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51.
Soltani Rad Mohammad Navid Behrouz Somayeh Mohammad-Javadi Mehdi Zarenezhad Elham 《Molecular diversity》2022,26(5):2503-2521
Molecular Diversity - The preparation, characterization and application of hydroxyapatite silica propyl bis aminoethoxy ethane cuprous complex (HASPBAEECC) as a novel hybrid nano-catalyst for... 相似文献
52.
Behrouz Kheirfam 《Journal of Optimization Theory and Applications》2014,161(3):853-869
In this paper, we first present a full-Newton step feasible interior-point algorithm for solving horizontal linear complementarity problems. We prove that the full-Newton step to the central path is quadratically convergent. Then, we generalize an infeasible interior-point method for linear optimization to horizontal linear complementarity problems based on new search directions. This algorithm starts from strictly feasible iterates on the central path of a perturbed problem that is produced by a suitable perturbation in the horizontal linear complementarity problem. We use the so-called feasibility steps that find strictly feasible iterates for the next perturbed problem. By using centering steps for the new perturbed problem, we obtain a strictly feasible iterate close enough to the central path of the new perturbed problem. The complexity of the algorithm coincides with the best known iteration bound for infeasible interior-point methods. 相似文献
53.
Behrouz Emamizadeh Mohsen Zivari-Rezapour 《Nonlinear Analysis: Theory, Methods & Applications》2011,74(16):5697-5704
This paper, motivated by Del Pezzo et al. (2006) [1], discusses the minimization of the principal eigenvalue of a nonlinear boundary value problem. In the literature, this type of problem is called Steklov eigenvalue problem. The minimization is implemented with respect to a weight function. The admissible set is a class of rearrangements generated by a bounded function. We merely assume the generator is non-negative in contrast to [1], where the authors consider weights which are positively away from zero, in addition to being two-valued. Under this generality, more physical situations can be modeled. Finally, using rearrangement theory developed by Geoffrey Burton, we are able to prove uniqueness of the optimal solution when the domain of interest is a ball. 相似文献
54.
The versatility of palladium(II) acetate and palladium on activated charcoal catalysts with triethylsilane has been investigated in the hydrogenation and the isomerization of carbon–carbon double bond of 1‐alkenes. The reduction of 1‐alkenes was carried out in the presence of triethylsilane, ethanol and a catalytic amount of palladium(II) acetate or palladium on activated charcoal, at room temperature. This facile and efficient method affords high yields for hydrogenation of unsaturated alkenes to the corresponding alkanes. Then the carbon–carbon double bond isomerization of 1‐alkenes was tested using the same catalysts in the absence of solvent. The system palladium(II) acetate‐triethylsilane was found to be more effective compared with palladium on an activated charcoal–triethylsilane system at room temperature, while comparable results were obtained at 50 °C for both catalysts. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
55.
Korbinian Riener Alexander Pthig Mirza Cokoja Wolfgang A. Herrmann Fritz E. Kühn 《Acta Crystallographica. Section C, Structural Chemistry》2015,71(8):643-646
In recent years, the use of copper N‐heterocyclic carbene (NHC) complexes has expanded to fields besides catalysis, namely medicinal chemistry and luminescence applications. In the latter case, multinuclear copper NHC compounds have attracted interest, however, the number of these complexes in the literature is still quite limited. Bis[μ‐1,3‐bis(3‐tert‐butylimidazolin‐2‐yliden‐1‐yl)pyridine]‐1κ4C2,N:N,C2′;2κ4C2,N:N,C2′‐dicopper(I) bis(hexafluoridophosphate), [Cu2(C19H25N5)2](PF6)2, is a dimeric copper(I) complex bridged by two CNC, i.e. bis(N‐heterocyclic carbene)pyridine, ligands. Each CuI atom is almost linearly coordinated by two NHC ligands and interactions are observed between the pyridine N atoms and the metal centres, while no cuprophilic interactions were observed. Very strong absorption bands are evident in the UV–Vis spectrum at 236 and 274 nm, and an emission band is observed at 450 nm. The reported complex is a new example of a multinuclear copper NHC complex and a member of a compound class which has only rarely been reported. 相似文献
56.
57.
Mohammad Akbar Ali Aminul Huq Mirza Ray J. Butcher Arun K. Chowdhury 《Transition Metal Chemistry》2011,36(5):471-479
A new tridentate ONS ligand, H2L, has been synthesized by condensing thenoyltrifluoroacetone(4,4,4-trifluoro-1-(2-thienyl)-2,4butaneanedione) with S-benzyldithiocarbazate
and its structure determined by X-ray diffraction. In the solid state, the Schiff base exists as the ketoamine-thioketo tautomer
but in solution and in the presence of copper(II), it converts to the enol-thiol form and deprotonates to give copper(II)
complexes of formula, [CuL] and [CuLL1] (L = doubly deprotonated form of the ligand; L1 = py, bipy or phen] which have been characterized by magnetic, spectroscopic, and X-ray diffraction studies. An X-ray crystallographic
analysis shows that [CuL(py)] has a square-planar geometry with the ligand coordinated to the copper(II) center via the enolate
oxygen, the azomethinic nitrogen and the thiolate sulfur, the fourth coordination position being occupied by pyridine. The
[CuL(bipy)] complex is five-coordinate with a structure close to square-pyramidal in which the Schiff base acts as a doubly
deprotonated tridentate ONS ligand and bipy is bidentate. 相似文献
58.
In the present study, a reverse-phase high performance liquid chromatography method was developed, validated and applied for the simultaneous determination of gliquidone, pioglitazone hydrochloride and verapamil in tablets and human serum. Chromatographic separation was achieved on a C18 column (5 μm, 25 × 0.46 cm) with a mobile phase consisting of methanol-water-acetonitrile (80:10:10 v/v/v) with a flow rate of 0.7 mL/min and pH adjusted to 3.50 with phosphoric acid at 230 nm. Glibenclamide was used as internal standard. The experimentally derived limit of detection and limit of quantitation were determined to be 0.24, 0.93, 0.40, and 0.80, 3.11, 1.36 μg/mL for gliquidone, pioglitazone, and verapamil, respectively. There were no interfering peaks due to the excipients present in the pharmaceutical tablets. Thus, the proposed method is simple and suitable for the simultaneous analysis of active ingredients in dosage forms and human serum. 相似文献
59.
Daniel Betz Philipp Altmann Mirza Cokoja Wolfgang A. Herrmann Fritz E. Kühn 《Coordination chemistry reviews》2011,255(13-14):1518-1540
Ionic liquids are an interesting alternative to classical solvents presenting several advantages. A variety of catalysts show good or even enhanced activities when applied in ionic liquids. Oxidation catalysis represents a large segment of industrial chemistry, providing both bulk chemicals and intermediates for high value added special products and pharmaceuticals. Particularly for the latter products organometallic and inorganic catalysts are being developed that can be applied in systems consisting of or containing ionic liquids. This work provides an overview on recent developments in this field. 相似文献
60.
Theoretical and Mathematical Physics - We present a supersymmetric generalization of a multicomponent coupled dispersionless (SUSY-MCD) integrable system. Expanding the superfields of the SUSY-MCD... 相似文献