Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4415
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dc.contributor.authorREJA, RAHI M.en_US
dc.contributor.authorMISRA, RAJKUMARen_US
dc.contributor.authorGOPI, HOSAHUDYA N.en_US
dc.date.accessioned2020-02-11T10:36:27Z
dc.date.available2020-02-11T10:36:27Z
dc.date.issued2019-01en_US
dc.identifier.citationChemNanoMat, 5(1), 51-54.en_US
dc.identifier.issn2199-692Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4415-
dc.identifier.urihttps://doi.org/10.1002/cnma.201800366en_US
dc.description.abstractA new approach for the construction of two-helix motifs from helix modules and planar 1,4,5,8-naphthalenetetracarboxylic diimide (NDI) is described. The single crystal conformations of two different types of two-helix motifs consisting of achiral alpha-peptide C-10-helix (3(10)) and chiral alpha,gamma-hybrid peptide C-12-helix revealed that the helices adopted antiparallel orientations across the planar NDI with 2-fold symmetry. The crystal conformations of two-helix motifs were further explored to design electrical conducting peptide foldamer by introducing electron rich pyrene (p-type) as a side-chain in the alpha,gamma-hybrid helix. The two-helix motif with charge transferable pyrene (p-type)-NDI (n-type) combination showed better electrical conductivity compared to the two-helix motif without pyrene side-chain. Moreover, the crystal conformations also provided molecular insight into the peptide orientation of NDI-peptide conjugates. The two-helix motifs described here may serve as potential molecular scaffolds to design novel conductive peptide foldamers and self-assembling biomaterials.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectPeptidesen_US
dc.subjectTwo-helix motifsen_US
dc.subjectCrystal conformationen_US
dc.subjectCharge transferen_US
dc.subjectConductivityen_US
dc.subject2019en_US
dc.titleEngineering Two-Helix Motifs through NDI Linker: A Modular Approach for Charge Transferable Conductive Foldamers Designen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemNanoMaten_US
dc.publication.originofpublisherForeignen_US
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