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Rearrangement of an aniline linked perylene bisimide under acidic conditions and visible to near-infrared emission from the intramolecular charge-transfer state of its fused derivatives

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dc.contributor.author Kojima, Mitsuru en
dc.contributor.author Tamoto, Akira en
dc.contributor.author Aratani, Naoki en
dc.contributor.author Yamada, Hiroko en
dc.date.accessioned 2017-12-14T05:13:19Z en
dc.date.available 2017-12-14T05:13:19Z en
dc.date.issued 2017-04-18 en
dc.identifier.issn 1359-7345 en
dc.identifier.uri http://hdl.handle.net/10061/12184 en
dc.description.abstract We have prepared a series of aniline-linked and fused perylene bisimides (PBIs) for making near-infrared (NIR) fluorophores. During this research, we found an unexpected rearrangement reaction on the PBI core for the first time. The aniline- and phenothiazine-fused PBIs exhibit excellent absorption ability and visible-to-NIR emission owing to their intramolecular charge transfer character. en
dc.language.iso en en
dc.publisher The Royal Society of Chemistry en
dc.rights Copyright c The Royal Society of Chemistry 2017 en
dc.rights 出版社許諾条件により本文は2018/4/18以降に公表する。 ja
dc.title Rearrangement of an aniline linked perylene bisimide under acidic conditions and visible to near-infrared emission from the intramolecular charge-transfer state of its fused derivatives en
dc.type.nii Journal Article en
dc.contributor.transcription アラタニ, ナオキ ja
dc.contributor.transcription ヤマダ, ヒロコ ja
dc.contributor.alternative 荒谷, 直樹 ja
dc.contributor.alternative 山田, 容子 ja
dc.textversion author en
dc.identifier.ncid AA12455105 en
dc.identifier.jtitle Chemical Communications en
dc.identifier.volume 53 en
dc.identifier.issue 42 en
dc.identifier.spage 5698 en
dc.identifier.epage 5701 en
dc.relation.doi 10.1039/C7CC01520H en
dc.identifier.NAIST-ID 73299042 en
dc.identifier.NAIST-ID 73293565 en
dc.relation.pmid 28447685 en


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