M. Caselli et al., MODELING OF THE CIS-TRANS PARTITIONING IN THE PHOTOISOMERIZATIONS OF CYANINES AND STILBENE DERIVATIVES, Chemical physics letters, 216(1-2), 1993, pp. 41-46
In the course of photoisomerization, polymethine cyanines as well as s
tilbene and its derivates decay from the S1 potential energy minimum,
corresponding to the perpendicular geometry, to yield either cis or tr
ans ground-state molecules. The fraction of cis isomers obtained, alph
a, spans a larger range of values for symmetric cyanines than for stil
bene derivatives. It is argued that such different behaviour for the t
wo classes of compounds should be traceable to the electronically diff
erent nature of their S1 perp species. Making use of radiationless tra
nsition theory results, it is shown that the relative location of the
S1 minimum and S0 maximum along the internal rotation coordinate is cr
ucial to the evaluation of alpha: even small differences between these
critical twisting angles, which are more reasonably expected for poly
methine cyanines than for stilbene-like compounds, may cause strong de
viations from equipartitioning (alpha = 0. 5 ).