Hypersilylsilylene-Supported Ni(0) Toluene and Ni(II) Complexes with Catalytic Application

The reaction of Ni(COD)2 with [PhC(NtBu)2SiSi(SiMe3)3] (1) in toluene results in the formation of an 18-electron silylene-Ni(0) toluene complex (2). The analogous reaction with 1,3-DFB instead of toluene affords the C–H activation followed by ring walking leading to the allylic cyclooctene adduct, the (η3-C8H13)Ni(II) complex (3). DFT calculations were carried out to elucidate the mechanism as well as to gain insight into why 1,3-DFB undergoes C–H bond activation instead of C–F bond activation. The use of NiCl2·DME permits access to 16-electron (tetrylene)2NiCl2 (Si(4) and Ge(5)) species, and 4 was later used as a catalyst for the C–N coupling reaction.

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Publication Details

Journal
Organometallics
Published
2025-11-13
DOI
https://doi.org/10.1021/acs.organomet.5c00303
Citations
1
Primary Topic
Synthesis and characterization of novel inorganic/organometallic compounds
Type
article
Field-Weighted Citation Impact
0.54
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article

Hypersilylsilylene-Supported Ni(0) Toluene and Ni(II) Complexes with Catalytic Application

Kumar Vanka, K. Vipin Raj, Sakya S. Sen, Milan Kumar Bisai et al.
1 citations
Organometallics
Synthesis and characterization of novel inorganic/organometallic compounds
0.54
article

Hypersilylsilylene-Supported Ni(0) Toluene and Ni(II) Complexes with Catalytic Application

Kumar Vanka, K. Vipin Raj, Sakya S. Sen, Milan Kumar Bisai, V. S. Ajithkumar, Pratiksha B. Ghanwat, Geetika Singh
article en
1 citations

Abstract

The reaction of Ni(COD)2 with [PhC(NtBu)2SiSi(SiMe3)3] (1) in toluene results in the formation of an 18-electron silylene-Ni(0) toluene complex (2). The analogous reaction with 1,3-DFB instead of toluene affords the C–H activation followed by ring walking leading to the allylic cyclooctene adduct, the (η3-C8H13)Ni(II) complex (3). DFT calculations were carried out to elucidate the mechanism as well as to gain insight into why 1,3-DFB undergoes C–H bond activation instead of C–F bond activation. The use of NiCl2·DME permits access to 16-electron (tetrylene)2NiCl2 (Si(4) and Ge(5)) species, and 4 was later used as a catalyst for the C–N coupling reaction.

OrganometallicsVol. 44(22)
National Chemical Laboratory (IN), Academy of Scientific and Innovative Research (IN)
Openalex Percentile: Top 28%
Synthesis and characterization of novel inorganic/organometallic compounds
0.54
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Hypersilylsilylene-Supported Ni(0) Toluene and Ni(II) Complexes with Catalytic Application — Kumar Vanka, K. Vipin Raj, et al. · Organometallics (2025) | TGRS Research Map | TGRS