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dc.contributor.authorSuzuki, Katsuakien
dc.contributor.authorUchida, Yoshiakien
dc.contributor.authorTamura, Ruien
dc.contributor.authorShimono, Satoshien
dc.contributor.authorYamauchi, Junen
dc.contributor.alternative田村, 類ja
dc.date.accessioned2013-02-04T07:51:52Z-
dc.date.available2013-02-04T07:51:52Z-
dc.date.issued2012-02-27-
dc.identifier.issn0959-9428-
dc.identifier.urihttp://hdl.handle.net/2433/169678-
dc.description.abstractThe generation of spin glass-like inhomogeneous magnetic interactions (the average spin–spin interaction constant: [J with combining macron] > 0 or [J with combining macron] < 0), which we refer to as positive or negative “magneto-LC effects”, respectively, was observed in the bulk liquid crystalline (LC) phases of chiral all-organic radical compounds 2 with a positive dielectric anisotropy (Δε > 0) under weak magnetic fields. The sign and magnitude of [J with combining macron] depended on the type of LC phase or superstructure; stronger positive interactions ([J with combining macron] > 0) operated in the chiral smectic A (SmA*) phase of (2S, 5S)-2b (89% ee) than in the chiral nematic (N*) phase of (2S, 5S)-2a (96% ee), whereas weak negative interactions ([J with combining macron] < 0) were observed in the achiral nematic (N) phase of (±)-2a. The origin of the positive magneto-LC effects operating in the SmA* and N* phases was interpreted in terms of the generation of ferromagnetic head-to-tail spin–spin dipole interactions, whereas antiferromagnetic interactions arising from the formation of the RS magnetic dipolar interaction were responsible for the negative magneto-LC effects in the N phase.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherRoyal Society of Chemistryen
dc.rights© The Royal Society of Chemistry 2012en
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.titleObservation of positive and negative magneto-LC effects in all-organic nitroxide radical liquid crystals by EPR spectroscopyen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA10822442-
dc.identifier.jtitleJournal of Materials Chemistryen
dc.identifier.volume22-
dc.identifier.spage6799-
dc.identifier.epage6806-
dc.relation.doi10.1039/c2jm16278d-
dc.textversionauthor-
dcterms.accessRightsopen access-
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