?-Diketones derived from cyclopentadienyl rhenium tricarbonyl
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.
Más información
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 |