4.8 Article

Nitric Oxide (NO) as a Reagent for Topochemical Framework Transformation and Controlled NO Release in Covalent Organic Frameworks

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 145, Issue 14, Pages 7800-7809

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c11967

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Covalent organic frameworks (COFs) are versatile platforms for gas separation and storage. In this study, nitric oxide (NO) is used as a reagent for the scalable gas-phase transformation of COFs. The study reveals the interaction and clean deamination of COFs by NO, providing a unique surface passivation strategy. Furthermore, NONOate-COFs show promise as tunable NO delivery platforms for bioregulatory NO release in biomedical applications.
Covalent organic frameworks (COFs) have emerged as versatile platforms for the separation and storage of hazardous gases. Simultaneously, the synthetic toolbox to tackle the COF trilemma has been diversified to include topochemical linkage transformations and post-synthetic stabilization strategies. Herein, we converge these themes and reveal the unique potential of nitric oxide (NO) as a new reagent for the scalable gas-phase transformation of COFs. Using physisorption and solid-state nuclear magnetic resonance spectroscopy on 15N-enriched COFs, we study the gas uptake capacity and selectivity of NO adsorption and unravel the interactions of NO with COFs. Our study reveals the clean deamination of terminal amine groups on the particle surfaces by NO, exemplifying a unique surface passivation strategy for COFs. We further describe the formation of a NONOate linkage by the reaction of NO with an amine-linked COF, which shows controlled release of NO under physiological conditions. NONOate-COFs thus show promise as tunable NO delivery platforms for bioregulatory NO release in biomedical applications.

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