基于金属卟啉的新型共价偶联结构与双金属催化中心通过协同模式催化环烷烃与 O2 的氧化反应

IF 3.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Jia-Ye Ni, Yan-Bo Ding, Jing Sun, Hong-Ke Wu, Hai-Min Shen, Yuan-Bin She
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引用次数: 0

摘要

建立了一种基于三(4-Cl)(4-OH)Co 和三(4-Cl)(4-OH)Zn 的新型双金属中心共价偶联催化体系 (Porp.Co@Zn-C6),以改善环烷烃的氧化。其中,部分氧化产物的选择性从 86.4% 提高到 97.5%,环己烷的转化率从 3.80% 提高到 4.41%。同时提高了转化率和选择性。在该系统中,Co(II) 被用来激活分子氧,Zn(II) 被用来加强环己基过氧化氢的利用,并避免其在无序状态下的热分解。这一建议也非常适用于其他环烷烃,可同时提高转化率和选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cycloalkanes oxidation with O2 catalyzed by a novel metalloporphyrin-based covalent coupling structure with bimetallic catalytic centers through synergistic mode

Cycloalkanes oxidation with O2 catalyzed by a novel metalloporphyrin-based covalent coupling structure with bimetallic catalytic centers through synergistic mode

A novel bimetallic central covalent coupling catalytic system (Porp.Co@Zn-C6) based on Tris(4-Cl)(4-OH)Co and Tris(4-Cl)(4-OH)Zn was established to improve cycloalkanes oxidation. In particular, the partially-oxidized product's selectivity rose from 86.4% to 97.5% and the cyclohexane conversion was boosted from 3.80% to 4.41%. Simultaneously achieved improvements in conversion and selectivity. In this system, Co(II) was employed to activate molecular oxygen, Zn(II) was utilized to strengthen the utilization of cyclohexyl hydroperoxide and to be avoided its thermal decomposition in disorder state. This proposal can be very suitable for other cycloalkanes as well, which will improve the conversion and selectivity concurrently.

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来源期刊
Catalysis Communications
Catalysis Communications 化学-物理化学
CiteScore
6.20
自引率
2.70%
发文量
183
审稿时长
46 days
期刊介绍: Catalysis Communications aims to provide rapid publication of significant, novel, and timely research results homogeneous, heterogeneous, and enzymatic catalysis.
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