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dc.contributor.authorNishino, Kentaen
dc.contributor.authorMorisaki, Yasuhiroen
dc.contributor.authorTanaka, Kazuoen
dc.contributor.authorChujo, Yoshikien
dc.contributor.alternative森崎, 泰弘ja
dc.contributor.alternative田中, 一生ja
dc.contributor.alternative中條, 善樹ja
dc.date.accessioned2020-02-10T06:36:45Z-
dc.date.available2020-02-10T06:36:45Z-
dc.date.issued2019-03-15-
dc.identifier.issn1861-4728-
dc.identifier.urihttp://hdl.handle.net/2433/245652-
dc.description.abstractTo obtain solid‐state emissive materials having stimuli‐responsive luminescent chromic properties without phase transition, benzobithiophenes modified with two o‐carborane units having various substituents in the adjacent phenyl ring in o‐carborane were designed and synthesized. Their emission colors were strongly affected not only by the substituents at the para‐position of the phenyl ring but also by molecular distribution in the solid state. In particular, the emission colors were changed by heating without crystal phase transition. It was proposed that their thermochromic properties were correlated not with isomerization but with the molecular motion at the distorted benzobithiophene moiety.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherWileyen
dc.rightsThis is the peer reviewed version of the following article: K. Nishino, Y. Morisaki, K. Tanaka, Y. Chujo, Chem. Asian J. 2019, 14, 789, which has been published in final form at https://doi.org/10.1002/asia.201801529. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.en
dc.rightsThis is not the published version. Please cite only the published version.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.subjectcarboranesen
dc.subjectcrystal packingen
dc.subjectluminescenceen
dc.subjectphotoluminescenceen
dc.subjectthermochromic materialsen
dc.subjectsolid-state emissionen
dc.titleDesign of Thermochromic Luminescent Dyes Based on the Bis(ortho-carborane)-Substituted Benzobithiophene Structureen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleChemistry - An Asian Journalen
dc.identifier.volume14-
dc.identifier.issue6-
dc.identifier.spage789-
dc.identifier.epage795-
dc.relation.doi10.1002/asia.201801529-
dc.textversionauthor-
dc.addressDepartment of Polymer Chemistry, Graduate School of Engineering, Kyoto Universityen
dc.addressDepartment of Polymer Chemistry, Graduate School of Engineering, Kyoto Universityen
dc.addressDepartment of Polymer Chemistry, Graduate School of Engineering, Kyoto Universityen
dc.addressDepartment of Polymer Chemistry, Graduate School of Engineering, Kyoto Universityen
dc.identifier.pmid30444302-
dcterms.accessRightsopen access-
datacite.awardNumberJP17H03067-
datacite.awardNumberJP17H01220-
datacite.awardNumberJP24102013-
datacite.awardNumberJP18H05356-
dc.identifier.pissn1861-4728-
dc.identifier.eissn1861-471X-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
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