Molecular and crystal structures of 1-methyl-2-Oxo-3-acetoxy-4-hydroxy-4-(Phenyl)piperidine, 1-ethyl-2-oxo-3,4-dihydroxy-4-(Pyridyl)piperidine, and 1-benzyl-2-oxo-3,4-dihydroxy-4-(Pyridyl)piperidine and the role of hydrogen bonds in molecular packing in crystals

The molecular and crystal structures of 1-methyl-2-oxo-3-acetoxy-4-hydroxy-4-(phenyl)hydropyridine, 1-ethyl-2-oxo-3,4-dihydroxy-4-(pyridyl)piperidine, and 1-benzyl-2-oxo-3,4-dihydroxy-4-(pyridyl)piperidine are determined by X-ray diffraction analysis. These three hydroxy derivatives of hydropyridine are the convenient model compounds in studies of the influence of intramolecular and intermolecular hydrogen bonds on the conformation and packing of molecules in crystals. The molecules of hydroxy derivatives possess a considerable conformational flexibility and can form an extended network of intramolecular and intermolecular hydrogen bonds. It is shown that these compounds more often than others form noncentrosymmetric and polysystem crystals. The role of the molecular association and the type of hydrogen-bonded associates (syntons) in crystal packing are discussed.     

溶剂蒸汽退火辅助微距升华法制备C8-BTBT单晶

有机半导体单晶由于具有内部长程有序的分子排列结构、缺陷及晶界少等优点,表现出优异的光电性能,是实现有机半导体器件实用化的一种重要材料。目前,研究者们已经发展出多种可应用于有机单晶的生长方法,其中,微距升华法是一种可以在大气环境下采用蒸镀的方式制备有机微/纳单晶的方法。然而,当将这种方法应用于C8-BTBT时发现,由于分子的熔点较低,蒸镀得到的是分子直接从液态凝固为无定形/多晶的结构。在本工作中,通过使用溶剂蒸汽退火的方式对其进行后处理,成功地将这种无定形/多晶结构转化为分立的单晶。为了表征所得到的晶体形貌和结构,分别使用光学显微镜、X射线衍射和原子力显微镜等仪器对其进行了表征,发现所制备的晶体结构具备单晶的典型特征。     

Solidification behaviour of organic nonlinear optical crystals

A representative rather than exhaustive review has been given on the solidification behaviour of organic nonlinear optical crystals. Many of the developments reported here represent quick experimental responses to the rapid theoretical advances made in the field of nonlinear optics. The article is divided into four parts. The first part deals with the characteristics of the organic nonlinear materials and need for large single crystals. The second and third parts are devoted to the thermophysical properties and experimental studies on crystallization processes. Here, recent work by authors is reviewed on the purification of source material, solidification behaviour and crystal growth. Various interactions between morphology, microsegregation, defects, growth velocity and temperature gradient are discussed. Specific examples of substituted anilines are presented. In the fourth section a stronger interaction is suggested between optical physicists and crystal growers to understand the problems of inhomogeneity, stress, damage threshold and doping in the organic crystals.     

X-ray diffraction studies of protein crystal disorder

Protein crystals contain many kinds of disorder, but only a small fraction of these are likely to be important in limiting the diffraction properties of interest to crystallographers. X-ray topography, high-angular-resolution reciprocal space measurements, and standard crystallographic data collection have been used to probe three factors that may produce diffraction-limiting disorder: (1) solution variations during crystal growth, (2) macromolecular impurities, and (3) post-growth crystal treatments. Variations in solution conditions that occur in widely used growth methods may lead to variations in equilibrium protein conformation and crystal packing as a crystal grows, and these may introduce appreciable disorder for sensitive proteins. Tetragonal lysozyme crystals subjected to abrupt changes in temperature, pH, or salt concentration during growth show increased disorder, consistent with this mechanism. Macromolecular impurities can have profound effects on protein crystal quality. A combination of diffraction measurements provides insight into the mechanisms by which particular impurities create disorder, and this insight leads to a simple approach for reducing this disorder. Substantial degradation of diffraction properties due to conformation and lattice constant changes can occur during post-growth crystal treatments such as heavy-atom compound and drug binding. Measurements of the time evolution of crystal disorder during controlled crystal dehydration – a simple model for such treatments – suggest that structural metastability conferred by the constraints of the crystal lattice plays an important role in determining the extent to which the diffraction properties degrade.     

Optical and mechanical properties of a new second order nonlinear optical crystal urea l‐threonine

A new second order non‐linear optical organic crystal Urea L‐threonine has been grown by aqueous solution slow cooling technique. The grown crystal is non hygroscopic and transparent in the visible region. The solubility of the grown crystal was found. The crystal structure and perfection were determined using powder XRD and High resolution XRD. The molecular structure was confirmed by ¹H‐NMR spectrum. Thermal properties of the crystal have been studied using thermogravimetric (TG) and differential thermal analysis (DTA). The dielectric response of the crystal with varying frequencies at different temperatures was studied. UV‐Visible spectrum was recorded to study the optical transparency of the grown crystals. The second order non linear optical property was examined by Kurtz powder technique and found that the second order susceptibilities is 1.2 KDP at wavelength 1064 nm. The mechanical behaviour was studied by Vickers Microhardness test. The results are discussed in detail. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

New organic molecular materials for nonlinear optics

We present four molecular organic crystals which were recently proposed for applications in nonlinear optics (three-wave-mixing and electrooptic effects) : methyl - (2,4 - dinitrophenyl) - aminopropanoate (MAP), 2 - methyl - 4 - nitroaniline (MNA), 3 - methyl - 4 - nitropyridine - 1 - oxyde (POM) and urea. The nonlinear efficiency of molecular organic crystals is seen to depend on the molecular hyperpolarizability and on the crystalline geometry. Both features are discussed and shown to lead, for crystal point groups of lower symmetry, to new structural relations between crystalline non linear coefficients. Each of the four molecular crystals discussed here are shown to have specific properties connected to different types of applications.     

X-ray diffraction study of fluorene, 9-fluorenone, and 9-dicyanomethylenefluorene derivatives

The results of a single-crystal X-ray diffraction analysis of fluorene, 9-fluorenone, and 9-dicyanomethylenefluorene derivatives as individual compounds, as well as their crystal solvates, molecular complexes, and charge-transfer complexes, are generalized. The most interesting features of the molecular geometry and conformation and the molecular packing in the crystals are discussed. The structural formula of 95 compounds and the R factors for X-ray diffraction analysis, which characterize the reliability of determining the structure, are summarized in three tables.     

Synthesis,growth and characterization of organic nonlinear optical bis-glycine maleate (BGM) single crystals

A new organic compound of bis-glycine maleate was synthesized in the alkaline medium of 10% ammonium hydroxide solution. The bulk single crystals of Bis-Glycine Maleate (BGM) have been grown by slow cooling method. The grown crystals were characterized by employing single crystal and powder X-ray diffraction, Fourier transform infrared, optical absorption spectral studies and thermo gravimetric analysis. The microhardness studies confirmed that the BGM has a fairly high Vicker’s hardness number value (41 kg mm⁻²) in comparison to other organic NLO crystals. Second harmonic generation efficiency of the crystal measured by Kurtz–Perry powder method using Nd:YAG laser is found to be comparable to that of potassium dihydrogen phosphate (KDP). Frequency dependent dielectric studies were carried out along the major growth axis.     

Structural and mechanical properties of KН2PО4 single crystals with embedded nanoparticles and organic molecules

Single crystals of KDP crystals with embedded Urea molecules and TiO₂ nanoparticles have been grown from aqueous solution by the temperature lowering method. The effect of the organic molecules and nanoparticles on the structural and mechanical properties has been studied. It has been observed that addition of Urea molecules improves laser induced damage threshold and mechanical strength of the crystal, while TiO₂ nanoparticles have the opposite effect. The structure and composition of KDP:Urea crystal are studied by three‐crystal X‐ray diffraction analysis, which reveals the existence of a correlation between the increase of the microhardness value and the change of the crystal lattice parameter. The surface features of KDP:TiO₂ crystals are analyzed by scanning electron microscopy that reveals the presence of quasi‐equidistant growth bands caused by capture of the nanoparticles. It is shown that the rise of TiO₂ nanoparticles concentration up to 10⁻⁴ wt.% and higher resulted in 3‐fold reduction of the laser damage threshold of KDP:TiO₂ relative to pure KDP in [001] and [100] crystallographic directions. It is found that microhardness and fracture toughness decrease at the nanoparticles concentration of 10⁻³ wt.% due to crack formation at crystal lattice discontinuities. The grown crystals also have been subjected to dielectric studies.     

Preparation and some properties of synthetic proustite single crystals

Conditions for the preparation of proustite single crystals are reported. For selecting these conditions temperature gradients in the crystallisation zone and in the melt, the rate of moving of the crystallisation front, the radial gradient, tube geometry, stabilisation of temperature, mechanisms of zone travelling, partial pressures were changed. – Differential-thermal, X-ray, and spectral-chemical analysis were applied to initial substances and final crystal bodies. To decrease the influence of spontaneous crystallisation an optimal temperature gradient was applied approaching maximum undercooling at the liquid-solid interface. – Optically transparent proustite crystals resulted. In the range from 1 to 12 μm they show 80% transparency. Microhardness was measured along the growth direction which deviated from the c-axis about 25°.     

Growth of high quality anthracene crystals by a simple solution technique

In recent years considerable effort has gone into the preparation and characterisation of high purity anthracene crystals, since anthracene is used as a model organic molecular crystal in studies of solid‐state properties. Studies of organic molecular crystals and their applications in optics and electronics have been increasing attractive interest. Several attempts have been made to grow single crystals of anthracene. This is the first attempt to grow high quality anthracene crystals by solution technique adopting slow evaporation method in different solvents like CS₂ and CCl₄. The harvested crystals were subjected to various characterization studies. The results of characterisation studies support the purity of solution grown anthracene crystals. The solubility of anthracene in various solvents like CS₂ and CCI₄ was determined. The crystals of anthracene were grown by systematic method of slow evaporation technique in various solvents. Different morphology is noted with varying solvents. The crystal was subjected to XRD studies, FTIR studies and thermal studies. © 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim     

Third-order NLO property of thienyl chalcone derivative: Physicochemical analysis and crystal structure determination

Good-quality single crystals of an efficient nonlinear optical (NLO) chalcone derivative 1-(5-chlorothiophen-2-yl)-3-(2,3-dichlorophenyl)prop-2-en-1-one (CTDCP) which meets many of the physicochemical requirements like transparency in the entire visible region, thermal stability, mechanical hardness have been achieved. The crystal belongs to orthorhombic system with the centrosymmetric space group Pbca. The third-order NLO properties were investigated using a single beam Z-scan technique with nanosecond laser pulses at 532 nm. The nonlinear refractive index is found to be of the order of 10^?11 cm²/W. The magnitude of third-order susceptibility is of the order of 10^?13 esu. The compound exhibits good optical limiting at 532 nm. The mechanical property of the crystals showed load dependent hardness. The static and frequency dependent molecular hyperpolarizabilities were computed using MOPAC 2012. Thermal study confirms that the crystal is dimensionally stable up to 179°C. The influence of direction of charge transfer on the nonlinearity of the molecule has been discussed in detail.     

掺杂对GaN晶体力学性能影响的研究

对GaN单晶力学性能的研究有助于解决其在生长、加工和器件应用中的开裂问题。本文围绕掺杂对GaN单晶力学性能的影响,通过纳米压痕法测试了不同掺杂类型(非掺、Si掺和Fe掺)GaN单晶的弹性模量和硬度,测试结果表明掺杂对GaN单晶的硬度有重要影响。Si掺、Fe掺GaN较非掺样品硬度有所提升,用重掺杂的氨热GaN单晶作为对照,也证明了这一结论。通过高分辨X射线衍射分析和原子力显微镜表征实验发现,晶体结晶质量、接触面积等因素对GaN单晶硬度的影响较小。对GaN表面纳米压痕滑移带长度和晶体晶格常数进行测试,结果表明,掺杂影响GaN单晶硬度的主要原因是缺陷对GaN位错增殖、滑移的阻碍作用和掺杂引起的GaN晶格常数的变化。     

Analysis of synthetic diamond single crystals by X-ray topography and double-crystal diffractometry

Structural features of diamond single crystals synthesized under high pressure and homoepitaxial films grown by chemical vapor deposition (CVD) have been analyzed by double-crystal X-ray diffractometry and topography. The conditions of a diffraction analysis of diamond crystals using Ge monochromators have been optimized. The main structural defects (dislocations, stacking faults, growth striations, second-phase inclusions, etc.) formed during crystal growth have been revealed. The nitrogen concentration in high-pressure/high-temperature (HPHT) diamond substrates is estimated based on X-ray diffraction data. The formation of dislocation bundles at the film-substrate interface in the epitaxial structures has been revealed by plane-wave topography; these dislocations are likely due to the relaxation of elastic macroscopic stresses caused by the lattice mismatch between the substrate and film. The critical thicknesses of plastic relaxation onset in CVD diamond films are calculated. The experimental techniques for studying the real diamond structure in optimizing crystal-growth technology are proven to be highly efficient.     

不同结构物质和有机基质对草酸钙晶体生长的促进作用

本文综述了有机大分子、小分子和有机基质对尿石矿物草酸钙(CaOxa)晶体成核、生长和聚集的促进作用.从促进物的分子结构和草酸钙晶体的晶面性质等方面讨论了不同类型促进物的作用机理.最后指出了该领域所面临的问题和将来的发展方向.     

Synthesis and mesomorphic properties of novel high birefringence azobenzene liquid crystals with lateral fluorosubstituent

In order to obtain liquid crystals with high birefringence (Δn), four azobenzene compounds based on lateral fluorinated bistolane moieties with trifluoromethyl terminal groups were synthesized with Hagihara–Sonogashira cross-coupling reaction. The molecular structures of the compounds were confirmed by Fourier transform infrared, ¹H-nuclear magnetic resonance. The transition temperatures, optical textures, and optical anisotropies were determined by differential scanning calorimetry, polarizing optical microscopy. The effect of the alkyl substituents on liquid crystal behavior is discussed in detail. The compounds have showed higher birefringence values.     

Growth and characterization of a novel NLO crystal bis-glycine hydrogen chloride (BGHC)

Single crystals of bis-glycine hydrogen chloride (BGHC), a semiorganic nonlinear optical (NLO) material, have been grown by slow solvent evaporation technique. Good optical quality single crystals with dimensions up to 33×5×5 mm³ are obtained. The crystals are characterized by optical transmission spectrum, FTIR and X-ray diffraction studies. The thermal stability of the crystal is studied by thermogravimetric analysis (TGA) and differential thermal analysis (DTA). The second harmonic generation (SHG) efficiency of BGHC was found to be 5.6 times that of KDP. The laser damage threshold values studied in single shot mode indicates that BGHC crystal possesses a fairly high value of 9.8 GW/cm² and thus the NLO studies confirmed the superiority of BGHC over KDP and urea crystals. The dielectric constant of the crystal was studied as a function of frequency and the results are discussed.     

Growth and characterization of organic nonlinear optical material: Benzilic acid

The organic nonlinear optical crystals of benzilic acid were grown by the slow evaporation method using ethanol as a solvent. Single-crystal X-ray diffraction (XRD), powder XRD studies and Fourier transform infrared (FTIR) spectral analysis were carried out to confirm the benzilic acid crystal. The optical transparency was studied by ultra violet (UV)–visible spectral analysis. Thermal properties of the grown crystals were studied by thermogravimetric and differential thermal analyses. The melting point of the grown crystal was confirmed by differential scanning calorimetry (DSC) analysis. The second harmonic generation (SHG) efficiency was found to be 2 times that of KDP.     

SiC单晶片的取向研磨

优质晶体生长常常需要籽晶或衬底偏离常规结晶取向.为便于按任意偏向角度研磨晶片,本实验室设计并应用了晶片取向研磨夹具及相应的研磨工艺.本文介绍了该夹具和工艺的工作原理、技术要点以及对技术指标的鉴定情况.测试结果表明,研磨取向误差范围可控制在5;之内,研磨片厚度偏差小于5 μm、粗糙度Ra=0.12 μm.     

Utilization and Modification of Perovskite-Type Layered Structures as Inorganic-Organic Hybrid Materials

Abstract

The aromatic ammonium-based layered halide compounds were obtained of bis(4-nitroanilinium)tetrachlorocadmate and bis(2-methyl-4-nitroanilinium) tetrachlorocadmate, aiming at a new type of inorganic-organic hybrid layered material. X-ray diffraction analyses of the single crystals revealed that both of the crystals take an alternate layered structure of the organic bilayer and the inorganic sheet. Cadmium ion and chloride anions form six-coordinated octahedra whose corner anions are shared with the neighboring octahedra for the crystal of bis(4-nitroanilinium)tetrachlorocadmate. In the case of bis(2-methyl-4-nitroanilinium) tetrachlorocadmate crystal the inorganic portion takes distorted four-coordinated tetrahedra. The structure of the inorganic portion for the latter crystal can be considered to be caused by the distortion of a perovskite-type octahedron due to the introduction of a bulky organic molecule.