Journal
CATALYSTS
Volume 7, Issue 4, Pages -Publisher
MDPI
DOI: 10.3390/catal7040101
Keywords
alkanes; amides; hydrogen peroxide; dinuclear complexes; iron complexes; metallasiloxanes
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Funding
- Ministry of Education and Science of the Russian Federation [02.a03.21.0008]
- RFBR [16-29-05180, 16-03-00254]
- RFBR-CNRS [16-53-150008]
- French Embassy in Moscow
- Balard Foundation
- Universite de Montpellier
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Two types of heterometallic (Fe(III),Na) silsesquioxanes-[Ph5Si5O10](2)[Ph10Si10O21]Fe-6(O2-)(2)Na-7 (H3O+)(MeOH)(2)(MeCN)(4.5).1.25(MeCN), I, and [Ph5Si5O10](2)[Ph4Si4O8](2)Fe6Na6(O2-)(3)(MeCN)(8.5)(H2O)(8.44), II-were obtained and characterized. X-ray studies established distinctive structures of both products, with pair of Fe(III)-O-based triangles surrounded by siloxanolate ligands, giving fascinating cage architectures. Complex II proved to be catalytically active in the formation of amides from alcohols and amines, and thus becoming a rare example of metallasilsesquioxanes performing homogeneous catalysis. Benzene, cyclohexane, and other alkanes, as well as alcohols, can be oxidized in acetonitrile solution to phenol-the corresponding alkyl hydroperoxides and ketones, respectively-by hydrogen peroxide in air in the presence of catalytic amounts of complex II and trifluoroacetic acid. Thus, the cyclohexane oxidation at 20 degrees C gave oxygenates in very high yield of alkanes (48% based on alkane). The kinetic behaviour of the system indicates that the mechanism includes the formation of hydroxyl radicals generated from hydrogen peroxide in its interaction with di-iron species. The latter are formed via monomerization of starting hexairon complex with further dimerization of the monomers.
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