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Thiophene-based covalent organic frameworks.


ABSTRACT: We report the synthesis and characterization of covalent organic frameworks (COFs) incorporating thiophene-based building blocks. We show that these are amenable to reticular synthesis, and that bent ditopic monomers, such as 2,5-thiophenediboronic acid, are defect-prone building blocks that are susceptible to synthetic variations during COF synthesis. The synthesis and characterization of an unusual charge transfer complex between thieno[3,2-b]thiophene-2,5-diboronic acid and tetracyanoquinodimethane enabled by the unique COF architecture is also presented. Together, these results delineate important synthetic advances toward the implementation of COFs in electronic devices.

SUBMITTER: Bertrand GH 

PROVIDER: S-EPMC3612668 | biostudies-literature | 2013 Mar

REPOSITORIES: biostudies-literature

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Thiophene-based covalent organic frameworks.

Bertrand Guillaume H V GH   Michaelis Vladimir K VK   Ong Ta-Chung TC   Griffin Robert G RG   Dincă Mircea M  

Proceedings of the National Academy of Sciences of the United States of America 20130311 13


We report the synthesis and characterization of covalent organic frameworks (COFs) incorporating thiophene-based building blocks. We show that these are amenable to reticular synthesis, and that bent ditopic monomers, such as 2,5-thiophenediboronic acid, are defect-prone building blocks that are susceptible to synthetic variations during COF synthesis. The synthesis and characterization of an unusual charge transfer complex between thieno[3,2-b]thiophene-2,5-diboronic acid and tetracyanoquinodim  ...[more]

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