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.
Authors
- Hajime Ito (ORCID: https://orcid.org/0000-0003-3852-6721)
- Kalipada Jana
- Koji Kubota (ORCID: https://orcid.org/0000-0003-1522-291X)
Institutions
- Hokkaido University (JP)
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
Funders
- 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