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Letter Cite This: J. Phys. Chem. Lett. 2018, 9, 6631−6637

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Characterization of Vibrational Coherence in Monomeric Bacteriochlorophyll a by Two-Dimensional Electronic Spectroscopy Veronica R. Policht, Andrew Niedringhaus, and Jennifer P. Ogilvie* Department of Physics, University of Michigan, Ann Arbor, Michigan 48108, United States

J. Phys. Chem. Lett. 2018.9:6631-6637. Downloaded from pubs.acs.org by IOWA STATE UNIV on 01/19/19. For personal use only.

S Supporting Information *

ABSTRACT: Bacteriochlorophyll a (BChla) is the most abundant pigment found in the Bacterial Reaction Center (BRC) and light-harvesting proteins of photosynthetic purple and green bacteria. Recent two-dimensional electronic spectroscopy (2DES) studies of photosynthetic pigment−protein complexes including the BRC and the Fenna−Matthews− Olson (FMO) complex have shown oscillatory signals, or coherences, whose physical origin has been hotly debated. To better understand the observations of coherence in larger photosynthetic systems, it is important to carefully characterize the spectroscopic signatures of the monomeric pigments. Prior spectroscopic studies of BChla have differed significantly in their observations, with some studies reporting little to no coherence. Here we present evidence of strong coherences in monomeric BChla in isopropanol using 2DES at 77 K. We resolve many modes with frequencies that correspond well with known vibrational modes. We confirm their vibrational origin by comparing the 2D spectroscopic signatures with expectations based on a purely vibrational model.

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the origin of these coherences by modeling the spectroscopic signatures of electronic, vibrational, and vibronic coherence to be expected in 2DES experiments.45−51 A number of studies have explored the effect of vibrational−electronic resonances on enhancing the processes of EET49,52−54 and CS.26,27,56 While many studies have observed coherences in bacterial PPCs, there have not been many complementary studies of the constituent monomer pigments. Of the studies that have been conducted thus far, there is disagreement as to whether or not coherences exist or are prominent in monomeric BChla. The earliest room-temperature coherence studies of monomeric BChla using ultrafast transient absorption (TA) spectroscopy did not resolve prominent coherent oscillations.57 Not long after this initial study, another TA study of BChla resolved a single low-frequency mode at 4.2 K but failed to see coherences at room temperature.29 In contrast, a three-pulse photon echo study observed several coherent modes in BChla at room temperature in several different solvents that were in the same frequency regime as low-frequency coherences observed in BRCs.37,38 The first 2DES study of BChla looked for coherences in several different solvents and concluded that two weak coherences at 550 and 730 cm−1 were present but that solvent contributions dominated the signals.41 This study was used to strengthen the assignment of coherence in the FMO complex as electronic in origin.41 Similarly, the earliest TA study of BChla, which did not resolve coherences, was used in the interpretation that BRC coherences were intermolecular in origin.8

hotosynthesis, the process wherein sunlight is converted into usable chemical energy by plants and other photosynthetic organisms, is responsible for the majority of life on Earth. In the initial steps following the absorption of sunlight, energy is rapidly and efficiently transferred between large pigment−protein complexes (PPCs) where it is converted into a long-lived charge separation.1 The main pigments involved in the excitation energy transfer (EET) and charge separation (CS) processes in bacterial photosynthesis are bacteriochlorophylls. Bacteriochlorophyll a (BChla) is the most prominent pigment in the Bacterial Reaction Center (BRC) protein of several species of purple bacteria as well as the Fenna−Matthews−Olson (FMO) antenna complex of green sulfur bacteria. For decades, spectroscopists and theorists have worked to better understand EET and CS processes in these systems, both studying the complexed PPCs1,2 and monomeric samples of the constituent pigments3,4 like BChla. Despite this intense research, many questions remain regarding the physical mechanisms that underlie the rapidity (fs−ps time scales) and efficiency of the primary steps of EET and CS, which can approach quantum efficiencies of unity.1 Following the first observation of coherences in a PPC using twodimensional electronic spectroscopy (2DES) in the FMO complex in 2007 by Engel et al.,5 the origin and role of longlived oscillatory coherences in EET and CS in PPCs has gripped the interest of the photosynthetic community. Coherent dynamics have been observed in a wide variety of systems using ultrafast spectroscopy techniques, including a variety of photosynthetic proteins including BRCs,6−25 the Photosystem II D1D2 reaction center,26−28 various antenna protein complexes,5,29−35 and monomeric molecular systems,36 including photosynthetic pigments.29,37−44 There have been numerous theoretical studies that have sought to characterize © 2018 American Chemical Society

Received: August 31, 2018 Accepted: October 30, 2018 Published: October 30, 2018 6631

DOI: 10.1021/acs.jpclett.8b02691 J. Phys. Chem. Lett. 2018, 9, 6631−6637

Letter

The Journal of Physical Chemistry Letters Coherences have previously been observed in Chlorophyll a (Chla), the plant analogue of BChla. An ultrafast pump−probe study of Chla showed a large number of oscillatory modes that were interpreted as intramolecular vibrations,40 and several 2DES studies of coherence in Chla observed strong coherence modes and reached similar conclusions.42,43 The vibrational properties of BChla and Chla are similar, with Huang−Rhys factors for strong vibrational modes on Qy in both molecules on the order of S ≅ 0.01.58,59 In a difference fluorescence linenarrowing experiment of BChla59 (Chla58) the Huang−Rhys factors for the 565 (573) and 727 (745) cm−1 vibrational modes were measured to be 0.0081 (0.018) and 0.0266 (0.035). Given these similarities, it might be expected that coherences would be present in BChla as they were seen in Chla. To this effect, a recent 2DES study of coherences on the red edge of the BChla Qy band showed several coherences that were assigned to vibrational origins;44 however, only a few lowfrequency modes were observed due to the bandwidth of the pulses used. Given the discrepancy in observations of coherences over the years and the need for proper comparison with signals seen in the PPCs, it is necessary to establish benchmark signatures of coherence in BChla. Here we present broad-band 2DES on monomeric BChla dissolved in isopropanol at 77 K. In this study, we observe many prominent coherences that correspond well with known vibrational modes of BChla. To characterize the distribution of coherence in the 2DES data, we present coherence maps (also called Fourier maps)60 for comparison with a simple displaced oscillator (DO) model for purely vibrational coherence.45,46 Our data show that vibrational coherences are indisputably present on monomeric BChla molecules. We also find some deviations from the expected behavior based on the simple DO model of purely vibrational coherence. These results serve as important benchmarks of coherence for improving our understanding of the more complex PPCS such as FMO and the BRC. Figure 1 shows the 77 K real absorptive 2DES spectrum and the 77 K linear absorption spectrum of BChla in isopropanol along with the pulse spectra. This experiment used isopropanol as the solvent because it has been suggested that the dielectric constant is similar to that experienced by BChla molecules in the BRC. Isopropanol is a five-coordinating solvent where one solvent molecule is ligated to the Mg2+ ion of each BChla.61 In contrast, six-coordinating solvents have two solvent molecules ligated to the Mg2+ on either side of the bacteriochlorin plane. As a control study for solvent dependence, we also performed 2DES at 77 K on BChla in ethanol, a predominantly sixcoordinating solvent62 with a significantly different resonance Raman (RR) spectrum from isopropanol, the results of which are presented in the SI and show similar results to what is presented in the main text. The 77 K real absorptive 2DES spectrum of BChla (Figure 1) shows a strong positive peak corresponding to ground-state bleach (GSB) and stimulated emission (SE) of the Q y band, which shows large inhomogeneous broadening along the diagonal, as well as negative excited-state absorption (ESA) signals above the diagonal and positive GSB signatures below the diagonal. The lifetime of the Qy excited state is on the order of tens of nanoseconds,63 significantly longer than the 3.5 ps scan analyzed here. The Qy band retains the inhomogeneous broadening for the entire 3.5 ps scan, indicating slow spectral diffusion. In order to analyze the weak oscillatory signals corresponding to coherences, we first perform a global kinetic

Figure 1. Real absorptive 2D spectrum of BChla in isopropanol at 77 K and t2 = 200 fs. The 77 K linear absorption spectrum (blue) is shown along with the pump (top, gray) and probe (right, gray) spectra used in the experiments. The pump pulse is centered to the blue of Qy so as to better access high-frequency excited-state coherences, while the probe spectrum is centered about Qy.

fit to the 2DES data set, fitting to a sum of complex exponentials. The exponential decay terms are then subtracted from the data, and the oscillatory residual is Fourier transformed with respect to t2 to yield the coherence frequency, ω2. Figure 2 shows the Frobenius or Fourier spectrum calculated by taking the Frobenius norm of the pseudo-three-dimensional frequency solid. The Frobenius spectrum shows several prominent peaks sitting atop a noise pedestal. Comparison of the peak frequencies from the Frobenius spectrum with known

Figure 2. Frobenius spectrum of the real rephasing signal of BChla in isopropanol at 77 K. The spectrum is normalized by the integrated amplitude. Several prominent peaks are labeled with their frequency. Blue lines above the spectrum indicate vibrational frequencies measured by RR.64−66 The RR spectra of BChla feature many prominent modes. In order to stringently compare our observed coherence frequencies, we select only those peaks in the Frobenius spectra above the background pedestal and search for matching vibrational modes from the RR experiments within our experimental resolution of Δω2 = 9.96 cm−1 and the reported resolutions in the RR studies. 6632

DOI: 10.1021/acs.jpclett.8b02691 J. Phys. Chem. Lett. 2018, 9, 6631−6637

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The Journal of Physical Chemistry Letters vibrational modes for monomeric BChla measured via RR64−66 shows that they are consistent with these modes being vibrational in origin. For several of these peaks, there are small differences in the frequency observed in the 2DES experiment versus the vibrational spectroscopy experiments; however, many of the observed modes in Figure 2 are within the experimental resolution of our experiment and the RR experiments referenced. This Frobenius spectrum shows reproducible peaks frequencies when compared across data sets from different experimental runs and when compared against different solvents (Figure S6), within the experimental Δω2 resolution, with peak amplitudes sensitive to the bandwidth of the pump and probe spectra. The two lowestfrequency peaks in Figure 2 are below the lowest resolved frequency in the RR experiments against which we are comparing.64−66 The normal vibrational modes of the BChla Qy state have been calculated by Rätsep et al., and the prominent modes identified in Figure 2 are assigned to skeletal stretching, in-plane bending, and torsional vibrational modes.59 Normal vibrations of BChla Qx states have also been assigned previously to skeletal vibrational modes.67 In order to better assign an origin to the coherence signals present in the BChla data, we plot the amplitude distribution of specific coherence frequencies as a function of the excitation and detection frequencies in coherence maps (Figure 3). Figure 3 shows both the real rephasing signal coherence maps, which show the same signatures in both ±ω2, along with the separated −ω2 and +ω2 coherence maps from the complex rephasing signal. The ±ω2 Frobenius spectrum of the complex rephasing signal is shown in Figure S1. Analyzing the complex rephasing signals allows us to better separate out distinct signals that may overlap in (ω1,ω3) but that oscillate with different signs. Analyzing coherences in this way was initially proposed by Seibt et al.68 and first performed by Song et al.69 and has been used in several recent coherence studies of PPCs.16,35 Analyzing the complex signals also allows us to differentiate ground- and excited-state vibrational frequencies (see Figure 4). Presenting the coherence data in coherence maps allows us to compare more directly to toy models for coherence of different origins. Coherences with a purely vibrational origin, where the coherence is between two vibrational states on the same electronic state, are frequently described by a displaced harmonic oscillator (DO) model (Figure 4).45,46 This model includes two electronic states (|g⟩ and |a⟩), each with two vibrational levels where the excited electronic state is displaced along the nuclear coordinate, q, by dimensionless displacement d. A similar model was used in the initial observations of coherences in the BRC using ultrafast TA spectroscopy.6 Given the simplicity of this model, we can easily determine which light−matter interaction pathways result in coherence during t2. There are eight rephasing coherence pathways, represented by double-sided Feynman diagrams in Figure 4, which are distributed in five distinct peaks in the 2D coherence map forming a characteristic “chair” pattern. The nonrephasing signal also has eight pathways, but we focus on the rephasing signals for signal-to-noise reasons. The first coherence map shown in Figure 3 is at ω2 = 160 cm−1, which is a weak peak in the Frobenius spectrum (Figure 2). This coherence map is shown for the purpose of comparison to a prominent mode observed in several coherence studies of FMO of about 160 cm−15,32,35 and shows three diagonally elongated peaks along the guiding

Figure 3. Real rephasing (left column) and −ω2 and +ω2 of the complex rephasing (center and right columns, respectively) coherence maps for several prominent modes in BChla in isopropanol. Diagonal lines are drawn at −ω1 = ω3 and at several values of −ω1 = ω3 ± n × ω2 to guide the eye for comparison to the DO model in Figure 4.

diagonal lines, similar to other more prominent low-frequency coherences (Figure S3). The high-frequency modes ω2 = 572 and 741 cm−1 show the best agreement with the DO model, showing nearly all of the expected signatures with the exception of the signature located at (−A,A − Ω) in Figure 4. The ω2 = 901 cm−1 mode also shows signals with the expected distribution (Figure 3) but with decreased signal strength in the off-diagonal signatures. The complex rephasing coherence maps allow us to further separate out pathways oscillating with opposite sign. Of the eight pathways predicted from the DO model (Figure 4), two oscillate with +ω2 and six 6633

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BRC in a study by Paleček et al.,16 where such features were attributed to ultrafast energy transfer between the pigments of the BRC. In the case of the spectrally isolated Qy band of monomeric BChla, we do not expect any energy transfer to occur, nor do the population dynamics show evidence for energy transfer. We can confirm that these signatures are due to destructive interference by looking at the complex rephasing coherence signal in Figure 3, which shows signal maxima along the diagonal. The nodal feature is also present in many weak coherence modes with similar destructive interference behavior as the ω2 = 901 cm−1 mode. There is also a nodal line in the ω2 = 349 cm−1 coherence map in Figure S3, but this seems to be due to a lack of amplitude on the diagonal rather than destructive interference effects. In an attempt to understand these nodal features, we have considered possible solvent effects, including excitation of solvent vibrations via coordinated solvent ligands.72,73 As a control study, we performed 2DES of BChla in ethanol, finding very similar results to the isopropanol studies, suggesting that solvent effects do not explain the observed nodal signature. The BChla in ethanol resultsaresummarizedintheSIalongwithadditionaldiscussionofdeviations from the DO model. Understanding the origin of the nodal signals and other deviations from the DO model is a work in progress that will be facilitated by ongoing theory collaborations. We note that the relative amplitudes and some of the frequencies of the dominant coherences found in our monomer data differ from those reported in 2DES studies of BChla-containing photosynthetic proteins. In the FMO complex, initial reports indicated frequencies ranging from ∼170 to 500 cm−1 present in analysis of a particular peak location in the 2D spectrum.5 More recent work in which coherences were characterized using coherence maps and polarization to suppress purely vibrational contributions has reported dominant frequencies of 170 and 210 cm−1 in FMO at 77 K.35 An LH1 dimer studied by Ferretti et al.55 reports dominant modes at 416 and 546 cm−1. In comparison, our monomer data show a peak at 414 cm−1, which is weak in the isopropanol data but is prominentin the ethanol data (Figure S6). RR studies are unable to resolve this peak possibly due to overlap with a broad multipeaked feature in the 300−400 cm−1 range.64−66 We observe a weak peak at 555 cm−1, though again this mode is not well characterized in RR studies. Studies of LH2 have reported a coherence dominating at ∼730−750 cm−1,74,75 consistent with our observation of a 741 cm−1 mode. In summary, we have characterized the coherences present upon excitation of the Qy band of BChla in isopropanol using 2DES with broad-band excitation and detection (Figure 1). Given the correspondence of peaks in the Frobenius spectrum (Figure 2) to well-characterized vibrational modes of BChla and the agreement of the coherence map amplitude distributions for prominent modes (Figure 3) with those expected for the DO model (Figure 4), the coherences observed in BChla are clearly vibrational in character. The characterization of the coherences in BChla is an important step in understanding the coherences present in the large PPCs and offers strong evidence that intramolecular vibrations are prominent in ultrafast spectroscopy of BChla and must be considered in the analysis of coherences in PPCs. Having established benchmark 2DES signatures of coherence of the monomer pigments, comparisons to 2DES coherences studies of the more complex PPCs can be made to improve our understanding of electronic−vibrational coupling and its

Figure 4. Toy model for purely vibrational coherences.45,46 DO model consisting of two electronic states (|g⟩ and |a⟩) with two vibrational states of frequency Ω (|g′⟩ and |a′⟩) displaced along the nuclear coordinate q by displacement d. This simple model yields eight possible rephasing light−matter interaction pathways, resulting in coherences during t2, illustrated with double-sided Feynman diagrams (below). These signals yield a characteristic chair pattern in the real rephasing signal when plotted in a 2D coherence map (top, right), two of which oscillate at +ω2 (red symbols) and six that oscillate at −ω2 (black symbols).

with −ω2. This behavior is present in the high-frequency coherence maps in Figure 3, strengthening our assignment that these coherences are due to intramolecular vibrations. Regarding the decreased signal strength of some signatures in the high-frequency coherence maps, several previous studies have discussed the filtering42,70 or even distorting71 effects that laser bandwidth can have on coherences probed. The effects that we see in the coherence maps, where expected signatures are attenuated in amplitude or missing from the maps shown in Figure 3, are related to the limited bandwidth of the pump spectrum (Figure 1). The pump spectrum in the experiment of BChla in ethanol (Figure S5) was tuned so as to better access these below-diagonal signals that are attenuated in Figure 3, with the trade-off of attenuated signatures at ω1 = −(A + Ω) (Figure S8). While the high-frequency coherence maps in Figure 3 match the expected 2D distribution predicted by the DO model well, the ω2 = 158 cm−1 and other low-frequency coherences prominent in the Frobenius spectrum (Figure S3) show distinct deviations from this model, suggesting that the DO model is insufficient to fully describe coherences in BChla. The coherence maps for ω2 = 202 and 349 cm−1 in Figure S3 show significant signal between the diagonal lines, which would indicate a vibronic coherence based on simulations of a mixed vibrational−electronic system.50,51 It is however unlikely that these low-frequency modes could be related to vibronic coherence as Qy is well isolated from the next-nearest electronic transition (Qx is ∼4000 cm−1 to the blue) and the samples are prepared with low enough concentration to assume that each molecule is an isolated monomer. Additional signatures not predicted in the DO model are present in the ω2 = 901 cm−1 in Figure 3, which features a nodal line in the diagonal peak where there is expected to be a maximum. The nodal signature appears similar to destructive interference signals recently observed in coherence maps of the 6634

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Formation of the Charge Pair P+H(L)- in Bacterial Reaction Centers. Biochemistry 2000, 39, 8353−8361. (11) Shuvalov, V. a.; Yakovlev, a. G. Coupling of Nuclear Wavepacket Motion and Charge Separation in Bacterial Reaction Centers. FEBS Lett. 2003, 540, 26−34. (12) Lee, H.; Cheng, Y.-C.; Fleming, G. R. Coherence Dynamics in Photosynthesis: Protein Protection of Excitonic Coherence. Science 2007, 316, 1462−1465. (13) Westenhoff, S.; Palecek, D.; Edlund, P.; Smith, P.; Zigmantas, D. Coherent Picosecond Exciton Dynamics in a Photosynthetic Reaction Center. J. Am. Chem. Soc. 2012, 134, 16484−16487. (14) Ryu, I. S.; Dong, H.; Fleming, G. R. Role of ElectronicVibrational Mixing in Enhancing Vibrational Coherences in the Ground Electronic States of Photosynthetic Bacterial Reaction Center. J. Phys. Chem. B 2014, 118, 1381−1388. (15) Flanagan, M. L.; Long, P. D.; Dahlberg, P. D.; Rolczynski, B. S.; Massey, S. C.; Engel, G. S. Mutations to R. Sphaeroides Reaction Center Perturb Energy Levels and Vibronic Coupling but Not Observed Energy Transfer Rates. J. Phys. Chem. A 2016, 120, 1479− 1487. (16) Paleček, D.; Edlund, P.; Westenhoff, S.; Zigmantas, D. Quantum Coherence as a Witness of Vibronically Hot Energy Transfer in Bacterial Reaction Center. Sci. Adv. 2017, 3, e1603141. (17) Ma, F.; Romero, E.; Jones, M. R.; Novoderezhkin, V. I.; van Grondelle, R. Vibronic Coherence in the Charge Separation Process of the Rhodobacter Sphaeroides Reaction Center. J. Phys. Chem. Lett. 2018, 9, 1827−1832. (18) Vos, M. H.; Jones, M. R.; Hunter, C. N.; Breton, J.; Martin, J. L. Coherent Nuclear Dynamics at Room Temperature in Bacterial Reaction Centers. Proc. Natl. Acad. Sci. U. S. A. 1994, 91, 12701− 12705. (19) Vos, M. H.; Jones, M. R.; Hunter, C. N.; Breton, J.; Lambry, J. C.; Martin, J. L. Coherent Dynamics during the Primary ElectronTransfer Reaction in Membrane-Bound Reaction Centers of Rhodobacter Sphaeroides. Biochemistry 1994, 33, 6750−6757. (20) Vos, M. H.; Jones, M. R.; McGlynn, P.; Hunter, C. N.; Breton, J.; Martin, J. L. Influence of the Membrane Environment on Vibrational Motions in Reaction Centres of Rhodobacter Sphaeroides. Biochim. Biophys. Acta, Bioenerg. 1994, 1186, 117−122. (21) Stanley, R. J.; Boxer, S. G. Oscillations in the Spontaneous Fluorescence from Photosynthetic Reaction Centers. J. Phys. Chem. 1995, 99, 859−863. (22) Jonas, D. M.; Lang, M. J.; Nagasawa, Y.; Joo, T.; Fleming, G. R. Pump−Probe Polarization Anisotropy Study of Femtosecond Energy Transfer within the Photosynthetic Reaction Center of Rhodobacter Sphaeroides R26. J. Phys. Chem. 1996, 100, 12660−12673. (23) Vos, M. H.; Breton, J.; Martin, J.-L. Electronic Energy Transfer within the Hexamer Cofactor System of Bacterial Reaction Centers. J. Phys. Chem. B 1997, 101, 9820−9832. (24) Vos, M. H.; Jones, M. R.; Martin, J. L. Vibrational Coherence in Bacterial Reaction Centers: Spectroscopic Characterisation of Motions Active during Primary Electron Transfer. Chem. Phys. 1998, 233, 179−190. (25) Rischel, C.; Spiedel, D.; Ridge, J. P.; Jones, M. R.; Breton, J.; Lambry, J. C.; Martin, J. L.; Vos, M. H. Low Frequency Vibrational Modes in Proteins: Changes Induced by Point-Mutations in the Protein-Cofactor Matrix of Bacterial Reaction Centers. Proc. Natl. Acad. Sci. U. S. A. 1998, 95, 12306−12311. (26) Fuller, F. D.; Pan, J.; Gelzinis, A.; Butkus, V.; Senlik, S. S.; Wilcox, D. E.; Yocum, C. F.; Valkunas, L.; Abramavicius, D.; Ogilvie, J. P. Vibronic Coherence in Oxygenic Photosynthesis. Nat. Chem. 2014, 6, 706−711. (27) Romero, E.; Augulis, R.; Novoderezhkin, V. I.; Ferretti, M.; Thieme, J.; Zigmantas, D.; van Grondelle, R. Quantum Coherence in Photosynthesis for Efficient Solar-Energy Conversion. Nat. Phys. 2014, 10, 676−682. (28) Novoderezhkin, V. I.; Romero, E.; Prior, J.; van Grondelle, R. Exciton-Vibrational Resonance and Dynamics of Charge Separation in

possible functional role in photosynthetic EET and CS. We note that during the review of this manuscript Irgen-Gioro et al. published a complementary report on coherence in BChla at room temperature.76



ASSOCIATED CONTENT

S Supporting Information *

The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.jpclett.8b02691.



Experimental methods, real and complex coherence analysis, coherence signal to noise comparison, deviations from the DO model, discussion of solvent dependence and Figures S1−S8, showing Frobenius spectra, coherence maps, linear absorption spectra, and real absorptive 2D spectra (PDF)

AUTHOR INFORMATION

Corresponding Author

*E-mail: [email protected]. ORCID

Veronica R. Policht: 0000-0002-1781-7258 Jennifer P. Ogilvie: 0000-0003-4060-5437 Notes

The authors declare no competing financial interest.



ACKNOWLEDGMENTS We thank Dewey Holten, Dave Bocian, and Kenneth Spears for helpful discussions. We gratefully acknowledge the support of the National Science Foundation through Grant #PHY1607570.



REFERENCES

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