Three series of compounds 1-21 were prepared by using 2-, 3-, and 4-pyridinemethanol as terminal group of calamitic liquid crystals. These compounds have some similarities in their phase behavior. They all exhibit SmA phase. A tilt smectic phase, SmC, will be formed when their flexible alkoxy chain is longer than hexoxy group. The profound difference between them is that the compounds 15-17 possess a short temperature range of N phase. The compounds 3 and 6 have the widest SmA phase, up to 94°C, and SmC phase, up to 46°C, respectively. . fore, three series of compounds 1-21 were derived from 2-, 3-, and 4-pyridinemethanol and their mesogenic properties were studied. The synthesis and structures of these compounds are shown in Fig. 1.
RESULTS AND DISCUSSIONThree series of compounds 1~21 were prepared by the esterification of seven analogous aromatic carboxylic acids and 2-pyridinemethanol, 3-pyridinemethanol, or 4-pyridinemethanol. Their structures were identified by IR, 1 H-NMR, 13 C-NMR, and MS. The spillting pattern and chemical shift of H-atom positioned ortho to hetero N-atom of pyridyl ring will give enough evidence to differentiate these three pyridyl ring system. The liquid crystal phases and phase transition temperatures of 1~21 were determined by DSC measurement and texture observation. These data