Photoreactions in the Gas-Phase Complexes of Mg•+−Dioxanes

Abstract

Photoreactions in the gas-phase complexes Mg(*+)(1,4-dioxane) (1) and Mg(*+)(1,3-dioxane) (1M) have been examined in the wavelength region of 230-440 nm. Photoproduct assignments are facilitated with the help of deuterium substitution experiments. The main energy relaxation channel for both photoexcited complexes is the evaporation of Mg(*+). Also observed from 1 are rich photoproducts with m/z 28, 41, 54-58, 67, 69, and 88; the most abundant one at m/z 54 is designated to Mg(*+)(O=CH(2)). In marked contrast, the photolysis of 1M yields only Mg(*+)(O=CH(2)) other than Mg(*+). Density functional calculations are performed to obtain optimized geometries and potential energy surfaces of 1 and 1M. Although Mg(*+)(chair-1,4-C(4)H(8)O(2)) (1a) and Mg(*+)(boat-1,4-C(4)H(8)O(2)) (1b) are comparable in energy, the much better agreement of the experimental action spectrum of Mg(*+)(1,4-C(4)H(8)O(2)) with the calculated absorption spectrum of 1a than with that of 1b indicates the predominance of 1a in the source due to the stability of the chair-1,4-dioxane. For photoreactions, the C-O bond is found to be much more prone to rupture than the C-C bond due to the coordination of O to Mg(+) in the parent complexes. Photoreaction mechanisms are discussed in terms of two key insertion complexes, which rationalize all of the observed photoproducts.