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One- and two-photon absorption properties of quadrupolar thiophene-based dyes with acceptors of varying strengths.


ABSTRACT: The one-photon (1P) and two-photon (2P) absorption properties of three quadrupolar dyes, featuring thiophene as a donor and acceptors of varying strengths, are determined by a combination of experimental and computational methods employing the density functional theory (DFT). The emission shifts in different solvents are well reproduced by time-dependent DFT calculations with the linear response and state specific approaches in the framework of the polarizable continuum model. The calculations show that the energies of both 1P- and 2P-active states decrease with an increase of the strength of the acceptor. The 2P absorption cross-sections predicted by the response theory are accounted for by considering just one intermediate state (S1) in the sum-over-states formulation. For the chromophore featuring the stronger acceptor, the energetic positions of the 1P- and 2P-active states prevent the exploitation of the theoretically predicted very high 2P activity due to the competing 1P absorption into the S1 state.

SUBMITTER: Canola S 

PROVIDER: S-EPMC6713623 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature

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One- and two-photon absorption properties of quadrupolar thiophene-based dyes with acceptors of varying strengths.

Canola Sofia S   Mardegan Lorenzo L   Bergamini Giacomo G   Villa Marco M   Acocella Angela A   Zangoli Mattia M   Ravotto Luca L   Vinogradov Sergei A SA   Di Maria Francesca F   Ceroni Paola P   Negri Fabrizia F  

Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20190228 9


The one-photon (1P) and two-photon (2P) absorption properties of three quadrupolar dyes, featuring thiophene as a donor and acceptors of varying strengths, are determined by a combination of experimental and computational methods employing the density functional theory (DFT). The emission shifts in different solvents are well reproduced by time-dependent DFT calculations with the linear response and state specific approaches in the framework of the polarizable continuum model. The calculations s  ...[more]

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