Full metadata record
DC FieldValueLanguage
dc.contributor.authorHsu, Ling-Huangen_US
dc.contributor.authorHsu, Shu-Minen_US
dc.contributor.authorWu, Fang-Yien_US
dc.contributor.authorLiu, Yu-Haoen_US
dc.contributor.authorNelli, Srinivasa Raoen_US
dc.contributor.authorYeh, Mei-Yuen_US
dc.contributor.authorLin, Hsin-Chiehen_US
dc.date.accessioned2019-04-03T06:41:31Z-
dc.date.available2019-04-03T06:41:31Z-
dc.date.issued2015-01-01en_US
dc.identifier.issn2046-2069en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c5ra00172ben_US
dc.identifier.urihttp://hdl.handle.net/11536/124604-
dc.description.abstractThe combination of a naphthalene diimide (NDI) group and a single amino-acid of serine (Ser) or lysine (Lys) can be used to promote the formation of a supramolecular hydrogel, which indicates the aromatic amino acid is not necessary to be used in the structural design of NDI-capped small molecule hydrogelators. An equimolar ratio of NDI-Ser and NDI-Lys can form a stable hydrogel under neutral conditions and its gel-to-sol transition temperature is higher than 37 degrees C. This work, as the first example of NDI-containing hydrogelators without aromatic rings in the side chains of amino acids, illustrates a new approach to design NDI-capped supramolecular hydrogels.en_US
dc.language.isoen_USen_US
dc.titleNanofibrous hydrogels self-assembled from naphthalene diimide (NDI)/amino acid conjugatesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c5ra00172ben_US
dc.identifier.journalRSC ADVANCESen_US
dc.citation.volume5en_US
dc.citation.issue26en_US
dc.citation.spage20410en_US
dc.citation.epage20413en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000350220400072en_US
dc.citation.woscount13en_US
Appears in Collections:Articles


Files in This Item:

  1. ee949f0b8f85fe01eecaa4cf51727049.pdf