Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2688
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dc.contributor.authorAdhikari, B.-
dc.date.accessioned2020-12-04T09:12:25Z-
dc.date.available2020-12-04T09:12:25Z-
dc.date.issued2017-
dc.identifier.citationNature Communications, 8.en_US
dc.identifier.other10.1038/ncomms15254-
dc.identifier.urihttps://www.nature.com/articles/ncomms15254-
dc.identifier.urihttp://hdl.handle.net/123456789/2688-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractUnlike classical covalent polymers, one-dimensionally (1D) elongated supramolecular polymers (SPs) can be encoded with high degrees of internal order by the cooperative aggregation of molecular subunits, which endows these SPs with extraordinary properties and functions. However, this internal order has not yet been exploited to generate and dynamically control well-defined higher-order (secondary) conformations of the SP backbone, which may induce functionality that is comparable to protein folding/unfolding. Herein, we report light-induced conformational changes of SPs based on the 1D exotic stacking of hydrogen-bonded azobenzene hexamers. The stacking causes a unique internal order that leads to spontaneous curvature, which allows accessing conformations that range from randomly folded to helically folded coils. The reversible photoisomerization of the azobenzene moiety destroys or recovers the curvature of the main chain, which demonstrates external control over the SP conformation that may ultimately lead to biological functions.en_US
dc.language.isoenen_US
dc.publisherNatureen_US
dc.subjectOne-dimensionally (1D)en_US
dc.subjectSupramolecularen_US
dc.subjectElongated polymersen_US
dc.subjectPolymersen_US
dc.titleLight-induced unfolding and refolding of supramolecular polymer nanofibresen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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