Journal of the American Chemical Society · 2005 · 47 citations · 14 references
Natural SciencesChemistryOrganic ChemistryPhysical ChemistryPolymer ChemistryHalogen ChemistryHeterocyclic ChemistryOrganic SynthesisRadical ReactionsReaction MechanismsFree Radical Chain ReactionsHalogen Atom ReactionsRadical Chain MechanismsRadical MechanismsSilylation Reactions
Reactions of stable silylenes 1 and 2 with a variety of halogenated organic compounds have been studied. Depending on the nature of the halocarbon, the products can be disilanes, LSiX-LSiR, or monosilanes, LSiXR, or a mixture of both types of products. Hexachloroethane reacts with the silylenes to give mainly the dichlorodisilane, LSiX-LSiX. The experimental results are rationalized in terms of several related free-radical chain mechanisms.
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Synthesis and Structure of a Stable Silylene
Michael Denk, Robert P. Lennon, Randy K. Hayashi et al. · Journal of the American Chemical Society · 1994 · 765 citations
Michael Haaf, Thomas A. Schmedake, Robert West · Accounts of Chemical Research · 2000 · 461 citations