Markovnikov-selective double hydrosilylation of challenging terminal aryl alkynes under cobalt and iron catalysis

被引:9
作者
Banach, Lukasz [1 ]
Brykczynska, Daria [2 ]
Gorczynski, Adam [2 ]
Wyrzykiewicz, Bozena [2 ]
Skrodzki, Maciej [1 ,2 ]
Pawluc, Piotr [1 ,2 ]
机构
[1] Adam Mickiewicz Univ, Ctr Adv Technol, Uniwersytetu Poznanskiego St 10, PL-61614 Poznan, Poland
[2] Adam Mickiewicz Univ, Fac Chem, Uniwersytetu Poznanskiego St 8, PL-61614 Poznan, Poland
关键词
GEMINAL BIS(SILANE); BOND FORMATION; SILICON; SI; REACTIVITY; HYDROSILANES; CARBON; DERIVATIVES; COMPLEXES; REAGENTS;
D O I
10.1039/d2cc04015h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Geminal bis(silanes) are unique compounds with interesting properties. The most straightforward way to access them is double hydrosilylation of alkynes, which was established only recently. Previous articles about transition metal-catalysed double hydrosilylation show that terminal aryl alkynes are a challenge. We report on cobalt(ii) and iron(iii) complexes with the easy-to-synthesise N,N,N-tridentate hydrazone ligand being active precatalysts in Markovnikov-selective double hydrosilylation of terminal aryl alkynes. The influence of the hydrazone ligand structure and the potential role of the sodium triethylborohydride activator were studied. Sets of geminal bis(silanes) with two identical or different silyl groups were synthesised, showing the applicability of the reported method.
引用
收藏
页码:13763 / 13766
页数:4
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