Crystal structure and optical properties of 4‐nitrophenyl 4‐butoxybenzoate

The title compound, C₁₇H₁₇N₁O₅, has been synthesized and characterized by single crystal X‐ray analysis and UV‐Vis spectra. The crystals are monoclinic, P 2₁/c, a = 17.994 (5) Å, b = 4.0592 (9) Å, c = 21.625 (5) Å, β = 99.634 (5)°, V = 1557.2 (6) ų and Z = 4. The molecule has an almost stretched form with a molecular length of 17.505 Å and an imbricated structure known for liquid crystals. The structure contains no direction‐specific intermolecular interactions like aromatic π‐π stacking and C‐H… π(arene) other than two weak C‐H…O hydrogen bonds. Good optical transmittance in the entire visible region of the UV‐Vis spectrum suggests that it is a potential candidate for optoelectronic applications. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Synthesis,growth and characterization of single crystals of pure and thiourea doped L‐glutamic acid hydrochloride

L(+)Glutamic acid hydrochloride [HOOC (CH₂)₂CH(NH₂) COOH·HCl], a monoamino dicarboxylic acid salt of L‐Glutamic acid was synthesized and the synthesis was confirmed by FTIR analysis. Solubility of the material in water was determined. Pure and Thiourea doped L‐Glutamic acid hydrochloride crystals were grown by low temperature solution growth using solvent evaporation technique. XRD, UV‐Vis‐NIR analyses were carried out for both pure and thiourea doped crystals. The crystals were qualitatively analyzed by EDAX analysis and the presence of thiourea was confirmed. The cell parameters of L‐Glutamic acid hydrochloride have been determined as a = 5.151 Å, b = 11.79 Å, c = 13.35 Å by X‐ray diffraction analysis and it crystallizes in orthorhombic space group P2₁2₁2₁. UV‐Vis‐NIR spectra analysis showed good optical transmission in the entire visible region for both pure and doped crystals. Micro hardness of both pure and doped crystals has been determined using Vickers micro hardness tester. The SHG efficiencies of both pure and doped crystals were determined using Kurtz powder test and pure L‐Glutamic acid hydrochloride crystal was found to possess better efficiency than thiourea doped L‐Glutamic acid hydrochloride crystals. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Nucleation kinetics and growth aspects of organic nonlinear optical L‐arginine trifluoroacetate single crystals

Experimental determination of solubility, metastable zonewidth and induction period for an organic nonlinear optical (NLO) L‐arginine trifluoroacetate (LATF) crystal is reported. The interfacial tension for different supersaturation conditions has been estimated for the LATF solution at 45°C. Bulk crystal of dimensions 57x5x3 mm³ has been grown by temperature lowering technique using optimized growth parameters. Powder X‐ray diffraction and FTIR studies confirm the crystalline nature and the functional groups of the grown crystals respectively. Linear optical property of the grown crystal has been studied by UV‐Vis spectrum. Thermal analyses have revealed that the compound is thermally stable upto 212°C. Kurtz powder SHG test confirm the nonlinear optical properties of the as‐grown LATF crystal. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Structural,thermal, mechanical and z‐scan studies on 4‐nitrophenol single crystals

4‐nitrophenol (4‐NP) single crystals have been grown by using slow evaporation and slow cooling techniques. A single crystal with size in the range of 7x3.4x1.8cm³ has been obtained by slow cooling method. The grown crystals have been subjected to various characterization studies. The powder XRD spectrum of 4‐NP reveals the good crystalline nature of the grown crystal. Single crystal XRD studies show that the crystal belongs to monoclinic system with cell parameters of a=6.09 Å, b=8.79 Å, c=11.61 Å, α=γ=90°, β=103.15°. The resultant FTIR spectrum confirms the various functional groups present in 4‐NP. Thermal analysis has been performed on the material to study the thermal stability of 4‐NP. The grown crystals belong to the category of soft materials as confirmed by Vickers Hardness tests. The optical transmiitance of 4‐NP single crystals has been measured from Vis‐IR spectroscopy study. The nonlinear optical properties have been analyzed by z‐scan technique and 4‐NP is found to be self defocusing because of its negative nonlinear refractive index. (© 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Powder second harmonic generation measurement and thermal decomposition mechanisms of a new organometallic compound [(18C6)Li][Cd(SCN)3]

Single crystals of a novel nonlinear optical organometallic compound CLTC, ([(18C6)Li][Cd(SCN)₃]), were grown from aqueous solutions via evaporation technique and characterized by IR spectroscopy, thermal gravimetric analysis and X‐ray single‐crystal diffraction. By X‐ray single‐crystal structural analysis it is revealed that the compound crystallized in a noncentrosymmetric space group Cmc2₁ of orthorhombic system with cell parameter a = 14.767(3) Å, b = 15.454(3) Å, c = 10.644(2) Å, V = 2429.0(8) ų and Z = 4. The thermal stability and thermal decomposition of CLTC crystal were investigated by means of thermogravimetry and differential thermal analysis. The second harmonic generation (SHG) efficiency was measured using the Kurtz and Perry powder technique. It was shown that the value of the SHG efficiency of CLCT powder was about 2 times higher than that of potassium dihydrogen phosphate (KDP). (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Preparation and Properties of a Novel Nonlinear Optical Crystal: MnHg(SCN)4(H2O)2.2(C3H6CONCH3)

In this article, diaquatetrakis (thiocyanato) manganese(II) mercury(II)‐N‐methyl‐2‐pyrrolidone, MnHg(SCN)₄(H2O)₂.2(C₃H₆CONCH₃), (abbreviated as MMTWMP), a new organometallic nonlinear optical crystal material is reported. The structure, optical and thermal characterizations were determined by elemental analysis, infrared and Raman spectroscopy, X‐ray powder diffraction, thermogravimetric analysis, differential scanning calorimetry, special heat, SHG measurements and UV/Vis/NIR optical transmission spectra. It belongs to the tetragonal crystallographic system, with cell parameters: a = 12.1294, c = 8.2238Å, V = 1211.27ų. Single crystals with dimensions up to 8 × 7 × 5 mm³ have been obtained. The morphology of the crystals was indexed. The MMTWMP crystal exhibits good physicochemical stability at normal temperature and pressure. Its UV transparency cutoff is 360 nm, which is shifted to the violet by 13 nm, as compared with MnHg(SCN)₄ (MMTC); the optical transmission is 44.82% at 404 nm, which is by 17.46% higher than that of MMTC.     

Growth and characterization of cadmium magnesium tetra thiocyanate crystals

Cadmium Magnesium Tetra Thiocyanate, CdMg(SCN)₄, [CMTC] belongs to bimetallic thiocyanate complexes. CMTC crystals has been grown by solution growth technique at room temperature. The morphologies of the grown crystals are identified by single crystal analysis. Also the Powder X‐ray Diffractogram of the crystal has been recorded and the various planes of reflection are identified. The title compound crystallizes under triclinic structure with lattice parameters a = 10.0976 Å, b = 7.5015 Å, c = 5.7720 Å and β = 90.2135°. The presence of magnesium and cadmium in the grown crystals were confirmed through Atomic Absorption Spectroscopy. The grown crystals are analysed qualitatively by Fourier Transform Infrared (FTIR) and Fourier Transform Raman spectral measurements. The transmittance spectrum of the crystal in the UV‐Visible region has been recorded and analysed. The dielectric measurements for the crystals were carried out in the microwave region. The thermal stabilities of the crystals were studied by using different thermal analyses like Thermo Gravimetric Analysis (TGA), Differential Thermal Analysis (DTA) and Differential Scanning Calorimetry (DSC). (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth and characterisation of potassium cobalt nickel sulfate hexahydrate for UV light filters

A new single crystal for ultraviolet light filter, KCNSH (Potassium Cobalt Nickel Sulfate Hexahydrate) was designed and its crystal structure was studied using X‐ray diffraction in this paper. The empirical of the title compound is K₂Co_0.1Ni_0.9(SO₄)₂.6H₂O with formula weight 437.15. KCNSH crystal belongs to the monoclinic space group P2(1)/c, a=6.1390(3)Å, b=12.1839(6)Å, c=9.0095(4)Å, α=γ=90°, β=105.060(2)°, V=650.74(5)ų, Z=2, Dc=2.231g/cm³. Using the cooling solution method, we have grown a deep green KCNSH crystal with dimension of 12×12×40mm³. The transmission spectrum of KCNSH in the range from UV to near IR wavelengths, its thermal properties, and the relationship between the structure and optical transmission properties are also studied and further discussed in this paper. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Crystal structure and properties of [Cu(sac)2(py)3], a new example of a mononuclear complex with both N‐ and O‐bonded saccharinate ligands

The crystal structure of the title complex has been determined by single X‐ray diffraction methods and refined to an R‐value of 0.0543. It crystallizes in the monoclinic P2₁/a space group with a = 21.1231(9), b = 9.4523(4), c = 16.1874(7) Å, β = 107.3706(3)° and Z = 4. The compound represents only the second known example of a simple mononuclear metal complex containing simultaneously N‐ and O‐bonded saccharinato ligands. Its infrared spectrum and thermal behavior are also briefly discussed.     

Structure and spectra character of cobalt nickel sulfate twelvehydrate (CNSH) single crystal

The title compound CoNi(SO₄)₂ · 12H₂O has been prepared and its crystal structure determined by single crystal X‐ray differaction at room temperature. The CNSH crystal structure belongs to the monoclinic space group C2/c,a = 9.966(2) Å, b = 7.2265(14) Å, c = 24.218(5) Å, β = 98.32(3)°, V = 1725.9(6) ų, z = 4, Dc = 2.024 gcm⁻³. The optical transmission character of CNSH crystal in aqueous solution is discontinuous in the range from ultraviolet to near IR wavelengths. The relationship between the structure and the optical transmission property is further discussed. (© 2003 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth and Characterization of a New Nonlinear Optical Crystal: Bis Thiourea Zinc Chloride

Bis Thiourea Zinc Chloride (BTZC) a new semiorganic nonlinear optical material has been synthesized. The solubility studies have been carried out in the temperature range 30°‐ 55°C. Single crystals of BTZC have been grown by slow evaporation of saturated aqueous solution at room temperature. The lattice parameters of the grown crystals have been determined by single crystal X‐ray diffraction technique. The UV‐Vis‐NIR transmittance spectrum has been recorded in the range 200‐2000 nm. The FT‐IR spectrum has been recorded in the range 400‐4000 cm^‐1 and the spectral bands have been compared with similar thiourea complexes.     

Growth,optical and thermal studies of nonlinear optical L‐arginine perchlorate single crystals

A potentially useful semiorganic nonlinear optical (NLO) material, L‐arginine perchlorate, has been synthesized and bulk crystals have been grown by slow cooling technique. The grown crystals were characterized by single crystal X‐ray diffraction, UV‐Vis‐NIR spectroscopy, FT‐IR, thermal analysis and SHG measurements. The grown crystals were thermally stable upto 153°C and exhibit SHG efficiency of about 0.17 with respect of Urea. The etching studies have been carried out on the grown crystal. LAPC has good optical transmission not only in the visible range, however, also in the near UV part of the spectra and hence it is a potential material for nonlinear frequency conversion. The refractive index was measured by the Brewster's angle method. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Investigations on the growth,optical behaviour and factor group of an NLO crystal: L‐alanine alaninium nitrate

Amino acid family crystals exhibit excellent nonlinear and electro‐optical properties. L‐alanine alaninium nitrate (LAAN) single crystal belonging to the amino acid group was grown by slow cooling solution growth technique. The High resolution X‐ray diffraction (HRXRD), Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, UV‐Vis., Photoluminescence (PL) and Factor group analyses were carried out. The factor group analysis reveals 183 internal vibrations for the title compound. The second harmonic generation property was tested by Kurtz‐Perry powder technique. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

The Crystal and Molecular Structure of 2‐[(3,4‐dimethoxybenzylidene)amino]adamantane

The crystal structure of the title compound, C₁₉H₂₅NO₂ was determined by single crystal X‐ray diffraction technique. The crystal data are Orthorombic, space group Pbca, with a = 9.2119(4), b = 9.5555(4), c = 37.6049(5) Å, Z = 8, T = 293(2) K, MoKα radiation, λ = 0.71073 Å, Mr = 299.40, R = 0.0839 for 1945 reflections with I > 2σ(I). The title compound shows intermolecular C‐H…O type interactions.     

Growth of tetrakis thiourea potassium iodide as new second order optical material

A novel organometallic nonlinear optical (NLO) crystal, namely thiourea complex of tetrakis thiourea potassium iodide (TTPI), has been grown by slow evaporation solution growth technique. The harvested crystal is large in size. To our knowledge there is no report is available for the bulk size single crystal of TTPI. This material has a positive temperature coefficient and has been grown by slow evaporation solution growth technique. The grown crystal have been characterized by employing several techniques such as single crystal and powder X‐ray diffraction, FTIR, UV‐Vis‐NIR spectra, thermo gravimetric analyses respectively. Etching studies have also been carried out in order to know the surface defects on the as grown specimen of TTPI. The relative second harmonic generation efficiency have been tested by using Nd:YAG laser as source. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Synthesis,spectral and thermal properties of non‐linear optical crystal ZnMg(SCN)4

Single crystals of zinc magnesium tetra thiocyanate [ZnMg(SCN)₄], a bimetallic thiocyanate complex, were grown by slow evaporation solution growth technique at room temperature. The bright, transparent and colourless crystals have well defined faces. The grown crystals were characterized through elemental analysis, powder X‐ray diffraction (XRD), thermogravimetric (TG) and differential thermal analysis (DTA), differential scanning calorimetric analysis (DSC), Fourier Transform Infra red (FTIR) and Optical studies. The elemental analysis confirms the stoichiometry of the synthesized crystals. The compound crystallizes under monoclinic structure with lattice parameters a = 10.055 Å, b = 7.44 Å, c = 6.00 Å and β = 90.113°. The TGA indicates 25 % weight loss at 205°C from which the decomposition pattern is formulated. The DSC study indicates that the crystal undergoes only first order phase transitions. The FTIR spectrum indicates among others the presence of metal‐nitrogen and metal‐sulphur bonds thus confirming the formation of the complex. The second harmonic‐generation (SHG) was confirmed by the emission of green radiation using Nd: YAG laser. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Synthesis,growth and characterization of S‐benzyl isothiouronium chloride single crystals

S‐Benzyl isothiouronium chloride single crystals were grown at room temperature by slow evaporation solution growth technique. Single crystal X‐ray diffraction study has been carried out to find the crystal system and unit cell parameters. Various functional groups present in the grown material have been identified using FTIR spectra. The transparency of crystal was tested using UV‐visible spectra. The grown crystal exhibits second harmonic generation (SHG). TGA/DTA analysis also carried out. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Si modified Ge10 cluster: the preparation and characterization of single crystal Na4(Ge,Si)9O20

A Si modified Ge₁₀ cluster with structure Na₄(Ge,Si)₉O₂₀ (denoted as HUT‐1) was synthesized by hydrothermal synthesis at 160 °C with a sodium silicate source. The compound was characterized by single crystal, powder X‐ray diffraction and TGA‐DSC analysis. HUT‐1 crystallizes in space group I4₁ (80) with calculated unit cell (a=14.966(5) Å, c=7.343(2) Å, V=1644.8(9) ų), which has the same structure as Na₄Ge₉O₂₀. HUT‐1 has a high Si/Ge ratio with an approximate formula of Na₄Ge_7.68Si_1.32O₂₀. Single crystal X‐ray structure refinements together with results from X‐ray powder diffraction (XRPD) confirm the occupancy of Si at two tetrahedral sites. (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Synthesis and characterization of (NH4)2CuBr2Cl2·2H2O crystals

Single crystals of a new compound, (NH₄)₂CuBr₂Cl₂.2H₂O, were grown from saturated aqueous solution at room temperature by slow evaporation method. The grown crystals were characterized through elemental, powder XRD, thermal and DSC analyses and FTIR and far IR spectra. The elemental analysis and the decomposition pattern formulated using the TG‐DTG studies confirm the stoichiometry of the compound. The crystallinity of the compound is confirmed from the powder XRD pattern. A preliminary single crystal X‐ray diffraction structural analysis reveals that the title compound belongs to the orthorhombic system with a = 7.7466 Å, b = 7.783 Å and c = 8.1211 Å. The low temperature DSC shows thermal anomalies at –161.1, –156.5, –152.4, –145.2, –134, –18.5, and 1.4°C during the heating run and at –4.3, –54.8, –66.1, –90.6, –109.7 and –147.2 °C during the cooling run. The thermal hysterses indicate first order phase transitions in the title compound at these temperatures. The FTIR spectra were used to assign the characteristic vibrational frequencies due to NH₄⁺, CuX₄^2– ions and other chemical bonds. The effect of substitution of two bromine atoms on the phase transitions of a closely related crystal, diammonium tetrachloro cuprate dihydrate is also discussed. (© 2005 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Synthesis,characterization and crystal structure of a 3‐D supramolecular Cu/Mn complex with pydc

A supramolecular compound, {[CuMn(pydc)₂(H₂O)₅]·2H₂O} ( 1 ) (pydc = pyridine‐2,6‐dicarboxylate dianion), has been synthesized and characterized by single‐crystal X‐ray diffraction. Single‐crystal X‐ray analysis reveals that it crystallizes in the triclinic space group P‐1, a = 8.4763(17) Å, b = 9.7715(19) Å, c = 13.909(3) Å, α =101.234(3)°, β =102.520(3)°, γ= 97.375(4)°. Two mixed‐metal ions exhibit similar coordinated geometries with octahedron. 1 possesses a 3‐D unusual supramolecular network featuring 1D water tape. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)