Please use this identifier to cite or link to this item: https://doi.org/10.1016/S1381-1169(03)00423-0
Title: Rh4(CO)12-derived functionalized MCM-41-tethered rhodium complexes: Preparation, characterization and catalysis for cyclohexene hydroformylation
Authors: Huang, L.
Wu, J.C.
Kawi, S. 
Keywords: Cyclohexene hydroformylation
Functionalization
MCM-41
Rh4(CO)12
Tethered catalyst
Issue Date: 1-Oct-2003
Citation: Huang, L., Wu, J.C., Kawi, S. (2003-10-01). Rh4(CO)12-derived functionalized MCM-41-tethered rhodium complexes: Preparation, characterization and catalysis for cyclohexene hydroformylation. Journal of Molecular Catalysis A: Chemical 206 (1-2) : 371-387. ScholarBank@NUS Repository. https://doi.org/10.1016/S1381-1169(03)00423-0
Abstract: The preparation of Rh4(CO)12-derived functionalized silicate MCM-41-tethered catalysts has been studied by infrared (IR) spectroscopy, X-ray diffraction (XRD) and N2 adsorption-desorption. Silicate MCM-41 is first functionalized with phosphine, amine and thiol donor ligand groups. Then the functionalized MCM-41 is reacted with Rh 4(CO)12 by coordination of surface donor ligands to the rhodium to produce phosphinated and aminated MCM-41-tethered unidentified rhodium carbonyl clusters and MCM-41-tethered [Rh(μ-S(CH2) 3Si(Os)3)(CO)2]2 (where Os, represents surface oxygen). The functionalized MCM-41 and Rh/functionalized MCM-41 possess the structural ordering of mesoporous MCM-41, but exhibit reduced pore sizes, total pore volumes and BET surface areas. The tethered rhodium carbonyl catalysts behave differently with different donor ligands attached in cyclohexene hydroformylation under equimolar CO and H 2 at 2.7 MPa and 100 °C. Only the aminated MCM-41-tethered catalyst displays good activity, selectivity and recycling for the formation of cyclohexane carboxaldehyde. The influences of supported donor ligands on the activity and stability of tethered catalysts for hydroformylation are discussed. The mesoporous structure of MCM-41 is maintained stable during the catalytic reaction. © 2003 Elsevier B.V. All rights reserved.
Source Title: Journal of Molecular Catalysis A: Chemical
URI: http://scholarbank.nus.edu.sg/handle/10635/92309
ISSN: 13811169
DOI: 10.1016/S1381-1169(03)00423-0
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