原位生成的单核半夹心[(η6-对-氰基)RuCl(酰胺)]配合物作为苯甲醇选择性氧化成苯甲醛的高效催化剂

IF 2.5 Q2 CHEMISTRY, MULTIDISCIPLINARY
G Veeranna , Venkata Ramana Reddy Chittireddy , Ravinder Vadde
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引用次数: 0

摘要

应用原位生成的单核 Ru(II)-organometallic complexes (1-7),即[(η6-p-cymene)RuCl(L)]、原位生成的单核 Ru(II) 有机金属配合物(1-7),即[(η6-p-cymene)RuCl(L)],由 Ru 二聚体[(p-cymene)RuCl2]2 与一些多官能团酰胺配体(L) 相互作用生成,可作为高效催化剂,在 CH3CN 中用叔丁基过氧化氢 (TBHP) 氧化剂氧化各种苯甲醇 (B-OL),从而高产率地选择性地生成苯甲醛 (B-AL)。研究发现,在 B-OL 氧化成 B-AL 的过程中,原位生成的催化剂比[(对-亚甲基)RuCl2]2 前体(二聚体)具有更高的活性。系统地监测了 B-OL 氧化过程中催化剂类型、反应温度、氧化剂和溶剂等各种反应参数的影响,以优化催化条件。为了证实在 B-OL 氧化过程中形成预测的原位生成的单核 Ru(II) 复合物催化剂,合成了其中一种 Ru(II) 复合物 (1),并通过元素分析 (EA)、红外 (IR)、质子-NMR 和质谱技术对其进行了表征,提出了其单核结构。此外,还观察到在将 B-OL 氧化成 B-AL 的过程中,原位生成的 Ru(II)催化剂和预合成的 Ru(II)催化剂的活性几乎相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In situ-generated mononuclear half-sandwich [(η6‐p‐cymene)RuCl(amide)] complexes as efficient catalysts in the selective oxidation of benzyl alcohol to benzaldehyde

In situ-generated mononuclear half-sandwich [(η6‐p‐cymene)RuCl(amide)] complexes as efficient catalysts in the selective oxidation of benzyl alcohol to benzaldehyde
The application of in situ-generated mononuclear Ru(II)-organometallic complexes (17) i.e., [(η6-p-cymene)RuCl(L)], produced by the interaction of Ru dimer [(p-cymene)RuCl2]2 with some polyfunctional amide ligands(L) as highly efficient catalystsin the oxidation of various benzyl alcohols (B-OLs) by tert-butyl hydroperoxide (TBHP) oxidant to produce selectively the benzaldehydes (B-ALs) in high yields in CH3CN is described. The in situ-generated catalysts were found to be highly active than the [(p-cymene)RuCl2]2 precursor (dimer) in the oxidation of B-OL to B-AL. The influence of various reaction parameters such as type of catalyst, reaction temperature, oxidant and solvent during the B-OL oxidation was systematically monitored to optimize the catalytic conditions. In order to confirm the formation of predicted in situ-generated mononuclear Ru(II) complex catalysts during the oxidation of B-OL, one of the Ru(II) complex (1) was synthesized and characterized by Elemental analysis (EA), Infrared (IR), Proton-NMR and Mass spectral techniques and its mono nuclear structure is proposed. Further, it was observed that the activity of in-situ generated and pre-synthesized Ru(II) catalyst was almost same in the oxidation of B-OL to B-AL.
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来源期刊
Results in Chemistry
Results in Chemistry Chemistry-Chemistry (all)
CiteScore
2.70
自引率
8.70%
发文量
380
审稿时长
56 days
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