Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9088
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dc.contributor.authorBiswas, Ankanen_US
dc.contributor.authorYadav, Jonuen_US
dc.contributor.authorDas, Apurba Kumaren_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:31:00Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:31:00Z-
dc.date.issued2017-
dc.identifier.citationReja, A., Biswas, A., Yadav, J., Dev, D., & Das, A. K. (2017). Induction of supramolecular helical handedness in a chemical reaction directed self-healable soft material. ChemistrySelect, 2(34), 10984-10989. doi:10.1002/slct.201702212en_US
dc.identifier.issn2365-6549-
dc.identifier.otherEID(2-s2.0-85041860494)-
dc.identifier.urihttps://doi.org/10.1002/slct.201702212-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9088-
dc.description.abstractThixotropic and self-healable supramolecular gel with nanohelical morphological features of discotic C3 symmetric benzene-1,3,5-tricarboxylic acid coupled with (L)- and (D)-phenylalanine were achieved by hydroxyl anion catalysed methyl ester hydrolysis in presence of lithium ions. The hydrolysis of methyl ester and subsequent formation of gel are highly dependent on metal ions. The arrangement of the molecular building blocks and increasing the structural complexity during the origin of the supramolecular structures from the monomeric units by a chemical reaction act as the executive parameters to determine the handedness of macroscopic chirality. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.sourceChemistrySelecten_US
dc.titleInduction of Supramolecular Helical Handedness in a Chemical Reaction Directed Self-Healable Soft Materialen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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