The cobalt(II) complex of a new tridentate Schiff-base ligand as a catalyst for hydrosilylation of olefins

被引:34
|
作者
Gorczynski, Adam [1 ]
Zaranek, Maciej [1 ,2 ]
Witomska, Samanta [1 ,2 ]
Bocian, Aleksandra [1 ]
Stefankiewicz, Artur R. [1 ,2 ]
Kubicki, Maciej [1 ]
Patroniak, Violetta [1 ]
Pawluc, Piotr [1 ,2 ]
机构
[1] Adam Mickiewicz Univ, Fac Chem, Umultowska 89b, PL-61614 Poznan, Poland
[2] Wielkopolska Ctr Adv Technol, Umultowska 89c, PL-61614 Poznan, Poland
关键词
Schiff-base; Complex; Cobalt; Hydrosilylation; Catalysis; Dehydrogenative silylation; ALKENE HYDROSILYLATION; IRON CATALYSTS; METAL-COMPLEXES; HYDROGENATION; MECHANISM; KETONES; STRANDS; FAMILY; ESTERS;
D O I
10.1016/j.catcom.2016.02.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Condensation of 1-methyl-2-imidazolecarboxaldehyde with 2-(1-methylhydrazinyl)pyridine results in the synthesis of new, tridentate Schiff-base ligand L, which readily reacts with CoCl2 to form a monometallic [CoLCl2] complex that, upon reduction, functions as active hydrosilylation catalyst. The ligand and the [CoLCl2] catalyst have been characterized spectroscopically (MS, NMR, FTIR) and by single crystal X-ray diffraction techniques. The results of preliminary catalytic experimentation show that the cobalt complex can induce hydrosilylation and dehydrogenative silylation of olefins, depending upon the hydrosilane substrate used. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:71 / 74
页数:4
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