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Royal Society of Chemistry, Chemical Communications, 25(50), p. 3356-3358, 2014

DOI: 10.1039/c4cc00251b

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Unusual formation of a N-heterocyclic germylene via homolytic cleavage of a C-C bond

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

Deutsche Forschungsgemeinschaft [RO 224/60-1]; Danish National Research Foundation [DNRF93]; Centre for Materials Crystallography; Norwegian Research Council through the CoE Centre for Theoretical and Computational Chemistry (CTCC) [179568/V30]; China Scholarship Council; Norwegian Supercomputing Program (NOTUR) [NN4654K] ; Reaction of the monoanionic radical salt IP center dot-K+ (IP = (Py)CH(=NR); Py = C5H4N, R = 2,6-iPr(2)C(6)H(3); alpha-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 CQC 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.