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Transformation of a Hydrazone-Linked Covalent Organic Framework into a Highly Stable Hydrazide-Linked One AITranslate

South China Normal University; South China Normal University; South China Normal University; South China Normal University; South China Normal University; South China Normal University; South China Normal University; Clark Atlanta University; South China Normal University; South China Normal University
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Publisher: ACS
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Abstract AITranslate

The development of covalent organic frameworks (COFs) with advanced linkages and exceptional chemical stability is of importance but remains a challenge. Herein, a hydrazone-linked COF (hydrazone-MTH-TFPB COF) was converted through mild oxidation into a hydrazide-linked one (hydrazide-MTH-TFPB COF). The hydrazide-linked COF exhibited high crystallinity, permanent porosity, and superb chemical stability in boiling water, strong acid, and strong base conditions. Moreover, hydrazide-MTH-TFPB COF displayed superior iodine uptake relative to hydrazone-MTH-TFPB COF, presumably due to the favorable interaction between iodine molecules and hydrazide moieties in the oxidized COF. This work delineates a facile approach for accessing hydrazide-linked COFs that are otherwise difficult to crystallize de novo.

KeyWords AITranslate

covalent organic frameworks hydrazonelinked COF hydrazidelinked COF linkage transformation robust COF iodine adsorption
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Basic Information:

DOI:https://doi.org/10.1021/acsapm.2c00543

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Citation Information:

The development of covalent organic frameworks (COFs) with advanced linkages and exceptional chemical stability is of importance but remains a challenge. Herein, a hydrazone-linked COF (hydrazone-MTH-TFPB COF) was converted through mild oxidation into a hydrazide-linked one (hydrazide-MTH-TFPB COF). The hydrazide-linked COF exhibited high crystallinity, permanent porosity, and superb chemical stability in boiling water, strong acid, and strong base conditions. Moreover, hydrazide-MTH-TFPB COF displayed superior iodine uptake relative to hydrazone-MTH-TFPB COF, presumably due to the favorable interaction between iodine molecules and hydrazide moieties in the oxidized COF. This work delineates a facile approach for accessing hydrazide-linked COFs that are otherwise difficult to crystallize de novo.

quote

GB/T 7714-2015 [1] YiXuan Yang, XiHao Tang, JiaLin Wu, et al. ACS Applied Polymer Materials, 2022(4). DOI:10.1021/acsapm.2c00543.
MLA [1] YiXuan Yang, et al., ACS Applied Polymer Materials, no. 4, 2022, https://doi.org/10.1021/acsapm.2c00543.
APA [1] YiXuan Yang, XiHao Tang, JiaLin Wu, ZhaoYi Dong, YiLun Yan, ShengRun Zheng, Jun Fan, Xinle Li, Songliang Cai, & WeiGuang Zhang. (2022). ACS Applied Polymer Materials(4). https://doi.org/10.1021/acsapm.2c00543
IEEE [1] YiXuan Yang, XiHao Tang, JiaLin Wu, ZhaoYi Dong, YiLun Yan, ShengRun Zheng, Jun Fan, Xinle Li, Songliang Cai, and WeiGuang Zhang, ACS Applied Polymer Materials, no. 4, 2022, doi: 10.1021/acsapm.2c00543. keywords: {covalent organic frameworks;hydrazonelinked COF;hydrazidelinked COF;linkage transformation;robust COF;iodine adsorption}