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两种钌(II)配合物实现 2-环己烯醇的高立体选择性异构化,反应中间体的合成与表征。

Good isomerization of 2-cyclohexenol by two Ru(ii) complexes, synthesis and characterization of a reaction intermediate.

机构信息

Área de Química Inorgánica-CIESOL, Facultad de Ciencias, Universidad de Almería, Almería, Spain.

出版信息

Dalton Trans. 2018 Nov 27;47(46):16398-16402. doi: 10.1039/c8dt02560f.

DOI:10.1039/c8dt02560f
PMID:30168829
Abstract

The catalytic activities of [RuClCp(PTA)2] (1) and [RuCp(PTA)2(H2O-κO)]OTf (2) were assessed for the redox isomerization of the cyclic allylic alcohol 2-cyclohexenol into cyclohexanone in water and biphasic media. Complex 2 showed unprecedented good TONs for the studied conversion both in water (TON = 647) and in the biphase of cyclohexene/H2O (TON = 3420) while 1 showed a lower but also good activity (water TON = 95, biphasic TON = 100). The catalytic reaction intermediate [RuCp(PTA)2(η2-C6H9OH)]CF3SO3 (3) was synthesized and characterized using NMR.

摘要

评估了[RuClCp(PTA)2](1)和[RuCp(PTA)2(H2O-κO)]OTf(2)在水相和两相介质中环状烯丙醇2-环己烯醇氧化异构化为环己酮的反应中的催化活性。配合物 2 在水相(TON = 647)和环己烯/H2O 的两相体系(TON = 3420)中对所研究的转化表现出前所未有的高TON 值,而 1 则表现出较低但仍良好的活性(水相 TON = 95,两相 TON = 100)。使用 NMR 合成并表征了催化反应中间体[RuCp(PTA)2(η2-C6H9OH)]CF3SO3(3)。

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