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Reduction in Crystal Symmetry of a Solid Solution: A Neutron Diffraction Study at 15 K of the Host/Guest System Asparagine/Aspartic Acid
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Crystallization of supramolecular materials: Perhydrotriphenylene (PHTP) inclusion compounds with nonlinear optical properties
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Hoss, R.; König, O.; Kramer-Hoss, V.; Berger, U.; Rogin, P.; Hulliger, J.: Crystallization of supramolecular materials: perhydrotriphenylene (PHTP) inclusion compounds with nonlinear optical properties. Angew. Chem. Int. Ed. Engl. 35 (1996) 1664-1666;
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Channel-type Inclusion Lattices of Perhydrotriphenylene: A New Route to Orientation Confined Nonlinear Optical Molecules
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Understanding and Control of Nucleation, Growth, Habit, Dissolution and Structure of Two- and Three-Dimensional Crystals Using 'Tailor-Made' Auxiliaries
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Weissbuch, I; Popovitz-Biro, R.; Lahav, M.; Leiserowitz, L.: Understanding and Control of Nucleation, Growth, Habit, Dissolution and Structure of Two- and Three-Dimensional Crystals Using 'Tailor-Made' Auxiliaries. Acta Crystallogr. B51 (1995) 115-148.
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0031168652
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The Crystallization of polar channel-type inclusion compounds: Property-directed supramolecular synthesis
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Hulliger, J.; Rogin, P.; Quintel, A.; Rechsteiner, P.; König, O.; Wübbenhorst, M.: The Crystallization of polar channel-type inclusion compounds: property-directed supramolecular synthesis. Adv. Mater. 9 (1997) 677-680.
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Theory and pyroelectric characterization of polar inclusion compounds of perhydrotriphenylene
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Hulliger, J.; Quintel, A.; Wübbenhorst, M.; Langley, P. J.; Roth, S. W.; Rechsteiner, P.: Theory and pyroelectric characterization of polar inclusion compounds of perhydrotriphenylene. Opt. Mater. 9 (1998) 259-264.
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17
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19544379948
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note
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w of ∼0.04 for drop-like objects would favour a translational movement in which the larger rounded part (b) is in front. Nevertheless, experiments show that the smaller tip section (t) enters the cylinder more frequently. This is because the b-section collides with the wall next to the hole more frequently than does the tip section.
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18
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19544363484
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note
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The Boltzmann factor results from a minimisation of the free energy F of an adlayer where a small number of dipoles undergo orientational disorder [1]. By this calculation we account only for a change in the attachment energy and for configurational entropy. As derived, Eq. (2) applies to cases where the equilibrium in Eq. (1) is on either side.
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19
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0000798431
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Sur la symétrie dans les phénomènes physique, symétrie d'un champ électrique et d'un champ magnétique
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0003077661
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Interface Structure
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Jackson, K.A.1
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23
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36849125451
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The distribution of solute in crystals grown from the melt
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24
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33845183311
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Centrosymmetric Crystals as Host Matrices for Second-Order Optical Nonlinear Effects
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25
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0009595503
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Second-harmonic generation from mixed crystals of p-nitroaniline
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26
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0032022983
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A supramolecular approach to the parallel alignment of nonlinear optical molecules
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Hulliger, J.; Langley, P. J.; König, O.; Roth, S. W.; Quintel, A.; Rechsteiner, P.: A supramolecular approach to the parallel alignment of nonlinear optical molecules. Pure Appl. Opt. 7 (1998) 221-227.
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27
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0002140018
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Comments on the elusive crystal structure of 4-iodo-4′-nitrobiphenyl
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0001385822
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Design of an SHG-active crystal, 4-iodo-4′-nitrobiphenyl: The role of supramolecular synthons
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Sarma, J. A. R. P.; Allen, F. H.; Hoy, V. J.; Howard, J. A. K.; Taimattam, R.; Biradha, K.; Desiraju, G. R.: Design of an SHG-active crystal, 4-iodo-4′-nitrobiphenyl: the role of supramolecular synthons. Chem. Commun. (1997) 101-102.
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The crystal structure of p-iodobenzonitrile
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0032494969
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On intrinsic and extrinsic defect-forming mechanisms determining the real-structure of 4-iodo-4′-nitrobiphenyl crystals
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Hulliger, J.; Langley, P. J.: On intrinsic and extrinsic defect-forming mechanisms determining the real-structure of 4-iodo-4′-nitrobiphenyl crystals. Chem. Commun. (1998) 2557-2558.
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Control of Symmetry and Asymmetry in Hydrogen-Bonded Nitroaniline Materials
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Materials for Nonlinear Optics (Chemical Perspectives), Marder, S. R.; Sohn, J. E.; Stucky, G. D. (eds.), chap. 29, Am. Chem. Soc., Washington, USA
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Second-Order Nonlinearity of Mixtures Including p-Nitroaniline Derivatives
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