Epoxidation of cyclooctene using soluble or MCM-41-supported molybdenum tetracarbonyl-pyridylimine complexes as catalyst precursors
authors Gomes, AC; Bruno, SM; Gago, S; Lopes, RP; Machado, DA; Carminatti, AP; Valente, AA; Pillinger, M; Goncalves, IS
nationality International
journal JOURNAL OF ORGANOMETALLIC CHEMISTRY
author keywords Molybdenum; Schiff base ligands; Carbonyl ligands; Supported catalysts; Oxidative decarbonylation; Olefin epoxidation
keywords MICROWAVE-ASSISTED SYNTHESIS; DERIVATIZED DIIMINE LIGANDS; TEMPERATURE IONIC LIQUIDS; TERT-BUTYL HYDROPEROXIDE; NITROGEN DONOR LIGANDS; SCHIFF-BASE LIGANDS; CARBONYL-COMPLEXES; OLEFIN EPOXIDATION; CRYSTAL-STRUCTURE; METHYL-METHACRYLATE
abstract The ligand N-(n-propyl)-2-pyridylmethanimine (pyim) and an immobilised analogue of this ligand (MCM-41-pyim) were prepared by the condensation reaction of 2-pyridinecarboxaldehyde with either propylamine or aminopropyl groups covalently attached to the ordered mesoporous silica MCM-41. Free and immobilised tetracarbonyl complexes of the type cis-[Mo(CO)(4)(L)] (L = pyim (1), MCM-41-pyim) were then prepared by microwave-assisted heating of a mixture of Mo(CO)(6) and the organic ligand or ligand-silica in toluene at 110 degrees C for 30-45 min. The products were characterised by NMR spectroscopy ((1)H, (13)C and (29)Si, in solution and in the solid state), elemental analysis, N(2) adsorption, and FT-IR spectroscopy. When used as catalyst precursors for the epoxidation of cis-cyclooctene by tert-butylhydroperoxide at 55 degrees C (1 mol% catalyst (Mo), no additional co-solvent), 1,2-epoxy-cyclooctane was obtained as the only reaction product in quantitative yield after 5 h for 1 and 36% yield after 24 h for the supported complex. The use of the ionic liquid (IL) 1-butyl-3-methylimidazolium tetrafluoroborate as co-solvent led to lower catalytic activities (epoxide selectivity was always 100%) but allowed the catalyst/IL mixtures (homogeneous mixture for IL+1 and a biphasic solid + IL system for IL+MCM-41-pyim/Mo) to be easily recovered and reused in subsequent runs without loss of catalytic performance. (C) 2011 Elsevier B. V. All rights reserved.
publisher ELSEVIER SCIENCE SA
issn 0022-328X
year published 2011
volume 696
issue 22
beginning page 3543
ending page 3550
digital object identifier (doi) 10.1016/j.jorganchem.2011.07.040
web of science category Chemistry, Inorganic & Nuclear; Chemistry, Organic
subject category Chemistry
unique article identifier WOS:000295717300013
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journal impact factor 1.946
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