Issue 11, 2012

Fluorescence and two-photon absorption of push–pull aryl(bi)thiophenes: structure–property relationships

Abstract

Photophysical and TPA properties of series of push–pull aryl(bi)thiophene chromophores bearing electron-donating (D) and electron-withdrawing (A) end-groups of increasing strength are presented. All compounds show an intense intramolecular charge transfer (ICT) absorption band in the visible region. Increasing the D and/or A strength as well as the length of the conjugated path induces bathochromic and hyperchromic shifts of the absorption band as reported for analogous push–pull polyenes. Yet, in contrast with corresponding push–pull polyenes, a significant increase in fluorescence is observed. In particular, chromophores built from a phenyl–bithienyl conjugated path and bearing strong D and A end-groups were found to combine very large one and two-photon brightness as well as strong emission in the red/NIR region. These molecules hold promise as biphotonic fluorescent probes for bioimaging.

Graphical abstract: Fluorescence and two-photon absorption of push–pull aryl(bi)thiophenes: structure–property relationships

Supplementary files

Article information

Article type
Paper
Submitted
19 Jul 2012
Accepted
31 Aug 2012
First published
17 Sep 2012

Photochem. Photobiol. Sci., 2012,11, 1756-1766

Fluorescence and two-photon absorption of push–pull aryl(bi)thiophenes: structure–property relationships

E. Genin, V. Hugues, G. Clermont, C. Herbivo, M. C. R. Castro, A. Comel, M. M. M. Raposo and M. Blanchard-Desce, Photochem. Photobiol. Sci., 2012, 11, 1756 DOI: 10.1039/C2PP25258A

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