White-Light initiated Mn2(CO)10/HFIP-Catalyzed anti-Markovnikov hydrosilylation of alkenes

被引:4
|
作者
Goncharova, Irina K. [1 ,2 ]
Filatov, Stepan A. [2 ,3 ]
Drozdov, Anton P. [1 ,2 ]
Tereshchenko, Andrei A. [4 ]
Knyazev, Pavel A. [5 ]
Guda, Alexander A. [4 ]
Beletskaya, Irina P. [6 ]
V. Arzumanyan, Ashot [1 ,2 ]
机构
[1] Russian Acad Sci, AV Topchiev Inst Petrochem Synth, 29 Leninsky Prospect, Moscow 119991, Russia
[2] Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, 28 Vavilov St, Moscow 119991, Russia
[3] Natl Univ Oil Gas Gubkin Univ, 65 Leninsky Prospect, Moscow 119991, Russia
[4] Southern Fed Univ, Smart Mat Res Inst, 178-24 Sladkov Str, Rostov Na Donu 344090, Russia
[5] Southern Fed Univ, Inst Phys & Organ Chem, 194-2 Stachki St, Rostov Na Donu, Russia
[6] Moscow MV Lomonosov State Univ, GSP-1, Leninskie Gory, Moscow 119991, Russia
关键词
Hydrosilylation; Anti -Markovnikov selectivity; Hydrosilanes; Alkenes; Manganese carbonyl; Hexafluoroisopropanol; White -light initiation; MANGANESE CATALYSIS; EFFICIENT HYDROSILYLATION; HOMOGENEOUS CATALYSIS; METAL; PLATINUM; OLEFINS; HYDROSILATION; COMPLEXES; MECHANISM; SILICA;
D O I
10.1016/j.jcat.2023.115269
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
This study presents a highly efficient and mild method for radical hydrosilylation of alkenes. The reaction proceeds under white-light, in the presence of Mn2(CO)10 pre-catalyst and HFIP as an additive, at r.t. and under air. Under white-light, [Mn]center dot is generated, which activates the Si-H-group to form Si center dot and trigger the autocatalytic process. HFIP acts as a unique activator which enables synthesis of the products with yields close to quantitative and with anti-Markovnikov selectivity. The method is applicable to terminal alkenes, including those with O-, N- and halogen-containing functional groups, styrene and allylbenzene derivatives, etc., as well as to a wide range of alkyl-, phenyl-, siloxy- and alkoxy-containing tertiary hydrosilanes. These conditions turned out to be most efficient for hydrosilylation of gaseous reagents such as ethylene and acetylene. In both cases the products showed quantitative yield at 1 atm and at r.t. The method is easily up-scalable in batch- and flowmodes.
引用
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页数:9
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