Hybrid Polyoxotungstates as Functional Comonomers in New Cross-Linked Catalytic Polymers for Sustainable Oxidation with Hydrogen Peroxide

被引:47
作者
Carraro, Mauro [1 ,2 ]
Fiorani, Giulia [1 ,2 ]
Mognon, Lorenzo [1 ,2 ]
Caneva, Francesca [1 ,2 ]
Gardan, Martino [1 ,2 ]
Maccato, Chiara [1 ,2 ]
Bonchio, Marcella [1 ,2 ]
机构
[1] Univ Padua, ITM CNR, I-35131 Padua, Italy
[2] Univ Padua, Dept Chem Sci, I-35131 Padua, Italy
关键词
biphasic catalysis; copolymerization; desulfurization; oxidation; polyoxometalates; MAIN-CHAIN-POLYOXOMETALATE; HIGHLY EFFICIENT; ORGANOSILYL DERIVATIVES; DEEP DESULFURIZATION; RECOVERABLE CATALYST; OPTICAL-PROPERTIES; IONIC LIQUIDS; EPOXIDATION; H2O2; COPOLYMERIZATION;
D O I
10.1002/chem.201201849
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Anchoring terminal octenyl tails on molecular polyoxotungstates yield polymerizable organicinorganic monomers with formula [{CH2?CH(CH2)6Si}xOySiWwOz]4- [x=2, w=11, y=1, z=39 (1); x=2, w=10, y=1, z=36 (2); and x=4, w=9, y=3, z=34 (3)]. These molecular hybrids can use aqueous hydrogen peroxide to catalyze the selective oxidation of organic sulfides in CH3CN. Copolymerization of 13 with methyl methacrylate and ethylene glycol dimethacrylate leads to porous materials with a homogeneous distribution of the functional monomers, as indicated by converging evidence from FTIR spectroscopy and electronic microscopy. The catalytic polymers activate hydrogen peroxide for oxygen transfer, as demonstrated by the quantitative and selective oxidation of methyl p-tolyl sulfide, which was screened as model substrate. The hybrid material containing monomer 2 was also tested in n-octane to evaluate its potential for the oxidation and removal of dibenzothiophene, a well-known gasoline contaminant.
引用
收藏
页码:13195 / 13202
页数:8
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