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Metal-Helix Frameworks from Short Hybrid Peptide Foldamers

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dc.contributor.author MISRA, RAJKUMAR en_US
dc.contributor.author SASEENDRAN, ABHIJITH en_US
dc.contributor.author DEY, SANJIT en_US
dc.contributor.author GOPI, HOSAHUDYA N. en_US
dc.date.accessioned 2019-02-27T04:39:39Z
dc.date.available 2019-02-27T04:39:39Z
dc.date.issued 2019-02 en_US
dc.identifier.citation Angewandte Chemie International Edition, 58(8), 2251-2255. en_US
dc.identifier.issn 1433-7851 en_US
dc.identifier.issn 1521-3773 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2119
dc.identifier.uri https://doi.org/10.1002/anie.201810849 en_US
dc.description.abstract The 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.iso en en_US
dc.publisher Wiley en_US
dc.subject Foldamers en_US
dc.subject Frameworks en_US
dc.subject Helices en_US
dc.subject Metal coordination en_US
dc.subject X-ray diffraction en_US
dc.subject TOC-FEB-2019 en_US
dc.subject 2019 en_US
dc.title Metal-Helix Frameworks from Short Hybrid Peptide Foldamers en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Angewandte Chemie International Edition en_US
dc.publication.originofpublisher Foreign en_US


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