Synthesis of Side-Chain-Free Hydrazone-Linked Covalent Organic Frameworks through Supercritical Carbon Dioxide Activation

Abstract Supercritical carbon dioxide (scCO2) activation provides milder conditions to process covalent organic frameworks (COFs) without compromising their crystallinity and porosity. To this end, three hydrazone COFs (TFPB-DHz COF, TFPT-DHz COF, Py-DHz COF) were synthesized with a terephthaloyl di...

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Bibliographic Details
Main Authors: Shashini D. Diwakara, Gregory T. McCandless, Sampath B. Alahakoon, Ronald A. Smaldone
Format: Article
Language:English
Published: Georg Thieme Verlag 2021-04-01
Series:Organic Materials
Subjects:
Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/a-1477-5123
Description
Summary:Abstract Supercritical carbon dioxide (scCO2) activation provides milder conditions to process covalent organic frameworks (COFs) without compromising their crystallinity and porosity. To this end, three hydrazone COFs (TFPB-DHz COF, TFPT-DHz COF, Py-DHz COF) were synthesized with a terephthaloyl dihydrazide linker (DHz) which has no substituents. To date, the synthesis of hydrazone COFs without a narrow range of alkoxy linkers has not been possible. The scCO2-activated hydrazone-linked COFs in this study were crystalline and had high surface areas (surface areas of TFPB-DHz COF, TFPT-DHz COF, and Py-DHz COF were 790, 1199, and 932 m2/g, respectively). This study shows the significance of using milder activation methods for making hydrazone-linked COF structures that were previously inaccessible.
ISSN:2625-1825