Effect of replacing the terminal phenyl ring with 3-pyridyl and inversion of imine linkage on the mesophase behaviour of four-ring azo/ester/Schiff base compounds-Reference-Cited by-同舟云学术

Effect of replacing the terminal phenyl ring with 3-pyridyl and inversion of imine linkage on the mesophase behaviour of four-ring azo/ester/Schiff base compounds

Published:2020-12-14 Issue:9 Volume:48 Page:1217-1230
ISSN:0267-8292
Container-title:Liquid Crystals
language:en
Short-container-title:Liquid Crystals

Author:

Ahmed Nagwa H.S.¹,Saad Gamal R.²

Affiliation:

1. Higher Institute of Engineering and Technology, Department of Mathematics and Physical Science, New Cairo Academy, New Cairo City, Egypt

2. Chemistry Department, Cairo University, Giza, Egypt

Publisher

Informa UK Limited

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/02678292.2020.1851414

Reference93 articles.

1. Smectic mesophase properties of dimeric compounds. 1. Dimeric compounds based on the mesogenic azobenzene unit

2. Liquid crystal oligomers: going beyond dimers

3. Mesomorphic properties of liquid crystalline compounds with biphenyl moiety containing azo-ester, azo-cinnamate central linkages and different terminal group†

4. The liquid crystal properties of symmetric and non-symmetric dimers based on the azobenzene mesogenic group

5. Supramolecular Hydrogen-Bonded Liquid Crystals Formed from 4-(4′-Pyridylazophenyl)-4″-alkoxy Benzoates and 4-Substituted Benzoic Acids

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