One-pot mechanochemical access to quinoline-linked covalent organic frameworks

Yizhou Zhan; Yuxuan Yang; Wei Zhao; Xi Wang; Xi Wang; Jiarong Qiu; Zhaonan Tang; Jiao He; Chenglong Deng; Heshen Xiao; Yiying Pang; Xiaoji Wang; Xiaoji Wang

doi:10.1039/d6ra01241h

January 1, 2026RSC AdvancesOpen Access

One-pot mechanochemical access to quinoline-linked covalent organic frameworks

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Key Points

To investigate the synthesis of quinoline-linked covalent organic frameworks using mechanochemical methods.
Utilized a one-pot mechanochemical approach for synthesis.
Transformed reversible imine bonds into irreversible quinoline linkages.
Analyzed the resulting frameworks for stability and structural characteristics.
Successfully formed quinoline-linked COFs demonstrating increased robustness.
Observed significant enhancement in structural stability compared to traditional COFs.
Framework showed improved performance metrics in application assessments.

Implication

One-pot synthesis of robust quinoline-linked COFs, enhancing stability and structural integrity.

Abstract

Quinoline-linked COFs are formed by transforming reversible imine bonds into irreversible, π-extended quinoline linkages, thereby enhancing framework robustness and structural stability.

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Cite This Study

Zhan et al. (2026) studied this question.

synapsesocial.com/papers/69e9baeb85696592c86ecce2 https://doi.org/10.1039/d6ra01241h

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One-pot mechanochemical access to quinoline-linked covalent organic frameworks

Key Points

Implication

Abstract

Discussion

Cite This Study

One-pot mechanochemical access to quinoline-linked covalent organic frameworks

Key Points

Implication

Abstract

Discussion

Cite This Study

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