| Literature DB >> 31398976 |
Hui Li1, Jianhong Chang1, Shanshan Li1, Xinyu Guan1, Daohao Li1, Cuiyan Li1, Lingxue Tang1, Ming Xue1, Yushan Yan2, Valentin Valtchev1,3, Shilun Qiu1, Qianrong Fang1.
Abstract
The functionalization of three-dimensional (3D) covalent organic frameworks (COFs) is essential to broaden their applications. However, the introduction of organic groups with electroactive abilities into 3D COFs is still very limited. Herein we report the first case of 3D tetrathiafulvalene-based COFs (3D-TTF-COFs) with non- or 2-fold interpenetrated pts topology and tunable electrochemical activity. The obtained COFs show high crystallinity, permanent porosity, and large specific surface area (up to 3000 m2/g). Furthermore, these TTF-based COFs are redox active to form organic salts that exhibit tunable electric conductivity (as high as 1.4 × 10-2 S cm-1 at 120 °C) by iodine doping. These results open a way toward designing 3D electroactive COF materials and promote their applications in molecular electronics and energy storage.Entities:
Year: 2019 PMID: 31398976 DOI: 10.1021/jacs.9b06908
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419