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壳聚糖促进的四(五氟苯基)钴卟啉在响应面法优化反应条件下对环己烷氧化的高活性催化作用

Highly Active Catalysis of Cobalt Tetrakis(pentafluorophenyl)porphyrin Promoted by Chitosan for Cyclohexane Oxidation in Response-Surface-Methodology-Optimized Reaction Conditions.

作者信息

Mo Lin-Qiang, Huang Xian-Fei, Huang Guan, Yuan Guang-Ping, Wei Su-Juan

机构信息

School of Chemistry and Chemical Engineering Guangxi University 530004 Nanning, Guangxi P.R.China.

School ofComputerandElectronicInformation Guangxi University 530004 Nanning, Guangxi P.R.China.

出版信息

ChemistryOpen. 2019 Jan 24;8(1):104-113. doi: 10.1002/open.201800268. eCollection 2019 Jan.

Abstract

We aimed at elevating catalytic performances of cobalt tetrakis(pentafluorophenyl)porphyrin (Co TPFPP) through axial coordination, nanocavities, and covalently grafting action. The Co TPFPP was immobilized onto nanoporous and nonporous chitosan, forming Co TPFPP/np- and nonp-CTS catalysts, respectively. The catalysts were characterized by various spectroscopic techniques. The catalytic performances of these catalysts for cyclohexane oxidation under response-surface-methodology-optimized oxidation reaction conditions were estimated and compared. Co TPFPP/np-CTS was an excellent catalyst at aspect of catalytic activity, exhibiting the considerable potential reusability, 24.2 mol % yields (KA oil : cyclohexanone and cyclohexanol) in average, and total turnover frequencies (TOFs) of 3.25×10 h. This is attributed to the structural characteristics of the Co TPFPP/np-CTS catalyst: the cobalt porphyrin molecules could be highly scattered on CTS, forming the independent active sites, and were not leached. The axial coordination exerted the most important effect on the catalytic activity, and the covalent grafting action had a decisive effect on the increase of the total TOFs and on the reusability of the catalyst.

摘要

我们旨在通过轴向配位、纳米腔和共价接枝作用提高四(五氟苯基)钴卟啉(Co TPFPP)的催化性能。将Co TPFPP固定在纳米多孔和无孔壳聚糖上,分别形成Co TPFPP/np-CTS和Co TPFPP/nonp-CTS催化剂。通过各种光谱技术对催化剂进行了表征。在响应面法优化的氧化反应条件下,评估并比较了这些催化剂对环己烷氧化的催化性能。Co TPFPP/np-CTS在催化活性方面是一种优异的催化剂,具有相当大的潜在可重复使用性,平均产率为24.2 mol%(KA油:环己酮和环己醇),总周转频率(TOF)为3.25×10 h⁻¹。这归因于Co TPFPP/np-CTS催化剂的结构特征:钴卟啉分子可以高度分散在CTS上,形成独立的活性位点,且不会浸出。轴向配位对催化活性起最重要的作用,共价接枝作用对总TOF的增加和催化剂的可重复使用性起决定性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/6345221/811ed7abdc31/OPEN-8-104-g001.jpg

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