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dc.contributor.advisorMcGrath, Dominic V.en_US
dc.contributor.authorBiswas, Soma
dc.creatorBiswas, Somaen_US
dc.date.accessioned2011-12-05T14:18:11Z
dc.date.available2011-12-05T14:18:11Z
dc.date.issued2008en_US
dc.identifier.urihttp://hdl.handle.net/10150/193436
dc.description.abstractAzobenzene upon photochemical E/Z isomerization changes both its shape and size. The E-azobenzene moiety falls in the class of calamitic liquid crystalline mesogens, producing a wide variety of mesophases. Two series of linear bis(azobenzene) compounds, one with phenyl benzoate linkage and the other with benzyl benzoate linkage were synthesized. The termini of these molecules ranged from a dodecyloxy chain to hydrophobic amphiphilic dendrons up to first generation. We determined the effects of both the linkages and generation number on the mesogenic properties of these compounds. Our results show that the mesogenic behavior of these bis(azobenzene) compounds are highly dependent on the linkages between individual azobenzenes and that for the bis(azobenzene) compounds of the phenyl benzoate series, generation number had an effect on the liquid crystalline mesophase of the compounds
dc.language.isoENen_US
dc.publisherThe University of Arizona.en_US
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en_US
dc.subjectAzobenzene Mesogenen_US
dc.subjectcalamitic (bis) azobenzeneen_US
dc.subjectDendronised materialsen_US
dc.subjectLiquid Crystalsen_US
dc.subjectpolycatenaren_US
dc.subjectsmectic C mesophaseen_US
dc.titleEFFECT OF LINKER CHEMISTRY AND TERMINAL SUBSTITUENTS ON THE LIQUID CRYSTALLINE PROPERTIES OF BIS(AZOBENZENE) MESOGENSen_US
dc.typetexten_US
dc.typeElectronic Thesisen_US
dc.contributor.chairMcGrath, Dominic V.en_US
dc.identifier.oclc659750766en_US
thesis.degree.grantorUniversity of Arizonaen_US
thesis.degree.levelmastersen_US
dc.contributor.committeememberMash, Eugeneen_US
dc.contributor.committeememberLichtenberger, Dennisen_US
dc.identifier.proquest10186en_US
thesis.degree.disciplineChemistryen_US
thesis.degree.disciplineGraduate Collegeen_US
thesis.degree.nameM.S.en_US
refterms.dateFOA2018-08-24T17:48:16Z
html.description.abstractAzobenzene upon photochemical E/Z isomerization changes both its shape and size. The E-azobenzene moiety falls in the class of calamitic liquid crystalline mesogens, producing a wide variety of mesophases. Two series of linear bis(azobenzene) compounds, one with phenyl benzoate linkage and the other with benzyl benzoate linkage were synthesized. The termini of these molecules ranged from a dodecyloxy chain to hydrophobic amphiphilic dendrons up to first generation. We determined the effects of both the linkages and generation number on the mesogenic properties of these compounds. Our results show that the mesogenic behavior of these bis(azobenzene) compounds are highly dependent on the linkages between individual azobenzenes and that for the bis(azobenzene) compounds of the phenyl benzoate series, generation number had an effect on the liquid crystalline mesophase of the compounds


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