Photoisomerization of 2,3-diphenylcyclopropane-1-carboxylic acid derivatives

Photochem Photobiol Sci. 2003 Nov;2(11):1101-6. doi: 10.1039/b306337m.

Abstract

Contrary to what is known about cis-1,2-diphenylcyclopropane and its derivatives, we find that they have triplet energies of ca. 311 kJ mol(-1), do not undergo intersystem crossing upon direct excitation, undergo the less common adiabatic photoisomerization to the corresponding trans isomers, and show emission from excited 1,3-diradical intermediates.