Relevant bibliographies by topics / Chiral crystal

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Chiral crystal'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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Journal articles on the topic "Chiral crystal"

1

Sasaki, Takeo, Satoshi Kajikawa, and Yumiko Naka. "Dynamic amplification of light signals in photorefractive ferroelectric liquid crystalline mixtures." Faraday Discuss. 174 (2014): 203–18. http://dx.doi.org/10.1039/c4fd00068d.

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The photorefractive effect in photoconductive ferroelectric liquid crystals that contain photoconductive chiral compounds was investigated. Terthiophene compounds with chiral structures were chosen as the photoconductive chiral compounds, and they were mixed with an achiral smectic C liquid crystal. The mixtures exhibit the ferroelectric chiral smectic C phase. The photorefractivity of the mixtures was investigated by two-beam coupling experiments. It was found that the ferroelectric liquid crystals containing the photoconductive chiral compound exhibit a large gain coefficient of over 1200 cm<sup>−1</sup> and a fast response time of 1 ms. Real-time dynamic amplification of an optical image signal of over 30 fps using the photorefractive ferroelectric liquid crystal was demonstrated.
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Ben-Moshe, Assaf, Alessandra da Silva, Alexander Müller, et al. "The chain of chirality transfer in tellurium nanocrystals." Science 372, no. 6543 (2021): 729–33. http://dx.doi.org/10.1126/science.abf9645.

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Despite persistent and extensive observations of crystals with chiral shapes, the mechanisms underlying their formation are not well understood. Although past studies suggest that chiral shapes can form because of crystallization in the presence of chiral additives, or because of an intrinsic tendency that stems from the crystal structure, there are many cases in which these explanations are not suitable or have not been tested. Here, an investigation of model tellurium nanocrystals provides insights into the chain of chirality transfer between crystal structure and shape. We show that this transfer is mediated by screw dislocations, and shape chirality is not an outcome of the chiral crystal structure or ligands.
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Lemmerer, Andreas, Nikoletta B. Báthori, and Susan A. Bourne. "Chiral carboxylic acids and their effects on melting-point behaviour in co-crystals with isonicotinamide." Acta Crystallographica Section B Structural Science 64, no. 6 (2008): 780–90. http://dx.doi.org/10.1107/s0108768108034526.

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The crystal structures of co-crystals of two systems of chiral carboxylic acids, optically active and racemic 2-phenylpropionic acid and 2-phenylbutyric acid, with isonicotinamide are reported to investigate the effects of the chirality of the chiral carboxylic acids on the melting point of the co-crystal complexes. It was found that the racemic co-crystal has a higher melting point than the optically active co-crystal, which correlates with the denser packing arrangement inherent in centrosymmetric space groups.
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Wu, Jian Yi, Li Zhang, Li Ling Cai, and Yang Zhang. "Catalyzing Synthesis of Chiral Nitrendipine." Advanced Materials Research 518-523 (May 2012): 3943–46. http://dx.doi.org/10.4028/www.scientific.net/amr.518-523.3943.

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This paper describes the chiral synthesis of R-2,6-dimethyl-4-(3-nitro phenyl)-1,4- dihydro-pyridine-3,5-dicarboxylic acid 3-ethyl ester 5-methyl ester (R-Nitrendipine) using chiral phase transfer catalyst. The structure of the obtained nitrendipine crystals was determined with single crystal X-ray diffraction. The crystal is monoclinic, with the space group of P21/c and unit cell constants of a=8.8577(15), b=15.581(3), c=12.999(2)Å, β=92.458(4)°, V=1792.3(5)Å3, Z=4, Dc =1.335g/cm3, F(000)=760. X-ray analysis reveals that the product is a chiral nitrendipine with R-configuration of the dihydropyridine ring. And measurement of polarimeter reveals that the synthesized nitrendipine is a chiral molecular.
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Wagner, Gabriele, Rudolf Herrmann, BjØrn Pedersen, and Wolfgang Scherer. "Synthesis and Structure of Chiral Silatranes Derived from Terpenes." Zeitschrift für Naturforschung B 56, no. 1 (2001): 25–38. http://dx.doi.org/10.1515/znb-2001-0105.

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Abstract Starting with the chiral pool compounds (-)-menthone, (-)-limonene, (-)-β-pinene, and (-)-carvone, new homochiral triethanolamine derivatives were obtained and converted to chi­ral silatranes. These silatranes were characterized by crystal structure analyses and NMR techniques. Conformational analyses in the solid state and in solution show that the chiral terpene residues determine the direction of the ring puckering of the silatrane moiety.
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Ozaki, M., Y. Matsuhisa, H. Yoshida, R. Ozaki, and A. Fujii. "Photonic crystals based on chiral liquid crystal." physica status solidi (a) 204, no. 11 (2007): 3777–89. http://dx.doi.org/10.1002/pssa.200776422.

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Bisht, Kamal Kumar, Priyank Patel, Yadagiri Rachuri, and Suresh Eringathodi. "Binary co-crystals of the active pharmaceutical ingredient 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene and camphoric acid." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 70, no. 1 (2014): 63–71. http://dx.doi.org/10.1107/s2052520613031260.

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Co-crystals comprising the active pharmaceutical ingredient 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene, C12H10N4, and the chiral co-formers (+)-, (−)- and (rac)-camphoric acid (cam), C10H16O4, have been synthesized. Two different stoichiometries of the API and co-former are obtained, namely 1:1 and 3:2. Crystallization experiments suggest that the 3:2 co-crystal is kinetically favoured over the 1:1 co-crystal. Single-crystal X-ray diffraction analysis of the co-crystals reveals N—H...O hydrogen bonding as the primary driving force for crystallization of the supramolecular structures. The 1:1 co-crystal contains undulating hydrogen-bonded ribbons, in which the chiral cam molecules impart a helical twist. The 3:2 co-crystal contains discrete Z-shaped motifs comprising three molecules of the API and two molecules of cam. The 3:2 co-crystals with (+)-cam, (−)-cam (space groupP21) and (rac)-cam (space groupP21/n) are isostructural. The enantiomeric co-crystals contain pseudo-symmetry consistent with space groupP21/n, and the co-crystal with (rac)-cam represents a solid solution between the co-crystals containing (+)-cam and (−)-cam.
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Sala, Filip. "Beam splitting in chiral nematic liquid crystals." Photonics Letters of Poland 10, no. 4 (2018): 109. http://dx.doi.org/10.4302/plp.v10i4.867.

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By lunching the beam into the chiral nematic liquid crystals it is possible to achieve a non-diffractive beam similar to a soliton. This effect is caused by the molecular reorientation i.e. nonlinear response of the material forming the areas of higher refractive index. Diffraction is suppressed by the focusing effect. For appropriate launching conditions it is also possible to achieve a beam which splits into two or more separate beams. Such phenomenon is discussed in this article and analyzed theoretical. To model this effect Fully Vectorial Beam Propagation Method coupled with the Frank-Oseen elastic theory is used. Simulations are performed for various input beam powers, widths, polarization angles and launching positions. Full Text: PDF ReferencesG. Assanto and M. A. Karpierz, "Nematicons: self-localised beams in nematic liquid crystals", Liq. Cryst. 36, 1161–1172 (2009) CrossRef G. Assanto, Nematicons: Spatial Optical Solitons in Nematic Liquid Crystals, John Wiley &amp; Sons Inc. Hoboken, New Jersey (2013) DirectLink A. Piccardi, A. Alberucci, U. Bortolozzo, S. Residori, and G. Assanto, "Soliton gating and switching in liquid crystal light valve", Appl. Phys. Lett. 96, 071104 (2010). CrossRef D. Melo, I. Fernandes, F. Moraes, S. Fumeron, and E. Pereira, "Thermal diode made by nematic liquid crystal", Phys. Lett. A 380, 3121 – 3127 (2016). CrossRef U. Laudyn, M. Kwaśny, F. A. Sala, M. A. Karpierz, N. F. Smyth, G. Assanto, "Curved optical solitons subject to transverse acceleration in reorientational soft matter", Sci. Rep. 7, 12385 (2017) CrossRef M. Kwaśny, U. A. Laudyn, F. A. Sala, A. Alberucci, M. A. Karpierz, G. Assanto, "Self-guided beams in low-birefringence nematic liquid crystals", Phys. Rev. A 86, 013824 (2012) CrossRef F. A. Sala, M. M. Sala-Tefelska, "Optical steering of mutual capacitance in a nematic liquid crystal cell", J. Opt. Soc. Am. B. 35, 133-139 (2018) CrossRef U. A. Laudyn, A. Piccardi, M. Kwasny, M. A. Karpierz, G. Assanto, "Thermo-optic soliton routing in nematic liquid crystals", Opt. Lett. 43, 2296-2299 (2018) CrossRef F. A. Sala, M. M. Sala-Tefelska, M. J. Bujok, J. "Influence of temperature diffusion on molecular reorientation in nematic liquid crystals", Nonlinear Opt. Phys. Mater. 27, 1850011 (2018) CrossRef I-C Khoo Liquid crystals John Wiley &amp; Sons, Inc (2007) DirectLink P. G. de Gennes, J. Prost, The Physics of Liquid Crystals, Clarendon Press (1995) DirectLink U. A. Laudyn, P. S. Jung, M. A. Karpierz, G. Assanto, "Quasi two-dimensional astigmatic solitons in soft chiral metastructures", Sci. Rep. 6, 22923 (2016) CrossRef J. Beeckman, A. Madani, P. J. M. Vanbrabant, P. Henneaux, S-P. Gorza, M. Haelterman, "Switching and intrinsic position bistability of soliton beams in chiral nematic liquid crystals", Phys. Rev. A 83, 033832 (2011) CrossRef A. Madani, J. Beeckman, K. Neyts, "An experimental observation of a spatial optical soliton beam and self splitting of beam into two soliton beams in chiral nematic liquid crystal", Opt. Commun. 298–299, 222-226, (2013) CrossRef G. D. Ziogos, E. E. Kriezis, "Modeling light propagation in liquid crystal devices with a 3-D full-vector finite-element beam propagation method", Opt. Quant. Electron 40, 10 (2008) CrossRef F. A. Sala, M. A. Karpierz, "Chiral and nonchiral nematic liquid-crystal reorientation induced by inhomogeneous electric fields", J. Opt. Soc. Am. B 29, 1465-1472 (2012) CrossRef F. A. Sala, M. A. Karpierz, "Modeling of molecular reorientation and beam propagation in chiral and non-chiral nematic liquid crystals", Opt. Express 20, 13923-13938 (2012) CrossRef F. A. Sala, "Design of false color palettes for grayscale reproduction", Displays, 46, 9-15 (2017) CrossRef
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Funahashi, Masahiro. "Chiral Liquid Crystalline Electronic Systems." Symmetry 13, no. 4 (2021): 672. http://dx.doi.org/10.3390/sym13040672.

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Liquid crystals bearing extended π-conjugated units function as organic semiconductors and liquid crystalline semiconductors have been studied for their applications in light-emitting diodes, field-effect transistors, and solar cells. However, studies on electronic functionalities in chiral liquid crystal phases have been limited so far. Electronic charge carrier transport has been confirmed in chiral nematic and chiral smectic C phases. In the chiral nematic phase, consisting of molecules bearing extended π-conjugated units, circularly polarized photoluminescence has been observed within the wavelength range of reflection band. Recently, circularly polarized electroluminescence has been confirmed from devices based on active layers of chiral conjugated polymers with twisted structures induced by the molecular chirality. The chiral smectic C phase of oligothiophene derivatives is ferroelectric and indicates a bulk photovoltaic effect, which is driven by spontaneous polarization. This bulk photovoltaic effect has also been observed in achiral polar liquid crystal phases in which extended π-conjugated units are properly assembled. In this manuscript, optical and electronic functions of these chiral π-conjugated liquid crystalline semiconductors are reviewed.
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Takanabe, Akifumi, Masahito Tanaka, Hideko Koshima, Motoo Shiro, and Toru Asahi. "Optical properties of chiral photomechanical salicylideneaniline crystal." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C379. http://dx.doi.org/10.1107/s205327331409620x.

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Mechanical motion caused by UV/VIS radiation onto bulk materials is called a photomechanical effect. In other words, the photomechanical effect is a type of energy conversion systems. Recently, a mechanical bending of photochromic diarylethene crystals was reported, and the molecular-scale motion was found to produce the macroscale bending of the crystals (Kobatake et al., 2007). Subsequently, several photomechanical crystals have been reported to provide promising opportunities for artificial molecular machinery. The mechanism of the conversion of light energy to mechanical energy, however, has not quantitatively been understood. In photomechanical effect, microscale structural change and stress should be involved with optical properties of anisotropy and chirality; linear birefringence (LB), linear dichroism (LD), circular dichroism (CD) and optical rotatory power (ORP). CD and ORP in a chiral anisotropic crystal are extremely difficult to be measured owing exclusively to the contribution of strong linear anisotropy. The High Accuracy Universal Polarimeter generalized by our group (G-HAUP) enables us to measure LB, LD, CD, and ORP simultaneously and quantitatively (Tanaka et al., 2012). The purpose of our study is to investigate the relationship between microscale structural change or stress induced by UV/VIS radiation and the four optical properties. We synthesized chiral N-3,5-di-tert-butylsalicylidene-1-phenylethylamine photochromic crystal, as shown in Scheme 1, because the mechanism of photomechanical effect in this crystal has been revealed qualitatively by analyzing single-crystal structure under UV/VIS radiation (Koshima et al., 2013). The LB, LD, CD, and ORP spectra in the direction perpendicular to (001) were successfully measured under VIS radiation. Furthermore, LD spectrum was found to change by UV radiation in 30mW/cm2. These results could contribute to an elucidation of the mechanism of photomechanical effect quantitatively.
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Dissertations / Theses on the topic "Chiral crystal"

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Wu, Haixia. "Anchoring Behavior of Chiral Liquid Crystal at Polymer Surface: In Polymer Dispersed Chiral Liquid Crystal Films." Thesis, Available online, Georgia Institute of Technology, 2004:, 2004. http://etd.gatech.edu/theses/available/etd-04082004-154054/unrestricted/wu%5Fhaixia%5F200405%5Fmast.pdf.

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Thesis (M.S.)--Textile and Fiber Engineering, Georgia Institute of Technology, 2004.<br>Griffin, Anselm, Committee Member; Srinivasarao, Mohan, Committee Chair; Park, Jung O., Committee Member. Includes bibliographical references (leaves 101-105).
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Payne, Jeffrey C. (Jeffrey Christopher) 1981. "Nanoparticle-chiral nematic liquid crystal composites." Thesis, Massachusetts Institute of Technology, 2006. http://hdl.handle.net/1721.1/36218.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2006.<br>Includes bibliographical references (leaves 76-79).<br>The advancement of the fabrication of a one-dimensional photonic crystal without time-reversal and space-inversion symmetries was pursued. Theoretical studies predict that such a system would exhibit unusual optical properties, including indirect photonic band gaps and backward wave propagating eigenmodes. Such a system can be created experimentally by combing magnetooptical nanoparticles with a chiral nematic liquid crystal. The fabrication of this material system was advanced through two distinct phases of research. The first phase seeks to produce magnetooptical yttrium iron garnet (YIG) nanoparticles with an average diameter on the order of 15-50 nm. It was determined that a commercially available yttrium iron oxide nanopowder (purchased from Sigma-Aldrich Corporation) exhibited YIG and orthorhombic yttrium iron oxide (YFeO3) phases after being calcined at 800 °C for two hours. These nanoparticles were slightly smaller than desired, having diameters on the order of 10-20 nm. Direct nanoparticle synthesis via coprecipitation in microemulsions produced superior results, resulting in a pure YIG material with diameters on the order of 30-50 nm.<br>(cont.) The second phase examines the manner in which nanoparticles co-assemble with a chiral nematic liquid crystal. It was determined that the addition of nanoparticles to a 5CB-COC system disrupts the system's helical structure. This disruption lowers the system's phase transition temperatures and inhibits the system's ability to form reflectivity peaks.<br>by Jeffrey Christopher Payne.<br>S.M.
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May, Alison. "Materials for chiral nematic liquid crystal applications." Thesis, University of Southampton, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273767.

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Remnant, Anna Marie. "Photoisomeric effect in chiral liquid crystal systems." Thesis, University of Southampton, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.274508.

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Birkett, John E. "Chiral HAN cells : a novel liquid crystal arrangement." Thesis, University of Exeter, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.438718.

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Park, Jinwoo. "Synthesis and Development of Helical Functional Polymers using Advanced Chiral Liquid Crystal Fields." 京都大学 (Kyoto University), 2015. http://hdl.handle.net/2433/199336.

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McLaren-Jones, Jennifer Sian Elizabeth. "Band edge lasing in chiral nematic liquid crystals." Thesis, University of Cambridge, 2019. https://www.repository.cam.ac.uk/handle/1810/288382.

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For the last 20 years, there has been considerable interest in chiral nematic liquid crystal band edge lasers. The birefringent molecules of chiral nematic liquid crystals form a periodic helical structure, which results in a photonic bandgap for circularly polarised light with the same sense of rotation as the helix. A large increase in effective gain is seen for a fluorescent gain medium within the liquid crystal at the band edges, resulting in lasing. Applications of liquid crystal lasers could include miniature medical diagnostic tools, large-area holographic laser displays, and environmental sensing. The wavelength of emission from dye-doped chiral nematic liquid crystals is highly flexible, with lasers demonstrated across the visible range and near infra-red. This thesis investigates two routes for improving the functionality of chiral nematic liquid crystal lasers, supported by mathematical modelling of expected lasing wavelengths based on reflection and transmission by anisotropic layers. Perovskite is tested as a replacement for fluorescent laser dyes as a gain medium,both in the form of quantum dots dispersed in liquid crystal, and as films placed in liquid crystal structures. It is shown that while the perovskite tested provides some emission, it is not compatible for lasing in these devices, and suggestions for building on these results are made. In-plane switching is tested and developed as a means to achieve tuning of the laser wavelength, demonstrating a continuous wavelength shift of 15 nm, from 600.71 nm to 585.03 nm, over a voltage range of 100 V. This is an improvement on previous tuning in related devices, and may be extended with optimisation of cell thickness,electrode geometry, and initial lasing wavelength. Accurate descriptions of the refractive index profile of the liquid crystal and perovskite are developed and included in mathematical modelling, in addition to descriptions of the wavelength-dependent gain of a laser dye and perovskite. Suggestions for developing this modelling are made, particularly by the inclusion of accurate modelling of the distortion caused by in-plane switching.
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Hylton, Rebecca Kathryn. "Crystal structure prediction and thermodynamic modelling of chiral molecules." Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10040863/.

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This thesis explores the potential of computed crystal energy landscapes as an aid in the rational design of chiral separation processes. Crystal structure prediction (CSP) methods have been used to explore the crystal energy landscapes of prototypical chiral systems and the corresponding lattice energies and properties are used to help explore the thermodynamics of these systems. The crystal energy landscape of two very different chiral systems is explored. The small, but very flexible 3-chloromandelic acid molecule which can form strong hydrogen bonding motifs, and the rigid lactide molecule where the crystal structures are dominated by weak van der Waals forces. These crystal energy landscapes highlight the complexity of chiral molecules, particularly the enantiopure structures which tend to be high Z’. These systems demonstrate that the factors which influences the kinetics of crystallisation and growth are not yet adequately understood. The accuracy of CSP methods was explored through the CCDC Blind Test on the supposedly rigid, pseudo-chiral structure XXII ([1,4]dithiino[2,3-c]isothiazole-3,5,6-tricarbonitrile). The crystal structure was successfully predicted within the submitted structures at a comparable rank to much more sophisticated prediction methods by other groups. This suggests that the CSP methods used in my research can give reliable results. The sublimation cycle is an approach which can be used to support the rational design of chiral separation process by crystallisation. Lattice energy calculations and k = 0 phonon calculations were performed for the 3-chloromandelic acid, lactide and naproxen experimental structures. These results have been used in conjunction with experimental methods, performed by experimentalists at the MPI, Magdeburg, to explore the sublimation cycle. The methods proposed show promise for aiding chiral separation process design.
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Ferris, Andrew J. PhD. "Chiral Induction and Defect Structures in Liquid Crystal Systems." Case Western Reserve University School of Graduate Studies / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case159293629900968.

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Peterson, Katherine Elizabeth. "Topics in supramolecular chemistry: nanococrystals, chiral cocrystals, and acoustic mixing." Diss., University of Iowa, 2019. https://ir.uiowa.edu/etd/7014.

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The synthesis of new molecules is often initiated with the desire to create unique materials that have specific functions and/or properties. The materials are often used in areas such as pharmaceuticals, medical imaging, and energetics. Preparation of these materials utilizes fundamental rules that define how molecules interact with each other in a solid. My research focuses on employing the established concepts to predict how certain molecules interact and assessing the solid form that results (crystal structure) from these interactions. The solids investigated in my research are composed of two different molecules that can combine in various ways based on complementary interactions. Once the two molecules interact to form a crystal structure, external stimuli, such as heat, can cause the atoms within the crystal to move in specific directions to allow for events such as water loss, or it can initiate atoms to rearrange completely to form a new molecule. My work evaluates how the crystal structure changes when the atoms move and how the interactions between the molecules are impacted. The results of my research indicate the crystal structure can be controlled by aspects such as physical size and the properties of the individual molecules within the crystal. Additionally, my work involves assessing new ways to synthesize the described molecules by using technology that avoids the use of harmful solvents. My research has demonstrated a new mixing method that can prepare molecules in the lab and production facilities that reduces the amount of solvent needed and improves sustainability through chemistry.
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Books on the topic "Chiral crystal"

1

Miller, Richard Jonathon. Structural studies of chiral frustrated liquid crystals. University of Manchester, 1994.

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Singh, Jag J. Positron lifetime measurements in chiral nematic liquid crystals. National Aeronautics and Space Administration, Office of Management, Scientific and Technical Information Program, 1991.

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Belyakov, V. A., and V. E. Dmitrienko. Optics of Chiral Liquid Crystals (Soviet Scientific Reviews Series, Section A). Routledge, 1989.

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Book chapters on the topic "Chiral crystal"

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Wang, Ling, Karla G. Gutierrez-Cuevas, and Quan Li. "Photochromic Chiral Liquid Crystals for Light Sensing." In Liquid Crystal Sensors. CRC Press, 2017. http://dx.doi.org/10.1201/9781315120539-2.

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Muševič, Igor. "Topological Particle-Like Structures in Chiral Nematics." In Liquid Crystal Colloids. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-54916-3_8.

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Chiellini, Emo, and Giancarlo Galli. "Chiral Thermotropic Liquid Crystal Polymers." In Recent Advances in Liquid Crystalline Polymers. Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-4934-8_2.

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Cachelin, Pascal, and Cees W. M. Bastiaansen. "Chiral Nematic Liquid Crystalline Sensors Containing Responsive Dopants." In Liquid Crystal Sensors. CRC Press, 2017. http://dx.doi.org/10.1201/9781315120539-3.

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Posnjak, Gregor. "Liquid Crystal Droplets." In Topological Formations in Chiral Nematic Droplets. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-98261-8_3.

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Imai, Yoshitane. "Circularly Polarized Luminescence from Solid-State Chiral Luminophores." In Advances in Organic Crystal Chemistry. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5085-0_16.

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Jin, Mingoo. "Mechano-Responsive Luminescence via Crystal-to-Crystal Phase Transitions Between Chiral and Non-chiral Space Groups." In Novel Luminescent Crystalline Materials of Gold(I) Complexes with Stimuli-Responsive Properties. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-4063-9_4.

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Horvath, Joshua D., Andrew J. Gellman, David S. Sholl, and Timothy D. Power. "Enantiospecific Properties of Chiral Single-Crystal Surfaces." In ACS Symposium Series. American Chemical Society, 2002. http://dx.doi.org/10.1021/bk-2002-0810.ch019.

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Imai, Yoshitane. "Solid-State Circularly Polarized Luminescence of Chiral Supramolecular Organic Fluorophore." In Advances in Organic Crystal Chemistry. Springer Japan, 2015. http://dx.doi.org/10.1007/978-4-431-55555-1_30.

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Coquerel, Gérard. "Chiral Discrimination in the Solid State: Applications to Resolution and Deracemization." In Advances in Organic Crystal Chemistry. Springer Japan, 2015. http://dx.doi.org/10.1007/978-4-431-55555-1_20.

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Conference papers on the topic "Chiral crystal"

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Evans, Julian S., Nan Wang, Sailing He, and Iam-Choon Khoo. "Self-assembly in chiral nematic liquid crystal." In Liquid Crystals XXI, edited by Iam Choon Khoo. SPIE, 2017. http://dx.doi.org/10.1117/12.2272574.

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Semnani, Behrooz, Jeremy Flannery, Zhenghao Ding, Rubayet Al Maruf, and Michal Bajcsy. "Spin-Preserving Chiral Photonic Crystal Mirror." In CLEO: QELS_Fundamental Science. OSA, 2019. http://dx.doi.org/10.1364/cleo_qels.2019.fm1b.1.

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Chen, Huang-Ming Philip, Yun-Yen Tsai, Chi-Wen Lin, and Han-Ping David Shieh. "Novel ferroelectric liquid crystals consisting glassy liquid crystal as chiral dopants." In SPIE Optics + Photonics, edited by Iam-Choon Khoo. SPIE, 2006. http://dx.doi.org/10.1117/12.679959.

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Clark, S. J., G. J. Ackland, and Jason Crain. "Electronic structure calculations of liquid crystal molecules: application to chiral solutes." In Liquid Crystals, edited by Jolanta Rutkowska, Stanislaw J. Klosowicz, Jerzy Zielinski, and Jozef Zmija. SPIE, 1998. http://dx.doi.org/10.1117/12.299962.

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Danilov, V. V., V. A. Smirnov, and Sergey V. Fedorov. "Doped chiral liquid crystal systems as photolimiters." In International Conference on Nonlinear Optics of Liquid and Photorefractive Crystals, edited by Gertruda V. Klimusheva. SPIE, 1998. http://dx.doi.org/10.1117/12.323694.

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Youn, Tae-Young, Kwang-Soo Bae, Jeoung-Yeon Hwang, Chang-Jae Yu, and Jae-Hoon Kim. "Tunable colors of chiral liquid crystal displays." In 2012 3rd IEEE International Conference on Network Infrastructure and Digital Content (IC-NIDC 2012). IEEE, 2012. http://dx.doi.org/10.1109/icnidc.2012.6418830.

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Omura, Rumi, Eri Suto, Naoki Nakamura, Ryuji Higashinaka, Tatsuma D. Matsuda та Yuji Aoki. "Single Crystal Growth and Anomalous Magnetoresistance of Chiral Crystal α-IrSn4". У Proceedings of the International Conference on Strongly Correlated Electron Systems (SCES2019). Journal of the Physical Society of Japan, 2020. http://dx.doi.org/10.7566/jpscp.30.011018.

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Danilovich, S. V., Vladimir E. Agabekov, A. I. Rusalovich, and Vladimir A. Chuiko. "New compensative chiral additives for liquid crystal compositions." In XIV Conference on Liquid Crystals, Chemistry, Physics, and Applications, edited by Jolanta Rutkowska, Stanislaw J. Klosowicz, and Jerzy Zielinski. SPIE, 2002. http://dx.doi.org/10.1117/12.472166.

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Iljin, A. G., P. P. Salo, and A. G. Tereshchenko. "Dynamic gratings in a chiral nematic liquid crystal." In SPIE Photonic Devices + Applications, edited by Iam Choon Khoo. SPIE, 2010. http://dx.doi.org/10.1117/12.860167.

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Cui, Zhenlu, Qi Wang, and Jianbing Su. "Oscillatory shear rheology of chiral liquid crystal polymers." In Second International Conference on Smart Materials and Nanotechnology in Engineering, edited by Jinsong Leng, Anand K. Asundi, and Wolfgang Ecke. SPIE, 2009. http://dx.doi.org/10.1117/12.838580.

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Reports on the topic "Chiral crystal"

1

Reichhardt, Cynthia. Skyrmions in Chiral Magnets, Liquid Crystals, and Beyond. Office of Scientific and Technical Information (OSTI), 2021. http://dx.doi.org/10.2172/1764165.

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Kemp, Richard Alan, and Ana M. Felix. Chiral multichromic single crystals for optical devices (LDRD 99406). Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/900406.

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