Two series of three ring esters with chiral chain (derivative of (S)-octanol-2) and achiral chain (the swallow type) with high tilted synclinic and anticlinic phases were chosen to studies. The aim of presented studies was to find how the changes of different molecule units influence the mesomorphic properties of the compounds (temperatures, enthalpies and the sequence of phase transitions) and to find members with the best properties for mixture formulation. The compounds were studied by polarising microscope, differential scanning calorimetry, miscibility and X-ray diffraction methods.
Mesomorphic properties (phase transitions enthalpies and temperatures) and the dependence of smectic layer spacings upon reduced temperature for eight homologous series of three ring ester such as: (S)-(+)-4-(1-methylheptyloxycarbonyl)phenyl or (S)-(+)-4-(1-methylheptyloxycarbonyl)-3-fluorophenyl or (S)-(+)-4-(1-methyl-heptyloxycarbonyl)-2-fluorophenyl 4'-(perfluoroalkanoyloxyhexyloxy)biphenylates and 4'-(alkanoyloxyhexyloxy)-biphenylates, and (S)-(+)-4-(1-methylheptyloxycarbonyl)biphenyl-4-yl 4'-(perfluoroalkanoyloxyhexyloxy)benzoates and 4'-(alkanoyloxyhexyloxy)benzoates were described. The terminal chain fluorinated compounds have SmC*anti-SmC*-SmA-Iso phase sequence and a high tilted (orthoconic) antiferroelectric phase in broad temperature range.
Homologous series of chiral (S) 4-(1-methylheptyloxycarbonyl)-phenyl and achiral 4-(4-heptyloxycarbonylphenyl 4-(perfluoroalkanoyloxyhexyloxy)biphenylates or 4-(alkanoyloxyhexyloxy)biphenylates, chiral (S) and racemic (R,S) 4′-(1-methyl heptyloxycarbonyl)biphenyl-4-yl 4-(perfluoroalkanoyloxyhexyloxy)benzoates or 4 (alkanoyloxyhexyloxy)benzoates have been prepared and their phase transitions have been investigated by DSC and polarizing thermomicroscopic methods. Moreover the temperature dependence of interlayer spacing by a small angle X-ray diffraction method has been studied. The chiral and achiral members exhibit a SmC anti. phase, while racemic members only exhibit SmC phase. Fluorinated compounds have lower melting points, lower melting enthalpy and broader range of the SmC anti. phase than earlier prepared series with shorter spacer group (CH 2 ) m , m < 6. They are very useful components for the formulation of orthoconic (interlayer tilt 90°) antiferroelectric mixtures with temperature range from (−20°C) to 100°C.
Two homologous series of mesogenic materials with molecules containing an amide moiety, cyclic or symmetrically branched, as the terminal group have been synthesized. Materials of both series form lamellar liquid crystal phases. It was observed that elongation of the amide chains in ‘fork-like’ compounds destabilizes the mesophases, while ‘cyclic’ materials, even with quite large terminal amide rings, exhibit enantiotropic liquid crystalline phases.
The optic and electrooptic properties of recently prepared orthoconic antiferroelectrics have been revieved. Relation between their chemical structure and mesogenic properties, smectic layer structure and helical pitch is discussed.
Tristate regular mixtures with different electro-optical properties such as threshold voltage, saturation voltage, holding ratio and response time are presented. The relation of properties with the structure of compounds is discussed. All of mixtures show only moderate dynamic and static contrast but big gray level scale without hysteresis for positive and negative field driving.
Homologous series of three ring esters (biphenylates and benzoates) – chiral (S), racemic (R,S) and achiral (either isopropyl or 4-heptyl chain) were tested by DSC, X-ray and electrooptic methods. It was found that in chiral, racemic and achiral homologous series with a 4-heptyl chain, the smectic A phase is a strongly tilted phase of de Vries type, and molecules in the anticlinic phase are highly tilted within the layers (up to 45°). The homologous series with an isopropyl chain gave a normal smectic A phase and low tilted synclinic or anticlinic phase. Chirality does not influence the smectic layer thickness or the molecular tilts in the smectic synclinic or anticlinic phase, but strongly influences the ability to form anticlinic order. The ability of the molecules to adopt anticlinic order is suppressed when a permanent helical structure or strong steric hindrance is absent.
Educational videos are very useful tools in HE in general and Chemistry in particular. They can show techniques such as handling a chemical reaction and equipment and at the same time can be very entertaining… or boring. Boring videos are rarely watched and only a very determined person will finish watching them and learn the lesson they are trying to teach. In education there is a need for shorter, more realistic and entertaining movies. You need to grasp the viewers’ attention and keep them engaged. We decided to use our Undergraduate students to help us to film educational videos and prepare the content of the Advanced Organic Laboratory webpage. Their enthusiasm, down-to-earth approach and experience helped us to prepare content that is more understandable, interesting and approachable for their fellow students. The project was successful in improving the students’ engagement and in creating new educational tools for the Chemistry Department. It was also fun for the students and staff involved. Students had an opportunity to learn more advanced techniques, deepen their own Chemistry knowledge and feed it back to teachers and their colleagues. Filming, music composing, teaching, presenting, learning Chemistry (theory and techniques) and acting – new ‘stars’ were born.
Compounds with the terminal swallow tailed chain have been synthesized. The prepared compounds were studied by thermomicroscopy, differential scanning calorimetry, miscibility and X-ray diffraction methods.