Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.336317
Title: Synthesis, structure and reaction studies of diphosphine rhodium complexes
Author: Crabtree, Simon Peter
ISNI:       0000 0001 3394 3097
Awarding Body: Durham University
Current Institution: Durham University
Date of Award: 1996
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Abstract:
A series of complexes of the type [Rh(diphos)(C(_7)H(_8))](BF(_4)) (1) have been synthesised and two of these species [diphos = Bu(^1)(_2)P(CH(_2))(_2)PBu(^1)(_2), Cy(_2)P(l,2-trans-cyclopentane)PCy(_2)] have been characterised by X-ray crystallography. The influence of the chelating diphosphine on the structural characteristics and NMR parameters of these compounds has been investigated. Complexes of the type (1) are active catalysts for the hydroformylation of l-hexene(120ºC, 450psi 2:1 H(_2):C0). However, they are inactive for the related hydroesterification process and this is attributed to the stability of [Rh(diphos)(CO)(_2)]^ under the reaction conditions. Detailed studies of the reactions of type (1) complexes with H(_2) have been undertaken. The products from these reactions are dependent on both the diphosphine and the solvent employed. In THF and CD(_2)Cl(_2), dimeric hydrides were observed, whilst in CDCl(_3) hydrido-chloro-complexes of the type [Rh(_z)(diphos)(_2)(|µCl)H(_2)](^2+) were formed. In the former solvents, three types of hydrides have been identified by NMR studies, namely [Rh(_2)(diphos)(_2)H(_6)], [Rh(_2)(diphos)(_2)H(_4)] and [Rh(_2)(diphos)(_2)H(_4)](^2+). The oxidative-addition reactions of alkyl-, acyl- and formyl-halide with Rh(I) complexes have been investigated. The reaction with ClCO(_2)Me with [Rh(dppe)Cl](_2) and [Rh(dppe)](_2)(BF(_4))(_2) led to the formation of diphosphine-rhodium(III)-halide species (H(_3)NOH)[Rh(dppe)Cl(_4)] and [Rh(_2)(dppe)(_2)(µ-Cl)(_3)Cl(_2)](BF(_4)) respectively. Alternative routes to these complexes have been investigated starting from RhCl(_3).3H(_2)O/diphosphines and a series of the novel halide bridged dimers have been characterised, including by X-ray crystallography and their reaction chemistry explored. In the synthesis of the cationic rhodium complexes from neutral chloro-complexes with AgBF(_4), the novel silver complexes [Ag(_2)(µ-Bu(^t)(_2)P(CH(_2))(_3)PBu(^t)(_2))(_2)](BF(_4))(_2), [{Ag(H(_2)O)}(_2)(µ-Bu(^t)(_2)P(CH(_2))(_2)PBu(^t)(_2))](BF(_4))(_2), and [Ag(C(_6)D(_6))(_3)BF(_4)] have been isolated as by-products and characterised by X-ray crystallography.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.336317  DOI: Not available
Keywords: Hydrides; X-ray crystal structure Chemistry, Inorganic Chemistry, Physical and theoretical Solid state physics
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