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)14(μ4-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.
Recommended Citation
Azam, Kazi A.; Bennett, Dennis W.; Hassan, Mohammad R.; Haworth, Daniel T.; Hogarth, Graeme; Kabir, Shariff E.; Lindeman, Sergey V.; Salassa, Luca; Simi, Sultana R.; and Siddiquee, Tasneem, "Double Carbon−Hydrogen Activation of 2-Vinylpyridine: Synthesis of Tri- and Pentanuclear Clusters Containing the μ-NC5H4CH═C Ligand" (2008). Chemistry Faculty Research and Publications. 617.
https://epublications.marquette.edu/chem_fac/617
Comments
Accepted version. Organometallics, Vol. 27, No. 19 (2008): 5163-5166. DOI. © 2008 American Chemical Society. Used with permission.