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1.
Axel Fischer Peter G. Jones Ion Neda Reinhard Schmutzler Igor V. Shevchenko 《无机化学与普通化学杂志》1994,620(5):908-913
Synthesis and Molecular Structure of new Ring Systems from 1,1,3,3-Tetrachloro-1,3-diphosphapropane 1,1,3,3-Tetrachloro-1,3-diphosphapropane 1 reacts in two different ways to form new heterocycles. Partial oxidation of 1 with tetrachloroorthobenzoquinone furnishes the methylene-bridged λ3P, λ5P species 3 . Subsequent reactions with di- and triethylamine lead to the condensed ring system 6 with the P?C bonds connected to a central four-membered ring. Compound 6 displays crystallographic inversion symmetry, a short transannular P? P distance and an extremely distorted tetrahedral coordination geometry at the four-membered ring phosphorus atoms. 1 reacts with 7 to give the heterocycle 8 with a central eight-membered ring involving four phosphorus atoms. The eight – membered ring shows a ?bent”? crown conformation, the condensed five – membered rings display envelope conformation. 相似文献
2.
Ion Neda Carsten Melnicky Alexander Vollbrecht Axel Fischer Peter G. Jones Reinhard Schmutzler 《无机化学与普通化学杂志》1996,622(6):1047-1059
The reaction of methylisatoic acid anhydride 1 with benzylamines led to the N-benzyl-N′-methylanthranilamide derivatives 2 – 4 . Their reaction with phosphorus trichloride furnished the 2-chloro-1-halobenzyl/benzyl-3-methyl-4(1 H)-1,3,2-benzodiazaphosphorin-4-ones 5 – 7 which, upon reaction with bis-(2-chloroethyl)ammonium chloride/triethylamine, were converted into the P-bis-(2-chloroethyl)amino-1-halobenzyl/benzyl-3-methyl-4(1 H)-1,3,2-benzodiazaphosphorin-4-ones 8 – 10 and 12 . With 2-chloroethylammonium chloride/triethyl-amine the P? NHCH2CH2Cl-substituted compound 11 was obtained from the PIIICl-species 6 . The reaction of 8 – 10 and 12 with hexafluoroacetone (HFA) took an unusual course: apart from the oxidative addition of HFA and formation of the perfluoropinacolyl ring system, one of the two CH2CH2Cl groups was found to alkylate the CH3N atom with formation of a five-membered (diazaphospholane) ring in the tricyclic phosphoranes 13 – 16 . The reaction of 11 with HFA also produced a spirophosphorane 17 which involved a λ5-oxazaphosphetidine ring system. In the reaction of 8, 10 and 12 with tetrachloro-o-benzoquinone, an oxidative addition reaction with concomitant N-alkylation and formation of the tricyclic phosphoranes 18 – 20 was found to take place. Single crystal X-ray structure determinations are described for the phosphoranes 13, 14 and 16 , and for the precursor compound 9 . The following features are common to the isostructural compounds 13 and 16 and the diethyl ether hemisolvate of 14 : the (λ5)-spiro phosphorus atom lies out of the plane of the other atoms of the rings to which it is common, and the dioxaphospholane rings display a twist conformation. In the λ3P-compound 9 the phosphorus atom also lies out of the plane of the other ring atoms. 相似文献
3.
Ali Reza Kazemizadeh Nahid Shajari Reza Shapouri Neda Adibpour Reza Teimuri‐Mofrad Parisa Dinmohammadi 《应用有机金属化学》2016,30(3):148-153
A four‐component reaction between aromatic carboxylic acids, (N‐isocyanimino)triphenylphosphorane, ferrocenecarbaldehyde and dibenzylamine is reported. This approach is an efficient, simple and high‐yield procedure for the synthesis of 1,3,4‐oxadiazole derivatives containing a ferrocene unit. The antimicrobial activities of the products were investigated against Staphylococcus aureus and Pseudomonas aeruginosa in in vitro and in vivo assays. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
4.
Neda Choodari Milani Yazdan Maghsoud Mahdieh Hosseini Abouzar Babaei Hamidreza Rahmani Stephen Mark Roe Khodayar Gholivand 《应用有机金属化学》2020,34(4):e5526
Seven novel complexes (C1–C7) were synthesized by the interaction between Cu(I) metal cation, L1, L2, L3, X and PPh3, where L1–L3 are derivatives of ((pyridine-2-ylmethylene)amino)phenol imine ligands and X = Cl−, Br−, I−, NCS−. All the complexes were characterized using infrared, 1H NMR and 31P NMR spectroscopies. The crystal structures of C1–C7 were also determined using single-crystal X-ray diffraction. The organization of the crystal structures and the intermolecular interactions are discussed. The supramolecular assemblies are driven by cooperative π…π interactions and hydrogen bonds, followed by CH…π linkages. The potential anticancer effect of C1–C7 was assessed for human glioblastoma cells using several anticancer experiments, which showed that these complexes have marked anticancer property against U87 cells. It was also found that the minimum and maximum anticancer effects are shown by C3- and C4-treated samples, respectively. Furthermore, theoretical approaches were used to investigate the nature of metal–ligand interactions which suggest a closed-shell and electrostatic character for Cu…N, Cu…P and Cu…X bonds. 相似文献
5.
Argus Adrian Dunca Kara E. Kohler Monika Neda Leo G. Rebholz 《Mathematical Methods in the Applied Sciences》2012,35(10):1205-1219
This work presents a rigorous analysis of mathematical and physical properties for solutions of multiscale deconvolution turbulence models. We show that solutions of these models exactly conserve model quantities for the integral invariants of fundamental physical importance: kinetic energy, helicity, and (in two dimensions) enstrophy. The kinetic energy conservation is the key that allows us to next apply the phenomenology of homogeneous, isotropic turbulence to establish the existence of a model energy cascade and, in particular, that the cascade exhibits enhanced energy dissipation in a secondary accelerated cascade, which ends at the model's microscale (which we establish is larger than the Kolmogorov microscale). We also prove that the model dissipates energy at the same rate as true turbulent flow, ~ O(U3 ∕ L), independent of Reynolds number. Lastly, we prove the existence of global attractors for the model solutions; the proof of which also shows that solutions are actually one degree of regularity higher than previously known. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
6.
Hamid Reza Shaterian Asghar Hosseinian Majid Ghashang Fahimeh Khorami Neda Karimpoor 《Phosphorus, sulfur, and silicon and the related elements》2013,188(9):2333-2338
An environmentally friendly procedure for the preparation of dihydropyrimidinone derivatives or their sulfur analogues under thermal solvent-free conditions in the presence of aluminium hydrogen sulfate [Al(HSO4)3] and alumina sulfuric acid (Al2O3-SO3H) as heterogeneous catalysts was developed. 相似文献
7.
A series of β‐hydroxynitriles were efficiently synthesized from the regioselective ring opening of oxiranes by cyanide anion in the presence of silica‐bound 3‐{2‐[poly(ethylene glycol)]ethyl}‐substituted 1‐methyl‐1H‐imidazol‐3‐ium bromide (SiO2? PEG? ImBr) as a novel recoverable phase‐transfer catalyst in H2O (Scheme 1 and Table 2). The workup procedure was straightforward, and the catalyst could be reused over four times with almost no loss of catalytic activity and selectivity. 相似文献
8.
Neda Seyedi 《Transition Metal Chemistry》2013,38(1):93-103
In this investigation, glycerol and [Fe(III)(salen)]Cl as a green catalyst system were used in multicomponent reactions for the synthesis of bis(indolyl)methanes, 3,4-dihydropyrimidinones, and 1,4-dihydropyridines, respectively. Excellent product yields and short reaction times were achieved. 相似文献
9.
There is a high overvoltage in the oxidation of methanol in fuel cells,and so modified electrodes are used to decrease it.A modified electrode that used Ni(II) loaded analcime zeolite to catalyze the electrooxidation of methanol in alkaline solution was proposed.Analcime zeolite was synthesized by hydrothermal synthesis,and Ni(II) ions were incorporated into the analcime structure,which was then mixed with carbon paste to prepare modified electrode.The electrocatalytic oxidation of methanol on the surface of the modified electrode in alkaline solution was investigated by cyclic voltammetry and chronoamperometry.The effects of the scan rate of the potential,concentration of methanol,and amount of zeolite were investigated.The rate constant for the catalytic reaction of methanol was 6 × 103 cm3 mol-1 s-1 from measurements using chronoamperometry.The proposed electrode significantly improved the electron transfer rate and decreased the overpotential for methanol oxidation. 相似文献
10.
Meysam Soltani Nejad Neda Samandari Najafabadi Sonia Aghighi Elena Pakina Meisam Zargar 《Molecules (Basel, Switzerland)》2022,27(4)
The aim of our study was to examine the different concentrations of AuNPs as a new antimicrobial substance to control the pathogenic activity. The extracellular synthesis of AuNPs performed by using Phoma sp. as an endophytic fungus. Endophytic fungus was isolated from vascular tissue of peach trees (Prunus persica) from Baft, located in Kerman province, Iran. The UltraViolet-Visible Spectroscopy (UV–Vis spectroscopy) and Fourier transform infrared spectroscopy provided the absorbance peak at 526 nm, while the X-ray diffraction and transmission electron microscopy images released the formation of spherical AuNPs with sizes in the range of 10–100 nm. The findings of inhibition zone test of Au nanoparticles (AuNPs) showed a desirable antifungal and antibacterial activity against phytopathogens including Rhizoctonia solani AG1-IA (AG1-IA has been identified as the dominant anastomosis group) and Xanthomonas oryzae pv. oryzae. The highest inhibition level against sclerotia formation was 93% for AuNPs at a concentration of 80 μg/mL. Application of endophytic fungus biomass for synthesis of AuNPs is relatively inexpensive, single step and environmentally friendly. In vitro study of the antifungal activity of AuNPs at concentrations of 10, 20, 40 and 80 μg/mL was conducted against rice fungal pathogen R. solani to reduce sclerotia formation. The experimental data revealed that the Inhibition rate (RH) for sclerotia formation was (15, 33, 74 and 93%), respectively, for their corresponding AuNPs concentrations (10, 20, 40 and 80 μg/mL). Our findings obviously indicated that the RH strongly depend on AuNPs rates, and enhance upon an increase in AuNPs rates. The application of endophytic fungi biomass for green synthesis is our future goal. 相似文献