μ-Borole三层配合物催化苯甲酸与炔烃的氧化偶联。杂化红环戊二烯/硼硼三层配合物的结构

IF 5.062
Dmitry A. Loginov, Dmitry V. Muratov, Yulia V. Nelyubina, Julia Laskova, Alexander R. Kudinov
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引用次数: 26

摘要

1-甲基-3-硼烯二甲胺加合物与[(C2H4)2RhCl]2反应生成三层络合物(η-C4H4BMe)Rh(μ-η:η-C4H4BMe)Rh(η-C4H4BMe) (1a),产率为62%,并生成微量(<1%)的杂化rhodycyclopentadienyl /borole三层络合物(η-C4H4BMe)Rh(μ-η:η-C4H4BMe)Rh((μ-η:η-C4H4BMe))Rh(η-C4H4BMe)(2)。在Cu(OAc)2, 1a和(η-C4H4BPh)Rh(μ-η:η-C4H4BPh)Rh(η-C4H4BPh) (1b)的存在下,苯甲酸与二苯乙炔选择性氧化偶联得到1,2,3,4-四苯基萘,收率为50-90%。在1a和[CpRhI2]2区催化下,苯甲酸与1-苯基-1-丁炔的类似反应选择性地得到1,4-二乙基-2,3-二苯萘。相应的三层配合物[(9- sme2 -7,8- c2b9h10)Rh(μ-η:η-C4H4BPh)Rh(9- sme2 -7,8- c2b9h10)]2+(3)和[Cp*Rh(μ-η:η-C4H4BPh)IrCp*]2+(4)也作为催化剂进行了测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

μ-Borole triple-decker complexes as catalysts for oxidative coupling of benzoic acid with alkynes. Structure of a hybrid rhodacyclopentadienyl/borole triple-decker complex

μ-Borole triple-decker complexes as catalysts for oxidative coupling of benzoic acid with alkynes. Structure of a hybrid rhodacyclopentadienyl/borole triple-decker complex

Reaction of dimethylamine adduct of 1-methyl-3-borolene with [(C2H4)2RhCl]2 gives the triple-decker complex (η-C4H4BMe)Rh(μ-η:η-C4H4BMe)Rh(η-C4H4BMe) (1a) in 62% yield and trace amount (<1%) of the hybrid rhodacyclopentadienyl/borole triple-decker complex (η-C4H4BMe)Rh(μ-η:η-C4H4Rh{(μ-η:η-C4H4BMe)Rh(η-C4H4BMe)})Rh(η-C4H4BMe) (2). The structure of 2 was determined by X-ray diffraction. In the presence of Cu(OAc)2, 1a and (η-C4H4BPh)Rh(μ-η:η-C4H4BPh)Rh(η-C4H4BPh) (1b) catalyze the oxidative coupling of benzoic acid with diphenylacetylene selectively giving 1,2,3,4-tetraphenylnaphtalene in 50–90% yields. Analogous reactions of benzoic acid with 1-phenyl-1-butyne catalyzed by 1a and [CpRhI2]2 regioselectively give 1,4-diethyl-2,3-diphenylnaphthalene. The related dicationic triple-decker complexes [(9-SMe2-7,8-C2B9H10)Rh(μ-η:η-C4H4BPh)Rh(9-SMe2-7,8-C2B9H10)]2+ (3) and [Cp*Rh(μ-η:η-C4H4BPh)IrCp*]2+ (4) were also tested as catalysts.

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期刊介绍: The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.
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