Journal of the American Chemical Society, volume 138, issue 16, pages 5283-5289
Reversible Isothermal Twist–Bend Nematic–Nematic Phase Transition Driven by the Photoisomerization of an Azobenzene-Based Nonsymmetric Liquid Crystal Dimer
Daniel A. Paterson
1, 2
,
Jie Xiang
2
,
Gautam Singh
3
,
Rebecca Walker
1
,
D. M. Agra-Kooijman
3
,
Cristina Moliner
4
,
Min Gao
2
,
John W. V. Storey
1
,
Satyendra Kumar
3
,
Oleg D. Lavrentovich
2
,
Corrie T Imrie
1
Publication type: Journal Article
Publication date: 2016-04-19
scimago Q1
SJR: 5.489
CiteScore: 24.4
Impact factor: 14.4
ISSN: 00027863, 15205126
PubMed ID:
27015140
General Chemistry
Catalysis
Biochemistry
Colloid and Surface Chemistry
Abstract
The liquid crystal nonsymmetric dimer, 1-(4-butoxyazobenzene-4'-yloxy)-6-(4-cyanobiphenyl-4'-yl) hexane (CB6OABOBu), shows enantiotropic twist-bend nematic, NTB, and nematic, N, phases. The NTB phase has been confirmed using polarized light microscopy, freeze fracture transmission electron microscopy, and X-ray diffraction. The helicoidal pitch in the NTB phase is 18 nm. The NTB-N (TNTBN) and N-I (TNI) transition temperatures are reduced upon UV light irradiation, with the reduction in TNTBN being much larger than that in TNI. An isothermal, reversible NTB-N transition may be driven photochemically. These observations are attributed to a trans-cis photoisomerization of the azobenzene fragment on UV irradiation, with the cis isomers stabilizing the standard nematic phase and the trans isomers stabilizing the NTB phase. The dramatic changes in TNTBN provide evidence that the transition between the normal nematic and twist-bend nematic with spontaneous breaking of chiral symmetry is crucially dependent on the shape of molecular dimers, which changes greatly during the trans-cis isomerization.
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