Hydrosilylation of Terminal Alkenes Catalyzed by a Scandium Metalloligand Supported Ni(0) Complex

Hydrosilylation of terminal alkenes catalyzed by a scandium metalloligand supported Ni(0) complex are studied. The anti ‐Markovnikov products are obtained in 62–89% yield, along with the alkanes and 1,1,2,2‐tetraphenyldisilane as minor products. The resting‐state complexes of hydrosilylation reactions are isolated and characterized by spectroscopic method and X‐ray diffraction studies, which represent rare‐example of Ni(0) silyl complexes supported by scandium ions via a Ni(0)→Sc(III) interaction. The catalytic cycle is proposed to be redox neutral with Ni(0) center, and is facilitated by metal‐ligand cooperation involving the Ni(0)Si bond.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-04-01
DOI
https://doi.org/10.1002/ejoc.202500069
Citations
4
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
3.74

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article

Hydrosilylation of Terminal Alkenes Catalyzed by a Scandium Metalloligand Supported Ni(0) Complex

Dongjing Hong, Lei Ma, Peng Cui
4 citations
European Journal of Organic Chemistry
Organoboron and organosilicon chemistry
3.74
article

Hydrosilylation of Terminal Alkenes Catalyzed by a Scandium Metalloligand Supported Ni(0) Complex

Dongjing Hong, Lei Ma, Peng Cui
article en
4 citations

Abstract

Hydrosilylation of terminal alkenes catalyzed by a scandium metalloligand supported Ni(0) complex are studied. The anti ‐Markovnikov products are obtained in 62–89% yield, along with the alkanes and 1,1,2,2‐tetraphenyldisilane as minor products. The resting‐state complexes of hydrosilylation reactions are isolated and characterized by spectroscopic method and X‐ray diffraction studies, which represent rare‐example of Ni(0) silyl complexes supported by scandium ions via a Ni(0)→Sc(III) interaction. The catalytic cycle is proposed to be redox neutral with Ni(0) center, and is facilitated by metal‐ligand cooperation involving the Ni(0)Si bond.

European Journal of Organic ChemistryVol. 28(20)
Anhui Normal University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 8%
Organoboron and organosilicon chemistry
3.74
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