Unusual formation of a N-heterocyclic germylene via homolytic cleavage of a C–C bond
Reaction of the monoanionic radical salt IP˙−K+ (IP = (Py)CH(=NR); Py = C5H4N, R = 2,6-iPr2C6H3; α-iminopyridine) with GeCl2(dioxane) afforded compound (IPGeCl)2 (1) which produced red blocks of IPGe: (2), when treated with KC8 in toluene. 1 is a digermylene formed via C–C coupling between two carbon-centered radicals. 2 can be considered as an analogue of a N-heterocyclic carbene, which exhibits a five-membered GeC2N2 ring with one CC double bond. 2 is formed by two-electron reduction of 1 with cleavage of the two Ge–Cl bonds and the central C–C single bond.