scholarly journals Growth and characterization of 4-(((4-aminophenyl)sulfonyl)oxy)-2,3-dihydroxy-4-oxobutanoic acid with Ce3+: for semiorganic nonlinear optical application

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
E. Vinoth ◽  
S. Vetrivel ◽  
S. Gopinath ◽  
R. Aruljothi ◽  
T. Suresh ◽  
...  
Keyword(s):  
Diffraction Study ◽  
Nonlinear Optical ◽  
Grown Crystal ◽  
Laser Source ◽  
Cutoff Wavelength ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxobutanoic Acid ◽  
Crystalline System

Abstract This work aims at the growth and characterization of novel semi-organometallic nonlinear optical (NLO) crystal 4-(((4-aminophenyl) sulfonyl) oxy)-2,3-dihydroxy-4-oxobutanoic acid (ASODA) with ammonium ceric (II) sulfate dehydrate (ACS). The crystal 4-(((4-aminophenyl) sulfonyl) oxy)-2,3-dihydroxy-4-oxobutanoic acid with Ce3+ (STA) was grown by slow evaporation solution growth technique using deionized water as a solvent. Crystalline system of the grown STA crystal was identified by a single crystal X-ray diffraction study and confirmed as monoclinic crystalline system with non-centrosymmetric space group P21/C. The powder X-ray diffraction study confirmed the purity and crystallinity of the crystal. The presence of functional groups and hydrogen bonds (–O–H–O–) was confirmed by FT-IR spectroscopy. UV-Vis spectra showed that the grown crystal had a low cutoff wavelength at 219 nm. The position of protons and carbons were determined by structural studies based on NMR technique. The grown crystal was thermally stable up to 130 °C and its melting point was 163 °C. The SHG studies were performed by Quanta Ray Model laser source using Kurtz powder technique. The NLO efficiency of the STA crystal was 0.5 times greater than that of standard KDP. The dielectric constant and dielectric loss of the grown crystal were studied at different temperatures. The surface morphology and the particle size of the crystal were determined by FE-SEM technique. From the mechanical studies, it was found that the grown crystal is a soft material.

scholarly journals Growth and Characterization of Adipic Acid Doped Potassium Hydrogen Phthalate: A Nonlinear Optical Single Crystal

2019 ◽  
Vol 32 (1) ◽  
pp. 79-83
Author(s):  
R. Manimekalai ◽  
S. Chidambaram
Keyword(s):  
Single Crystal ◽  
Adipic Acid ◽  
Nonlinear Optical ◽  
Grown Crystal ◽  
Cutoff Wavelength ◽  
Potassium Hydrogen Phthalate ◽  
Hydrogen Phthalate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Potassium Hydrogen

Adipic acid doped potassium hydrogen phthalate (AAKHP) and pure potassium hydrogen phthalate single crystals were grown by slow evaporation method. Single crystal X-ray diffraction analysis was carried out to determine the lattice parameters in a = 6.47 Å, b = 9.59 Å, c = 13.25 Å and space group of Pca21. This confirms the grown AAKHP belongs to the orthorhombic system. Various diffracting planes of the grown crystal were indexed using powder X-ray diffraction study. Fourier-transform infrared studies confirm the presence of various functional groups in the grown crystal. The transmittance spectrum shows that the lower cutoff wavelength is around 290 nm. The nonlinear optical property of the grown crystal has been studied by Kurtz powder second harmonic generation (SHG) analysis. EDAX analysis confirms the presence of various elements in the AAKHP crystal. Vickers micro-hardness studies are used for the analysis of mechanical behaviour of the grown crystal. The paramagnetic nature of the grown crystal was confirmed by vibration spectrum magnetometer technique.

Synthesis, Growth and Characterization of Organic Nonlinear Optical L-Asparagine L-Tartrate Single Crystals

2012 ◽  
Vol 584 ◽  
pp. 13-17 ◽  
Author(s):  
G. Peramaiyan ◽  
P. Pandi ◽  
B.M. Sornamurthy ◽  
R. Mohan Kumar
Keyword(s):  
Nonlinear Optical ◽  
Grown Crystal ◽  
Second Harmonic ◽  
Bulk Single Crystal ◽  
X Ray Diffraction ◽  
Ftir Studies ◽  
Slow Evaporation Technique ◽  
Evaporation Technique ◽  
Generation Test

L-asparagine L-tartrate (LAT), an organic compound has been synthesized from aqueous solution and bulk single crystal has been grown by slow evaporation technique. Powder X-ray diffraction studies confirmed the monoclinic structure of the grown LAT crystal. The presence of functional groups of the grown crystal was identified by FTIR studies. Linear optical property of the grown crystal was studied by UV-Vis spectral analysis. Microhardness studies reveal that the crystal possesses relatively higher hardness compared to other organic nonlinear optical crystals. Dielectric response of the L-asparagine L-tartrate crystal was analyzed for different frequencies at various temperatures. Kurtz-Perry powder second harmonic generation test confirmed the nonlinear optical properties of the as-grown LAT crystal.

Synthesis, crystal growth and characterization of di-valine maleic – a new nonlinear optical material

RSC Advances ◽  
2016 ◽  
Vol 6 (101) ◽  
pp. 99139-99148 ◽  
Author(s):  
Soma Adhikari ◽  
Tanusree Kar ◽  
Saikat Kumar Seth
Keyword(s):  
Dipole Moment ◽  
Crystal Growth ◽  
Nonlinear Optical ◽  
Dft Method ◽  
Nonlinear Optical Material ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order ◽  
Shg Efficiency

A new NLO material namely di-valine maleic (VM) was synthesized and characterized by X-ray diffraction analysis. The SHG efficiency of VM was investigated and dipole moment, polarizability, first order hyperpolarizability were calculated by DFT method.

scholarly journals Synthesis and Characterization of New Diiron and Diruthenium μ-Aminocarbyne Complexes Containing Terminal S-, P- and C-Ligands

2007 ◽  
Vol 62 (3) ◽  
pp. 427-438 ◽  
Author(s):  
Vincenzo G. Albano ◽  
Luigi Busetto ◽  
Fabio Marchetti ◽  
Magda Monari ◽  
Stefano Zacchini ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Diffraction Study ◽  
Coordination Mode ◽  
Bond Cleavage ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dithiocarbamate Ligand ◽  
High Yields

The diiron aminocarbyne complexes [Fe2{μ-CN(Me)(R)}(μ-CO)(CO)(NCMe)(Cp)2][SO3CF3] (R = Xy1, 1a; R = Me, 1b; R = CH2Ph, 1c; Xy1 = 2,6-Me2C6H3) undergo replacement of the coordinated nitrile by halides, diethyldithiocarbamate, and dicyanomethanide to give [Fe2{μ-CN(Me) (R)}(μ-CO)(CO)(X)(Cp)2] complexes (R = Me, X = Br, 4a; R = Me, X = I, 4b; R = CH2Ph, X = Cl, 4c; R = CH2Ph, X = Br, 4d; R = CH2Ph, X = I, 4e; R = Xy1, X = SC(S)NEt2, 5a; R = Me, X = SC(S)NEt2, 5b; R = Xy1, X = CH(CN)2, 7), in good yields. The molecular structure of 5a shows an unusual η1 coordination mode of the dithiocarbamate ligand. Similarly, treatment of [M2{μ-CN(Me) (R)}(μ-CO)(CO)(NCMe)(Cp)2][SO3CF3] (M = Fe, R = Xy1, 1a; M = Fe, R = Me, 1b; M = Ru, R = Xy1, 2a; M = Ru, R = Me, 2b) with a series of phosphanes generates the cationic complexes [M2{μ- CN(Me)(R)}(μ-CO)(CO)(P)(Cp)2][SO3CF3] (M = Fe, R = Xy1, P = PPh2H, 6a; M = Fe, R = Xy1, P = PPh3, 6b; M = Fe, R = Xy1, P = PMe3, 6c; M = Fe, R = Me, P = PMe2Ph, 6d; M = Fe, R = Me, P = PPh3, 6e; M = Fe, R = Me, P = PMePh2, 6f; M = Ru, R = Xy1, P = PPh2H, 6g; M = Ru, R = Me, P = PPh2H, 6h), in high yields. The molecular structure of 6a has been elucidated by an X-ray diffraction study. The reactions of [Fe2{μ-CN(Me)(Xyl)}(μ-CO)(CO)(NCR′)(Cp)2][SO3CF3] [R′ = Me, 1a; R′ = tBu, 3] with PhLi and PPh2Li yield [Fe2{μ-CN(Me)(Xy1)}(μ-CO)(CO)(Ph)(Cp)2] (8) and [Fe2{μ-CN(Me)(Xy1)}(μ-CO)(CO)(PPh2)(Cp)2] (9), respectively. The molecular structure of 8 has been ascertained by X-ray diffraction. Conversely, the reaction of 1a with MeLi generates the aminoalkylidene compound [Fe2{C(Me)N(Me)(Xy1)}(μ-CO)2(CO)(Cp)2] (10).Finally, the acetone complex [Fe2{μ-CN(Me)(Xy1)}(μ-CO)(CO)(OCMe2)(Cp)2][SO3CF3] (12) reacts with lithium acetylides to give complexes [Fe2{μ-CN(Me)(Xy1)}(μ-CO)(CO)(C≡CR)(Cp)2] (R = p-C6H4Me, 11a; R = Ph, 11b; R = SiMe3, 11c), in high yields. Filtration through alumina of a solution of 11a in CH2Cl2 results in hydration of the acetylide group and C-Si bond cleavage, affording [Fe2{μ-CN(Me)(Xy1)}(μ-CO)(CO){C(O)Me}(Cp)2] (12).

X-ray diffraction study of an as-grown crystal of a two-phase sample of Lu0.65Ca0.35F2.65

2014 ◽  
Vol 59 (6) ◽  
pp. 874-877
Author(s):  
T. S. Chernaya ◽  
N. B. Bolotina ◽  
I. A. Verin ◽  
B. P. Sobolev
Keyword(s):  
Diffraction Study ◽  
Grown Crystal ◽  
X Ray Diffraction ◽  
Two Phase ◽  
X Ray ◽  
Phase Sample

scholarly journals Studies on the growth and characterization of L-cysteine hydrogen fluoride single crystal

2019 ◽  
Vol 37 (3) ◽  
pp. 304-309
Author(s):  
Azeezaa Varsha Mohammed ◽  
Suresh Sagadevan
Keyword(s):  
Single Crystal ◽  
Hydrogen Fluoride ◽  
Grown Crystal ◽  
Optical Band Gap ◽  
Second Harmonic ◽  
X Ray Diffraction ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Ft Ir

AbstractL-cysteine hydrogen fluoride (LCHF) single crystals were grown from aqueous solution. Single crystal X-ray diffraction, FT-IR, UV-Vis-NIR, and TG-DTA were used to test the grown crystals. The specimen dielectric and mechanical behaviors were also studied. Powder X-ray diffraction of the grown crystal was recorded and indexed. The optical properties of the LCHF crystal were determined using UV-Vis spectroscopy. It was found that the optical band gap of LCHF was 4.8 eV. The crystal functional groups were identified using FT-IR. Second harmonic generation (SHG) efficiency of the LCHF was three times higher than that of KDP. The dielectric constant, dielectric loss and AC conductivity were measured at different frequencies and temperatures.

scholarly journals Synthesis, Crystal Growth, Structure, Crystalline Perfection, Thermal, Linear and Nonlinear Optical Investigations on 2-Amino-5-Nitropyridine 4-Chlorobenzoic Acid (1:1): A Novel Organic Single Crystal for NLO and Optical Limiting Optical Applications

2021 ◽  
Author(s):  
Sivasubramani Vediyappan ◽  
Arumugam Raja ◽  
Ro Mu Jauhar ◽  
Ramachandran Kasthuri ◽  
Vishwanathan Vijayan ◽  
...  
Keyword(s):  
Solid State ◽  
Single Crystal ◽  
Single Crystals ◽  
Nonlinear Optical ◽  
Grown Crystal ◽  
Solid State Laser ◽  
X Ray Diffraction ◽  
Chlorobenzoic Acid ◽  
X Ray ◽  
532 Nm

Abstract 2-amino-5-nitropyridine 4-chlorobenzoic acid (1:1) (2A5NP4CBA), a potentially useful organic adduct compound has been synthesized and grown as optically transparent single crystals by conventional slow evaporation solution technique (SEST) for the first time in the literature. The formation of the new crystalline material was confirmed by the single-crystal X-ray diffraction (SXRD) analysis and the crystal structure of the grown crystal was found to be monoclinic. Fourier transform infrared (FTIR) spectrum has been recorded by the KBr pellet technique to determine the various vibrational functional groups in the title material. The powder X-ray diffraction (PXRD) and high-resolution X-ray diffraction (HRXRD) analyses have been carried out and the obtained results reveal that the grown crystal has a single-phase and is free from structural grain boundaries. The obtained less value (32 arc-s) of full width at half maximum (FWHM) for (001) plane indicates the excellent crystalline quality of the title 2A5NP4CBA single crystal. The linear optical properties were evaluated by the UV-vis-NIR absorption and transmittance analyses and the obtained results reveal that the grown crystal possesses more than 70% of optical transmittance window with the cut-off edge at 419 nm. The thermal analysis discloses that the grown crystal possesses good thermal stability of about 187°C. To determine the appropriateness of the grown crystal for the high-power laser application, laser damage threshold (LDT) analysis has been carried out by Nd: YAG laser of a wavelength of 1064 nm. The third-order nonlinear optical coefficients such as nonlinear absorption (β), nonlinear refraction (n 2 ) and nonlinear susceptibility (χ (3) ) have been evaluated by utilizing the single beam Z-scan technique using a solid-state laser of wavelength 532 nm. The calculated ꭓ (3) value is found to be reasonably good compared to other organic single crystals which are reported in the literature. The optical limiting (OL) behavior of the title crystal was evaluated using a solid-state laser at 532 nm and the limiting threshold was found to be 7.8 mW/cm 2 .

Sign in / Sign up

Export Citation Format

Share Document