Mechanism of Thioether Oxidation over Di- and Tetrametic Ti Centers: Kinetic and DFT Studies Based on Model Ti-Containing Polyoxometalates Full article
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Chemistry - A European Journal
ISSN: 0947-6539 , E-ISSN: 1521-3765 |
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| Output data | Year: 2015, Volume: 21, Number: 41, Pages: 14496-14506 Pages count : 11 DOI: 10.1002/chem.201501157 | ||||||
| Tags | density functional calculations, homogenous catalysis, kinetic modeling, polyoxometalates, sulfoxidation, titanium | ||||||
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| Affiliations |
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Funding (5)
| 1 | Russian Foundation for Basic Research | 13-03-12042 |
| 2 | European Commission | |
| 3 | Rovira i Virgili University | |
| 4 | Ministry of Economic Affairs and Digital Transformation | CTQ2011-29054-C02-01 |
| 5 | Government of Catalonia | 2014SGR199 |
Abstract:
The oxidation of thioethers by the green oxidant aqueous H2O2 catalysed by the tetratitanium-substituted Polyoxometalate (POM) (Bu4N)8[{γ-SiTi2W10O36(OH)2}2(μ-O)2], as a model catalyst comprising tetrameric titanium centres, was investigated by kinetic modelling and DFT calculations. Several mechanisms of sulfoxidation were evaluated by using methyl phenyl sulfide (PhSMe) as a model substrate in the experiments and dimethyl sulfide in the calculations. The first mechanism assumes that the active hydroperoxo species forms directly through interaction of the Ti2(μ-OH)2 group in [{γ-SiTi2W10O36(OH)2}2(μ-O)2]8− (1 D) with H2O2. The second mechanism includes hydrolysis of Ti-O-Ti bonds linking two γ-Keggin units in structure 1 D to produce the monomer [(γ-SiW10Ti2O38H2)(OH)2]4− (1 M), followed by the formation of an active hydroperoxo species upon interaction of the Ti hydroxo group with H2O2. Both kinetic modelling and DFT calculations support the mechanism through the monomeric species that involves the hydrolysis step. According to the DFT studies the activation of H2O2 by compound 1 M is preferred by 6.5 kcal mol−1 with respect to anion 1 D due to the more flexible Ti environment of the terminal Ti hydroxo group in 1 M. The calculations also indicate that for the „monomeric“ mechanism two pathways are operative: the mono- and the multinuclear pathway. In the mononuclear mechanism, the active group is the terminal Ti[BOND]OH group, whereas in the multinuclear path the active group is the bridging Ti2(μ-OH) moiety. Moreover, unlike previous studies, the sulfoxidation is preferred through a β-oxygen atom transfer from the Ti hydroperoxo group because the α-oxygen atom transfer leads to an unfavourable seven-fold coordinated Ti environment in the transition state. Finally, we have generalised these results to other Ti-containing POMs: the Ti-monosubstituted α-Keggin ion [α-PTi(OH)W11O39]4− and the dititanium-substituted sandwich-type ion [Ti2(OH)2As2W19O67]8−.
Cite:
Skobelev I.Y.
, Zalomaeva O.V.
, Kholdeeva O.A.
, Poblet J.M.
, Carbo J.J.
Mechanism of Thioether Oxidation over Di- and Tetrametic Ti Centers: Kinetic and DFT Studies Based on Model Ti-Containing Polyoxometalates
Chemistry - A European Journal. 2015. V.21. N41. P.14496-14506. DOI: 10.1002/chem.201501157 WOS Scopus РИНЦ ANCAN PMID OpenAlex
Mechanism of Thioether Oxidation over Di- and Tetrametic Ti Centers: Kinetic and DFT Studies Based on Model Ti-Containing Polyoxometalates
Chemistry - A European Journal. 2015. V.21. N41. P.14496-14506. DOI: 10.1002/chem.201501157 WOS Scopus РИНЦ ANCAN PMID OpenAlex
Dates:
| Submitted: | Mar 24, 2015 |
| Published online: | Aug 13, 2015 |
| Published print: | Oct 5, 2015 |
Identifiers:
| Web of science: | WOS:000363331600034 |
| Scopus: | 2-s2.0-84942292972 |
| Elibrary: | 24950866 |
| Chemical Abstracts: | 2015:1528791 |
| Chemical Abstracts (print): | 163:489643 |
| PMID: | 26384744 |
| OpenAlex: | W2164532034 |