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21.
In this report, we try to show the importance of incorporation of name reactions in the sequential cascade reaction in which significantly decreasing the number of steps towards an ideal and practical multi-step synthesis of natural products as well showing virtually all the advantages already mentioned for “Click Chemistry”. In addition, since the chiral inductions are desired for most of these sequential name reactions, their asymmetric catalyzed reactions were also described. 相似文献
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Somayeh Khosravinia Mahmood A. Mahdavi Reza Gheshlaghi Hesam Dehghani 《Applied biochemistry and biotechnology》2018,184(3):885-896
Numerous desulfurizing bacteria from the Rhodococcus genus harbor conserved dsz genes responsible for the degradation of sulfur compounds through 4S pathway. This study describes a newly identified desulfurizing bacterium, Rhodococcus sp. FUM94, which unlike previously identified strains encodes a truncated dsz operon. DNA sequencing revealed a frameshift mutation in the dszA gene, which led to an alteration of 66 amino acids and deletion of other C-terminal 66 amino acids. The resulting DszA polypeptide was shorter than DszA in Rhodococcus sp. IGTS8 reference strain. Despite the truncation, desulfurizing activity of the operon was observed and attributed to the removal of an overlap of dszA and dszB genes, and lack of active site in the altered region. Desulfurization experiments resulted in specific production rate of 6.3 mmol 2-hydroxy biphenyl (kgDCW)?1 h?1 at 2 g l?1 biocatalyst concentration and 68.8% biodesulfurization yield at 20 g l?1 biocatalyst concentration, both at 271 μM dibenzothiophene concentration which is comparable to similar wild-type biocatalysts. 相似文献
23.
Kinetics of the substitution reaction of solvent molecule in uranyl(VI) Schiff base complexes by tri‐n‐butylposphine as the entering nucleophile in acetonitrile at 10–40°C was studied spectrophotometrically. The second‐order rate constants for the substitution reaction of the solvent molecule were found to be (8.8 ± 0.5) × 10?3, (5.3 ± 0.2) × 10?3, (7.5 ± 0.3) × 10?3, (6.1 ± 0.3) × 10?3, (13.5 ± 1.6) × 10?3, (13.2 ± 0.9) × 10?3, (52.9 ± 0.2) × 10?3, and (88.1 ± 0.6) × 10?3 M?1 s?1 at 40°C for [UO2(Schiff base)(CH3CN)], where Schiff base = L1–L8, respectively. In a temperature dependence study, the activation parameters ΔH# and ΔS# for the reaction of uranyl complexes with PBu3 were determined. From the linear rate dependence on the concentration of PBu3, the span of k2 values and the large negative values of the activation entropy, an associative (A) mechanism is deduced for the solvent substitution. By comparing the second‐order rate constants k2, it was concluded that the steric and the electronic properties of the complexes were important for the rate of the reactions. 相似文献
24.
Numerical Algorithms - 相似文献
25.
Sevda Dehghani Samahe Sadjadi Naeimeh Bahri‐Laleh Mehdi Nekoomanesh‐Haghighi Albert Poater 《应用有机金属化学》2019,33(5)
Taking advantage of computational chemistry, the best diamine for the synthesis of a multi‐dentate ligand from the reaction with 3‐(trimethoxysilyl) propylisocyanate (TEPI) was selected. Actually, predictive Density Functional Theory (DFT) calculations provided the right diamino chain, i.e. ethylenediamine, capable to sequester a palladium atom, together with the relatively polar solvent toluene, and then undergo the experiments as a selective catalytic agent. The ligand was then prepared and applied for the decoration of the halloysite (Hal) outer surface to furnish an efficient support for the immobilization of Pd nanoparticles. The resulting catalyst exhibited high catalytic activity for hydrogenation of nitroarenes. Moreover, it showed high selectivity towards nitro functional group. The study of the catalyst recyclability confirmed that the catalyst could be recycled for several reaction runs with only slight loss of the catalytic activity and Pd leaching. Hot filtration test also proved the heterogeneous nature of the catalysis. 相似文献
26.
Dehghani A. Mojaveri B. Alenabi A. A. 《International Journal of Theoretical Physics》2021,60(10):3885-3895
International Journal of Theoretical Physics - Two new configurations of superposition of quantum states corresponding to the angular momentum of spin-1 quantum system is proposed in this article.... 相似文献
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28.
Hossein Dehghani Mohammad Reza Mansournia 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2009,74(2):324-328
The sitting-atop complexation of meso-tetraarylporphyrins and its para-substituted derivatives (H2t(4-X)pp, X:H, Br, Cl, CH(CH3)2, OCH3, CH3), as electron donors, with zirconyl, as an electron acceptor, have been investigated spectrophotometrically in chloroform. The mole ratio studies based on physicochemical techniques were employed clearly and revealed the formation of 1:1 sitting-atop complexes which was confirmed by UV–vis, 1H NMR and IR spectroscopic data. The value of the formation constant was estimated for each complex using a nonlinear optimization of the complex absorbance vs. mole ratio data by package KINFIT. The results showed that the stability of these complexes decreases with the temperature enhancement. Thermodynamic parameters, ΔG°, ΔH° and ΔS°, of the SAT complexes have been determined from the temperature dependence of formation constants by Van’t Hoff equation. Also, the influence of the substituents of the aryl rings in H2t(4-X)pp on the stability of the SAT complexes is discussed. 相似文献
29.
The reaction of meso-tetraarylporphyrins (H2t(Xp)p) with SbCl3 under free solvent conditions affords green complexes with a 1:1 H2t(X)pp:SbCl3 ratio. These complexes have dimeric structures with a (μ-Cl)2bridge. UV–VIS, 1H NMR and 13C NMR spectra data show that the porphyrin core of [(H2t(Xp)p)2Sb2Cl6], similar to 1:2 (donor:acceptor) molecular complexes of meso-tetraarylporphyrins and porphyrin diacid, is distorted, thus two nitrogen atoms of pyrrolenine in a side of the porphyrin plane act as electron donors to an antimony atom of SbCl3. Molecular complexation of meso-tetraarylporphyrins with SbCl3 produces a large downfield shift for the NH signal, although there is no hydrogen bonding present. 相似文献
30.
Mohammad Mazloum Ardakani Parvaneh Rahimi Hossein Dehghani Payam Ebrahimi Karami Hamid Reza Zare Somayeh Karami 《Electroanalysis》2007,19(21):2258-2263
The preparation and electrocatalytic behavior of glassy carbon electrodes modified with three different cobalt porphyrin complexes were investigated. The electrocatalytic ability of the modified electrodes for the reduction of dioxygen to hydrogen peroxide and water in air‐saturated aqueous solutions was examined by cyclic voltammetry and chronoamperometry techniques. The porphyrin‐adsorbed glassy carbon electrodes possess excellent electrocatalytic abilities for dioxygen reduction with overpotential about 0.5 V lower than that at a plain glassy carbon electrode. The experimental parameters were optimized and the mechanism of the catalytic process was discussed. The possible effects of the electron‐donating properties of groups in the meso‐position of the porphyrin ring were investigated. 相似文献