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Ionothermal Synthesis of Imide-Linked Covalent Organic Frameworks

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dc.contributor.author Banerjee, Tanmay
dc.date.accessioned 2021-11-11T11:20:38Z
dc.date.available 2021-11-11T11:20:38Z
dc.date.issued 2020-06-23
dc.identifier.uri https://onlinelibrary.wiley.com/doi/full/10.1002/anie.202007372
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3466
dc.description.abstract Covalent organic frameworks (COFs) are an extensively studied class of porous materials, which distinguish themselves from other porous polymers in their crystallinity and high degree of modularity, enabling a wide range of applications. COFs are most commonly synthesized solvothermally, which is often a time-consuming process and restricted to well-soluble precursor molecules. Synthesis of polyimide-linked COFs (PI-COFs) is further complicated by the poor reversibility of the ring-closing reaction under solvothermal conditions. Herein, we report the ionothermal synthesis of crystalline and porous PI-COFs in zinc chloride and eutectic salt mixtures. This synthesis does not require soluble precursors and the reaction time is significantly reduced as compared to standard solvothermal synthesis methods. In addition to applying the synthesis to previously reported imide COFs, a new perylene-based COF was also synthesized, which could not be obtained by the classical solvothermal route. In situ high-temperature XRPD analysis hints to the formation of precursor–salt adducts as crystalline intermediates, which then react with each other to form the COF. en_US
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Chemistry en_US
dc.subject Ionothermal en_US
dc.subject Synthesis en_US
dc.subject Covalent Organic en_US
dc.title Ionothermal Synthesis of Imide-Linked Covalent Organic Frameworks en_US
dc.type Article en_US


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