This research demonstrates copper-catalyzed carbon-carbon bond formation in arylboronic acids, suggesting an innovative approach to organic synthesis.
The formation of carbon–carbon bonds is essential in organic synthesis, making the development of new catalysts for CC bond formation a demanding task. Functionalization with specific structures in covalent organic frameworks (COFs) imparts them with unique properties. Their highly ordered pores, large surface area, and naturally low density make COFs excellent components of heterogeneous catalysts. When combined with transition metals, they deliver outstanding catalytic performance in organic reactions. In this study, we designed and synthesized a new COF, BTT‐BD(OH) 2 , which contains benzo[1,2‐b:3,4‐b′:5,6‐b″]trithiophene (BTT) and phenol hydroxyl groups derived from 4,4′‐diaminobiphenyl‐3,3′‐diol (BD(OH) 2 ), with a transition metal copper complexed to serve as a heterogeneous catalyst, Cu@COF. Here, we report on the catalysis of the synthesis of sp 2 ‐sp 2 linkages from arylboronic acids. The catalytic performance evaluation shows that the C–C coupling reaction catalyzed by Cu@COF proceeds smoothly under mild, environmentally friendly conditions (at room temperature, in methanol solvent, without alkali, in open air). A variety of symmetrical biaryl compounds has been successfully synthesized. The Cu@COF demonstrated high catalytic activity, broad substrate applicability, and good recyclability.
No takes yet. Share an insight, caveat, or question.
Huo et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: