Добірка наукової літератури з теми "Mesogenic systems"
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Статті в журналах з теми "Mesogenic systems"
Chao, C. Y., X. Li, and C. K. Ober. "Directing self-assembly in macromolecular systems: Hydrogen bonding in ordered polymers." Pure and Applied Chemistry 76, no. 7-8 (January 1, 2004): 1337–43. http://dx.doi.org/10.1351/pac200476071337.
Повний текст джерелаVora, R. A., and S. J. Rajput. "Binary Mesogenic Systems Comprised of Ester Mesogens and Non-Mesogens." Molecular Crystals and Liquid Crystals 209, no. 1 (December 1991): 265–77. http://dx.doi.org/10.1080/00268949108036201.
Повний текст джерелаKoßmehl, Gerhard, and Jürgen Bahr. "Liquid Crystalline Azomethines and Polyazomethines Containing Azobenzene and Stilbene Units." Zeitschrift für Naturforschung B 46, no. 2 (February 1, 1991): 245–54. http://dx.doi.org/10.1515/znb-1991-0219.
Повний текст джерелаMirnaya, T. A., G. G. Yaremchuk, and S. V. Volkov. "Phase Diagrams of Binary Alkanoate Systems with Common Cation: Potassium Isobutyrate-Propionate, and Sodium Butyrate-Isobutyrate." Zeitschrift für Naturforschung A 51, no. 8 (August 1, 1996): 957–59. http://dx.doi.org/10.1515/zna-1996-0811.
Повний текст джерелаDolden, J. G., and P. T. Alder. "The Mesogenic Index: An Empirical Method for Predicting Polymeric Liquid Crystallinity." High Performance Polymers 10, no. 3 (September 1998): 249–72. http://dx.doi.org/10.1088/0954-0083/10/3/004.
Повний текст джерелаMirnaya, T. A., G. G. Yaremchuk, and S. V. Volkov. "Phase Diagrams of Binary Systems of Some Alkali Iso–Butyrates with One Mesogenic Component." Zeitschrift für Naturforschung A 50, no. 9 (September 1, 1995): 893–96. http://dx.doi.org/10.1515/zna-1995-0917.
Повний текст джерелаMirnaya, T. A., Y. V. Bereznitski, and S. V. Volkov. "Liquid Crystals and Glasses in Binary Systems from Sodium and Alkali-Earth Metal Butyrates." Zeitschrift für Naturforschung A 51, no. 7 (July 1, 1996): 867–70. http://dx.doi.org/10.1515/zna-1996-0711.
Повний текст джерелаKrigbaum, William R. "Phase studies of binary mesogenic systems." Faraday Discussions of the Chemical Society 79 (1985): 133. http://dx.doi.org/10.1039/dc9857900133.
Повний текст джерелаBubnov, Alexej, Martin Cigl, Deyvid Penkov, Marek Otruba, Damian Pociecha, Hsiu-Hui Chen, and Věra Hamplová. "Design and Self-Assembling Behaviour of Calamitic Reactive Mesogens with Lateral Methyl and Methoxy Substituents and Vinyl Terminal Group." Polymers 13, no. 13 (June 30, 2021): 2156. http://dx.doi.org/10.3390/polym13132156.
Повний текст джерелаLi, Qian Yue, Jun Xu, Wen Zheng Zhang, and Peng Li. "Preparation and Characterization of Chiral Cyclosiloxane-Based Liquid-Crystalline Elastomers Bearing Menthyl Groups." Advanced Materials Research 466-467 (February 2012): 445–48. http://dx.doi.org/10.4028/www.scientific.net/amr.466-467.445.
Повний текст джерелаДисертації з теми "Mesogenic systems"
Haldar, Sripada. "Investigation on some achiral and chiral mesogemic systems by different experimental techniques." Thesis, University of North Bengal, 2013. http://hdl.handle.net/123456789/1481.
Повний текст джерелаTamba, Maria Gabriela [Verfasser], W. [Akademischer Betreuer] Weißflog, and R. [Akademischer Betreuer] Zentel. "Design of liquid crystal dimers and trimers : synthesis and characterization of novel systems containing bent-core and calamitic mesogenic units / Maria Gabriela Tamba. Betreuer: W. Weißflog ; R. Zentel." Halle, Saale : Universitäts- und Landesbibliothek Sachsen-Anhalt, 2014. http://d-nb.info/1069814741/34.
Повний текст джерелаElliott, Alice Margaret Sophie. "The physical structure of a system of mesogenic side chain polymers." Thesis, University of Cambridge, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388435.
Повний текст джерелаLian, Qing. "Structural investigation of a mesogen-chitosan graft copolymer system." Thesis, Georgia Institute of Technology, 1996. http://hdl.handle.net/1853/8598.
Повний текст джерелаHarwood, Simon M. "Novel chiral thermochromic mesogens derived from cholest-5-en-3#beta#-ol and related systems." Thesis, University of Hull, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327294.
Повний текст джерелаThompson, Neil James. "The synthesis and liquid-crystalline properties of metallo-mesogens : copper (II) complexes of #beta#-diketones and ferrocene-containing systems." Thesis, University of Hull, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.259771.
Повний текст джерелаPiovesan, Annie. "Contribution a l'etude de la structure moleculaire de mesogenes thermotropes hautement ordonnes : transitions monocouche-bicouche dans des composes polaires." Clermont-Ferrand 2, 1986. http://www.theses.fr/1986CLF21042.
Повний текст джерелаGuo, Chang-yi, and 郭昶邑. "Wide blue phase range observed in simple binary mixture systems containing biphenyl mesogens with 2-octyloxy tail." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/54061303021332896775.
Повний текст джерела大同大學
化學工程學系(所)
104
Four series of simple and rodlike racemic biphenyl mesogens possessing 2-octyloxy tail and different substituents at inner-core position of phenyl ring were easily prepared. In general, cubic BPs can be induced by adding appropriate ratio of chiral additive S811 or ISO(6OBA)2 into these racemic biphenyl mesogens during the heating and cooling processes. Interestingly, BPIII (5-6 K) easily dominates in high chirality condition for the blending mixture composed of mono-substituted biphenyl mesogens and chiral dopant S811. In addition, formation temperature of BPIII is near room temperature (36°C) when compound C6OBiPhI-OH is blend with 35 wt% S811 during the cooling process. Stable BPs with more than 20 K present in the blending mixture system composed of chiral dopant ISO(6OBA)2 and no substituted biphenyl mesogens CnOBiPhI-H or difluoro substituted CnOBiPhI-FF. Notably, the widest temperature range of BP (~34 K) can be induced by adding only 10 wt% chiral dopant ISO(6OBA)2 with high HTP into the biphenyl compound C6OBiPhI-H. The properties of BPs were characterized by POM, DSC and reflection spectra. On the basis of our experimental results and molecular modeling, we demonstrated that the appearance and temperature range of BPs in this simple type of biphenyl mesogen with 2-octyloxy tail are affected by the molecular dipole moment and biaxiality.
Wu, Zong-Ye, and 吳宗燁. "The effect of functional groups of racemic rodlike Schiff base mesogens on the stabilization of blue phase in binary mixture system." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/41890230015479625079.
Повний текст джерела大同大學
化學工程學系(所)
104
Four series of rodlike racemic Schiff base mesogens possessing different alkyl chains and two types of linkage, ester and alkynyl groups were synthesized and applied to induce cubic blue phases (BPs) in simple binary mixture systems. The mesophases of these Schiff base mesogens were confirmed by variable-temperature XRD and the characteristic texture of POM. In general, when chiral additive S811 with the ratio of 20-40 wt% is added into the rodlike racemic Schiff base mesogens possessing hydroxyl group, the temperature range of cubic BPs could be induced more than 20 K. The widest temperature range of cubic BP (35 K) presents in the blending mixture composed of rodlike racemic salicylaldimine-based mesogen OH-TIn possessing alkynyl linkage and 35-40 wt% S811. However, Schiff base mesogens with alkynyl linkage and no hydroxyl group show direct isotropic to chiral nematic transition when equal chiral dopants is added. Interestingly, wide BPs (>30 K) also can be induced by adding chiral additive ISO(6OBA)2 with high HTP into the racemic Schiff base mesogen with ester linkage. Cubic BPI and BPII can be confirmed by reflectance spectra and polarized optical microscopy (POM). The results of reflectance spectra indicate that Schiff base mesogens possessing alkoxy chain exhibit wider BPII range than Schiff base mesogens possessing alkyl chain due to larger super-cooling effect in the binary mixture system containing chiral dopant S811. However, only BPII can be induced in the blending mixture system composed of Schiff base mesogen and ISO(6OBA)2 both on heating and cooling processes. On the basis of our experimental results and molecular modeling, the appearance and temperature range of BPs are affected by the values of biaxiality, the polarizability and dipole moment of geometry.
Lobo, Nitin Prakash. "NMR Methods For The Study Of Partially Ordered Systems." Thesis, 2012. https://etd.iisc.ac.in/handle/2005/2588.
Повний текст джерелаЧастини книг з теми "Mesogenic systems"
Shibaev, V. P., Ya S. Freidzon, and S. G. Kostromin. "Molecular Architecture and Structure of Thermotropic Liquid Crystal Polymers with Mesogenic Side Groups." In Partially Ordered Systems, 77–120. New York, NY: Springer New York, 1994. http://dx.doi.org/10.1007/978-1-4613-8333-8_3.
Повний текст джерелаDong, Ronald Y. "Internal Dynamics of Flexible Mesogens." In Partially Ordered Systems, 233–62. New York, NY: Springer New York, 1997. http://dx.doi.org/10.1007/978-1-4612-1954-5_8.
Повний текст джерелаDong, Ronald Y. "Internal Dynamics of Flexible Mesogens." In Partially Ordered Systems, 213–35. New York, NY: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4684-0208-7_8.
Повний текст джерелаI. Shabatina, Tatyana. "Self-Assembled Nanostructures Formation in Hybrid Metal-Mesogenic Systems." In Nanostructures in Energy Generation, Transmission and Storage. IntechOpen, 2019. http://dx.doi.org/10.5772/intechopen.83003.
Повний текст джерелаCairns, Darran, Matthew Sousa, and Gregory Crawford. "Responsive Reactive Mesogen Microstructures." In Cross-Linked Liquid Crystalline Systems, 69–90. CRC Press, 2011. http://dx.doi.org/10.1201/b10525-5.
Повний текст джерелаStrohriegl, Peter. "Reactive Mesogens in Organic Light-Emitting Devices." In Cross-Linked Liquid Crystalline Systems, 319–46. CRC Press, 2011. http://dx.doi.org/10.1201/b10525-13.
Повний текст джерелаAmimori, Ichiro, and Tokuju Oikawa. "Viewing Angle Compensation Films for LCD Using Reactive Mesogens." In Cross-Linked Liquid Crystalline Systems, 91–118. CRC Press, 2011. http://dx.doi.org/10.1201/b10525-6.
Повний текст джерела"Self-Assembly and Biomimetics." In Nanoscopic Materials: Size-Dependent Phenomena and Growth Principles, 296–326. 2nd ed. The Royal Society of Chemistry, 2014. http://dx.doi.org/10.1039/bk9781849739078-00296.
Повний текст джерелаТези доповідей конференцій з теми "Mesogenic systems"
Larichev, A. V., A. N. Simonov, and V. P. Shibaev. "Real time holography and phase conjugation in films of azo dye containing side-chain LC polymers." In The European Conference on Lasers and Electro-Optics. Washington, D.C.: Optica Publishing Group, 1998. http://dx.doi.org/10.1364/cleo_europe.1998.cfk7.
Повний текст джерелаIlavský, Michal, Jan Nedbal, Lenka Poláková, Zdeňka Sedlákova, Michio Tokuyama, Irwin Oppenheim, and Hideya Nishiyama. "Thermal and Dielectric Behavior of Liquid-Crystalline Polybutadiene-Diols with Mesogenic Groups in Side Chains." In COMPLEX SYSTEMS: 5th International Workshop on Complex Systems. AIP, 2008. http://dx.doi.org/10.1063/1.2897834.
Повний текст джерелаMihara, Takashi, Hiroyuki Kohno, and Naoyuki Koide. "Physical properties of regioregular polythiophene derivatives containing mesogenic or ionic group in the side chain." In Smart Materials, Nano-, and Micro-Smart Systems, edited by Alan R. Wilson. SPIE, 2004. http://dx.doi.org/10.1117/12.585047.
Повний текст джерелаTorres, Yanira, Timothy White, Amber McClung, and William Oates. "Photoresponsive Azobenzene Liquid Crystal Polymer Networks: In Situ Photogenerated Stress Measurement." In ASME 2010 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. ASMEDC, 2010. http://dx.doi.org/10.1115/smasis2010-3656.
Повний текст джерела