Preparation, Structural Characterization, and Photochemical Reactions of Silyl- and Germylborates

Silylborates (Li[PhnMe3-nSiBPh3], n = 1−3) and germylborates (Li[PhnMe3-nGeBPh3], n = 1−3; M[Et3GeBPh3], M = Li, Na, K) were prepared by the reaction of the corresponding silyl- and germylalkali
metals with triphenylborane in a hexane/benzene mixed solvent. The silyl- and germylborates were fully
identified by 1H, 13C, 11B, and 7Li NMR spectroscopic methods. The solid-state structure of germylborates
Li[Ph3GeBPh3] and M[Et3GeBPh3] (M = Li and Na) were determined by X-ray diffraction analyses.
The polymeric structure of M[Et3GeBPh3] was observed in the solid state and in hydrocarbon solution.
The alkali metal atoms were located near the center of the benzene ring of triphenylborane and interacted
with the neighboring borate molecules by Li+−π interaction. The polymeric structure was broken by the
addition of MeOH. However, M[Et3GeBPh3] was coordinated by three MeOH molecules to form a dimeric
structure without methanolysis reaction. The primary processes in photochemical reactions of silyl- and
germylborates were investigated by chemical trapping experiments and the CIDEP (chemical-induced
dynamic electron polarization) method. The cleavage of the Ge−B (or Si−B) bonds of germylborates
(or silylborates) was considered most probably to occur from their triplet states.