Syntheses, Characterisation And Mesophase Investigation Of A New Class Of Hydrazine-Based Liquid Crystal Dimers

dc.contributor.authorAbd Rani, Umairah
dc.date.accessioned2017-02-10T01:57:24Z
dc.date.available2017-02-10T01:57:24Z
dc.date.issued2016-02
dc.description.abstractFour new series of non-symmetric dibenzylidenehydrazine-based liquid crystal dimers, N-{4[10-(16-decyloxyphenylimino)methyl)phenoxy] alkyloxybenzy lidene}-N'-(4'-decyloxybenzylidene)hydrazines (SB-(CH2)n-HZ), N-{4[10-(16-decyl oxyphenyldiazenyl)phenoxy]alkyloxybenzylidene}-N'-(4'-decyloxybenzylidene) hyd razines (AZ-(CH2)n-HZ), N-[4-{12-[18-((S)-(-)-23-methylbutyloxy)carbonylphenyl] phenoxy} alkyloxybenzylidene]-N'-(4'-decyloxybenzylidene) hydrazines (BP-(CH2)n -HZ) and N-(4-alkylxybenzylidene)-N'-[4'-(cholesteryloxycarbonyl)alkyloxybenzylid ene]hydrazines (Chol-(CH2)m-HZ-(CH2)n) had been synthesised and characterised. All dimers incorporated dibenzylidenehydrazine as one of the mesogenic arms and differ in terms of the other side arms and spacer parity. The molecular structures of these dimers were elucidated by CHN, FT-IR, 1D and 2D-NMR spectroscopy. Their liquid crystalline properties were investigated using POM, DSC and XRD. Phase behavior of the dimers was structure and spacer parity dependent. Various mesophases including nematic (N), cholesteric (N*), smectic A (SmA), chiral smectic A (SmA*), smectic C (SmC), chiral smectic C (SmC*) and smectic J (SmJ) were observed when one of the mesogenic side arms was changed. A pronounced odd-even effect in transitional properties (melting and clearing temperatures as well as entropy changes) were seen in SB-(CH2)n-HZ, AZ-(CH2)n-HZ and BP-(CH2)n- HZ upon varying the spacer length.en_US
dc.identifier.urihttp://hdl.handle.net/123456789/3700
dc.language.isoenen_US
dc.publisherUniversiti Sains Malaysiaen_US
dc.subjectLiquid crystals dimersen_US
dc.titleSyntheses, Characterisation And Mesophase Investigation Of A New Class Of Hydrazine-Based Liquid Crystal Dimersen_US
dc.typeThesisen_US
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