (Figure S7). If the growth of PAHs was allowed only into planar shapes, the mass peaks at m/z = 300 and 398 could be assigned to corresponding representative planar PAHs, such as coronene (C24H12) and ovalene (C32H14), respectively. Considering the spatial restriction of αcage, the molecular dimensions of ovalene correspond to the limiting size of planar PAH that can reside inside the cage (Figure S8 & S9). In the present study, however, we do not rule out the possibility of the

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formation of curved PAHs based on several experimental and calculation results. In particular, in the mass spectra of the products formed at 400 °C, many peaks were observed in region of m/z ≥ 398, where PAHs should grow in curved shapes rather than planar ones (Figure 3b). Moreover, the products synthesized at 400 °C exhibited the enhanced population of hydrogenated species at m/z ≥ 398 (Figure 3b), which are likely to have the polycyclic network of nonplanar geometries. In addition, the mass spectrum of the products synthesized at 520 °C also showed relatively very small peaks in the region of m/z ≥ 398. In light of these theoretical results and experimental observations, it is proposed that the products obtained at 400 °C would be composed of PAHs with a wide range of m/z from small planar molecules to large curved PAHs, whereas the products synthesized at 520 °C would be PAH molecules mainly of m/z = 300 (C24H12), 374 (C30H14) and 398 (C32H14) (Figure S3 & S10). The growth of PAH molecules. To see how the synthesized PAH molecules reside within the confined α-cage nanoreactor, we investigated the atomic distribution of carbons inside the CaA zeolite, using single crystal X-ray diffraction data. An electrondensity map for carbon atomic positions in the products was derived by a difference Fourier method.27 The electron-density map showed that carbon atoms were distributed only inside each α-cage, not through the

narrow cage apertures (Figure 5a). This result visualized that the products were entrapped within the α-cage nanoreactor, as a ship-in-bottle synthesis. A hexagonallike carbon ring was located near the Ca2+-center (Figure 5b). It showed that the Ca2+ ion had an interaction with π-electron clouds of the benzene-like ring.34 Apart from the hexagonal ring, it was difficult to precisely assign carbon positions. We attribute this to various random orientations of the molecules generated in a cage nanoreactor, resulting in the average electrondensity overlapping various carbon atomic positions.

Figure 5. Electron-density maps of LTA zeolite after PAH formation at 400 °C. They include the zeolite framework (yellow), from different viewpoints along (a) (100) and (b) (100) axes. The iso-surface level of the electron density is set to 0.47 electrons per Å3 (cyan) and 0.5 electrons per Å3 (purple). Small gray balls represent Ca2+ ions.

Figure 6. The catalytic effects of Ca2+ on energy barriers for the reaction pathway from 1,12-benzoperylene (C22H12) to coronene (C24H12). (a) Calculated energy profile for acetylene addition and dehydrogenation without Ca2+ (black, upper) and with Ca2+ (red, down) by DFT calculations. (b) Calculated reaction energy barriers for Ca2+ migration between center and peripheral benzene rings.

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To understand the PAH growth inside the CaA zeolite in the molecular level, we calculated energetics for the reaction pathways using a DFT method (Figure 6a). As a model reaction, we chose a pathway from 1,12benzoperylene (C22H12) to coronene (C24H12), which corresponds to simple acetylene addition followed by hydrogen abstraction. Without Ca2+ ions, the addition of acetylene to 1,12-benzoperylene proceeds via [4+2] cycloaddition, exhibiting the highest energy barrier of 35 kcal/mol. In comparison, owing to the strong

interaction between Ca2+ and π-electron clouds, Ca2+ attracts both reactants, 1,12-benzoperylene and acetylene, giving more chances of reactive collisions between them. At the same time, the Ca2+catalyst lowers the energy barrier to nearly five-fold (38 vs 8 kcal/mol) via sequential C-C bond formation. In addition, Ca2+ stabilizes hydrogenated coronene, which is an intermediate for coronene formation. For the hydrogen abstraction, however, the energy barrier for dehydrogenation is almost unaffected by the presence of Ca2+. This result shows good agreement with the observations in mass spectra, where a substantial amount of the hydrogenated species was detected at low synthesis temperature (400 °C). Besides, the calculated energies required for Ca2+ migrations between center and peripheral benzene rings in 1,12benzoperylene were less than 3 kcal/mol (Figure 6b). It indicates that Ca2+ ions freely migrate from one benzene ring to the others under the present conditions. Such (almost) barrierless migration of Ca2+ would effectively lead to the rapid growth of PAHs by placing the Ca2+ nearby peripheral carbon sites, where acetylene is added.

Figure 7. Schematic representation of the proposed mechanism of PAH formation and further growth in the αcage of CaA zeolite. The cage frameworks are displayed by red and blue balls and sticks.

Based on the experimental and calculation results, we propose the formation/growth mechanism of PAH molecules inside the LTA nanoreactor containing Ca2+-

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catalysts (Figure 7). As we already mentioned, the Ca2+ catalyst significantly lowers the energy barriers by providing an alternative effective pathway for C-C bond formation. As shown in the electron density map (Figure 7), the initial growth of PAHs would preferentially occur near the Ca2+ catalysts, which are embedded in corners of α-cage (near sodalite-site). The small PAHs, such as benzene, are expected to be easily formed near the Ca2+ catalytic center by not only increased collisions of attracted acetylenes by Ca2+, but also large thermodynamic stability of benzene-ring. By continuous Ca2+-mediated reactive collisions of acetylene molecules, small PAH molecules will spontaneously grow until its molecular dimension reaches the size of coronene that tightly fits the dimension of α-cage corner. When the energy is not sufficient to complete abstraction of hydrogen (400 °C in current system), the hydrogenated PAHs will induce various curvatures in molecular topologies and thus lead to grow further in strained curved shapes along the cage wall, enabling formation of the orange-light-emitting PAHs. In contrast, with sufficient energy to actively promote the dehydrogenation process (520 °C), small PAH molecules that have grown near the Ca2+ ions would be liberated from the cage corner to further grow into planar shapes or keep growing into curved PAH molecules along the wall of cage. The growth would be restricted by the finite size of α-cage.

Figure 8. (a) Emission spectra of the products before (black dotted line) and after the separation (corresponding colors), dispersed in NMP. (b) Photographs of NMP solutions (upper), LED devices (middle) and luminescent PMMA films (bottom) under a UV lamp. (c) Mass spectra of the total product produced at 400 °C (upper), group B fraction (lower left) and group G (lower right). (d) Absorption (Abs) and fluorescence (FL) spectra of coronene (black) and B (blue).

Separation into distinct color emitters. We employed silica column chromatography to separate the white-light emitting product synthesized at 400 °C (See SI for the experimental details.). The product was

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separated into four distinct groups exhibiting violet (V), blue (B), green (G), and orange (O) of fluorescence in NMP, under a single wavelength of UV excitation (Figure 8a). The fluorescence quantum yield, which was calibrated against quinine sulfate as a standard sample (54% in 0.1 M H2SO4),35 of the white emission was determined to 13.7 % under 340 nm excitation in NMP solution. The fluorescence quantum yields were also determined to 20.6, 9.3, 5.9, and 6.5% for V, B, G, and O, respectively, under the same conditions. In Figure 8c, the mass spectrum of the 400 °Csynthesized product is compared with the mass spectra of the separated group B and group G fractions. The result indicates that the mass range between 270 and 350 amu in the synthesized product corresponds to the mass peaks of the group B, while the range of 350-450 amu corresponds to the mass signals coming from the group G component. The group V and O components were difficult to assign in the total mass spectrum of the product, which seemed to be due to their low concentrations. The separated group B component was further characterized by absorption and fluorescence spectroscopy, and 1H and 13C solution NMR spectroscopy. The absorption spectrum of B was very similar to that of coronene. The fluorescence spectra in the range of 420-520 nm wavelength exhibited the emission peaks assignable to coronene. The fluorescence of 350-420 nm range was somewhat different from that of coronene, indicating the possibility of presence of other compounds (Figure 8d). 1 H NMR spectrum of the group B showed a very strong single peak at 8.93 ppm. 13C NMR spectrum exhibited three distinct peaks at 122.84, 125.58, and 129.17 ppm. The main peaks in both NMR spectra were well matched to the chemical shifts of coronene (Figure S11). Hence, we conclude that the major component of the group B is coronene. As mentioned in the previous section, the group G component gave a mass spectrum with the major signal at 398 amu, which coincided with the molecular weight of ovalene. However, neither 1H NMR nor 13C NMR spectra could be assigned to ovalene. The group G was very sparingly soluble in NMR solvents, causing low signal intensities in the NMR spectra. Nonetheless, the 1H NMR spectrum could resolve two peaks in the range of 7.5-8.0 ppm, and several peaks in 2.5-4.0 ppm. The 13C NMR spectrum exhibited two small peaks in 125-135 ppm (Figure S12). Because of this discrepancy, we searched the possibility for other molecules with 398 amu. Thereby, it was possible to suggest diindenocorannulenes, bowl-shaped PAH compounds, as a candidate. The NMR and absorption spectra of these two isomeric compounds were similar to those of the group G.36 Based on the elution order, we speculate that the group V would be smaller molecules than coronene, while the group O could include PAHs which are larger than the group G and have curved molecular topologies with a permanent dipole moment (Figure S8). This is in

good agreement with the results from mass spectral analyses. Moreover, this rationale explains why the products synthesized at 400 °C and 520 °C have white and green emission, respectively. Since the product formed at 520 °C does have a very small amount of the orange-emitters, the resulting additive emission is green. In comparison, the white-light-emitting product synthesized at 400 °C shows an additive ensemble behavior of the all four distinct fluorescent groups. For their optical applications, the separated PAHs were directly employed as fluorophores to fabricate flexible free-standing luminescent polymer composite film and LED devices (Figure 8b). The polymer films were prepared by mixing a few drops of each material dispersed in NMP and poly(methyl methacrylate) (PMMA) at appropriate ratios. The LED devices were made by coating each fluorophore in NMP on the light unit comprised of a 365 nm excitation light emitting chip. The PMMA films and LED devices successfully generated blue, green and orange illumination, demonstrating their potential as promising fluorophores in practical applications. CONCLUSIONS We reported a simple and scalable method to synthesize PAH molecules via Ca2+-catalyzed polymerization of acetylene inside the α-cage of LTA zeolite, generating the products of 0.30 g g-1 zeolite. The dimension of the cage nanoreactors imposed spatial restriction on the growth of PAH molecules, so that the obtained products had a narrow range of molecular sizedistribution. The experimental results and DFT calculations suggested that the Ca2+-catalyzed condition induced acetylene addition first followed by hydrogen abstraction, which is a reverse order of the reaction steps of the HACA mechanism. 28-33 With sufficient energy to actively promote the dehydrogenation process (520 °C), planar PAH and small curved PAH molecules, which are mainly blue and green fluorophores, preferentially grow until the growth is restricted by the finite size of α-cage. However, at a lower temperature of 400 °C, PAH molecules could grow into large curved shapes as well, which have been identified as the orange-fluorescent component, along the wall of the cage due to the shortage of thermal energy. We believe that our strategy established the groundwork for the synthesis of PAHs, which may further contribute to rationally synthesize nanographenes as synthetic precursors, using zeolite nanoreactors.

ASSOCIATED CONTENT Supporting Information. The Supporting Information is available free of charge on the ACS Publications website at DOI:

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Detailed experimental procedures; additional characterizations of the products; calculation results.

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AUTHOR INFORMATION

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Corresponding Authors

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*[email protected] *[email protected]

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ORCID

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Seung Hyeon Ko: 0000-0003-2875-1095 Taekyoung Lee: 0000-0001-6733-4732 Hongjun Park: 0000-0002-8978-7342 Doo-Sik Ahn: 0000-0001-9154-1029 Kyoungsoo Kim: 0000-0002-2042-0913 Yonghyun Kwon: 0000-0002-2703-3692 Ryong Ryoo: 0000-0003-0047-3329

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Notes The authors declare no competing financial interest.

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ACKNOWLEDGMENT

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This work was supported by IBS-R004. The authors are grateful to Ms. Min Sun Kim at Korea Basic Science Institute on mass spectrum measurement.

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Nanocage-confined synthesis of fluorescent polycyclic aromatic

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