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541.
J. Volke P. Kratochvíl E. Naumann A. Sippel E. Ühlein H. Reiher E. Best W. Schermann H. Schäfer 《Colloid and polymer science》1966,209(2):182-189
Ohne Zusammenfassung 相似文献
542.
E. Ühlein 《Colloid and polymer science》1969,232(1):713-727
Ohne Zusammenfassung 相似文献
543.
The title compound, bis[N-(2-fluoro-3-methoxy)-salicylideneaminato]copper(II) [Cu(C14H12O2FN)2] was synthesized and its crystal structure was determined. The title compound is triclinic, space group P
with a = 8.552(1), b = 9.645(1), c = 7.871(1) Å, = 108.708(1), = 93.769(1), = 79.429(1), V = 1208.98(1) Å3, Z = 2, D
c = 1.696 gcm–3, (Mo K) = 1.815 mm–1, R = 0.0369 for 2963 reflections [I>2(I)]. The title compound has crystallographic inversion symmetry with two bidentate Schiff base ligand coordinated to the Cu atom in a square-planar arrangement. The Cu–N1 and Cu–O2 distances are 1.995(1) and 1.885(1) Å, respectively. 相似文献
544.
The crystal and molecular structure of the title complex, C18H19N2O2Ni, has been determined by direct methods. The compound crystallizes in the monoclinic crystal system witha=22.973(1),b=5.212(1),c=27.076(1)Å, β=106.46(1)°, space groupC2/c,V=3109.1(6)Å3, Z=8, andD x=1.51g cm?3. The nickel atom is in a slightly distorted square-planar environment of two oxygens [Ni(1)?O(1) 1.824(3) and Ni(1)?O(2) 1.856(3)Å] and two nitrogens [Ni(1)?N(1) 1.849(3) and Ni(1)?N(2) 1.932(3)Å] with O?Ni?N angles between 85.7(1) and 97.1(1)°. The nickel atom is 0.006 Å out of the plane of its ligands. 相似文献
545.
In this study, interelement interferences were evaluated for the determination of arsenic in aqueous samples through laser-induced breakdown spectroscopy (LIBS) hyphenated with a hydride generation sample introduction system. Optimum instrumental and chemical parameters were selected and variation in LIBS signal intensity was recorded for As solution in the presence of comparable concentrations of interfering elements. No significant change in the signal intensity of As(I) 228.8?nm line was observed in the presence of alkali/alkali earth metals; however, the presence of hydride-forming elements has shown a noticeable decrease in the line emission strength of arsenic. The least variation in arsenic signal was observed in the presence of Ge, the most volatile of all. However, the signal has decreased to a greater extent in the presence of Sn, Sb, and Pb. The presence of interfering elements on electron temperature and electron number density of arsenic plasma has also been studied. Plasma temperatures calculated using both As and Ar emission lines in the Boltzmann equation were similar, being around 5000?K. The McWhirter criterion for stationary and homogenous plasmas was utilized for the establishment of the local thermodynamic equilibrium under the plasma conditions studied. Applicability of the technique for multielemental analysis of water samples was tested through spiking experiments. Arsenic signal showed 26% decrease in the multielemental mixture solution. LIBS is among a few atomic spectroscopic techniques that facilitate rapid and simultaneous multielemental analysis without extensive sample preparation steps. However, the analytical performance of the technique still requires more serious efforts to compete with other conventional techniques for routine analysis of environmental samples. 相似文献
546.
Ayhan Üngördü 《International journal of quantum chemistry》2020,120(6):e26128
Porphyrin and M-Porphyrin (M = Fe2+, Co2+, Ni2+, Cu2+, and Zn2+) complexes were designed to examine their organic light-emitting diode (OLED) properties. All calculations were performed in different media, which are gas, benzene, DMSO, and water phases. The calculations of both porphyrin and its metal complexes as a monomer form were performed at B3LYP/6-31G(d) level by using the Gaussian 16 and GaussView 6 package programs. On the other hand, emission calculations for the monomer form and dimer form computations of the studied compounds were carried out at PBE0/TZP and B3LYP/TZP levels, respectively, by using Amsterdam density functional (ADF) 2019 package program. The OLED tensors of the mentioned molecules, which are emission energies, reorganization energies (λe and λh), the ionization potentials and the electron affinities (adiabatic and vertical), the effective transfer integrals (Ve and Vh), and the charge transfer rates (We and Wh), were calculated to evaluate the OLED behaviors and determine the best OLED structure. 相似文献
547.
Let F be a free Lie algebra of rank n ≥ 2 and A be a free abelian Lie algebra of rank m ≥ 2. We prove that the test rank of the abelian product F ×A is m. Morever we compute the test rank of the algebra F/gk( F) ¢F/\gamma _{k}\left( F\right) ^{^{\prime }}. 相似文献
548.
We focused on the determination of biologically active secondary metabolites in wild hops over the course of the vegetation period in four selected sites in Pie??any. Hop was collected in four collection periods in 2010. The objects of research were the leaves of male and female plants, and female cones. Analysis of the extracts from wild hop confirmed differences in total content of polyphenols, flavonoids between the localities and in the growing seasons over the vegetation period. The extracts from leaves from the first harvest in localities “gSládkovi?ova” and the river Vah showed higher levels of polyphenols (4.91–6.93 mg g?1 of dry mass), flavonoids (2.28–2.99 mg g?1 of dry mass) than the extracts from cones collected at the end of the vegetation period (polyphenols 3.63–5.33 mg g?1 of dry mass, flavonoids 1.86–2.16 mg g?1 of dry mass). The extracts from leaves from the first harvest from the “tennis court” site showed lower values of polyphenols and flavonoids. Our findings were that the leaves from the first harvest at the beginning of the growing season contained higher amounts of the secondary metabolites investigated than the cones at the end of the growing season. The content of α-bitter acids in wild hop cones ranged from 1.64 % to 2.91 %, in leaves from 0.11 % to 0.99%. Concentration of β-bitter acids in cones varied from 1.63 % to 1.93 % and in leaves from 0.02 % to 0.61 %. 相似文献
549.
Ş. Hakan Üngören Mustafa Saçmacı Cengiz Arıcı Ertan Şahin Taner Arslan Fatma Kandemirli 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):2877-2890
Novel alkyl substituted 3-(4-benzoyl-1,5-diphenyl-2,3-dihydro-1H-pyrazol-3-yl)-3-oxo-2-(triphenylphosphoranylidene) propanoates (3) were synthesized from 4-benzoyl-1,5-diphenyl-1H-pyrazole-3-carbonylchloride (1) and alkyl (triphenylphosphoranylidene) acetates (2a–b). The synthesized compounds were characterized by elemental analysis, spectroscopic studies (3a–b), and single crystal X-ray diffraction (3a). The mechanism of the reaction between (1) and (2a) was studied by AM1, and the geometrical parameters of the studied molecules were also carried out in B3LYP methods with the standard 6–31G (d,p) basis set. NBO analysis were studied for 1 and 2a B3LYP methods with the standard 6–31G (d,p) basis set. 相似文献
550.
Composites of a polyindole (PIN) and poly(vinyl acetate) (PVAc) were prepared chemically using FeCl3 as an oxidant agent in anhydrous media. The composite compositions were altered by varying the indole monomer during preparation. The composites were characterized by FTIR and UV‐visible spectroscopies, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), stress‐strain experiments and conductivity measurements. Moreover, the film of PVAc and PIN/PVAc composites were prepared by casting on glass Petri dishes to examine their stress‐strain properties. PIN/PVAc composites are thermally more stable than PIN. It was found that the conductivities of PIN/PVAc composites depend on the indole content in the composites. 相似文献