Home >

news Help

Publication Information


Title
Japanese:Synthesis and oxidation catalysis of a Ti-substituted phosphotungstate, and identification of the active oxygen species. 
English:Synthesis and oxidation catalysis of a Ti-substituted phosphotungstate, and identification of the active oxygen species. 
Author
Japanese: Eri Takahashi, Keigo Kamata, Yuji Kikukawa, Sota Sato, Kosuke Suzuki, Kazuya Yamaguchi, Noritaka. Mizuno.  
English: Eri Takahashi, Keigo Kamata, Yuji Kikukawa, Sota Sato, Kosuke Suzuki, Kazuya Yamaguchi, Noritaka. Mizuno.  
Language English 
Journal/Book name
Japanese:Catalysis Science & Technology 
English:Catalysis Science & Technology 
Volume, Number, Page Vol. 5    No. 10    pp. 4778-4789
Published date 2015 
Publisher
Japanese:Royal Society of Chemistry 
English:Royal Society of Chemistry 
Conference name
Japanese: 
English: 
Conference site
Japanese: 
English: 
DOI https://doi.org/10.1039/C5CY01031D
Abstract In this paper, we report the synthesis of a Ti-substituted phosphotungstate, TBA6[(ホウ-PW10O36)2Ti4(ホシ-O)2(ホシ-OH)4] (I, TBA = tetra-n-butylammonium), and its application to H2O2-based oxidn. Firstly, an org. solvent-sol. dilacunary phosphotungstate precursor, TBA3[ホウ-PW10O34(H2O)2] (PW10), has been synthesized. By the reaction of PW10 and TiO(acac)2 (acac = acetylacetonate) in an org. medium (acetonitrile), I can be obtained. Compd. I possesses a tetranuclear Ti core which can effectively activate H2O2 and shows high catalytic performance for several oxidn. reactions, such as epoxidn. of alkenes, oxygenation of sulfides, oxidative bromination of unsatd. compds., and hydroxylation of anisole, giving the corresponding oxidn. products with high efficiencies and selectivities. The catalytic performance of I is much superior to those of previously reported Ti-substituted polyoxometalates. In addn., I is highly durable during catalysis and can be reused several times while keeping its high catalytic performance. Furthermore, we have successfully isolated the truly catalytically active species for the present I-catalyzed oxidn., TBA6[(ホウ-PW10O36)2Ti4(ホシ-ホキ2:ホキ2-O2)4] (II), and its anion structure has been detd. by X-ray crystallog. anal. All of the four Ti2-ホシ-ホキ2:ホキ2-peroxo species in II are active for stoichiometric oxidn. (without H2O2), and II is included in the catalytic cycle for I-catalyzed oxidn. [on SciFinder(R)]

©2007 Tokyo Institute of Technology All rights reserved.