2015
DOI: 10.1063/1.4907758
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Valence-bond non-equilibrium solvation model for a twisting monomethine cyanine

Abstract: We propose and analyze a two-state valence-bond model of non-equilibrium solvation effects on the excited-state twisting reaction of monomethine cyanines. Suppression of this reaction is thought responsible for environment-dependent fluorescence yield enhancement in these dyes. Fluorescence is quenched because twisting is accompanied via the formation of dark twisted intramolecular charge-transfer (TICT) states. For monomethine cyanines, where the ground state is a superposition of structures with different bo… Show more

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Cited by 4 publications
(3 citation statements)
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References 91 publications
(126 reference statements)
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“…As is well known, dark twisted intramolecular charge-transfer (TICT) states controlled by the conical intersections are essential in photophysics of monomeric cyanines. 52,53 In addition, the involvement of dark electronic states in the LHNs’ excited state dynamics was previously postulated in ref. 32, where narrow band excitation pump–probe experiments were performed at cryogenic temperature.…”
Section: Resultsmentioning
confidence: 81%
“…As is well known, dark twisted intramolecular charge-transfer (TICT) states controlled by the conical intersections are essential in photophysics of monomeric cyanines. 52,53 In addition, the involvement of dark electronic states in the LHNs’ excited state dynamics was previously postulated in ref. 32, where narrow band excitation pump–probe experiments were performed at cryogenic temperature.…”
Section: Resultsmentioning
confidence: 81%
“…However, TPAHPyMe was almost non-emissive in any solvent (Figures S15 and S16, Supporting Information), which might be due to its more twisted conformation and the absence of strong intramolecular hydrogen bond. [11] The quenching effect of the pyridinium salt can be further verified by the lower fluorescence intensity of TPAHPy in the acidic environment (Figures S17-S19, Supporting Information).…”
Section: Resultsmentioning
confidence: 81%
“…There is a large family of related monomethyne dyes which share a similar bridging motif and electronic structure to p -HBDI. 74 This promises a range of possibilities to both modify MEPs to optimise isomerization yield and to design sites which allow the proposed light driven torsion couple to be incorporated into molecular machines.…”
Section: Discussionmentioning
confidence: 99%