Journal
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
Volume 285, Issue 1-2, Pages 92-100Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.molcata.2008.01.022
Keywords
rhenium; cyclohexane; dioxygen; carboxylic acids; radical mechanism; cyclohexanol; cyclohexanone
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The pyrazole complexes [ReCl2{N2C(O)Ph}(Hpz)(PPh3)(2)] 2 (Hpz = pyrazole), [ReCl2{N2C(O)Ph}(Hpz)(2)(PPh3)] 3 and [ReClF{N2C(O)Ph}(Hpz)(2)(PPh3)] 4, and their precursor [ReOCl3(PPh3)(2)] 1, immobilized on 3-aminopropyl functionalized silica, catalyze the cyclohexane oxidation with dioxygen, to cyclohexanol and cyclohexanone (the main product), in the absence of solvent and additives and under relatively mild conditions. Complex 4, whose synthesis and characterization are reported herein for the first time, provides the best activity (ca. 16% overall conversion towards the ketone and alcohol, at the 02 pressure of 19 atm, at 150 degrees C, 8 h reaction time). The reaction is further promoted by pyrazinecarboxylic acid. TGA analysis shows that the supported complexes are stable up to ca. 200 degrees C. The use of radical traps supports the involvement of a free-radical mechanism via carbon- and oxygen-centred radicals. The effects of various factors were studied towards the optimization of the processes. Complex 4 also catalyzes the oxidation of other cycloalkanes to the corresponding cycloalkanols and cycloalkanones. (c) 2008 Elsevier B.V. All rights reserved.
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