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NEW JOURNAL OF CHEMISTRY · 2025 · IF 2.5

Hydrosilylation of olefins catalyzed with cobalt(II)-dehydroacetic acid complexes and self-supported catalysts

Xinyu Wang,Luoqi Liu,Weihong Huang,Ying Bai,Jiayun Li,Jiajian Peng

Dehydroacetic acid [3-acetyl-4-hydroxy-6-methyl-2H-pyran-2-one, DHA] can provide O,O′-bidentate coordination sites, and the conjugated π system (CC–CO) in the dehydroacetic acid molecules can effectively stabilize the electronic state of the metal center. This characteristic makes dehydroacetic acid an important ligand in the fields of coordination chemistry and catalysis. A series of cobalt(II)-dehydroacetic acid complexes have been successfully prepared and utilized insoluble cobalt salts to support dehydroacetic acid, creating self-supported catalysts. These two types of catalysts can efficiently catalyze the hydrosilylation reaction of various olefins under mild conditions. Compared to traditional catalysts, these two types of catalysts not only exhibit significantly enhanced catalytic activity but also show superior selectivity for the reaction products.

CAS / MDL: 111-66-0
研究领域: 无机化学 · 配位化学 · 催化化学 · 有机合成方法学 · 金属有机化学
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JOURNAL OF APPLIED POLYMER SCIENCE · 2017 ·Vol. 134 ·期 46 ·45484 · IF 1.86

Copper(I) bromide coordinated by the ionic liquid 1-[(diethyl amine)amine]ethyl-3-methyl imidazolium chloride to catalyze the atom transfer radical polymerization of methyl methacrylate in 1-allyl-3-methyl imidazolium chloride

Teng Xue,Erjun Tang,Jian Zhou,Ruitao Han,Shaojie Liu

A coordinating ionic liquid (IL), 1-[(diethyl amine)amine]ethyl-3-methyl imidazolium chloride ([N 3 MIM]Cl), was prepared as an alternative to a simple organic ligand to coordinate to copper(I) bromide (CuBr). We, thereby, obtained a novel catalyst for atom transfer radical polymerization (ATRP) reactions. This catalyst was applied to the ATRP of methyl methacrylate in the IL 1-allyl-3-methyl imidazolium chloride ([AMIM]Cl). The chemical structures of the ILs obtained were confirmed by Fourier transform infrared spectroscopy, mass spectrometry, and 1 H-NMR analyses. The coordination ability of [N 3 MIM]Cl was assessed by cyclic voltammetry, and the redox potential of [N 3 MIM]Cl–CuBr was −0.507 V. The [N 3 MIM]Cl–CuBr complex was expected to be a markedly more active catalyst than the amine DETA–CuBr complex. The coordination mode toward CuBr was also examined. The [N 3 MIM]Cl–CuBr catalyst system showed good controllability in the aforementioned ATRP reaction in [AMIM]Cl. The Cu catalyst was easily separated from the obtained polymer with the coordinating IL as a ligand. Consequently, the coordinating IL overcame the shortcomings of traditional organic ligands, such as poor compatibility with IL media and poor separation of the catalyst from the polymer; this makes it highly promising for applications in the ATRP field. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45484.

研究领域: 高分子化学 · 催化化学 · 功能材料 · 绿色溶剂 · 配位化学 · 电化学
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