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dc.contributor.authorOhtani, Shunsukeen
dc.contributor.authorNakamura, Masashien
dc.contributor.authorGon, Masayukien
dc.contributor.authorTanaka, Kazuoen
dc.contributor.authorChujo, Yoshikien
dc.contributor.alternative大谷, 俊介ja
dc.contributor.alternative中村, 将志ja
dc.contributor.alternative権, 正行ja
dc.contributor.alternative田中, 一生ja
dc.contributor.alternative中條, 善樹ja
dc.date.accessioned2020-08-21T01:22:05Z-
dc.date.available2020-08-21T01:22:05Z-
dc.date.issued2020-06-18-
dc.identifier.issn1359-7345-
dc.identifier.issn1364-548X-
dc.identifier.urihttp://hdl.handle.net/2433/254052-
dc.description.abstractWe describe herein a robust π-conjugated molecules with solid-state emission in the near-infrared (NIR) region (ΦF = 0.03–0.06). Initially, the diastereomers of bisboron azomethine complexes having phenyl groups in the same and opposite directions to the π-plane were synthesized. These diastereomers showed emission properties with larger red-shifts (>200 nm) and 10 times larger emission efficiencies than those of the mononuclear complex. Theoretical calculation data indicate that superior optical properties of the bisboron complexes should be attributable to efficient expansion of the π-conjugated system. In addition, the bisboron compounds and their conjugated polymers exhibited intense NIR emissions even in the solid state.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherRoyal Society of Chemistryen
dc.rightsThis is the accepted manuscript of the article, which has been published in final form at https://doi.org/10.1039/d0cc02301a.en
dc.rightsThe full-text file will be made open to the public on 18 June 2021 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.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.titleSynthesis of fully-fused bisboron azomethine complexes and their conjugated polymers with solid-state near-infrared emissionen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleChemical Communicationsen
dc.identifier.volume56-
dc.identifier.issue48-
dc.identifier.spage6575-
dc.identifier.epage6578-
dc.relation.doi10.1039/d0cc02301a-
dc.textversionauthor-
dc.addressDepartment of Polymer Chemistry, Graduate School of Engineering, Kyoto University Katsuraen
dc.addressDepartment of Polymer Chemistry, Graduate School of Engineering, Kyoto University Katsuraen
dc.addressDepartment of Polymer Chemistry, Graduate School of Engineering, Kyoto University Katsuraen
dc.addressDepartment of Polymer Chemistry, Graduate School of Engineering, Kyoto University Katsuraen
dc.addressDepartment of Polymer Chemistry, Graduate School of Engineering, Kyoto University Katsuraen
dc.identifier.pmid32400769-
dcterms.accessRightsopen access-
datacite.date.available2021-06-18-
datacite.awardNumber18K14275-
datacite.awardNumber17H03067-
datacite.awardNumber17H01220-
datacite.awardNumber24102013-
datacite.awardNumber18H05356-
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
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
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