Issue 10, 2022

Synthesis of phenol esters by direct C–H activation of aldehydes using a highly efficient and reusable copper-immobilized polyimide covalent organic framework (Cu@PI-COF)

Abstract

In the present study, we report the design and fabrication of a thermally and chemically stable copper-based polyimide covalent organic framework (Cu@PI-COF) via a facile and straightforward synthetic approach. The as-synthesized Cu@PI-COF proves its supremacy in the synthesis of biologically significant phenol esters by the reaction of 2-hydroxyacetophenone with a series of aldehydes. The obtained catalyst was thoroughly investigated by various physico-chemical techniques, such as FT-IR, XRD, SEM, TEM, AAS, TGA, EDX, 13C NMR, BET and ED-XRF. The superior prowess of Cu@PI-COF was demonstrated in the synthesis of phenol esters with good to excellent yields, a wider substrate scope and shorter reaction times under ambient reaction conditions. Besides showcasing remarkable catalytic activity, the catalyst also exhibited excellent recoverability and recyclability in up to seven consecutive runs with no reduction in its catalytic performance, which offers the potential for scale-up in various pharmaceutical applications.

Graphical abstract: Synthesis of phenol esters by direct C–H activation of aldehydes using a highly efficient and reusable copper-immobilized polyimide covalent organic framework (Cu@PI-COF)

Supplementary files

Article information

Article type
Paper
Submitted
20 Dec 2021
Accepted
03 Feb 2022
First published
04 Feb 2022

New J. Chem., 2022,46, 4715-4723

Synthesis of phenol esters by direct C–H activation of aldehydes using a highly efficient and reusable copper-immobilized polyimide covalent organic framework (Cu@PI-COF)

P. Yadav, R. Gupta, G. Arora, A. Srivastava and R. K. Sharma, New J. Chem., 2022, 46, 4715 DOI: 10.1039/D1NJ06055D

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