Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2119
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dc.contributor.authorMISRA, RAJKUMARen_US
dc.contributor.authorSASEENDRAN, ABHIJITHen_US
dc.contributor.authorDEY, SANJITen_US
dc.contributor.authorGOPI, HOSAHUDYA N.en_US
dc.date.accessioned2019-02-27T04:39:39Z
dc.date.available2019-02-27T04:39:39Z
dc.date.issued2019-02en_US
dc.identifier.citationAngewandte Chemie International Edition, 58(8), 2251-2255.en_US
dc.identifier.issn1433-7851en_US
dc.identifier.issn1521-3773en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2119-
dc.identifier.urihttps://doi.org/10.1002/anie.201810849en_US
dc.description.abstractThe potential of structured peptides has not been explored much in the design of metal‐organic frameworks (MOFs). This is partly due to the difficulties in obtaining stable secondary structures from the short α‐peptide sequences. Here we report the design, crystal conformations, coordination site dependent different silver coordinated frameworks of short α,γ‐hybrid peptide 12‐helices consisting of terminal pyridyl moieties and the utility of metal‐helix frameworks in the adsorption of CO2. Upon silver ion coordination the 12‐helix terminated by the 3‐pyridyl derivatives adopted a 2:2 macrocyclic structure, while the 12‐helix terminated by the 4‐pyridyl derivatives displayed remarkable porous metal‐helix frameworks. Both head‐to‐tail intermolecular H‐bonds of the 12‐helix and metal ion coordination have played an important role in stabilizing the ordered metal‐helix frameworks. The studies described here open the door to design a new class of metal‐organic‐frameworks from peptide foldamers.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectFoldamersen_US
dc.subjectFrameworksen_US
dc.subjectHelicesen_US
dc.subjectMetal coordinationen_US
dc.subjectX-ray diffractionen_US
dc.subjectTOC-FEB-2019en_US
dc.subject2019en_US
dc.titleMetal-Helix Frameworks from Short Hybrid Peptide Foldamersen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleAngewandte Chemie International Editionen_US
dc.publication.originofpublisherForeignen_US
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