Issue 35, 2005

Reactivity of electrophilic μ-phosphinidene complexes with heterocumulenes: formation of the first σ-π-aminophosphaimine complexes [Mn2(CO)8{μ-η12-P(NiPr2)[double bond, length as m-dash]NR}] and diazoalkane insertions into metal–phosphorus bonds

Abstract

The bridging phosphinidene complexes [Mn2(CO)8(μ-PNiPr2)] and [Co2(CO)4(μ-dppm)( μ-PNR2)] (NR2 = NiPr2, TMP) react with heterocumulenes RN3, CH2N2 and Ph2C[double bond, length as m-dash]N[double bond, length as m-dash]N to form complexes with μ-η12-aminophosphaimine, μ-η12-aminophosphaalkene and μ-η12-aminophosphadiphenylmethylazaimine ligands, respectively.

Graphical abstract: Reactivity of electrophilic μ-phosphinidene complexes with heterocumulenes: formation of the first σ-π-aminophosphaimine complexes [Mn2(CO)8{μ-η1,η2-P(NiPr2) [[double bond, length as m-dash]] NR}] and diazoalkane insertions into metal–phosphorus bonds

Supplementary files

Article information

Article type
Communication
Submitted
18 Apr 2005
Accepted
24 Jun 2005
First published
29 Jul 2005

Chem. Commun., 2005, 4441-4443

Reactivity of electrophilic μ-phosphinidene complexes with heterocumulenes: formation of the first σ-π-aminophosphaimine complexes [Mn2(CO)8{μ-η12-P(NiPr2)[double bond, length as m-dash]NR}] and diazoalkane insertions into metal–phosphorus bonds

T. W. Graham, K. A. Udachin and A. J. Carty, Chem. Commun., 2005, 4441 DOI: 10.1039/B505472A

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