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Chemically Stable Carbazole-Based Imine Covalent Organic Frameworks with Acidochromic Response for Humidity Control Applications.

ABSTRACT: Isoreticular chemically stable two-dimensional imine covalent organic frameworks (COFs), further denoted as DUT-175 and DUT-176, are obtained in a reaction of 4,4'-bis(9H-carbazol-9-yl)biphenyl tetraaldehyde with phenyldiamine and benzidine. The crystal structures, solved and refined from the powder X-ray diffraction data and confirmed by high-resolution transmission electron microscopy, indicate AA-stacked layer structures. Both structures feature distorted hexagonal channel pores, assuring remarkable porosity (S_BET = 1071 m² g^-1 for DUT-175 and S_BET = 1062 m² g^-1 for DUT-176), as confirmed by adsorption of gases and vapors. The complex conjugated π system of the COFs involves electron-rich carbazole building units, which in combination with the imine groups allow reversible pH-dependent protonation of the frameworks, accompanied by charge transfer and shift of the absorption bands in the UV-vis spectrum. The sigmoidal shape of the water vapor adsorption and desorption isotherms with a steep adsorption step at p/p₀ = 0.4-0.6 in combination with excellent stability over dozens of adsorption and desorption cycles ranks these COFs among the best materials for indoor humidity control applications.

SUBMITTER: Gilmanova L

PROVIDER: S-EPMC8587605 | biostudies-literature | 2021 Nov

REPOSITORIES: biostudies-literature

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Chemically Stable Carbazole-Based Imine Covalent Organic Frameworks with Acidochromic Response for Humidity Control Applications.

Gilmanova Leisan L Bon Volodymyr V Shupletsov Leonid L Pohl Darius D Rauche Marcus M Brunner Eike E Kaskel Stefan S

Journal of the American Chemical Society 20211102 44

Isoreticular chemically stable two-dimensional imine covalent organic frameworks (COFs), further denoted as DUT-175 and DUT-176, are obtained in a reaction of 4,4'-bis(9<i>H</i>-carbazol-9-yl)biphenyl tetraaldehyde with phenyldiamine and benzidine. The crystal structures, solved and refined from the powder X-ray diffraction data and confirmed by high-resolution transmission electron microscopy, indicate AA-stacked layer structures. Both structures feature distorted hexagonal channel pores, assur ...[more]

PMID: 34726056

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Project description: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 N2 porosimetry. The evolution of COF crystallinity during the solvothermal depolymerization and repolymerization processes was characterized by in situ wide angle X-ray scattering, and the concentrations of free COF monomers as a function of temperature were quantified by variable temperature 1H 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 to TAPB-PDA COF and 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.

Dataset Information

Chemically Stable Carbazole-Based Imine Covalent Organic Frameworks with Acidochromic Response for Humidity Control Applications.

Publications

Chemically Stable Carbazole-Based Imine Covalent Organic Frameworks with Acidochromic Response for Humidity Control Applications.

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