A Supramolecular Catalyst Self-Assembled From Polyoxometalates and Cationic Pillar[5]arenes for the Room Temperature Oxidation of Aldehydes

被引:16
|
作者
Zeng, Mengyan [1 ]
Chen, Kun [1 ]
Tan, Junyan [2 ]
Zhang, Jie [2 ]
Wei, Yongge [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Key Lab Organ Optoelect & Mol Engn, Minist Educ, Beijing, Peoples R China
[2] Peking Univ, Beijing Natl Lab Mol Sci, Coll Chem & Mol Engn, Key Lab Polymer Chem & Phys,Minist Educ, Beijing, Peoples R China
来源
FRONTIERS IN CHEMISTRY | 2018年 / 6卷
基金
中国国家自然科学基金;
关键词
pillar[5]arenes; chromium centered Anderson polyoxometalates; nanospheres; supramolecular catalyst; aldehyde oxidation; AEROBIC OXIDATION; OXIDE CLUSTERS; WATER; SURFACTANTS; CHEMISTRY; COMPLEX; VESICLE; FILMS; ACIDS;
D O I
10.3389/fchem.2018.00457
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oxidizing aldehydes to generate carboxylic acids is a crucial reaction in nature and in chemical industry. The aldehyde oxidation, an easily achieved process in liver cells, is inert toward autoxidation in industrial production and difficultly achieved under enzymatic condition (in water, at pH 7, at room temperature). Herein, we prepared a supramolecular catalyst which are nanospheres assembled in aqueous media by chromium centered Anderson polyoxometalates Na-3[CrMo6O18(OH)(3)] (namely, CrMo6) and cationic pillar[5]arenes (namely, P5A) with 10 positive charges which can be used as the phase transfer catalysts (PTCs). This supramolecular catalyst was exploited on aldehydes oxidation under enzymatic condition with relatively good conversion. Through DLS monitoring, the diameters of nanospheres were variable while changing the charge ratios of the ionic complexes (P5A-CrMo6), and it is probably because of the closer charge ratios causing the more compact assemblies. Also, the nano-morphologies were monitored by TEM and SEM, and the nanostructures were characterized by zeta potential, the X-ray energy-dispersive spectroscopy (EDS), elemental analysis.
引用
收藏
页数:8
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