Photoisomerisation of α-(thiopyran-2-ylidene) ketones; substituent effects
Abstract
In a series of ten substituted α-(thiopyran-2-ylidene) ketones, the stable Z-form is transformed into the E-isomer upon irradiation. The photoproduct reverts to the starting material by a dark process, which obeys first-order kinetics. The rate constants for the EZ-isomerization are controlled mainly by steric factors. The activation energy for the thermal reversion is ca. 10 kcal mol–1.