Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2666
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dc.contributor.authorThote, Jayshrien_US
dc.contributor.authorAiyappa, Harshitha Barikeen_US
dc.contributor.authorKUMAR, RAYA RAHULen_US
dc.contributor.authorKandambeth, Sharathen_US
dc.contributor.authorBiswal, Bishnu P.en_US
dc.contributor.authorShinde, Digambar Balajien_US
dc.contributor.authorRoy, Neha Chakien_US
dc.contributor.authorBanerjee, Rahulen_US
dc.date.accessioned2019-04-29T10:14:35Z
dc.date.available2019-04-29T10:14:35Z
dc.date.issued2016-09en_US
dc.identifier.citationIUCrJ, 3(6), 402-407.en_US
dc.identifier.issn2052-2525en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2666-
dc.identifier.urihttps://doi.org/10.1107/S2052252516013762en_US
dc.description.abstractThe formation of keto-enamine based crystalline, porous polymers in water is investigated for the first time. Facile access to the Schiff base reaction in water has been exploited to synthesize stable porous structures using the principles of Dynamic Covalent Chemistry (DCC). Most credibly, the water-based Covalent Organic Frameworks (COFs) possess chemical as well as physical properties such as crystallinity, surface area and porosity, which is comparable to their solvothermal counterparts. The formation of COFs in water is further investigated by understanding the nature of the monomers formed using hydroxy and non-hydroxy analogues of the aldehyde. This synthetic route paves a new way to synthesize COFs using a viable, greener route by utilization of the DCC principles in conjunction with the keto–enol tautomerism to synthesize useful, stable and porous COFs in water.en_US
dc.language.isoenen_US
dc.publisherInternational Union of Crystallographyen_US
dc.subjectCrystalline porous polymersen_US
dc.subjectHydrothermalen_US
dc.subjectPorous organic solidsen_US
dc.subjectHydrogen bondingen_US
dc.subjectMicroporous materialsen_US
dc.subject2016en_US
dc.titleConstructing covalent organic frameworks in water via dynamic covalent bondingen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleIUCrJen_US
dc.publication.originofpublisherForeignen_US
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