2-PHOTON CHEMISTRY IN THE LASER JET - GENERATION OF RADICAL INTERMEDIATES AND THEIR PHOTOCHEMICAL-TRANSFORMATIONS

The novel laser jet technique provides sufficiently high photon densities to permit the observation of the photochemistry of photochemically generated radicals (two-photon chemistry) in the liquid phase. Four recent applications of this novel, photochemically useful method are presented: these include the photochemistry of hydroxydiphenylmethyl, 9-hydroxyxanthenyl, diphenylmethyl, and benzoyl radicals under laser jet and normal photolysis conditions. The regioselectivity of cross-coupling reactions of hydroxydiphenylmethyl or 9-hydroxyxanthenyl radicals with solvent-derived radicals changes when these species are electronically excited, i.e. under the high-intensity conditions of the laser jet, cross-coupling at the para position (head-to-tail combination) is significantly enhanced relative to the normal coupling mode at the hydroxy-bearing radical site (head-to-head combination). Semiempirical calculations of the spin density distributions for the ground and first excited states of the radicals confirm the change in spin density from the hydroxy-bearing carbon atom to the conjugating benzene rings in these radical species on photoexcitation. For the diphenylmethyl radical, two reaction pathways have been observed under the high photon densities of the laser jet: the electronically excited diphenylmethyl radical can either abstract a chlorine atom from carbon tetrachloride through an electron transfer process or can be photoionized on further photoexcitation (multiphoton chemistry). The resulting benzhydryl cation was trapped by methanol as the corresponding ether product, which unequivocally demonstrates that carbene formation by photoejection of a hydrogen atom does not take place under laser jet photolysis conditions. An advantage of the high photon densities produced in laser jet photolysis is the high steady state concentration of short-lived transients that are generated, which enable unprecedented intermolecular reactions to be observed. Thus, about a millimolar concentration of tert-butoxy radicals can be obtained in the laser jet photocleavage of tert-butyl peroxide. When the tert-butoxy radicals are produced in the presence of benzaldehyde, the main product is tert-butyl benzoate. If carbon tetrachloride is also present, chlorobenzene can be detected. This is rationalized as the product derived from chlorine abstraction by phenyl radicals, which are presumably produced by the photodecarbonylation of benzoyl radicals. An alternative method of obtaining benzoyl radicals is the two-photon cleavage of benzil. The laser jet photolysis of benzil in tert-butyl peroxide yields mainly tert-butyl benzoate, whereas in carbon tetrachloride, benzoyl chloride, chlorobenzene and alpha,alpha,alpha-trichloroacetophenone are observed. The first two products result from chlorine atom abstraction by the photochemically generated benzoyl and phenyl radicals, and the last product from in-cage cross-coupling between benzoyl and trichloromethyl radicals. Such product studies provide detailed mechanistic information on the photochemical behaviour of electronically excited, short-lived transients which complements nicely the kinetic and spectral data of time-resolved laser flash studies. Consequently, the laser jet technique constitutes a valuable tool for determining the mechanism of two-photon reactions.