Synthesis and catalytic activity of N-heterocyclic silylene (NHSi) iron (II) hydride for hydrosilylation of aldehydes and ketones

被引:6
|
作者
Du, Xinyu [1 ]
Qi, Xinghao [1 ]
Li, Kai [1 ]
Li, Xiaoyan [1 ]
Sun, Hongjian [1 ]
Fuhr, Olaf [2 ,3 ]
Fenske, Dieter [2 ,3 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Key Lab Special Funct Aggregated Mat, Minist Educ, Shanda Nanlu 27, Jinan 250100, Peoples R China
[2] Karlsruher Inst Technol KIT, Inst Nanotechnol INT, Eggenstein Leopoldshafen, Germany
[3] Karlsruher Inst Technol KIT, Karlsruher Nanomicrofacil KNMF, Eggenstein Leopoldshafen, Germany
基金
中国国家自然科学基金;
关键词
aldehyde; hydrosilylation; iron hydride; ketone; silylene; COMPLEXES BEARING; LIGANDS; ACTIVATION; REACTIVITY; DONOR; ACCESS; COBALT;
D O I
10.1002/aoc.6286
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel silylene supported iron hydride [Si, C]FeH (PMe3)(3) (1) was synthesized by C (sp(3))-H bond activation with zero-valent iron complex Fe (PMe3)(4). Complex 1 was fully characterized by spectroscopic methods and single crystal X-ray diffraction analysis. To the best of our knowledge, 1 is the first example of silylene-based hydrido chelate iron complex produced through activation of the C (sp(3))-H bond. It was found that complex 1 exhibited excellent catalytic activity for hydrosilylation of aldehydes and ketones. The catalytic system showed good tolerance and catalytic activity for the substrates with different functional groups on the benzene ring. It is worth mentioning that, the experimental results showed that both ketones and aldehydes could be reduced in good to excellent yields under the same catalytic conditions. Based on the experiments and literature reports, a possible catalytic mechanism was proposed.
引用
收藏
页数:10
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