Solvent tuning of photochemistry upon excited-state symmetry breaking.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
21 04 2020
Historique:
received: 09 01 2020
accepted: 20 03 2020
entrez: 23 4 2020
pubmed: 23 4 2020
medline: 23 4 2020
Statut: epublish

Résumé

The nature of the electronic excited state of many symmetric multibranched donor-acceptor molecules varies from delocalized/multipolar to localized/dipolar depending on the environment. Solvent-driven localization breaks the symmetry and traps the exciton in one branch. Using a combination of ultrafast spectroscopies, we investigate how such excited-state symmetry breaking affects the photochemical reactivity of quadrupolar and octupolar A-(π-D)

Identifiants

pubmed: 32317631
doi: 10.1038/s41467-020-15681-3
pii: 10.1038/s41467-020-15681-3
pmc: PMC7174366
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1925

Références

Yong, C.-K. et al. Ultrafast delocalization of excitation in synthetic light-harvesting nanorings. Chem. Sci. 6, 181–189 (2015).
pubmed: 28553466 doi: 10.1039/C4SC02424A pmcid: 28553466
Alvertis, A. M. et al. Switching between coherent and incoherent singlet fission via solvent-induced symmetry breaking. J. Am. Chem. Soc. 141, 17558–17570 (2019).
pubmed: 31604015 doi: 10.1021/jacs.9b05561 pmcid: 31604015
Sung, J., Kim, P., Fimmel, B., Würthner, F. & Kim, D. Direct observation of ultrafast coherent exciton dynamics in helical π-stacks of self-assembled perylene bisimides. Nat. Commun. 6, 8646 (2015).
pubmed: 26492820 pmcid: 4639892 doi: 10.1038/ncomms9646
Kaufmann, C. et al. Ultrafast exciton delocalization, localization, and excimer formation dynamics in a highly defined perylene bisimide quadruple π-stack. J. Am. Chem. Soc. 140, 4253–4258 (2018).
pubmed: 29502406 doi: 10.1021/jacs.7b11571 pmcid: 29502406
Lim, J. M. et al. Exciton delocalization and dynamics in helical π-stacks of self-assembled perylene bisimides. Chem. Sci. 4, 388–397 (2013).
doi: 10.1039/C2SC21178E
Aggarwal, A. V. et al. Fluctuating exciton localization in giant π-conjugated spoked-wheel macrocycles. Nat. Chem. 5, 964–970 (2013).
pubmed: 24153376 doi: 10.1038/nchem.1758 pmcid: 24153376
Bakulin, A. A. et al. The role of driving energy and delocalized states for charge separation in organic semiconductors. Science 335, 1340–1344 (2012).
pubmed: 22362882 doi: 10.1126/science.1217745 pmcid: 22362882
Collini, E. & Scholes, G. D. Coherent intrachain energy migration in a conjugated polymer at room temperature. Science 323, 369–373 (2009).
pubmed: 19150843 doi: 10.1126/science.1164016 pmcid: 19150843
Reid, O. G., Pensack, R. D., Song, Y., Scholes, G. D. & Rumbles, G. Charge photogeneration in neat conjugated polymers. Chem. Mater. 26, 561–575 (2014).
doi: 10.1021/cm4027144
Banerji, N. Sub-picosecond delocalization in the excited state of conjugated homopolymers and donor–acceptor copolymers. J. Mater. Chem. C 1, 3052–3066 (2013).
doi: 10.1039/c3tc00005b
Fidler, A. F., Singh, V. P., Long, P. D., Dahlberg, P. D. & Engel, G. S. Dynamic localization of electronic excitation in photosynthetic complexes revealed with chiral two-dimensional spectroscopy. Nat. Commun. 5, 3286 (2014).
pubmed: 24504144 pmcid: 3976994 doi: 10.1038/ncomms4286
Scholes, G. D. & Smyth, C. Perspective: detecting and measuring exciton delocalization in photosynthetic light harvesting. J. Chem. Phys. 140, 110901 (2014).
pubmed: 24655162 doi: 10.1063/1.4869329
Jang, S. J. & Mennucci, B. Delocalized excitons in natural light-harvesting complexes. Rev. Mod. Phys. 90, 035003 (2018).
doi: 10.1103/RevModPhys.90.035003
Albota, M. et al. Design of organic molecules with large two-photon absorption cross sections. Science 281, 1653–1656 (1998).
pubmed: 9733507 doi: 10.1126/science.281.5383.1653
Pawlicki, M., Collins, H. A., Denning, R. G. & Anderson, H. L. Two-photon absorption and the design of two-photon dyes. Angew. Chem. Int. Ed. 48, 3244–3266 (2009).
doi: 10.1002/anie.200805257
Geng, Q., Wang, D., Chen, P. & Chen, S.-C. Ultrafast multi-focus 3-D nano-fabrication based on two-photon polymerization. Nat. Commun. 10, 2179 (2019).
pubmed: 31097713 pmcid: 6522551 doi: 10.1038/s41467-019-10249-2
Kawata, S., Sun, H.-B., Tanaka, T. & Takada, K. Finer features for functional microdevices. Nature 412, 697–698 (2001).
pubmed: 11507627 doi: 10.1038/35089130
LaFratta, C. N., Fourkas, J. T., Baldacchini, T. & Farrer, R. A. Multiphoton fabrication. Angew. Chem. Int. Ed. 46, 6238–6258 (2007).
doi: 10.1002/anie.200603995
Mahou, P., Vermot, J., Beaurepaire, E. & Supatto, W. Multicolor two-photon light-sheet microscopy. Nat. Methods 11, 600–601 (2014).
pubmed: 24874570 doi: 10.1038/nmeth.2963
Helmchen, F. & Denk, W. Deep tissue two-photon microscopy. Nat. Methods 2, 932–940 (2005).
pubmed: 16299478 doi: 10.1038/nmeth818
Denk, W., Strickler, J. & Webb, W. Two-photon laser scanning fluorescence microscopy. Science 248, 73–76 (1990).
pubmed: 2321027 doi: 10.1126/science.2321027
Zong, W. et al. Fast high-resolution miniature two-photon microscopy for brain imaging in freely behaving mice. Nat. Methods 14, 713–719 (2017).
pubmed: 28553965 doi: 10.1038/nmeth.4305
Tang, C. et al. Two-photon absorption and optical power limiting properties of ladder-type tetraphenylene cored chromophores with different terminal groups. J. Mater. Chem. C 1, 1771 (2013).
doi: 10.1039/c2tc00780k
Pascal, S. et al. Unraveling the two-photon and excited-state absorptions of Aza-BODIPY dyes for optical power limiting in the SWIR band. J. Phys. Chem. C 123, 23661–23673 (2019).
doi: 10.1021/acs.jpcc.9b08376
Korzycka, K. A. et al. Two-photon sensitive protecting groups operating via intramolecular electron transfer: uncaging of GABA and tryptophan. Chem. Sci. 6, 2419–2426 (2015).
pubmed: 28706657 pmcid: 5488212 doi: 10.1039/C4SC03775H
Nakanotani, H. et al. High-efficiency organic light-emitting diodes with fluorescent emitters. Nat. Commun. 5, 4016 (2014).
pubmed: 24874292 doi: 10.1038/ncomms5016
Data, P. et al. Dibenzo[a,j]phenazine-cored donor-acceptor-donor compounds as green-to-red/NIR thermally activated delayed fluorescence organic light emitters. Angew. Chem. Int. Ed. 55, 5739–5744 (2016).
doi: 10.1002/anie.201600113
Stennett, T. E. et al. Near-infrared quadrupolar chromophores combining three-coordinate boron-based superdonor and superacceptor units. Angew. Chem. Int. Ed. 58, 6449–6454 (2019).
doi: 10.1002/anie.201900889
Schierl, C. et al. Quadrupolar cyclopenta[Hi]aceanthrylene-based electron donor-acceptor-donor conjugates: charge transfer versus charge separation. Angew. Chem. Int. Ed. 58, 14644–14652 (2019).
doi: 10.1002/anie.201906206
Dereka, B., Rosspeintner, A., Li, Z., Liska, R. & Vauthey, E. Direct visualization of excited-state symmetry breaking using ultrafast time-resolved infrared spectroscopy. J. Am. Chem. Soc. 138, 4643–4649 (2016).
pubmed: 26986957 doi: 10.1021/jacs.6b01362
Dereka, B., Koch, M. & Vauthey, E. Looking at photoinduced charge transfer processes in the IR: answers to several long-standing questions. Acc. Chem. Res. 50, 426–434 (2017).
pubmed: 28068061 doi: 10.1021/acs.accounts.6b00538
Dereka, B., Rosspeintner, A., Krzeszewski, M., Gryko, D. T. & Vauthey, E. Symmetry-breaking charge transfer and hydrogen bonding: toward asymmetrical photochemistry. Angew. Chem. Int. Ed. 55, 15624–15628 (2016).
doi: 10.1002/anie.201608567
Dereka, B. & Vauthey, E. Solute–solvent interactions and excited-state symmetry breaking: beyond the dipole–dipole and the hydrogen-bond interactions. J. Phys. Chem. Lett. 8, 3927–3932 (2017).
pubmed: 28786689 doi: 10.1021/acs.jpclett.7b01821
Dereka, B. et al. Excited-state symmetry breaking in a quadrupolar molecule visualized in time and space. J. Phys. Chem. Lett. 8, 6029–6034 (2017).
pubmed: 29190104 doi: 10.1021/acs.jpclett.7b02944
Söderberg, M., Dereka, B., Marrocchi, A., Carlotti, B. & Vauthey, E. Ground-state structural disorder and excited-state symmetry breaking in a quadrupolar molecule. J. Phys. Chem. Lett. 10, 2944–2948 (2019).
pubmed: 31081644 doi: 10.1021/acs.jpclett.9b01024
Beckwith, J. S. et al. Specific monitoring of excited-state symmetry breaking by femtosecond broadband fluorescence upconversion spectroscopy. J. Phys. Chem. Lett. 8, 5878–5883 (2017).
Kim, W., Sung, J., Grzybowski, M., Gryko, D. T. & Kim, D. Modulation of symmetry-breaking intramolecular charge-transfer dynamics assisted by pendant side chains in π-linkers in quadrupolar diketopyrrolopyrrole derivatives. J. Phys. Chem. Lett. 7, 3060–3066 (2016).
pubmed: 27455383 doi: 10.1021/acs.jpclett.6b01248
Markovic, V., Villamaina, D., Barabanov, I., Lawson Daku, L. M. & Vauthey, E. Photoinduced symmetry-breaking charge separation: the direction of the charge transfer. Angew. Chem. Int. Ed. 50, 7596–7598 (2011).
doi: 10.1002/anie.201102601
Carlotti, B. et al. Photoinduced symmetry-breaking intramolecular charge transfer in a quadrupolar pyridinium derivative. Phys. Chem. Chem. Phys. 16, 13984–13994 (2014).
pubmed: 24898848 doi: 10.1039/C4CP00631C
Wu, Y. et al. Ultrafast photoinduced symmetry-breaking charge separation and electron sharing in perylenediimide molecular triangles. J. Am. Chem. Soc. 137, 13236–13239 (2015).
pubmed: 26418462 doi: 10.1021/jacs.5b08386
Cooper, T. M. et al. Two-photon spectroscopy of a series of platinum acetylides: conformation-induced ground-state symmetry breaking. J. Phys. Chem. A 121, 5442–5449 (2017).
pubmed: 28650633 doi: 10.1021/acs.jpca.7b04784
Kim, T. et al. Symmetry-breaking charge transfer in the excited-state in directly linked push-pull porphyrin arrays. Phys. Chem. Chem. Phys. 19, 13970–13977 (2017).
Carlotti, B. et al. Efficient excited-state symmetry breaking in a cationic quadrupolar system bearing diphenylamino donors. ChemPhysChem 17, 136–146 (2016).
pubmed: 26510394 doi: 10.1002/cphc.201500784
Zhou, J. et al. Asymmetric charge separation and recombination in symmetrically functionalized σ–π hybrid oligosilanes. Dalton Trans. 46, 8716–8726 (2017).
Terenziani, F., Painelli, A., Katan, C., Charlot, M. & Blanchard-Desce, M. Charge instability in quadrupolar chromophores: symmetry breaking and solvatochromism. J. Am. Chem. Soc. 128, 15742–15755 (2006).
pubmed: 17147384 doi: 10.1021/ja064521j
Amthor, S., Lambert, C., Dümmler, S., Fischer, I. & Schelter, J. Excited mixed-valence states of symmetrical donor−acceptor−donor π systems. J. Phys. Chem. A 110, 5204–5214 (2006).
pubmed: 16610844 doi: 10.1021/jp056728p
Megerle, U., Selmaier, F., Lambert, C., Riedle, E. & Lochbrunner, S. Symmetry-dependent solvation of donor-substituted triarylboranes. Phys. Chem. Chem. Phys. 10, 6245 (2008).
pubmed: 18936848 doi: 10.1039/b806131a
Terenziani, F., Sissa, C. & Painelli, A. Symmetry breaking in octupolar chromophores: solvatochromism and electroabsorption. J. Phys. Chem. B 112, 5079–5087 (2008).
pubmed: 18376886 doi: 10.1021/jp710241g
Kim, T., Kim, W., Mori, H., Osuka, A. & Kim, D. Solvent and structural fluctuations induced symmetry-breaking charge transfer in a porphyrin triad. J. Phys. Chem. C 122, 19409–19415 (2018).
doi: 10.1021/acs.jpcc.8b05363
Scholes, G. D. et al. Using coherence to enhance function in chemical and biophysical systems. Nature 543, 647–656 (2017).
pubmed: 28358065 doi: 10.1038/nature21425
Dereka, B. et al. Direct observation of a photochemical alkyne–allene reaction and of a twisted and rehybridized intramolecular charge-transfer state in a donor–acceptor dyad. J. Am. Chem. Soc. 139, 16885–16893 (2017).
pubmed: 29068229 doi: 10.1021/jacs.7b09591
Kasha, M., Rawls, H. R. & Ashraf El-Bayoumi, M. The exciton model in molecular spectroscopy. Pure Appl. Chem. 11, 371–392 (1965).
doi: 10.1351/pac196511030371
Ivanov, A. I., Dereka, B. & Vauthey, E. A simple model of solvent-induced symmetry-breaking charge transfer in excited quadrupolar molecules. J. Chem. Phys. 146, 164306 (2017).
pubmed: 28456195 doi: 10.1063/1.4982067
Ivanov, A. I. Theory of vibrational spectra of excited quadrupolar molecules with broken symmetry. J. Phys. Chem. C 122, 29165–29172 (2018).
doi: 10.1021/acs.jpcc.8b10985
Ivanov, A. I. & Tkachev, V. G. Exact solution of three-level model of excited state electron transfer symmetry breaking in quadrupolar molecules. J. Chem. Phys. 151, 124309 (2019).
pubmed: 31575174 doi: 10.1063/1.5116015
Horng, M. L., Gardecki, J., Papazyan, A. & Maroncelli, M. Subpicosecond measurements of polar solvation dynamics: coumarin 153 revisited. J. Phys. Chem. 99, 17311–17337 (1995).
doi: 10.1021/j100048a004
Wang, Y., Jiang, Y., Hua, J., Tian, H. & Qian, S. Optical limiting properties and ultrafast dynamics of six-branched styryl derivatives based on 1,3,5-triazine. J. Appl. Phys. 110, 033518 (2011).
doi: 10.1063/1.3619796
Wang, Y. et al. Probing ultrafast excited state dynamics and nonlinear absorption properties of three star-shaped conjugated oligomers with 1,3,5-triazine core. RSC Adv. 4, 10960–10967 (2014).
doi: 10.1039/c3ra45544k
Cho, Y. J. et al. The influence of π-conjugation on competitive pathways: charge transfer or electron transfer in new D-π-A and D-π-Si-π-A dyads. Phys. Chem. Chem. Phys. 18, 22921–22928 (2016).
pubmed: 27485173 doi: 10.1039/C6CP03259A
Del Sesto, R. E. et al. Chemical reduction of 2,4,6-tricyano-1,3,5-triazine and 1,3,5-tricyanobenzene. Formation of novel 4,4’,6,6’-tetracyano-2,2’-bitriazine and its radical anion. J. Org. Chem. 68, 3367–3379 (2003).
pubmed: 12713334 doi: 10.1021/jo025833h
Shida, T. Electronic Absorption Spectra of Radical Ions (Elsevier, Amsterdam, 1988).
Osterbacka, R., An, C. P., Jiang, X. M. & Vardeny, Z. V. Two-dimensional electronic excitations in self-assembled conjugated polymer nanocrystals. Science 287, 839–842 (2000).
pubmed: 10657294 doi: 10.1126/science.287.5454.839
Peeks, M. D. et al. Electronic delocalization in the radical cations of porphyrin oligomer molecular wires. J. Am. Chem. Soc. 139, 10461–10471 (2017).
pubmed: 28678489 pmcid: 5543395 doi: 10.1021/jacs.7b05386
Zamadar, M., Asaoka, S., Grills, D. C. & Miller, J. R. Giant infrared absorption bands of electrons and holes in conjugated molecules. Nat. Commun. 4, 2818 (2013).
doi: 10.1038/ncomms3818
Cravino, A. et al. Positive and negative charge carriers in doped or photoexcited polydithienothiophenes: a comparative study using raman, infrared, and electron spin resonance spectroscopy. J. Phys. Chem. B 106, 3583–3591 (2002).
doi: 10.1021/jp013351o
Yin, J., Wang, Z., Fazzi, D., Shen, Z. & Soci, C. First-principles study of the nuclear dynamics of doped conjugated polymers. J. Phys. Chem. C 120, 1994–2001 (2016).
doi: 10.1021/acs.jpcc.5b11764
Harbach, P. H. P. & Dreuw, A. A fresh look at excitonically coupled chromophores from a jahn–teller perspective. Chem. Phys. 377, 78–85 (2010).
doi: 10.1016/j.chemphys.2010.08.018
Saggu, M., Fried, S. D. & Boxer, S. G. Local and global electric field asymmetry in photosynthetic reaction centers. J. Phys. Chem. B 123, 1527–1536 (2019).
pubmed: 30668130 doi: 10.1021/acs.jpcb.8b11458
Serdiuk, I. E. & Roshal, A. D. Exploring double proton transfer: a review on photochemical features of compounds with two proton-transfer sites. Dye. Pigment. 138, 223–244 (2017).
doi: 10.1016/j.dyepig.2016.11.028
Lin, C.-C., Chen, C.-L., Chung, M.-W., Chen, Y.-J. & Chou, P.-T. Effects of multibranching on 3-hydroxyflavone-based chromophores and the excited-state intramolecular proton transfer dynamics. J. Phys. Chem. A 114, 10412–10420 (2010).
pubmed: 20822165 doi: 10.1021/jp105542z pmcid: 20822165
Zhang, Y., Sun, M. & Li, Y. How was the proton transfer process in bis-3, 6-(2-benzoxazolyl)-pyrocatechol, single or double proton transfer? Sci. Rep. 6, 25568 (2016).
pubmed: 27157994 pmcid: 4860645 doi: 10.1038/srep25568
Delor, M. et al. Toward control of electron transfer in donor-acceptor molecules by bond-specific infrared excitation. Science 346, 1492–1495 (2014).
pubmed: 25525241 doi: 10.1126/science.1259995 pmcid: 25525241
Delor, M. et al. On the mechanism of vibrational control of light-induced charge transfer in donor–bridge–acceptor assemblies. Nat. Chem. 7, 689–695 (2015).
pubmed: 26291939 doi: 10.1038/nchem.2327 pmcid: 26291939
Delor, M. et al. Directing the path of light-induced electron transfer at a molecular fork using vibrational excitation. Nat. Chem. 9, 1099–1104 (2017).
pubmed: 29064501 doi: 10.1038/nchem.2793 pmcid: 29064501
Stensitzki, T. et al. Acceleration of a ground-state reaction by selective femtosecond-infrared-laser-pulse excitation. Nat. Chem. 10, 126–131 (2018).
pubmed: 29359754 doi: 10.1038/nchem.2909

Auteurs

Bogdan Dereka (B)

Department of Physical Chemistry, University of Geneva, 30 Quai Ernest-Ansermet, 1211, Geneva, Switzerland.
Department of Chemistry and Institute for Biophysical Dynamics, James Franck Institute, The University of Chicago, 929 E. 57th St., Chicago, IL, 60637, USA.

Denis Svechkarev (D)

Department of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, NE, 68198-6858, USA.

Arnulf Rosspeintner (A)

Department of Physical Chemistry, University of Geneva, 30 Quai Ernest-Ansermet, 1211, Geneva, Switzerland.

Alexander Aster (A)

Department of Physical Chemistry, University of Geneva, 30 Quai Ernest-Ansermet, 1211, Geneva, Switzerland.

Markus Lunzer (M)

Institute of Applied Synthetic Chemistry, TU Wien, Getreidemarkt 9/163/MC, 1060, Vienna, Austria.

Robert Liska (R)

Institute of Applied Synthetic Chemistry, TU Wien, Getreidemarkt 9/163/MC, 1060, Vienna, Austria.

Aaron M Mohs (AM)

Department of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, NE, 68198-6858, USA.
Department of Biochemistry and Molecular Biology, Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, 68198-6858, USA.

Eric Vauthey (E)

Department of Physical Chemistry, University of Geneva, 30 Quai Ernest-Ansermet, 1211, Geneva, Switzerland. eric.vauthey@unige.ch.

Classifications MeSH