Issue 42, 2023

Exploring amine-rich supramolecular silver(i) metallogels for autonomous self-healing and as catalysts for a three component coupling reaction

Abstract

A series of Ag(I) supramolecular organo-aqueous gels have been synthesized in the presence of an amine-rich triazole ligand as a gelator. Judicious choice of the triazole derivative and counter anion allows a desired spatial orientation of the pendant amine functionality to accentuate the gelation ability and autonomous self-healability via hydrogen bonding. In addition, the hydrogen bond donors, i.e. pendant –NH2 groups, offer a critical proximity of counter anions to the Lewis acidic Ag(I) and the reactants for promoting a three component coupling reaction of an aldehyde, a terminal alkyne and an amine, giving expedient access to propargyl amines, with remarkable functional group tolerance for both aromatic and aliphatic aldehydes, and aryl acetylenes. Experiments substantiate the pivotal role of counter anions and H-bonding interactions in the observed preference for propargylamines over the diacetylene by-product. Our catalyst is robust, bench-stable, and recyclable, and demonstrates a catalytic efficiency comparable to or better than those of reported systems. The catalyst was found equally effective for the gram-scale synthesis of propargylamines. Our approach lies at the intersection of metal-based, H-bond-mediated counter anion-tuned catalysis, evincing a potential for the development of purpose-built supramolecular gels for desired catalytic applications in the future.

Graphical abstract: Exploring amine-rich supramolecular silver(i) metallogels for autonomous self-healing and as catalysts for a three component coupling reaction

Supplementary files

Article information

Article type
Paper
Submitted
31 май 2023
Accepted
22 авг 2023
First published
23 авг 2023

Dalton Trans., 2023,52, 15530-15538

Exploring amine-rich supramolecular silver(I) metallogels for autonomous self-healing and as catalysts for a three component coupling reaction

E. Saha, A. Rahaman, S. Bhadra and J. Mitra, Dalton Trans., 2023, 52, 15530 DOI: 10.1039/D3DT01654D

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