Header menu link for other important links
X
Unusual formation of a N-heterocyclic germylene via homolytic cleavage of a C–C bond
Li Yan, , Stollberg Peter, Zhu Hongping, W. Roesky Herbert, Herbst-Irmer Regine, Stalke Dietmar, Fliegl Heike
Published in Royal Society of Chemistry (RSC)
2014
Volume: 50
   
Issue: 25
Pages: 3356 - 3358
Abstract

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 C=C 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.

About the journal
JournalData powered by TypesetChemical Communications
PublisherData powered by TypesetRoyal Society of Chemistry (RSC)
Open AccessNo