Hydroformylation of synthetic naphtha catalyzed by a dinuclear gem-dithiolato-bridged rhodium(I) complex
Resumen: This work focuses on the use of a gem-dithiolato-bridged rhodium(I) Rh 2(µ-S 2CBn 2)(cod) 2 complex (cod = 1,5-cyclooctadiene, Bn 2CS 2 2- = 1,3-diphenyl-2,2-dithiolatopropane) dissolved in toluene in the presence of monodentate phosphite P-donor ligand (P(OPh) 3) under carbon monoxide/hydrogen (1:1, syngas) atmosphere as an effective catalyst for hydroformylation of some olefins (oxo-reactions). The capability of this system to catalyze the hydroformylation of hex-1-ene, cyclohexene, 2,3-dimethyl-but-1-ene and 2-methyl-pent-2-ene and their quaternary mixture (synthetic naphtha) has been demonstrated. This innovative method to perform the in situ hydroformylation of the olefins present in naphthas to oxygenated products would be a promissory work for a future industrial catalytic process applicable to gasoline improving based on oxo-reactions. An important observation is that variation of CO/H 2 pressure (6.8-34.0 atm), temperature (60-80 oC), reaction time (2-10 h), rhodium concentration ((1.0-1.8)x10 -3 mol/L) affect hydroformylation reaction rates. Optimal conversion to oxygenated products were achieved under Rh = 1.8 x10 -2 mol/L, P(CO/H 2) = 34 atm (CO/H 2 = 1:1) at 80 oC for 10 h.
Idioma: Inglés
DOI: 10.2174/1876214X01003010044
Año: 2010
Publicado en: Open catalysis journal 3, 1 (2010), 44-49
ISSN: 1876-214X

Factor impacto SCIMAGO:

Financiación: info:eu-repo/grantAgreement/ES/MINECO-FEDER/CTQ2006-03973
Tipo y forma: Article (Published version)
Área (Departamento): Química Inorgánica (Departamento de Química Inorgánica)
Exportado de SIDERAL (2017-05-04-10:19:22)

Este artículo se encuentra en las siguientes colecciones:
articulos > articulos-por-area > quimica_inorganica



 Notice créée le 2016-04-08, modifiée le 2017-05-04


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