Issue 12, 2011

Stille-type aryl–aryl cross-coupling catalysis using triarylphosphine ligands with electron-rich Fe(ii)-alkynyl substituents

Abstract

The synthesis of four new phosphane ligands featuring electron-rich Fe(II) “(η2-dppe)(η5-C5Me5)FeC[triple bond, length as m-dash]C-” substituents in para and meta position(s) on the aryl rings (1–4) is reported along with those of the corresponding PdCl2(PAr3)2 precatalysts (7–10). These precatalysts have then been tested in a Stille-type aryl–aryl cross coupling reaction. It is shown that these new ligands survive the reaction conditions and perform at least as well as the classic triphenylphosphine ligand for this transformation.

Graphical abstract: Stille-type aryl–aryl cross-coupling catalysis using triarylphosphine ligands with electron-rich Fe(ii)-alkynyl substituents

Supplementary files

Article information

Article type
Letter
Submitted
03 Jun 2011
Accepted
19 Sep 2011
First published
10 Oct 2011

New J. Chem., 2011,35, 2740-2742

Stille-type aryl–aryl cross-coupling catalysis using triarylphosphine ligands with electron-rich Fe(II)-alkynyl substituents

G. Grelaud, A. Tohmé, G. Argouarch, T. Roisnel and F. Paul, New J. Chem., 2011, 35, 2740 DOI: 10.1039/C1NJ20480G

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