Homeotropic Alignment of Dendritic Columnar Liquid Crystal Induced by Hydrogen-Bonded Triphenylene Core Bearing Fluoroalkyl Chains
Shinsuke Ishihara, Yusuke Furuki, Jonathan P. Hill, Katsuhiko Ariga, Shinji Takeoka
Abstract
Shinsuke Ishihara, Yusuke Furuki, Jonathan P. Hill, Katsuhiko Ariga, Shinji Takeoka
Abstract
A 1:3 molar complex of the fluoroalkyl side chain-substituted 2,6,10-tris-carboxymethoxy-3,7,11-tris(4,4,5,5,6,6,7,7,7-nonafluoroheptyloxy)triphenylene (TPF4) with the second generation dendron 3,5-bis(3,4-bis-dodecyloxybenzyloxy)-N-pyridin-4-yl-benzamide (DN) assembled through complementary hydrogen bonding to form a supramolecular columnar liquid crystal, which exhibited homeotropic alignment when sandwiched between octadecyltrichlorosilane (OTS)-coated or indium tin oxide (ITO)-coated glass plates due to specific interactions between the fluoroalkyl side chains and the substrates.
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A 1:3 molar complex of the fluoroalkyl side chain-substituted 2,6,10-tris-carboxymethoxy-3,7,11-tris(4,4,5,5,6,6,7,7,7-nonafluoroheptyloxy)triphenylene (TPF4) with the second generation dendron 3,5-bis(3,4-bis-dodecyloxybenzyloxy)-N-pyridin-4-yl-benzamide (DN) assembled through complementary hydrogen bonding to form a supramolecular columnar liquid crystal, which exhibited homeotropic alignment when sandwiched between octadecyltrichlorosilane (OTS)-coated or indium tin oxide (ITO)-coated glass plates due to specific interactions between the fluoroalkyl side chains and the substrates.
Key concepts: Homeotropic alignment, Triphenylene, Materials science, Octadecyltrichlorosilane, Supramolecular chemistry, Side chain, Hydrogen bond, Indium tin oxide