A Thermally Stable and Sterically Unprotected Terminal Electrophilic Phosphinidene Complex of Cobalt and Its Conversion to an η-Phosphirene-Reference-Cited by-同舟云学术

A Thermally Stable and Sterically Unprotected Terminal Electrophilic Phosphinidene Complex of Cobalt and Its Conversion to an η-Phosphirene

Published:2003-02-07 Issue:9 Volume:125 Page:2404-2405
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Sánchez-Nieves Javier¹,Sterenberg Brian T.¹,Udachin Konstantin A.¹,Carty Arthur J.¹

Affiliation:

1. Steacie Institute for Molecular Sciences, National Research Council of Canada, 100 Sussex Drive, Ottawa, Ontario, Canada K1A 0R6, and Ottawa-Carleton Chemistry Research Institute, Department of Chemistry, University of Ottawa, Ottawa, Ontario, Canada K1N 6N5

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja028303b

Reference33 articles.

1. The first stable transition metal (molybdenum or tungsten) complexes having a metal–phosphorus(III) double bond: the phosphorus analogues of metal aryl- and alkyl-imides; X-ray structure of [Mo(η-C5H5)2(PAr)](Ar = C6H2But3-2,4,6)

2. Terminal Phosphinidene and Heavier Congeneric Complexes. The Quest Is Over

3. Cleavage of a phosphorus-carbon double bond and formation of a linear terminal phosphinidene complex

4. Phosphinidene Transfer Reactions of the Terminal Phosphinidene Complex Cp2Zr(:PC6H2-2,4,6-t-Bu3)(PMe3)

5. Arsinidene, Phosphinidene, and Imide Formation via 1,2-H2-Elimination from (silox)3HTaEHPh (E = N, P, As): Structures of (silox)3Ta:EPh (E = P, As)

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