Ruthenium Arene Derivatives of Chiral Ferrocene-Based P,N or P,O Ligands. Transformation of Chloro–Alcohol into Hydrido–Carbonyl Complexes
Autor: | M. Carmen Carrión, Javier Rodríguez Torres, Afrooz Zirakzadeh, Blanca R. Manzano, M. Angeles de la Peña, A. E. Mucientes, Francisco Sepúlveda, Félix A. Jalón, Ana M. Rodríguez, Walter Weissensteiner |
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Rok vydání: | 2011 |
Předmět: | |
Zdroj: | Organometallics. 30:3490-3503 |
ISSN: | 1520-6041 0276-7333 |
DOI: | 10.1021/om1008132 |
Popis: | Several ferrocene-based chiral nonracemic aminophosphine and racemic hydroxyphosphine ligands have been used in the synthesis of RuII(arene) derivatives (arene = p-cymene, benzene). The reaction of suitable ruthenium complexes with the aminophosphine (P,N) ligands and NaBPh4 led to chelate complexes [RuCl(arene)(P,N)]BPh4 in which the ferrocenyl ligand is coordinated in a bidentate fashion. When these reactions were carried out with the hydroxyphosphine (P,O) ligands the alcohol functionality was oxidized, and hydrido–ketone (or hydrido–aldehyde) derivatives of the type [RuH(arene)(PC═O)]BPh4 were obtained. The structures of two derivatives containing either an aminophosphine or a ketophosphine ligand were determined by X-ray diffraction. The reaction of the hydroxyphosphine ligands with the ruthenium precursors was studied in detail. Derivatives with coordinated hydroxyphosphine ligands were isolated and, in the case of a p-cymene hydroxyphosphine derivative, the rate constants and also the thermal and t... |
Databáze: | OpenAIRE |
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