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Activation and selective oxy-functionalization of alkanes with metal complexes: Shilov reaction and some new aspects
- Source :
- Journal of Molecular Catalysis A: Chemical. 426:305-315
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- The quest of selective catalytic reactions for direct conversion of alkanes into valued products remains to be the most important task objective of modern chemistry and metal complex catalysis. Nowadays it is adopted that the formation of metal–alkyl intermediates (M R) is a necessary condition for activation and functionalization of alkanes on metal complexes but the mechanism of subsequent reactions of metal alkyls remain obscure, so that effective catalytic systems of this kind are still rare and uncommon. Although it is widely adopted that alkane σ-complexes (M·RH) most frequently are primary hydrocarbon intermediates in these processes, low profile in the literature is given to their reactivity and these are often considered simply just as some ‘collision complexes’. Nevertheless, theoretical and experimental studies provide more and more evidence that the С Н bonds in such complexes may be markedly weakened and/or polarized, thus opening wide horizons for occurrence of subsequent direct homolytic or heterolytic reactions of alkanes. This review addresses the discussion of new routes for activation and oxygenation of saturated hydrocarbons, including those via alkane σ-complexes, without formation of metal–alkyl intermediates.
- Subjects :
- chemistry.chemical_classification
Alkane
Primary (chemistry)
010405 organic chemistry
Process Chemistry and Technology
010402 general chemistry
Photochemistry
01 natural sciences
Heterolysis
Catalysis
0104 chemical sciences
Homolysis
Metal
Hydrocarbon
chemistry
Computational chemistry
visual_art
visual_art.visual_art_medium
Reactivity (chemistry)
Physical and Theoretical Chemistry
Subjects
Details
- ISSN :
- 13811169
- Volume :
- 426
- Database :
- OpenAIRE
- Journal :
- Journal of Molecular Catalysis A: Chemical
- Accession number :
- edsair.doi...........7be2433c7688836927af5043f8c50b54