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  4. Solvothermal depolymerization and recrystallization of imine-linked two-dimensional covalent organic frameworks
 
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Solvothermal depolymerization and recrystallization of imine-linked two-dimensional covalent organic frameworks

Journal
Chemical Science
Journal Volume
12
Journal Issue
48
Start Page
16014
End Page
16022
ISSN
2041-6520
2041-6539
Date Issued
2021
Author(s)
Ji, Woojung
Hamachi, Leslie S.
Natraj, Anusree
Flanders, Nathan C.
Li, Rebecca L.  
Chen, Lin X.
Dichtel, William R.
DOI
10.1039/d1sc03963f
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/732161
Abstract
Mechanistic understanding into the formation and growth of imine-linked two-dimensional (2D) covalent organic frameworks (COFs) is needed to improve their materials quality and access larger crystallite sizes, both of which limit the promise of 2D COFs and 2D polymerization techniques. Here we report a previously unknown temperature-dependent depolymerization of colloidal 2D imine-linked COFs, which offers a new means to improve their crystallinity. 2D COF colloids form at room temperature but then depolymerize when their reaction mixtures are heated to 90 °C. As the solutions are cooled back to room temperature, the 2D COFs repolymerize and crystallize with improved crystallinity and porosity, as characterized by X-ray diffraction, infrared spectroscopy and N2porosimetry. The evolution of COF crystallinity during the solvothermal depolymerization and repolymerization processes was characterized byin situwide angle X-ray scattering, and the concentrations of free COF monomers as a function of temperature were quantified by variable temperature1H NMR spectroscopy. The ability of a 2D COF to depolymerize under these conditions depends on both the identity of the COF and its initial materials quality. For one network formed at room temperature (TAPB-PDA COF), a first depolymerization process is nearly complete, and the repolymerization yields materials with dramatically enhanced crystallinity and surface area. Already recrystallized materials partially depolymerize upon heating their reaction mixtures a second time. A related 2D COF (TAPB-DMTA COF) forms initially with improved crystallinity compared toTAPB-PDA COFand then partially depolymerizes upon heating. These results suggest that both high materials quality and network-dependent properties, such as interlayer interaction strength, influence the extent to which 2D COFs resist depolymerization. These findings offer a new means to recrystallize or solvent anneal 2D COFs and may ultimately inform crystallization conditions for obtaining large-area imine-linked two-dimensional polymers from solution.
Publisher
Royal Society of Chemistry (RSC)
Type
journal article

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