2-(对烷氧基苯甲酸酯基或对烷氧基苯丙烯酸酯基)-5-氧-2,5-二氢呋喃化合物的合成与液晶性质研究

Two series of p-alkoxybenzoates Ia-If and p-alkoxycinnamates IIa-IIf, each species beating one terminal furanone, have been synthesized and characterized by IR, ^13C NMR, ^1H NMR, MS spectra and elemental analysis. The mesogenic properties of both series of furanones have been studied by polarizing optical microscopy and differential scanning calorimetry （DSC）. The relationship between structures and mesogenic properties was discussed. The results show that the increased alkoxy chain length （C7-C12） and the bridging groups between the benzene ring and the furanone ring affected the mesomorphic properties greatly, and the two series of furanones might display monotropic or enantiotropic nematic （N） or semetic C （SmC） mesophases and different mesomorpic phase temperature ranges corresponding to different carbon chain length.

Synthesis and Mesomorphic Properties of 2‐(4‐Alkoxybenzoyloxy or 4‐Alkoxycinnamoyloxy)‐5‐oxo‐2,5‐dihydrofurans

Two series of p‐alkoxybenzoates Ia–If and p‐alkoxycinnamates IIa–IIf , each species bearing one terminal furanone, have been synthesized and characterized by IR, ¹³C NMR, ¹H NMR, MS spectra and elemental analysis. The mesogenic properties of both series of furanones have been studied by polarizing optical microscopy and differential scanning calorimetry (DSC). The relationship between structures and mesogenic properties was discussed. The results show that the increased alkoxy chain length (C₇–C₁₂) and the bridging groups between the benzene ring and the furanone ring affected the mesomorphic properties greatly, and the two series of furanones might display monotropic or enantiotropic nematic (N) or semetic C (SmC) mesophases and different mesomorpic phase temperature ranges corresponding to different carbon chain length.