Autor: |
Mohammed Rafiq H. Siddiqui, M.M.Taqui Khan, K. Venkatasubramanian, M.A. Moiz, Hari C. Bajaj, S.D. Bhatt, Debabrata Chatterjee |
Rok vydání: |
1993 |
Předmět: |
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Zdroj: |
Polyhedron. 12:1443-1451 |
ISSN: |
0277-5387 |
DOI: |
10.1016/s0277-5387(00)84580-5 |
Popis: |
The catalytic oxidation of tertiary phosphines, PR 3 (R = p -fluorophenyl, phenyl and cyclohexyl), by molecular oxygen to the corresponding phosphine oxide, (PR 3 O), catalysed by Ru III (EDTA-H)(H 2 O) is reported as a function of catalyst, substrate (PR 3 ) and molecular oxygen concentration at a constant pH 3.0 in water-dioxan (50% v/v) medium. The reactivity of PR 3 towards catalytic oxidation by molecular oxygen decreases in the order tris( p -fluorophenyl)phosphine triphenylphosphine tris-(cyclohexyl)-phosphine. A reverse reactivity order was observed in the case of stoichiometric oxidation of PR 3 by [ORu V (EDTA)] − . The proposed mixed-ligand complex Ru III -EDTA-PR 3 intermediate in the catalytic oxidation of PR 3 with molecular oxygen has been isolated and its structure solved by single-crystal X-ray diffraction. The experimental results are discussed in terms of the σ-basic and π-acidic character of the phosphine substrates in the homolytic bond cleavage of OO bonds of the μ-peroxo intermediate and oxygen atom transfer to the substrate. The bond dissociation energy for OO bond cleavage is computed by the kinetic data obtained for oxygen atom transfer from the oxo complex [ORu V (EDTA)] − . |
Databáze: |
OpenAIRE |
Externí odkaz: |
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