7 research outputs found
ELECTRON-DEFICIENT VANADIUM ALKYL COMPLEXES - SYNTHESIS AND MOLECULAR-STRUCTURE OF THE VANADIUM(III) DINITROGEN COMPLEX [(ME3CCH2)3V]2(MU-N2)
Formation and structure of the oxygen-centered lead thiolate cluster Pb5O(SRF)(8)center dot 2C(7)H(8) [R-F=2,4,6-tris(trifluoromethyl)phenyl]
The unusual pentanuclear lead thiolate cluster PbsO(SRF)(8).C2H8 (3) (C7H8 = toluene) has been obtained by oxidation of Pb(SRF)(2) (2) with dry air and structurally characterized. The central oxygen atom is coordinated to three lead atoms in a trigonal planar fashion. The coordination sphere of the other two lead atoms is completed by coordination of toluene molecules
.alpha.-, .beta.-, and .delta.-Hydrogen abstraction in the thermolysis of paramagnetic vanadium(III) dialkyl complexes
CATALYTIC EPOXIDATION OF CYCLOHEXENE WITH TERT-BUTYLHYDROPEROXIDE USING AN IMMOBILIZED MOLYBDENUM CATALYST
This work describes the synthesis of molybdenum complexes immobilized on a silica support and their performance in the epoxidation reaction of cyclohexene using tert-butylhydroperoxide (TBHP) as the oxidizing agent. The catalyst synthesis included solubilization of variable amounts of bis-oxomolybdenum (VI) acetylacetonate precursor in different solvents such as tetrahydrofuran (THF), ethanol, THF/water and ethanol/water mixtures and contact with the silica support. Characterization techniques demonstrated that the nature of the incorporated molybdenum species depends markedly on the solvent employed. If the solvent employed is an ethanol:water mixture, physical adsorption of the Mo-species onto the support surface occurs; however, when THF is used as the solvent (THF catalyst series), molybdenum is grafted on the silica surface via chemical bonding with the surface hydroxyl groups of silica. Specifically, these latter catalysts show similar performance to that of the homogeneous catalyst, although long-term experiments showed deactivation by leaching of the active phase.Peer reviewe