Issue 95, 2024

Carboxylative cyclization of atmospheric CO2 with alkynol catalyzed by a 1-methylhydantoin anion-functionalized ionic liquid via chelative interactions

Abstract

Metal- and solvent-free carboxylative cyclization of atmospheric CO2 with alkynol can be achieved using a 1-methylhydantoin anion-functionalized ionic liquid. 1H NMR, in situ FT-IR and DFT calculations indicate that the 1-methylhydantoin anion acts as a “pincer ligand” to form chelative interactions with the hydroxyl group, thereby effectively activating the alkynol.

Graphical abstract: Carboxylative cyclization of atmospheric CO2 with alkynol catalyzed by a 1-methylhydantoin anion-functionalized ionic liquid via chelative interactions

Supplementary files

Article information

Article type
Communication
Submitted
18 Jul 2024
Accepted
04 Nov 2024
First published
05 Nov 2024

Chem. Commun., 2024,60, 14089-14092

Carboxylative cyclization of atmospheric CO2 with alkynol catalyzed by a 1-methylhydantoin anion-functionalized ionic liquid via chelative interactions

Y. Guo, T. Chen and Y. Xu, Chem. Commun., 2024, 60, 14089 DOI: 10.1039/D4CC03586K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements