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Liquid Crystalline Conjugated Polymers and Their Applications in Organic Electronics

dc.citation.epage2733en_US
dc.citation.issue11en_US
dc.citation.spage2713en_US
dc.citation.volume47en_US
dc.citation.woscount34
dc.contributor.authorYang, Sheng-Hsiungen_US
dc.contributor.authorHsu, Chain-Shuen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:09:22Z
dc.date.available2014-12-08T15:09:22Z
dc.date.issued2009-06-01en_US
dc.description.abstractThis article describes the syntheses and electro-optical applications of liquid crystalline (LC) conjugated polymers, for example, poly(p-phenylenevinylene), polyfluorene, polythiophene, and other conjugated polymers. The polymerization involves several mechanisms: the Gilch route, Heck coupling, or Knoevenagel condensation for poly(p-phenylenevinylene)s, the Suzukior Yamamoto-coupling reaction for polyfluorenes, and miscellaneous coupling reactions for other conjugated polymers. These LC conjugated polymers are classified into two types: conjugated main chain polymers with long alkyl side chains, namely main-chain type LC polymers, and conjugated polymers grafting with mesogenic side groups, namely side-chain type LC conjugated polymers. In general, the former shows higher transition temperature and only nematic phase: the latter possesses lower transition temperature and more mesophases, for example. smectic and nematic phases, depending on the structure of mesogenic side chains. The fully conjugated main chain promises them as good candidates for polarized electroluminescent or field-effect devices. The polarized emission can be obtained by surface rubbing or thermal annealing in liquid crystalline phase, with maximum dichroic ratio more than 20. In addition, conjugated oligomers with LC properties are also included and discussed in this article. Several oligo-fluorene derivatives show outstanding polarized emission properties and potential use in LCD backlight application. (c) 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47:2713-2733, 2009en_US
dc.identifier.doi10.1002/pola.23342en_US
dc.identifier.issn0887-624Xen_US
dc.identifier.journalJOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRYen_US
dc.identifier.urihttp://dx.doi.org/10.1002/pola.23342en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/7152
dc.identifier.wosnumberWOS:000266388100001
dc.language.isoen_USen_US
dc.subjectconducting polymersen_US
dc.subjectconjugated polymersen_US
dc.subjectfield effect transistoren_US
dc.subjectlight-emitting diodesen_US
dc.subjectliquid crystallineen_US
dc.subjectliquid-crystalline polymers (LCP)en_US
dc.subjectpolarized electroluminescenceen_US
dc.subjectpolyfluoreneen_US
dc.subjectpoly(p-phenylenevinylene)en_US
dc.subjectpolythiopheneen_US
dc.titleLiquid Crystalline Conjugated Polymers and Their Applications in Organic Electronicsen_US
dc.typeReviewen_US

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