Issue 39, 2016

Insertion of phenyl isothiocyanate into a P–P bond of a nickel-substituted bicyclo[1.1.0]tetraphosphabutane

Abstract

A new reaction mode for bicyclo[1.1.0]tetraphosphabutanes is reported. The C[double bond, length as m-dash]S and C[double bond, length as m-dash]N bonds of phenyl isothiocyanate reversibly insert into a P–P bond of [{CpNi(IMes)}2(μ-η11-P4)] (1Mes, IMes = 1,3-bis(2,4,6-trimethylphenyl)imidazolin-2-ylidene), forming isomers 2a and 2b. X-ray crystallography and 31P{1H} NMR spectroscopy revealed similar bicyclo[3.1.0]heterohexane structures for these compounds.

Graphical abstract: Insertion of phenyl isothiocyanate into a P–P bond of a nickel-substituted bicyclo[1.1.0]tetraphosphabutane

Supplementary files

Article information

Article type
Communication
Submitted
21 Feb 2016
Accepted
11 Apr 2016
First published
11 Apr 2016
This article is Open Access
Creative Commons BY license

Chem. Commun., 2016,52, 6601-6604

Author version available

Insertion of phenyl isothiocyanate into a P–P bond of a nickel-substituted bicyclo[1.1.0]tetraphosphabutane

S. Pelties, A. W. Ehlers and R. Wolf, Chem. Commun., 2016, 52, 6601 DOI: 10.1039/C6CC01572G

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