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dc.contributor.authorYoshida, Yukihiroen
dc.contributor.authorNakamura, Yutoen
dc.contributor.authorKishida, Hideoen
dc.contributor.authorHayama, Hiromien
dc.contributor.authorNakano, Yoshiakien
dc.contributor.authorYamochi, Hidekien
dc.contributor.authorSaito, Gunzien
dc.contributor.alternative中野, 義明ja
dc.contributor.alternative矢持, 秀起ja
dc.date.accessioned2018-03-16T02:46:28Z-
dc.date.available2018-03-16T02:46:28Z-
dc.date.issued2017-06-02-
dc.identifier.issn1466-8033-
dc.identifier.urihttp://hdl.handle.net/2433/230179-
dc.description.abstractSingle crystals of racemic charge-transfer complexes comprising a helical polycyclic aromatic hydrocarbon molecule, [6]helicene, as the electron donor (D) and 7, 7, 8, 8-tetracyano-p-quinodimethane (TCNQ) analogs as the electron acceptor (A) were obtained via either co-sublimation or solvent evaporation. All complexes consist of heterochiral DA-type alternating π-columns with a [⋯(P)-[6]helicene⋯TCNQ⋯(M)-[6]helicene⋯TCNQ⋯] repeating unit, which show a peculiar wavy feature primarily related to the nonplanar geometry of the [6]helicene molecules. [6]Helicene molecules form a two-dimensional sheet intersecting the columns, and the molecular arrangement (namely, either homochiral or heterochiral arrangement) in the sheets depends on the TCNQ analog. Theoretical calculations were carried out to discuss the origin of the molecular deformation of [6]helicene molecules in the CT solids in terms of intermolecular interactions.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherRoyal Society of Chemistry (RSC)en
dc.rightsThis is the accepted version of the article, which has been published in final form at http://doi.org/10.1039/c7ce00763aen
dc.rightsThe full-text file will be made open to the public on 01 Jun 2018 in accordance with publisher's 'Terms and Conditions for Self-Archiving'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.rightsThis is not the published version. Please cite only the published version.en
dc.titleRacemic charge-transfer complexes of a helical polycyclic aromatic hydrocarbon moleculeen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleCrystEngCommen
dc.identifier.volume19-
dc.identifier.issue26-
dc.identifier.spage3626-
dc.identifier.epage3632-
dc.relation.doi10.1039/c7ce00763a-
dc.textversionauthor-
dc.addressFaculty of Agriculture, Meijo University・Division of Chemistry, Graduate School of Science, Kyoto Universityen
dc.addressDepartment of Applied Physics, Nagoya University /Department of Applied Physics, Nagoya Universityen
dc.addressFaculty of Agriculture, Meijo Universityen
dc.addressDivision of Chemistry, Graduate School of Science, Kyoto University・Research Center for Low Temperature and Materials Sciences, Kyoto Universityen
dc.addressDivision of Chemistry, Graduate School of Science, Kyoto University・Research Center for Low Temperature and Materials Sciences, Kyoto Universityen
dc.addressFaculty of Agriculture, Meijo University・Toyota Physical and Chemical Research Instituteen
dcterms.accessRightsopen access-
datacite.date.available2018-06-01-
datacite.awardNumber25288041-
datacite.awardNumber26288035-
datacite.awardNumber15K17901-
datacite.awardNumber16H00964-
datacite.awardNumber16H04139-
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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