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

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Abstract

A new reaction mode for bicyclo[1.1.0]tetraphosphabutanes is reported. The CS and CN bonds of phenyl isothiocyanate reversibly insert into a P-P bond of [{CpNi(IMes)}2(μ-η1:η1-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.

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Pelties, S., Ehlers, A. W., & Wolf, R. (2016). Insertion of phenyl isothiocyanate into a P-P bond of a nickel-substituted bicyclo[1.1.0]tetraphosphabutane. Chemical Communications, 52(39), 6601–6604. https://doi.org/10.1039/c6cc01572g

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