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Synthesis of laterally substituted alpha-methylstilbene-tolane liquid crystals

dc.citation.epage9en_US
dc.citation.issue1en_US
dc.citation.spage1en_US
dc.citation.volume35en_US
dc.citation.woscount5
dc.contributor.authorChang, Chin-Yenen_US
dc.contributor.authorChien, Szu-Yuanen_US
dc.contributor.authorHsu, Chain-Shuen_US
dc.contributor.authorGauza, Sebastianen_US
dc.contributor.authorWu, Shin-Tsonen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:12:47Z
dc.date.available2014-12-08T15:12:47Z
dc.date.issued2008en_US
dc.description.abstractThree series of alpha-methylstilbene-tolane liquid crystals, 4-[2-(4-alkylphenyl)-1-ethynyl]-4'-fluoro-alpha-methylstilbene (3a-3e), 4-[2-(4-alkylphenyl)-1-ethynyl]-2'-methyl-4'-fluoro-alpha-methylstilbene (4a-4e) and 4-[2-(4-alkylphenyl)-1-ethynyl]-3'-methyl-4'-fluoro-alpha-methylstilbene (5a-5e), were synthesized and their phase transition temperatures characterized. All the alpha-methylstilbene-tolane liquid crystals exhibit an enantiotropic nematic phase. Compounds 5a-5e, which contain a lateral methyl group at the 3 position of the middle phenyl ring, display low melting points, a wide nematic range and a small enthalpy of fusion. Their potential applications for displays and laser-beam steering are noted.en_US
dc.identifier.doi10.1080/02678290701743027en_US
dc.identifier.issn0267-8292en_US
dc.identifier.journalLIQUID CRYSTALSen_US
dc.identifier.urihttp://dx.doi.org/10.1080/02678290701743027en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/9846
dc.identifier.wosnumberWOS:000252356000001
dc.language.isoen_USen_US
dc.titleSynthesis of laterally substituted alpha-methylstilbene-tolane liquid crystalsen_US
dc.typeArticleen_US

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