期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 142, 期 19, 页码 8862-8870出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c01990
关键词
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资金
- U.S. Army Research Office [W911NF-17-1-0126]
- NSERC of Canada
- FQRNT PBEEE international postdoctoral fellowship
- NSERC
- FQRNT
We report the first transformation between crystalline vinylene-linked two-dimensional (2D) polymers and crystalline cyclobutane-linked three-dimensional (3D) polymers. Specifically, absorption-edge irradiation of the 2D poly(arylenevinylene) covalent organic frameworks (COFs) results in topological [2 + 2] cycloaddition cross-linking of the pi-stacked layers in 3D COFs. The reaction is reversible, and heating to 200 degrees C leads to a cycloreversion while retaining the COF crystallinity. The resulting difference in connectivity is manifested in the change of mechanical and electronic properties, including exfoliation, blue-shifted UV-vis absorption, altered luminescence, modified band structure, and different acid-doping behavior. The Li-impregnated 2D and 3D COFs show a significant room : temperature ion conductivity of 1.8 x 10(-4) S/cm and 3.5 X 10(-5) S/cm, respectively. Even higher room-temperature proton conductivity of 1.7 x 10(-2) S/cm and 2.2 x 10(-3) S/cm was found for H2SO4-treated 2D and 3D COFs, respectively.
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