Heterobimetallic RePd complexes bridged by ? 1: ? 5-Ph 2PC 5H 4 ligand. Synthesis, electronic and crystal structure of (CO) 2(PR 3) (? 5-C 5H 4PPh 2)Re-PdCl 2, R = Me and OMe

Sierra D.; Klahn A.H.; Ramirez-Tagle, R; Arratia-Perez, R; Fuentealba, M; Godoy, F; Teresa Garland M.

Keywords: complexes, spectroscopy, distance, ligands, crystal, density, complexation, synthesis, bond, palladium, structure, ray, rhenium, infrared, ir, theory, bimetallic, crystallography, compounds, calculation, X, (chemical), Functional, Metallic, Hetero, Heterobimetallics

Abstract

The new rhenium complexes (? 5-C 5H 4PPh 2)Re(CO) 2(PR 3) (R = Me (1) and OMe (2)) were prepared photochemically from (? 5-C 5H 4PPh 2)Re(CO) 3 in the presence of PMe 3 or P(OMe) 3. Further reaction of these ligands with PdCl 2(NCPh) 2 in chloroform, produces the heterobimetallic complexes (CO) 2(PMe 3)(? 5-C 5H 4PPh 2)Re-PdCl 2 (3) and (CO) 2(P(OMe) 3)(? 5-C 5H 4PPh 2)Re-PdCl 2 (4). IR spectroscopy reveals that both complexes possess a Re-Pd interaction which was confirmed by X-ray crystallography (Re-Pd bond distance = 2.762 Å in 3 and 2.774 Å in 4). Relativistic functional density theory calculations have also been carried out in order to probe the bonding in these compounds. © 2010 The Royal Society of Chemistry.

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Título de la Revista: DALTON TRANSACTIONS
Volumen: 39
Número: 27
Editorial: ROYAL SOC CHEMISTRY
Fecha de publicación: 2010
Página de inicio: 6295
Página final: 6301
URL: http://www.scopus.com/inward/record.url?eid=2-s2.0-77954283453&partnerID=q2rCbXpz