Polyether Functionalized Isonitrile Enhanced Nickel‐Catalyzed Hydrosilylation of Olefins

ABSTRACT The hydrosilylation reaction is the core conversion process for synthesizing organosilicon compounds and/or polymers, and the choice of catalyst is crucial for reaction efficiency and selectivity. Isonitrile as a ligand, cannot only stabilize the low valence metal center, but also directly participate in the process of bond formation and cleavage. This study reported that a series of polyether functionalized isonitrile was prepared. The effectiveness of polyether functionalized isonitrile as ligand for nickel pivalate catalyzed hydrosilylation of olefins had been investigated.

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Publication Details

Journal
Applied Organometallic Chemistry
Published
2026-09-08
DOI
https://doi.org/10.1002/aoc.70648
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
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article

Polyether Functionalized Isonitrile Enhanced Nickel‐Catalyzed Hydrosilylation of Olefins

来国桥, Jiajian Peng, Weihong Huang, Ying Bai et al.
Applied Organometallic Chemistry
Organoboron and organosilicon chemistry
article

Polyether Functionalized Isonitrile Enhanced Nickel‐Catalyzed Hydrosilylation of Olefins

来国桥, Jiajian Peng, Weihong Huang, Ying Bai, Jiayun Li, Zhijun Yuan
article en

Abstract

ABSTRACT The hydrosilylation reaction is the core conversion process for synthesizing organosilicon compounds and/or polymers, and the choice of catalyst is crucial for reaction efficiency and selectivity. Isonitrile as a ligand, cannot only stabilize the low valence metal center, but also directly participate in the process of bond formation and cleavage. This study reported that a series of polyether functionalized isonitrile was prepared. The effectiveness of polyether functionalized isonitrile as ligand for nickel pivalate catalyzed hydrosilylation of olefins had been investigated.

Applied Organometallic ChemistryVol. 40(10)
Hangzhou Normal University (CN), Jiangxi University of Technology (CN)
Openalex Percentile: Top 20%
Organoboron and organosilicon chemistry
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