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Constitutional isomerism of the linkages in donor–acceptor covalent organic frameworks and its impact on photocatalysis

  • When new covalent organic frameworks (COFs) are designed, the main efforts are typically focused on selecting specific building blocks with certain geometries and properties to control the structure and function of the final COFs. The nature of the linkage (imine, boroxine, vinyl, etc.) between these building blocks naturally also defines their properties. However, besides the linkage type, the orientation, i.e., the constitutional isomerism of these linkages, has rarely been considered so far as an essential aspect. In this work, three pairs of constitutionally isomeric imine-linked donor-acceptor (D-A) COFs are synthesized, which are different in the orientation of the imine bonds (D-C=N-A (DCNA) and D-N=C-A (DNCA)). The constitutional isomers show substantial differences in their photophysical properties and consequently in their photocatalytic performance. Indeed, all DCNA COFs show enhanced photocatalytic H2 evolution performance than the corresponding DNCA COFs. Besides the imine COFs shown here, it can be concluded that theWhen new covalent organic frameworks (COFs) are designed, the main efforts are typically focused on selecting specific building blocks with certain geometries and properties to control the structure and function of the final COFs. The nature of the linkage (imine, boroxine, vinyl, etc.) between these building blocks naturally also defines their properties. However, besides the linkage type, the orientation, i.e., the constitutional isomerism of these linkages, has rarely been considered so far as an essential aspect. In this work, three pairs of constitutionally isomeric imine-linked donor-acceptor (D-A) COFs are synthesized, which are different in the orientation of the imine bonds (D-C=N-A (DCNA) and D-N=C-A (DNCA)). The constitutional isomers show substantial differences in their photophysical properties and consequently in their photocatalytic performance. Indeed, all DCNA COFs show enhanced photocatalytic H2 evolution performance than the corresponding DNCA COFs. Besides the imine COFs shown here, it can be concluded that the proposed concept of constitutional isomerism of linkages in COFs is quite universal and should be considered when designing and tuning the properties of COFs.show moreshow less

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Author details:Jin YangORCiD, Samrat GhoshORCiD, Jérôme Roeser, Amitava AcharjyaORCiD, Christopher PenschkeORCiDGND, Yusuke TsutsuiORCiD, Jabor RabeahORCiDGND, Tianyi Wang, Simon Yves Djoko TameuORCiD, Meng-Yang Ye, Julia Grüneberg, Shuang LiORCiD, Changxia LiORCiD, Reinhard SchomaeckerORCiDGND, Roel Van de KrolORCiDGND, Shu SekiORCiD, Peter SaalfrankORCiDGND, Arne ThomasORCiDGND
DOI:https://doi.org/10.1038/s41467-022-33875-9
ISSN:2041-1723
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/36274186
Title of parent work (English):Nature Communications
Publisher:Nature Publishing Group UK
Place of publishing:[London]
Publication type:Article
Language:English
Date of first publication:2022/10/23
Publication year:2022
Release date:2024/01/22
Volume:13
Issue:1
Article number:6317
Number of pages:10
Funding institution:China Scholarship Council (CSC); Berlin Graduate School of Natural; Sciences and Engineering (BIG-NSE); Deutsche Forschungsgemeinschaft; (DFG, German Research Foundation) under Germany's Excellence Strategy; [EXC 2008-390540038-UniSysCat]; BMBF [033RC024]; Alexander von Humboldt; foundation; Projekt DEAL
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie
DDC classification:5 Naturwissenschaften und Mathematik / 50 Naturwissenschaften / 500 Naturwissenschaften und Mathematik
Peer review:Referiert
Publishing method:Open Access / Gold Open-Access
DOAJ gelistet
License (German):License LogoCC-BY - Namensnennung 4.0 International
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