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dc.contributor.advisorDarkwa, J
dc.contributor.authorMoutloali, R.M
dc.date.accessioned2023-06-14T16:43:57Z
dc.date.available2023-06-14T16:43:57Z
dc.date.issued2003
dc.identifier.urihttp://hdl.handle.net/11394/10256
dc.descriptionPhilosophiae Doctor - PhDen_US
dc.description.abstractThermal analysis data of compounds A, C, F and I established that they were nonmesogenic while E and G were found to be mesogenic. The lack of mesogenic behaviour of A could be attributed to hydrogen bonding. The non-mesogenic behaviour of C and F is due to reduced molecular anisotropy as a result of large lateral substituents. Complexes I decomposed at high temperatures and before melting and hence no liquid crystalline behaviour was found. It is likely that the high decomposition temperature is the result of increased molecular interactions. We found that removing the phosphine ligands and increasing molecular length induced liquid crystalline behaviour in complexes E. The more planar complexes G were also found to be liquid crystallineen_US
dc.language.isoenen_US
dc.publisherUniversity of the Western Capeen_US
dc.subjectthiolatoen_US
dc.subjectschiffen_US
dc.subjectnickelen_US
dc.subjectpalladiumen_US
dc.subjectmesogensen_US
dc.titleThiolato schiff base complexes of nickel and palladium as mesogens and molecular wiresen_US
dc.rights.holderUniversity of the Western Capeen_US


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