Structure-Kinetics Correlations in Isostructural Crystals of α-[ortho-Tolyl)-acetophenones: Pinning Down Electronic Effects Using Laser-Flash Photolysis in the Solid State

摘要

Aqueous suspensions of nanocrystals in the 200-500 run size range of isostructural α-(ortho-tolyl)-acetophenone (1a) and α-(ortho-tolyl)-para-methylacetophe-none (1b) displayed good absorption characteristics for flash photolysis experiments in a flow system, with transient spectra and decay kinetics with a quality that is similar to that recorded in solution. In contrast to solution measurements, reactions in the solid state were characterized by a rate limiting hydrogen transfer reaction from the triplet excited state and a very shortlived biradical intermediate, which does not accumulate. Notably, the rate for δ-hydrogen atom transfer of la (2.7 × 10~7 s~(-1)) in the crystalline phase is 18-fold larger than that of lb (1.5 × 10~6 s~(-1)). With nearly identical molecular and crystal structures, this decrease in the rate of δ-hydrogen abstraction can be assigned unambiguously to an electronic effect by the para-methyl group in 1b, which increases the contribution of the ~3π, π~* configuration relative to the reactive ~3π, π~* configuration in the lowest triplet excited state. These results highlight the potential of relating single crystal X-ray structural data with absolute kinetics from laser flash photolysis.