화학공학소재연구정보센터
Journal of the American Chemical Society, Vol.142, No.19, 8862-8870, 2020
Transformation between 2D and 3D Covalent Organic Frameworks via Reversible [2+2] Cycloaddition
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.