Epoxidation of Limonene by Tert-butyl Hydroperoxide Catalyzed by Polybenzimidazole-supported Mo(VI) Complex
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چکیده
منابع مشابه
Oxidation of Alkenes with tert-Butyl Hydroperoxide Catalyzed by Mn(II), Cu(II) and VO(IV) Schiff Base Complexes Encapsulated in the Zeolite-Y: A Comparative Study
Oxovanadium(IV), manganese(II) and copper(II) complexes of a Schiff base ligand derived from 2,4-dihydroxyacetophenone and 1,2-diaminocyclohexane have been encapsulated in the nanocavity of zeolite-Y by flexible ligand method and characterized by metal analysis, IR spectroscopic studies and X-ray diffraction patterns. The encapsulated complexes abbreviated here as CuL-Y, MnL-Y and VOL-Y catalyz...
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In the present work, highly efficient oxidation of sulfides catalyzed by MoO2(acac)2 supported on multi-wall carbon nanotubes, MWCNTs, modified with 1,2-diaminobenzene (DAB) and 2-aminophenol (AP), at room temperature are reported. The effects of various parameters such as reaction time, solvent, catalyst amount, oxidant, etc, were studied. These heterogenized catalysts showed high activity in ...
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The epoxidation of limonene with hidrogen peroxide was studied over zeolite Tibeta (a large pore material) and heteropoly acids on carbono and alumina supported. PW11/C was catalyst the best tested. Introduction In the last years, the increase in environmental restrictions lead to the search for new oxydant systems to replace the traditionals in order to avoid the generation of polluting efflue...
متن کاملSelective catalytic oxidation of organosulfur compounds with tert-butyl hydroperoxide.
Rates and selectivities for the oxidation of various organosulfur compounds with tert-butyl hydroperoxide were measured on CoAPO-5 (APO = aluminophosphate; Co/P = 0.05), Co/H-Y (Co/Al = 0.15), and MoO(x)/Al2O3 (15 % wt MoO3). Rates increased with increasing electron density at the sulfur atom (methyl phenyl sulfide>diphenyl sulfide>4-methyldibenzothiophene>2,5-dimethyl thiophene). Rates (per me...
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ژورنال
عنوان ژورنال: Journal of Ion Exchange
سال: 2007
ISSN: 1884-3360,0915-860X
DOI: 10.5182/jaie.18.598