钴叔丁基过氧配合物催化苯乙烯选择性好氧过氧化反应。

IF 8.5 Q1 CHEMISTRY, MULTIDISCIPLINARY
JACS Au Pub Date : 2025-02-28 eCollection Date: 2025-03-24 DOI:10.1021/jacsau.5c00139
Yunzhou Chen, Huiying Song, Yiming Hao, Matthew Y Lui, Wing-Leung Wong, William W Y Lam, Bun Chan, Huatian Shi, Wai-Lun Man
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引用次数: 0

摘要

苯乙烯的选择性氧化是必要的和具有挑战性的。在这项研究中,我们阐明了在环境条件下,由钴(III)叔丁基过氧配合物[CoIII(OO t Bu)(qpy)(NCCH3)]2+(1)催化苯乙烯选择性氧化成聚苯乙烯过氧物质的独特途径。通过x射线分析和理论计算,对二过氧络合物[CoIII(qpy)(OOCH(Ph) 2oo to Bu)(NCCH3)]2+(2)的结构进行了研究,结果表明该反应始于苯乙烯在1中的CoIII- oo to Bu部分的亲核加成。这一步之后,与一个O2分子加成,形成一个二过氧自由基(PhCOO•(H)CH2OOtBu),随后与CoII(qpy)反弹生成2。在过量O2存在的情况下,配合物2可以进一步与额外的苯乙烯分子反应,导致形成钴(III)聚苯乙烯过氧物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Selective Aerobic Peroxidation of Styrene Catalyzed by a Cobalt tert-Butylperoxo Complex.

Selective oxidation of styrene to desired products is essential and challenging. In this study, we elucidate a unique pathway for the selective oxidation of styrene to polystyrene peroxo species, catalyzed by the cobalt(III) tert-butylperoxo complex, [CoIII(OO t Bu)(qpy)(NCCH3)]2+ (1), under ambient conditions. Mechanistic investigations, including the structural determination of the diperoxo complex, [CoIII(qpy)(OOCH(Ph)CH2OO t Bu)(NCCH3)]2+ (2), by X-ray analysis and theoretical calculations reveal that the reaction begins with the nucleophilic addition of styrene to the CoIII-OO t Bu moiety in 1. This step is followed by an addition with an O2 molecule, forming a diperoxyl radical (PhCOO(H)CH2OOtBu), which subsequently rebounds with CoII(qpy) to yield 2. In the presence of excess O2, complex 2 can further react with additional styrene molecules, leading to the formation of cobalt(III) polystyrene peroxo species.

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来源期刊
CiteScore
9.10
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