Issue 8, 2003

Diastereoselective formation of a dipalladium(i) complex supported by a bridging tetradentate ligand, and oxidative addition of RS–H across a phosphine-bridged PdI–PdI bond

Abstract

The ligand CH2(P(o-C6H4NMe2)2)2 (dmapm) gives access to the first example of a dipalladium(I) complex supported by a tetradentate ligand, Pd2Cl2(μ-N,P,P,N-dmapm), which, unlike the well-known Pd2X2(μ-dppm)2 complexes (X = halide, dppm = bis(diphenylphosphino)methane), reacts with thiols to give addition of RS–H across a phosphine-bridged Pd–Pd bond.

Graphical abstract: Diastereoselective formation of a dipalladium(i) complex supported by a bridging tetradentate ligand, and oxidative addition of RS–H across a phosphine-bridged PdI–PdI bond

Supplementary files

Article information

Article type
Communication
Submitted
07 Jan 2003
Accepted
06 Mar 2003
First published
20 Mar 2003

Chem. Commun., 2003, 988-989

Diastereoselective formation of a dipalladium(I) complex supported by a bridging tetradentate ligand, and oxidative addition of RS–H across a phosphine-bridged PdI–PdI bond

S. Jo Ling Foo, N. D. Jones, B. O. Patrick and B. R. James, Chem. Commun., 2003, 988 DOI: 10.1039/B300177F

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