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Synthesis and mesomorphic properties of Schiff base esters possessing terminal chloro substituent

dc.citation.epage640en_US
dc.citation.issue6en_US
dc.citation.spage637en_US
dc.citation.volume21en_US
dc.citation.woscount6
dc.contributor.authorHa, Sie Tiongen_US
dc.contributor.authorOng, Lay Khoonen_US
dc.contributor.authorLee, Siew Lingen_US
dc.contributor.authorLin, Hong Cheuen_US
dc.contributor.authorWin, Yip Fooen_US
dc.contributor.authorOng, Siew Tengen_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.date.accessioned2014-12-08T15:06:49Z
dc.date.available2014-12-08T15:06:49Z
dc.date.issued2010-06-01en_US
dc.description.abstractA homologous series of Schiff base esters, 4-chlorobenzylidene-4'-n-alkanoyloxyanilines, containing even number of carbons at the end groups of the molecules (C(n-1)H(2n-1)COO-, n = 4, 6, 8, 10, 12, 14, 16) were synthesized. The mesomorphic properties were investigated by differential scanning calorimetry (DSC) and polarizing optical microscopy (POM). It was found that the end groups of the molecules had an effect on the mesomorphic properties. n-Butanoyloxy was found non-mesogenic, whilst n-hexanoyloxy exhibited monotropic smectic phase. The higher members in this homologous series were enantiotropic smectogens. (C) 2010 Sie Tiong Ha. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.en_US
dc.identifier.doi10.1016/j.cclet.2010.01.023en_US
dc.identifier.issn1001-8417en_US
dc.identifier.journalCHINESE CHEMICAL LETTERSen_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cclet.2010.01.023en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/5343
dc.identifier.wosnumberWOS:000278442300002
dc.language.isoen_USen_US
dc.subjectSchiff base estersen_US
dc.subjectSmectic Aen_US
dc.subjectSmectic Ben_US
dc.subjectLiquid crystalen_US
dc.titleSynthesis and mesomorphic properties of Schiff base esters possessing terminal chloro substituenten_US
dc.typeArticleen_US

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