UNIGE document Scientific Article
previous document  unige:96318  next document
add to browser collection

Ultrafast Elementary Photochemical Processes of Organic Molecules in Liquid Solution

Published in Chemical Reviews. 2017, vol. 117, no. 16, p. 10826-10939
Abstract Ultrafast photochemical reactions in liquids occur on similar or shorter time scales compared to the equilibration of the optically populated excited state. This equilibration involves the relaxation of intramolecular and/or solvent modes. As a consequence, the reaction dynamics are no longer exponential, cannot be quantified by rate constants, and may depend on the excitation wavelength contrary to slower photochemical processes occurring from equilibrated excited states. Such ultrafast photoinduced reactions do no longer obey the Kasha–Vavilov rule. Nonequilibrium effects are also observed in diffusion-controlled intermolecular processes directly after photoexcitation, and their proper description gives access to the intrinsic reaction dynamics that are normally hidden by diffusion. Here we discuss these topics in relation to ultrafast organic photochemical reactions in homogeneous liquids. Discussed reactions include intra- and intermolecular electron- and proton-transfer processes, as well as photochromic reactions occurring with and without bond breaking or bond formation, namely ring-opening reactions and cis–trans isomerizations, respectively.
Full text
Research group Groupe Vauthey
(ISO format)
KUMPULAINEN, Tatu Samuli et al. Ultrafast Elementary Photochemical Processes of Organic Molecules in Liquid Solution. In: Chemical Reviews, 2017, vol. 117, n° 16, p. 10826-10939. https://archive-ouverte.unige.ch/unige:96318

91 hits



Deposited on : 2017-08-28

Export document
Format :
Citation style :