Effect of the size of polycyclic aryl groups on the competition between adiabatic/diabatic photoisomerization mechanisms of cis-styrylarenes.
Alessio CesarettiBenedetta CarlottiFausto EliseiAnna SpallettiPublished in: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology (2019)
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 cis-trans photoisomerization has been determined and found to increase when increasing the size of the polycyclic chromophore.