Issue 10, 2003

The truly symmetrical doubly-bridging mode of trimethylphosphine in a dinuclear rhodium complex

Abstract

The dinuclear complex [Rh2I2(μ-CPh2)2(μ-PMe3)] was prepared from the Rh2(acac)2 counterpart and Me3SiI and shown crystallographically to contain the PMe3 ligand in a truly symmetrical bridging position; a new synthetic route to migrate more bulky phosphines such as PPh3 and PiPr3 from a terminal into a bridging site is also described.

Graphical abstract: The truly symmetrical doubly-bridging mode of trimethylphosphine in a dinuclear rhodium complex

Supplementary files

Article information

Article type
Communication
Submitted
30 Jan 2003
Accepted
14 Mar 2003
First published
16 Apr 2003

Chem. Commun., 2003, 1136-1137

The truly symmetrical doubly-bridging mode of trimethylphosphine in a dinuclear rhodium complex

T. Pechmann, C. D. Brandt and H. Werner, Chem. Commun., 2003, 1136 DOI: 10.1039/B301251D

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