Synthesis and Photoswitching Properties of Liquid Crystals Derived from Myo-Inositol

A new series of unconventional liquid crystal molecules derived from myo-inositol core were synthesized by linking six azobenzene units having terminal double bonds as polymerizable functional groups to myoinositol. Differential scanning calorimetry, polarizing optical microscopy and X-ray diffracti...

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Main Authors: Lutfor, M. R., M. M., Yusoff, Kumar, Sandeep
Format: Article
Published: Royal Society of Chemistry 2014
Subjects:
Online Access:http://umpir.ump.edu.my/id/eprint/8079/
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author Lutfor, M. R.
M. M., Yusoff
Kumar, Sandeep
author_facet Lutfor, M. R.
M. M., Yusoff
Kumar, Sandeep
author_sort Lutfor, M. R.
building UMP Institutional Repository
collection Online Access
description A new series of unconventional liquid crystal molecules derived from myo-inositol core were synthesized by linking six azobenzene units having terminal double bonds as polymerizable functional groups to myoinositol. Differential scanning calorimetry, polarizing optical microscopy and X-ray diffraction studies were carried out to determine mesomorphism in these materials. Thus, all compounds showed stable enantiotropic SmA phase which was independent of the chain length and chain parity. The photoswitching behaviour of these molecules in solutions showed E to Z isomerization in 8–10 s, whereas the reverse process took about 270–305 min. In solid film, the E–Z photoisomerization took 5 s, while the reverse transformation from Z to E state took 120 min. The photoswitching behaviour of these materials represents one of the fastest switching times so far observed in such materials and,therefore, they are good candidates for molecular switches.
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spelling ump-80792018-02-06T07:36:10Z http://umpir.ump.edu.my/id/eprint/8079/ Synthesis and Photoswitching Properties of Liquid Crystals Derived from Myo-Inositol Lutfor, M. R. M. M., Yusoff Kumar, Sandeep QD Chemistry A new series of unconventional liquid crystal molecules derived from myo-inositol core were synthesized by linking six azobenzene units having terminal double bonds as polymerizable functional groups to myoinositol. Differential scanning calorimetry, polarizing optical microscopy and X-ray diffraction studies were carried out to determine mesomorphism in these materials. Thus, all compounds showed stable enantiotropic SmA phase which was independent of the chain length and chain parity. The photoswitching behaviour of these molecules in solutions showed E to Z isomerization in 8–10 s, whereas the reverse process took about 270–305 min. In solid film, the E–Z photoisomerization took 5 s, while the reverse transformation from Z to E state took 120 min. The photoswitching behaviour of these materials represents one of the fastest switching times so far observed in such materials and,therefore, they are good candidates for molecular switches. Royal Society of Chemistry 2014-07-29 Article PeerReviewed Lutfor, M. R. and M. M., Yusoff and Kumar, Sandeep (2014) Synthesis and Photoswitching Properties of Liquid Crystals Derived from Myo-Inositol. RSC Advances, 4 (66). pp. 35089-35098. ISSN 2046-2069. (Published) http://dx.doi.org/10.1039/C4RA05568C DOI: 10.1039/c4ra05568c
spellingShingle QD Chemistry
Lutfor, M. R.
M. M., Yusoff
Kumar, Sandeep
Synthesis and Photoswitching Properties of Liquid Crystals Derived from Myo-Inositol
title Synthesis and Photoswitching Properties of Liquid Crystals Derived from Myo-Inositol
title_full Synthesis and Photoswitching Properties of Liquid Crystals Derived from Myo-Inositol
title_fullStr Synthesis and Photoswitching Properties of Liquid Crystals Derived from Myo-Inositol
title_full_unstemmed Synthesis and Photoswitching Properties of Liquid Crystals Derived from Myo-Inositol
title_short Synthesis and Photoswitching Properties of Liquid Crystals Derived from Myo-Inositol
title_sort synthesis and photoswitching properties of liquid crystals derived from myo-inositol
topic QD Chemistry
url http://umpir.ump.edu.my/id/eprint/8079/
http://umpir.ump.edu.my/id/eprint/8079/
http://umpir.ump.edu.my/id/eprint/8079/