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A series of 1-methyl-1H-benzimidazole-based compounds, 2-(4ʹ-alkoxy-1,1ʹ-biphenyl-4-yl)-1-methyl- 1H-1,3-benzimidazole derivatives (nPPMx-M) with terminal hydrogen, methyl and nitro moieties (coded as nPPMH-M, nPPMM-M and nPPMN-M, respectively), were prepared and their structures were characterised. The compounds display enantiotropic smectic mesophases for hydrogen and methyl terminated compounds (nPPMH-M and nPPMM-M), and enantiotropic nematic mesophases for nitro terminated compounds (nPPMN-M) with short alkoxy chain below than 10 carbon atoms, where the mesophase ranges are 24-72°C and 74-104°C on heating and cooling processes for nPPMH-M, 90-119°C and 110-135°C for nPPMM-M, and 102-129°C and 113-207°C for nPPMN-M, respectively. It is noted that the compounds nPPMx-M exhibit much lower melting points and much wider mesophase range both in heating and cooling than non-1-methyl substituted analogs, which are ascribed to the disruption of hydrogen bonding among the molecules caused by methyl substitution at 1-position of benzimidazole. Meanwhile, among the compounds nPPMx-M, much wider mesophase ranges are obtained for nPPMM-M and nPPMN-M, indicating a much high mesophase stability for the compounds bearing terminal moiety (CH3 and NO2). [ABSTRACT FROM AUTHOR]

Fluorinated aromatics is generally chosen as mesogenic cores to design novel liquid crystal compounds. Here, a series of benzoxazole derivatives with laterally multifluorinated biphenyl units, 2-(3′,3-difluoro −4′-alkoxy-1,1′-biphenyl-4-yl)-benzoxazole derivatives (coded as nPF(3)PF(3)Bx), are synthesized and characterized, where methyl and nitro moieties are selected as terminal groups to investigate the effects of different polar substituents on the liquid crystal properties. The compounds nPF(3)PF(3)Bx show enantiotropic mesophases with mesophase ranges of 0-40°C and 0-63°C on heating and cooling for hydrogen-terminated derivatives (nPF(3)PF(3)BH), 43-93°C and 54-123°C for methyl-terminated ones (nPF(3)PF(3)BM), 60-108°C and 74-152°C for nitro terminated ones (nPF(3)PF(3)BN), respectively. They exhibit photoluminescence emission peaks at 390-392 nm and UV-vis absorption bands with maxima at 327-330 nm, respectively. The results reveal that lateral multifluoro substituents lead to a decrease in melting/clearing points, while electron-withdrawing terminal nitro moiety results in increases in both melting point and mesophase range. [ABSTRACT FROM AUTHOR]

Series of laterally multifluorinated heterocyclic compounds, 2-(2ʹ,3-difluoro-4ʹ-alkoxy-1,1ʹ-biphenyl-4-yl)-benzoxazole derivatives (nPF(2)PF(3)Bx), are prepared and characterised. They mainly display enantiotropic nematic mesophases with wider mesophase ranges of 12–107°C (heating process) and 22–134°C (cooling process) than the corresponding analogues. The enhanced nematic mesophase stability is achieved via slightly increasing inter-ring twist angle with inter-ring lateral fluorine substitute in biphenyl unit, as well as through improving the molecular polarity with multifluorine substitutes. Meanwhile, two inter-ring lateral fluorine atoms lead to a decrease in melting/clearing points and a wide nematic mesophase range, which makes it possible for heterocyclic mesogens nPF(2)PF(3)Bx to use in nematic liquid crystal display mixtures. [ABSTRACT FROM PUBLISHER]

Series of laterally monofluorinated compounds, 2-(4ʹ-alkoxy-3-fluorobiphenyl-4-yl)-1H-benzimidazole derivatives (nPPF(3)Mx) bearing different substituents (H, CH3, NO2, coded as nPPF(3)MH, nPPF(3)MM and nPPF(3)MN, respectively) at 5-position, were prepared and their structures were characterised. According to the results from differential scanning calorimetry and polarising optical microscopy, the present compounds nPPF(3)Mx exhibit enantiotropic smectic mesophases, for which the mesophase ranges are 13–67 and 47–111°C on heating and cooling for nPPF(3)MH, 84–112 and 126–154°C for nPPF(3)MM, and 23–102 and 49–117°C for nPPF(3)MN, respectively. Compared to non-fluorinated analogues, monofluorinated nPPF(3)Mx have low melting/clearing points and display enhanced mesophase range both in heating and cooling, which are attributed to the disruption of the side-to-side intermolecular packing caused by theortholateral fluoro substituents and the increased dipole–dipole interaction between the polar fluoro-substituted molecules, respectively. It is noted that nPPF(3)MM and nPPF(3)MN show a much wider mesophase range than nPPF(3)MH, which suggest that the substituent at benzimidazole moiety can improve the mesophase stability. [ABSTRACT FROM PUBLISHER]