A mechanochemical [2+2+2] cycloaddition facilitated by a cobalt(<scp>ii</scp>) catalyst and piezoelectric materials

In this study, we present the first general mechanochemical protocol for the catalytic [2+2+2] cycloaddition of alkynes <i>via</i> a simple and inexpensive cobalt(ii)-based catalytic system. The key to achieving the high efficiency of this mechanochemical transformation is the use of piezoelectric BaTiO<sub>3</sub> as a reductant in combination with an amine additive to facilitate the generation of a catalytically active low-valent cobalt species. This method is characterized by a broad substrate scope, short reaction times, solvent-less conditions, and the feasibility of reacting poorly soluble substrates. Thus, we provide a more efficient, broadly applicable, and sustainable alternative to existing solution-based protocols.

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Publication Details

Journal
Chemical Science
Published
2025-01-01
DOI
https://doi.org/10.1039/d5sc02074c
Citations
3
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
2.37

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article

A mechanochemical [2+2+2] cycloaddition facilitated by a cobalt(ii) catalyst and piezoelectric materials

Hajime Ito, Kalipada Jana, Koji Kubota
3 citations
Chemical Science
Fluorine in Organic Chemistry
2.37
article

A mechanochemical [2+2+2] cycloaddition facilitated by a cobalt(ii) catalyst and piezoelectric materials

Hajime Ito, Kalipada Jana, Koji Kubota
article en
3 citations

Abstract

In this study, we present the first general mechanochemical protocol for the catalytic [2+2+2] cycloaddition of alkynes <i>via</i> a simple and inexpensive cobalt(ii)-based catalytic system. The key to achieving the high efficiency of this mechanochemical transformation is the use of piezoelectric BaTiO<sub>3</sub> as a reductant in combination with an amine additive to facilitate the generation of a catalytically active low-valent cobalt species. This method is characterized by a broad substrate scope, short reaction times, solvent-less conditions, and the feasibility of reacting poorly soluble substrates. Thus, we provide a more efficient, broadly applicable, and sustainable alternative to existing solution-based protocols.

Chemical ScienceVol. 16(25)
Hokkaido University (JP)
Japan Science and Technology Corporation, Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science, Core Research for Evolutional Science and Technology
Openalex Percentile: Top 12%
Fluorine in Organic Chemistry
2.37
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A mechanochemical [2+2+2] cycloaddition facilitated by a cobalt(<scp>ii</scp>) catalyst and piezoelectric materials — Hajime Ito, Kalipada Jana, et al. · Chemical Science (2025) | TGRS Research Map | TGRS