Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/5256
Title: Synthesis, reactivity and catalytic properties of rhodium complexes of (R,R)-1-benzyl-3,4-dithioetherpyrrolidines
Authors: Diéguez, M. 
Ruiz, A. 
Claver, C. 
Pereira, M. M. 
Flor, M. T. 
Bayón, J. C. 
Serra, M. E. S. 
Rocha Gonsalves, A. M. d'A. 
Keywords: Rhodium complexes; Dithioether ligands; Hydroformylation; Hydrogenation; Hydroboration
Issue Date: 1999
Citation: Inorganica Chimica Acta. 295:1 (1999) 64-70
Abstract: Complexes [Rh(cod)(degusR)]ClO4, where cod is 1,5-cyclooctadiene and degusR represents the homochiral dithioethers (R,R)-1-benzyl-3,4-bis(methylsulfanyl)pyrrolidine, (R,R)-1-benzyl-3,4-bis(isopropylsulfanyl)pyrrolidine and (R,R)-1-benzyl-3,4-bis(phenylsulfanyl)pyrrolidine were prepared and characterized. Their reactivity with CO and PPh3 was investigated. The complexes were assayed as catalysts in hydroformylation of styrene, hydrogenation of acrylic acids and hydroboration of styrene. Although these complexes containing dithioethers behave as catalytic precursors in hydroformylation reaction, the results suggest that mononuclear hydride rhodium carbonyl species is responsible for the catalytic activity. The cationic complexes are not active in the hydrogenation of acrylic acids in the conditions tested. These complexes are moderately active in the hydroboration of styrene with catecholborane, but their selectivities are not satisfactory.
URI: http://hdl.handle.net/10316/5256
DOI: 10.1016/S0020-1693(99)00309-6
Rights: openAccess
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais

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