Issue 9, 2009

Synthesis and structure of indenyl rhodium(I) complexes containing unsaturated phosphines: catalyst precursors for alkene hydroboration

Abstract

The indenyl compound (η5-C9H7)Rh(coe)2 (1, coe = cis-cyclooctene) has been prepared as a thermally stable alternative to the diethylene derivative (η5-C9H7)Rh(η2-H2C[double bond, length as m-dash]CH2)2. Compound 1 reacts with unsaturated phosphines Ph2PR (R = CH[double bond, length as m-dash]CH2, 2; CH2CH[double bond, length as m-dash]CH2, 3; and C[triple bond, length as m-dash]C-tert-Bu, 4) to give complexes of the type (η5-C9H7)Rh(Ph2PR)2, where bonding occurs through the phosphorus atom. Addition of Ph2PC[triple bond, length as m-dash]CPPh2 to 1 gave the dimer [(η5-C9H7)Rh(μ-Ph2PC[triple bond, length as m-dash]CPPh2)]2 (5). Solution and solid state data showed that these new phosphine complexes have only a moderate amount of distortion within the indenyl ring. These compounds were found to catalyse the hydroboration of vinylarenes and the first example of an internal hydroboration of diphenylvinylphosphine has been reported.

Graphical abstract: Synthesis and structure of indenyl rhodium(I) complexes containing unsaturated phosphines: catalyst precursors for alkene hydroboration

Supplementary files

Article information

Article type
Paper
Submitted
17 Jul 2008
Accepted
12 Nov 2008
First published
20 Jan 2009

Dalton Trans., 2009, 1624-1631

Synthesis and structure of indenyl rhodium(I) complexes containing unsaturated phosphines: catalyst precursors for alkene hydroboration

C. N. Garon, D. I. McIsaac, C. M. Vogels, A. Decken, I. D. Williams, C. Kleeberg, T. B. Marder and S. A. Westcott, Dalton Trans., 2009, 1624 DOI: 10.1039/B812259H

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