4.5 Article

Photo-Responsive Behavior of Azobenzene Based Polar Hockey-Stick-Shaped Liquid Crystals

期刊

CHEMPHYSCHEM
卷 22, 期 13, 页码 1361-1370

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cphc.202100215

关键词

azobenzene; hockey-stick-shaped liquid crystals; polar liquid crystals; photoisomerization; X-ray diffraction

资金

  1. SERB Project [CRG/2019/000901/OC]
  2. CSIR [09/947(0254)/2020-EMR-I]
  3. IISER Mohali
  4. DST, India [SR-WOS-A-CS-26-2017]
  5. DST-SERB, India [NPDF/2016/000560]

向作者/读者索取更多资源

The study presented here investigates the photoswitching behavior of azobenzene-based polar hockey-stick-shaped liquid crystals (HSLCs) by synthesizing two new series of phenyl-ring based polar HSLCs. The synthesized materials exhibited decent photochromic behavior and different potential applications. The thermal phase behavior of the superstructural assembly was characterized using various techniques, revealing the formation of nematic and partially bilayer smectic A phases depending on the length of the terminal alkyl chain.
A study on the photoswitching behavior of azobenzene-based polar hockey-stick-shaped liquid crystals (HSLCs) has been presented. Two new series of five phenyl rings based polar HSLCs have been designed and synthesized. Solution state photoisomerization of the synthesized materials was investigated thoroughly via UV-visible and H-1 NMR spectroscopic techniques, whereas solid-state photochromic behavior was elucidated via physical color change of the materials, solid-state UV-visible study, powder XRD, and FE-SEM techniques. The materials exhibited decent photochromic behavior for different potential applications. The thermal phase behavior of the superstructural assembly has been characterized via polarizing optical microscopy (POM), differential scanning calorimetry (DSC), and temperature-dependent small and wide-angle X-ray scattering (SAXS/WAXS) studies. Depending upon the length of the terminal alkyl chain, nematic (N) and partially bilayer smectic A (SmA(d)) phases were observed. DFT calculations revealed the favorable anti-parallel arrangement of the polar molecules that substantiate the formation of SmA(d) phase.

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