Issue 9, 2019

Effect of the size of polycyclic aryl groups on the competition between adiabatic/diabatic photoisomerization mechanisms of cis-styrylarenes

Abstract

The occurrence of adiabatic photoisomerization in the singlet manifold directly from 1Z* to 1E* has been found to be more common than expected. This mechanism has been experimentally evidenced through a detailed fluorimetric study for a large series of styrylarenes. Its weight on the overall cistrans photoisomerization has been determined and found to increase when increasing the size of the polycyclic chromophore.

Graphical abstract: Effect of the size of polycyclic aryl groups on the competition between adiabatic/diabatic photoisomerization mechanisms of cis-styrylarenes

Supplementary files

Article information

Article type
Paper
Submitted
04 janv. 2019
Accepted
25 mars 2019
First published
29 mars 2019

Photochem. Photobiol. Sci., 2019,18, 2125-2135

Effect of the size of polycyclic aryl groups on the competition between adiabatic/diabatic photoisomerization mechanisms of cis-styrylarenes

A. Cesaretti, B. Carlotti, F. Elisei and A. Spalletti, Photochem. Photobiol. Sci., 2019, 18, 2125 DOI: 10.1039/C9PP00009G

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