Nickel-catalyzed dehydrogenative Zn–Zn coupling to a Zn( <scp>i</scp> ) dimer and its reactivity

High-yield access to a bis-guanidinate zinc(I) dimer was achieved <i>via</i> nickel-catalyzed dehydrocoupling of a zinc(II) hydride. Reactions of Zn(I) dimer with diphenyl dichalcogenides and sulfur resulted in the formation of zinc chalcogenolates and a rare zinc(II) hexasulfide, respectively. Protonolysis of the zinc chalcogenolates afforded zinc hydroxide or phenoxide complexes.

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Publication Details

Journal
Chemical Communications
Published
2025-11-27
DOI
https://doi.org/10.1039/d5cc06233k
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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Nickel-catalyzed dehydrogenative Zn–Zn coupling to a Zn( i ) dimer and its reactivity

Sagrika Rajput, Sharanappa Nembenna, Sayantan Mukhopadhyay, Smrutirani Padhan et al.
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Sulfur-Based Synthesis Techniques
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Nickel-catalyzed dehydrogenative Zn–Zn coupling to a Zn( i ) dimer and its reactivity

Sagrika Rajput, Sharanappa Nembenna, Sayantan Mukhopadhyay, Smrutirani Padhan, Nithya M. Thilakan
article en

Abstract

High-yield access to a bis-guanidinate zinc(I) dimer was achieved <i>via</i> nickel-catalyzed dehydrocoupling of a zinc(II) hydride. Reactions of Zn(I) dimer with diphenyl dichalcogenides and sulfur resulted in the formation of zinc chalcogenolates and a rare zinc(II) hexasulfide, respectively. Protonolysis of the zinc chalcogenolates afforded zinc hydroxide or phenoxide complexes.

Chemical CommunicationsVol. 62(2)
National Institute of Science Education and Research (IN), Homi Bhabha National Institute (IN)
National Institute of Science Education and Research, Homi Bhabha National Institute, Science and Engineering Research Board
Openalex Percentile: Top 72%
Sulfur-Based Synthesis Techniques
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