A Tetrathiafulvalene-Based Electroactive Covalent Organic Framework

Two‐dimensional covalent organic frameworks (2D COFs) provide a unique platform for the molecular design of electronic and optoelectronic materials. Here, the synthesis and characterization of an electroactive COF containing the well‐known tetrathiafulvalene (TTF) unit is reported. The TTF‐COF cryst...

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Published inChemistry : a European journal Vol. 20; no. 45; pp. 14614 - 14618
Main Authors Ding, Huimin, Li, Yonghai, Hu, Hui, Sun, Yimeng, Wang, Jianguo, Wang, Caixing, Wang, Cheng, Zhang, Guanxin, Wang, Baoshan, Xu, Wei, Zhang, Deqing
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 03.11.2014
WILEY‐VCH Verlag
Wiley
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Summary:Two‐dimensional covalent organic frameworks (2D COFs) provide a unique platform for the molecular design of electronic and optoelectronic materials. Here, the synthesis and characterization of an electroactive COF containing the well‐known tetrathiafulvalene (TTF) unit is reported. The TTF‐COF crystallizes into 2D sheets with an eclipsed AA stacking motif, and shows high thermal stability and permanent porosity. The presence of TTF units endows the TTF‐COF with electron‐donating ability, which is characterized by cyclic voltammetry. In addition, the open frameworks of TTF‐COF are amenable to doping with electron acceptors (e.g., iodine), and the conductivity of TTF‐COF bulk samples can be improved by doping. Our results open up a reliable route for the preparation of well‐ordered conjugated TTF polymers, which hold great potential for applications in fields from molecular electronics to energy storage. An electroactive COF: A two‐dimensional covalent organic framework (COF) containing well‐known tetrathiafulvalene (TTF) units is synthesized (see figure). The presence of TTF units endows the TTF‐COF with electron‐donating ability, and the open frameworks of TTF‐COF are amenable to doping with electron acceptors (e.g., iodine). In addition, the conductivity of TTF‐COF bulk samples can be improved by doping.
Bibliography:Chinese Academy of Sciences
ArticleID:CHEM201405330
ark:/67375/WNG-R2TQ3SBL-5
NSFC
National Natural Science Foundation of China - No. 21203140
istex:B3A85B1CCEA153CBABD5E7D4816B5369F0F53403
Wuhan University - No. 203273642
State Basic Program
Research Fund for the Doctoral Program of Higher Education of China - No. 20130141110008
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SourceType-Scholarly Journals-1
ObjectType-Feature-2
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ISSN:0947-6539
1521-3765
1521-3765
DOI:10.1002/chem.201405330