?-Diketones derived from cyclopentadienyl rhenium tricarbonyl

Cautivo, T; Godoy, F; Klahn A.H.; Buono-Core G.E.; Sierra D.; Fuentealba, M; Garland M.T.

Abstract

The acetyl complex (?5-C5H4COCH3)Re(CO)3 reacts with KOtBu and an excess of appropriate ester to provide cyrhetrenyl-?-diketones complexes (?5-C5H4COCH2COR)Re(CO)3 (R = CF3, 1a; CH3, 1b; Ph, 1c). These new 1,3-diketones exist predominantly as enol tautomer, although a enol/keto mixture of approx. 10:1 is present in complexes 1b-c, in chloroform-d solution. The complexes have been characterized by spectroscopic techniques IR, 1H and 13C NMR and mass spectrometry. X-ray crystallography of complex 1b shows that only the enol form occurs in the solid state. The O-C-C-C-O fragment of the molecule is planar with asymmetric enolisation in the direction furthest from the cyrhetrenyl group. © 2007 Elsevier B.V. All rights reserved.

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Título de la Revista: INORGANIC CHEMISTRY COMMUNICATIONS
Volumen: 10
Número: 9
Editorial: Elsevier
Fecha de publicación: 2007
Página de inicio: 1031
Página final: 1034
URL: http://www.scopus.com/inward/record.url?eid=2-s2.0-34547839718&partnerID=q2rCbXpz