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Conversion of a singlet silylene to a stable biradical
, Roesky H.W., Schwarzer M.C., Frenking G., Tkach I., Wolf H., Kratzert D., Herbst-Irmer R., Niepötter B., Stalke D.
Published in Wiley Online Library
2013
Volume: 52
   
Issue: 6
Pages: 1801 - 1805
Abstract
Silicon becomes colored: Stable biradicals were prepared from an N-heterocyclic carbene stabilized SiCl2 and a cyclic alkyl(amino)carbene, and characterized as two polymorphs. The deep-blue crystals of one polymorph are stable upon exposure to air for about a week, while the solution in THF decomposes rapidly when exposed to air. In a side reaction, the different carbene species react with each other under C-H activation and C-C bond formation in the presence of the biradical. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
About the journal
JournalData powered by TypesetAngewandte Chemie - International Edition
PublisherData powered by TypesetWiley Online Library
ISSN14337851
Open AccessNo