Journal
SOFT MATTER
Volume 9, Issue 4, Pages 1172-1177Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2sm26807h
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Funding
- National Natural Science Fund for Distinguished Young Scholar [51025313]
- National Natural Science Foundation [50973010, 53373003, 51272026, 51273022]
- Important Project of Ministry of Education [313002]
- National Natural Science Foundation Youth Fund of China [61007016]
- China Postdoctoral Science Foundation [20100470205]
- Fundamental Research Funds for the Central Universities of China [FRF-TP-12-035A]
- China Infovision Optoelectronics (Kun Shan) Co. Ltd.
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Several kinds of tolane cyano derivatives with different lateral fluoro substituents are doped with chiral additives to induce the blue phase (BP). Fluoro substituents are found to exert a great effect on the BP ranges for biphenyl mesogens. The laterally difluorinated compounds exhibit wider BP ranges than their corresponding mono-fluorinated homologues when equal chiral dopant is added, while the non-fluorinated compounds show direct isotropic (Iso) to chiral nematic (N-star) transitions, even in highly chiral systems. By adjusting the concentrations of the chiral dopant ISO(6OBA)(2) in the fluorinated liquid crystals, the BP ranges can be broadened to more than 12 degrees C. Competition between the steric repulsions caused by the lateral fluoro substituents and pi-pi interactions of the aromatic cores is supposed to be the main factor that leads to the above results. Apart from this, a weak C-H center dot center dot center dot F interaction may have also been conducive to the BP stabilization.
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