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dc.contributor.authorHu, Yien_US
dc.contributor.authorWu, Kuan-Yien_US
dc.contributor.authorZhu, Tiantianen_US
dc.contributor.authorShen, Pengen_US
dc.contributor.authorZhou, Yien_US
dc.contributor.authorLi, Xiaohongen_US
dc.contributor.authorWang, Chien-Lungen_US
dc.contributor.authorTu, Yingfengen_US
dc.contributor.authorLi, Christopher Y.en_US
dc.date.accessioned2019-04-02T06:00:33Z-
dc.date.available2019-04-02T06:00:33Z-
dc.date.issued2018-10-08en_US
dc.identifier.issn1433-7851en_US
dc.identifier.urihttp://dx.doi.org/10.1002/anie.201805717en_US
dc.identifier.urihttp://hdl.handle.net/11536/148247-
dc.description.abstractWe report herein a series of tetrablock-mimic azobenzene-containing [60]fullerene dyads that form supramolecular liquid crystals (LCs) from phase-segregated two-dimensional (2D) crystals. The unique double-, triple-, and quadruple-layer packing structure of fullerenes in the 2D crystals leads to different smectic supramolecular LC phases, and novel LC phase transitions were observed upon changes in the fullerene packing layer number in the 2D crystals. Interestingly, by combining the LC properties with 2D crystals, these materials show excellent electron mobility in the order of 10(-3) cm(2) V-1 s(-1), despite their relatively low fullerene content. Our results provide a novel method to manipulate 2D crystal layer thickness, with promising applications in optoelectronic devices.en_US
dc.language.isoen_USen_US
dc.subjectelectron mobilityen_US
dc.subjectfullerenesen_US
dc.subjectliquid crystalsen_US
dc.subjectsupramolecular chemistryen_US
dc.subjecttwo-dimensional crystalsen_US
dc.titleUnique Supramolecular Liquid-Crystal Phases with Different Two-Dimensional Crystal Layersen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/anie.201805717en_US
dc.identifier.journalANGEWANDTE CHEMIE-INTERNATIONAL EDITIONen_US
dc.citation.volume57en_US
dc.citation.spage13454en_US
dc.citation.epage13458en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000446306600011en_US
dc.citation.woscount1en_US
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