Polyoxometalate-based Gemini ionic catalysts for selective oxidation of benzyl alcohol with hydrogen peroxide in water

被引:35
作者
Hao, Pengbo [1 ]
Zhang, Mingjie [1 ]
Zhang, Wei [1 ]
Tang, Zhiyang [1 ]
Luo, Ni [1 ]
Tan, Rong [1 ]
Yin, Donghong [1 ]
机构
[1] Hunan Normal Univ, Natl & Local Joint Engn Lab New Petrochem Mat & F, Minist Educ, Key Lab Chem Biol & Tradit Chinese Med Res, Changsha 410081, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOSPHOTUNGSTIC ACID; PHASE OXIDATION; SOLVENT-FREE; LIQUID; BENZALDEHYDE; TOLUENE; NANOPARTICLES; HYBRID; H2O2; DESULFURIZATION;
D O I
10.1039/c8cy01191e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Keggin-type phosphotungstic acid (H3PW12O40, HPW)-based di-imidazolium ionic liquid (IL) hybrids were prepared by exchanging the protons of HPW with PEG-bridged di-imidazolium cations in water. Characterization results suggested that intact Keggin-type [PW12O40](3-) anions were incorporated with various PEG-modified di-imidazolium cations through ionic interaction, giving PW-based ionic catalysts with a Gemini structure. PEG-bridged di-imidazolium cations could not only fine-tune the redox properties of PW anions but also enhanced the compatibility of the catalyst in the aqueous system, which in turn improved its catalytic performance. Furthermore, combination of double catalytic sites into a single molecule enforced an intramolecular, cooperative reaction pathway resulting in a further enhanced reaction rate and higher selectivity in the selective oxidation of benzyl alcohol with H2O2 in water. More importantly, the di-imidazolium IL cations imparted a reaction controlled phase transfer function to the PW hybrids. The catalysts were thus precipitated from the aqueous system upon consumption of H2O2 and could be reused several times without loss of activity and selectivity.
引用
收藏
页码:4463 / 4473
页数:11
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