Reactivity of Terminal Electrophilic Phosphinidene Complexes: Synthesis of the First Rhenium Phosphinidene, [Re(CO)5(η1-PNiPr2)][AlCl4], and Novel Reactions with Azobenzene
Author:
Affiliation:
1. Steacie Institute for Molecular Sciences, National Research Council of Canada, 100 Sussex Drive, Ottawa, Ontario, Canada K1A 0R6, and The Ottawa-Carleton Chemistry Institute, University of Ottawa, Ottawa, Ontario, Canada K1N 6N5
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om0401307
Reference27 articles.
1. Terminal chloroaminophosphido and aminophosphinidene complexes of molybdenum
2. Electrophilic “Fischer Type” Phosphinidene Complexes of Molybdenum, Tungsten, and Ruthenium
3. Group Transfer from Nickel Imido, Phosphinidene, and Carbene Complexes to Ethylene with Formation of Aziridine, Phosphirane, and Cyclopropane Products
4. Formation of Phosphirenes by Phosphinidene Group-Transfer Reactions from (dtbpe)NiP(dmp) to Alkynes
5. A Thermally Stable and Sterically Unprotected Terminal Electrophilic Phosphinidene Complex of Cobalt and Its Conversion to an η-Phosphirene
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