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611.
In this work, we synthesized Ni2+-containing 1-methyl-3-(3-trimethoxysilylpropyl) imidazolium chloride ionic liquid on magnetic Fe3O4 nanoparticles. The catalytic activity of these novel nanocomposites was finally evaluated for the Heck reaction at 100 °C, and can be reused after washing without loss in activity. The immobilized ionic liquid catalysts proved to be effective and easily separated from the reaction media by applying an external magnetic field. This procedure has many obvious advantages compared to those reported in the previous literature, including avoidance of the use of the expensive Pd catalysts, mild reaction conditions, high yields, and simplicity of the methodology.  相似文献   
612.
A catalyst-free and convenient approach for the preparation of substituted dihydro-2-oxypyrrole is described. This three-component reaction between primary amines, dialkyl acetylenedicarboxylate, and N,N′-bis(phenylmethylidene)phenylmethane proceeds in MeOH under reflux conditions in good to excellent yields.  相似文献   
613.
Structural, bonding and electronic characteristics of complexes of anthraquinone and 1-arylazo-2-naphtol dyes and cellulose I β are studied using B3LYP density functional method with 6-31G** basis set based on the partially and fully optimized structures. Results reveal that for both partially and fully optimized complexes, there is a stabilizing attraction between dyes and cellulose surface. The hydrazone (Hy) tautomer in anionic state (Hy–SO3 ?) shows the strongest interaction with the cellulose surface. Natural bond orbital (NBO) and atoms-in-molecules (AIM) analyses have been carried out to study the nature of azo dyes-cellulose bonds in detail. According to NBO analysis, a remarkable charge transfer occurs between the –SO3 ? and –SO3H functional groups of the dye and the cellulose surface which can be regarded as the main source of the large dye–cellulose interaction energy. AIM analysis confirms the existence of hydrogen and van der Waals bonds between the azo dyes and cellulose. Furthermore, a very good agreement is observed between the number of hydrogen bonding sites and dye–cellulose interaction energies.  相似文献   
614.

The reaction of the title ylide {PhCOCHP(p-tolyl)3} with Pd(II), Pt(II). Hg(II), and Ag(I) in equimolar ratios using CH3CN, CH3OH, and CH2Cl2 as solvents have yielded [{(p-tolyl)3PCHCOC6H5} PdCl2]2 (I), [{(p-tolyl)3 PCHCOC6H5} PtCl2]2(2), [Hg(NO3)2 {(p-tolyl)3 PCHCOC6H5}](3), and [Ag{(p-tolyl)3 PCHCOC6H5 < eqid1 > 2]+ (4). The IR, 1H 13C, and 31P NMR together with micro analysis data of the products were obtained.  相似文献   
615.
616.
Abstract

The reaction of Ph2PCH2PPh2 (dppm) with 4-methylphenacyl bromide and 2-(bromoacetyl)naphthalene in chloroform produce the new phosphonium salts [Ph2PCH2PPh2CH2C(O)C6H4Me]Br (1) and [Ph2PCH2PPh2CH2C(O)C10H7]Br (2). Further, by reaction of the monophosphonium salts of dppm with the strong base Et3N the corresponding bidentate phosphorus ylides, Ph2PCH2P(Ph)2 = C(H)C(O)C6H4Me (3) and Ph2PCH2P(Ph)2 = C(H)C(O)C10H7 (4) were obtained. The reaction of these ligands with mercury(II) halides in dry methanol led to the formation of the mononuclear complexes {HgX 2[(Ph2PCH2PPh2C(H)C(O)C6H4Me)]} [X = Cl (5), Br (6), and I (7)] and {HgX 2[(Ph2PCH2PPh2C(H)C(O)C10H7)]} [X = Cl (8), Br (9), and I (10)]. Characterization of the obtained compounds was performed by elemental analysis, IR, 1H, 31P, and 13C NMR spectra. The structure of compounds 3 and 10 are unequivocally determined by single crystal X-ray diffraction techniques. X-ray analysis of 10 reveals the presence of mononuclear complex containing Hg atom in a distorted tetrahedral environment. In all complexes, the title ylides are coordinated through the ylidic carbon and the phosphine phosphorus. Computational studies on ligand 4 and complexes 8, 9, and 10 at DFT (B3LYP) level of theory are also reported. It was shown that the formation of P,C-coordinated 1+1 complex 10 is energetically more favored than corresponding P,P-coordinated 1+2 product.

[Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the following free supplemental files: Additional figures]  相似文献   
617.
Jiang et al. proposed an algorithm to solve the inverse minimum cost flow problems under the bottleneck-type weighted Hamming distance [Y. Jiang, L. Liu, B. Wuc, E. Yao, Inverse minimum cost flow problems under the weighted Hamming distance, European Journal of Operational Research 207 (2010) 50–54]. In this note, it is shown that their proposed algorithm does not solve correctly the inverse problem in the general case due to some incorrect results in that article. Then, a new algorithm is proposed to solve the inverse problem in strongly polynomial time. The algorithm uses the linear search technique and solves a shortest path problem in each iteration.  相似文献   
618.
We describe a new chemiluminescence (CL) system based on the oxidation of rhodamine B (RhoB) with alkaline potassium permanganate in the presence of gold nanoparticles (Au-NPs) and anionic detergent sodium dodecyl sulfate. Free RhoB is weakly chemiluminescent when oxidized with permanganate at alkaline pH values. However, a remarkably strong enhancement of CL is observed in the presence of Au-NPs, probably due to a strong interaction between RhoB and the NPs. The possible mechanism was studied via recording the CL emission. It is also found that the intensity of CL gradually decreases in the presence of cyanide due to its interaction with the Au-NPs. The relation between the decreased CL intensity and cyanide concentration was exploited to develop a method for the determination of cyanide in the 0.01–0.5 μM concentration range, with a detection limit of 2.8 nM. The method was used to determine cyanide in spiked water, urine, and serum. Figure
Alkaline permanganate-rhodamine B-SDS CL reaction is dramatically enhanced by gold nanoparticles. Based on the inhibiting effect of cyanide on this system, a sensitive CL method was developed for its determination  相似文献   
619.
Calcium in the form of tricalcium phosphate was encapsulated in the inner water phase of water-in-oil-in-water emulsion. Efficiency and payload of microcapsules were optimized using a D-optimal mixture design with four components (gelatin, agar, primary water-in-oil emulsion, and water in outer phase). Release profiles of calcium from microcapsules were determined at 4°C over 12 days. It was found that microencapsulation efficiency increased by increasing of water-in-oil emulsion to 45% and then decreased at higher contents of this portion. However, payload increased continuously with increase of water-in-oil fraction. Less calcium was released when both biopolymers and water-in-oil emulsion contents were increased.  相似文献   
620.

In the present article, a terminal sliding mode control strategy has been proposed in order to address the synchronization problem for a class of perturbed nonlinear systems with fixed convergence time and input quantization. The proposed protocol guarantees the fixed-time convergence of the sliding manifold to the origin, which means that the convergence time of the proposed sliding manifold does not change on the variations of initial values, different from typical control methods. Here, the hysteresis quantizer, as a specific type of quantizer with nonlinear sector-bounded, is applied in order to quantize the input signal. The proposed quantized control scheme vigorously prevents the potential adverse chattering phenomenon which is experienced in the common quantization methods. The proposed controller does not need the limiting criteria related to considered parameters of quantization compared to recent control approaches. Finally, the designed controller is implemented on the perturbed Genesio–Tesi (G–T) chaotic systems to verify effectiveness and strength of the proposed method.

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