Synthesis of silyl iron hydride via Si-H activation and its dual catalytic application in the hydrosilylation of carbonyl compounds and dehydration of benzamides

被引:25
作者
Ren, Shishuai [1 ]
Xie, Shangqing [1 ]
Zheng, Tingting [1 ,2 ]
Wang, Yangyang [1 ,3 ]
Xu, Shilu [1 ]
Xue, Benjing [1 ]
Li, Xiaoyan [1 ]
Sun, Hongjian [1 ]
Fuhr, Olaf [4 ,5 ]
Fenske, Dieter [4 ,5 ]
机构
[1] Shandong Univ, Minist Educ, Key Lab Special Funct Aggregated Mat, Sch Chem & Chem Engn, Shanda Nanlu 27, Jinan 250199, Shandong, Peoples R China
[2] Capital Normal Univ, Dept Chem, Beijing 100037, Peoples R China
[3] Northwest Normal Univ, Coll Chem & Chem Engn, Lanzhou 730070, Gansu, Peoples R China
[4] KIT, Inst Nanotechnol INT, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
[5] KIT, KNMF, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
关键词
BOND ACTIVATION; PINCER COMPLEXES; PRIMARY AMIDES; ASYMMETRIC HYDROGENATION; ALKANE HYDROXYLATION; NICKEL-COMPLEXES; COBALT COMPLEXES; RUTHENIUM; LIGANDS; REDUCTION;
D O I
10.1039/c8dt00289d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The hydrido silyl iron complex (o-Ph2PC6H4SiMe2)Fe(PMe3)(3)H (2) was obtained via the activation of the Si-H bond of the bidentate silyl ligand o-Ph2P(C6H4)SiMe2H (1) by Fe(PMe3)(4). 2 showed good to excellent catalytic activity in both the reduction of aldehydes/ketones and the dehydration of benzamide. In addition, with complex 2 as a catalyst, ,-unsaturated carbonyls could be selectively reduced to the corresponding ,-unsaturated alcohols. The mechanisms of the formation of 2 and the catalytic dehydration process are proposed and partly experimentally verified.
引用
收藏
页码:4352 / 4359
页数:8
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