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Synthesis and mesomorphic properties and optical behaviour analysis of homologous series azobenzene liquid crystal monomer with polar substituents.
- Source :
- Liquid Crystals; Jan2020, Vol. 47 Issue 2, p155-168, 14p
- Publication Year :
- 2020
-
Abstract
- Twenty novel azobenzene liquid crystal micromolecular compounds named ω-[4-(p-substituted azobenzeneoxy carbonyl]acid (X-ABCnA) have been designed and synthesised, followed by studies on the thermal performance and mesomorphic properties of the compounds. The liquid crystal compounds were divided into five homologous series based on the terminal substituents R (R = CH<subscript>3</subscript>O, CH<subscript>3</subscript>, H, Cl, NO<subscript>2</subscript>). In each series, the number of carbons on flexible chain was 4, 6, 8 and 10, respectively. Fourier-transform infrared, proton nuclear magnetic resonance and elementary analysis demonstrated that the structure of the synthesised azobenzene liquid crystal compounds was consistent with the molecular design. The mesomorphic properties were tested, analysed and characterised by using differential scanning calorimetry and polarised optical microscopy. The melting transition (T<subscript>m</subscript>) of all the compounds in homologous series with different substituents appeared to decrease with the increase of carbon numbers on flexible chains. The same held true for the temperature of isotropic-mesophase/crystalline transition. The compounds with stronger polarity of terminal substituents were more likely to form broader mesogenic ranges. The liquid crystal compounds discussed in this work can be regarded as a reference for the synthesis of mesogenic arms participating in the synthesis of novel multi-arm liquid crystalline macromolecules and polymers. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 02678292
- Volume :
- 47
- Issue :
- 2
- Database :
- Complementary Index
- Journal :
- Liquid Crystals
- Publication Type :
- Academic Journal
- Accession number :
- 141877065
- Full Text :
- https://doi.org/10.1080/02678292.2019.1633480