Abstract
Don't count on counterions: The cyclic five-membered CSi(3)P cation 1 is synthesized in the reaction of benzamidinato-stabilized chlorosilylene and methyl phosphaalkyne. The presence of four π electrons in 1 means it can be considered as a formal, heavier analogue of the cyclopentadienyl cation. Surprisingly the small counteranion (Cl(-)) does not contribute to the ring stability.
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Anions / chemistry
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Cations / chemistry
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Chlorides / chemistry*
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Cyclobutanes / chemical synthesis
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Cyclobutanes / chemistry*
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Models, Molecular
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Molecular Structure
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Organophosphorus Compounds / chemical synthesis
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Organophosphorus Compounds / chemistry*
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Silanes / chemical synthesis
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Silanes / chemistry*
Substances
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Anions
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Cations
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Chlorides
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Cyclobutanes
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Organophosphorus Compounds
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Silanes