Issue 48, 2019

Synthesis of metallophosphaalkenes by reaction of organometallic nucleophiles with a phosphaethynolato-borane

Abstract

We describe the reaction of a phosphaethynolato-borane [B]OCP ([B] = N,N′-bis(2,6-diisopropylphenyl)-2,3-dihydro-1H-1,3,2-diazaboryl) with the organometallic nucleophile Na[Cp*Fe(CO)2] (Cp* = pentamethylcyclopentadienyl). The electrophilic character of [B]OCP allows for a new route towards the formation metal–phosphorus bonds affording a metallophosphaalkene that can be functionalised at both the oxygen and phosphorus atoms depending on the reagents employed.

Graphical abstract: Synthesis of metallophosphaalkenes by reaction of organometallic nucleophiles with a phosphaethynolato-borane

Supplementary files

Article information

Article type
Communication
Submitted
18 Apr 2019
Accepted
14 May 2019
First published
14 May 2019

Chem. Commun., 2019,55, 6842-6845

Synthesis of metallophosphaalkenes by reaction of organometallic nucleophiles with a phosphaethynolato-borane

D. W. N. Wilson and J. M. Goicoechea, Chem. Commun., 2019, 55, 6842 DOI: 10.1039/C9CC03040A

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