Document Type

Article

Language

eng

Publication Date

2008

Publisher

American Chemical Society

Source Publication

Organometallics

Source ISSN

0276-7333

Abstract

Reactions of 2-vinylpyridine with the triruthenium complexes [Ru3(CO)12] and [Ru3(CO)10(μ-dppm)] leads to a previously unknown double carbon−hydrogen bond activation of the β-carbon of the vinyl group to afford the pentaruthenium and triruthenium complexes [Ru5(CO)144-C5H4CH═C)(μ-H)2] (1) and [Ru3Cl(CO)5(μ-CO)(μ-dppm)(μ3-NC5H4CH═C)(μ-H)] (2), respectively. Crystal structures reveal two different forms of bridging of the dimetalated 2-vinylpyridyl ligand, capping a square face in 1 and a triangular face in 2.

Comments

Accepted version. Organometallics, Vol. 27, No. 19 (2008): 5163-5166. DOI. © 2008 American Chemical Society. Used with permission.

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