首页 | 本学科首页   官方微博 | 高级检索  
     


Origin of the Director Tilt in the Lyotropic Smectic C* Analog Phase: Hydration Interactions and Solvent Variations
Authors:Dr. Johanna R. Bruckner  Friederike Knecht  Prof. Dr. Frank Giesselmann
Affiliation:Institute of Physical Chemistry, University of Stuttgart, Stuttgart, Germany
Abstract:The origin and long‐range correlation of the director tilt in the recently discovered urn:x-wiley:14394235:media:cphc201500673:cphc201500673-math-0001 phase, which is the lyotropic analog of the thermotropic smectic C* (SmC*) liquid crystalline phase, are investigated. Polarized micro‐Raman spectroscopy reveals that the director tilt in the urn:x-wiley:14394235:media:cphc201500673:cphc201500673-math-0002 phase originates from a tilting of the aromatic 2‐phenylpyrimidine cores of the surfactant molecules. Optical measurements of the tilt angle show that its magnitude decreases with increasing solvent concentration, suggesting that the long‐range inter‐lamellar correlation of the tilt directions is reduced at increasing thickness of the solvent layers. The phase diagrams with four different solvents (water, formamide, N‐methylformamide, N,N‐dimethylformamide) are investigated, showing that the urn:x-wiley:14394235:media:cphc201500673:cphc201500673-math-0003 phase is only formed with those solvents that exhibit a dense network of hydrogen bonds. This observation suggests that these hydrogen bond networks play an essential role in the long‐range correlation of the director tilt between adjacent surfactant layers. To verify this assumption, mixtures with deuterated solvents are investigated, showing that the tilt angle in the urn:x-wiley:14394235:media:cphc201500673:cphc201500673-math-0004 phase is indeed reduced by this modification of the solvent′s hydrogen bond network.
Keywords:amphiphiles  hydration interactions  liquid crystals  Raman spectroscopy  solvent effects
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号