Synthesis of 4-substituted pyrano[4,3-b]pyran-2,5-diones in an ionic liquid

The mildly basic ionic liquid N,N,N,N-tetramethylguanidinium triflate (TMGTf) was found to be a very effective solvent for the reaction between 4-hydroxy-6-methyl-2H-pyran-2-one, Meldrum's acid, and aldehydes to afford some novel pyrano[4,3-b]pyran-2,5-diones in high yields at room temperature. The stages, through which these reactions might proceed, depend largely on the nature of the aldehyde substrates. The reaction of aliphatic aldehydes has given access to some novel carboxylated products.     

Surface nanostructural modifications of Ti implanted by N+ ions as a function of energy

The surface modification of titanium foil/sheet samples (0.5?mm thickness) implanted by nitrogen ions of different energy and fluence of 1?×?10^18?N^+?cm^?2 was studied using X-ray diffraction (XRD), atomic force microscopy (AFM), scanning electron microscopy and secondary-ion mass spectrometry (SIMS). XRD patterns showed the development of titanium nitride with different compositions in the implanted samples, and the presence of different titanium compositions such as titanium oxides was also observed. AFM images at 16 and 20?keV showed the formation of grains, which were attributed to the initial sputtering of grain boundaries. The morphology of the surface changed at 25?keV showing granular structure with an almost uniform background and lowest surface roughness relative to lower and higher implantation energies. A correlation was obtained between all results for XRD, SIMS and AFM except the titanium nitride maximum intensity at 25?keV N⁺ implantation. In order to achieve more detailed information about the role of N⁺ energy in this kind of work it is proposed that a further investigation is needed on both N⁺ energy and substrate temperature as well as some theoretical studies.     

PSOHS: an efficient two-stage approach for data clustering

Cluster analysis is an important task in data mining and refers to group a set of objects such that the similarities among objects within the same group are maximal while similarities among objects from different groups are minimal. The particle swarm optimization algorithm (PSO) is one of the famous metaheuristic optimization algorithms, which has been successfully applied to solve the clustering problem. However, it has two major shortcomings. The PSO algorithm converges rapidly during the initial stages of the search process, but near global optimum, the convergence speed will become very slow. Moreover, it may get trapped in local optimum if the global best and local best values are equal to the particle’s position over a certain number of iterations. In this paper we hybridized the PSO with a heuristic search algorithm to overcome the shortcomings of the PSO algorithm. In the proposed algorithm, called PSOHS, the particle swarm optimization is used to produce an initial solution to the clustering problem and then a heuristic search algorithm is applied to improve the quality of this solution by searching around it. The superiority of the proposed PSOHS clustering method, as compared to other popular methods for clustering problem is established for seven benchmark and real datasets including Iris, Wine, Crude Oil, Cancer, CMC, Glass and Vowel.     

Silica sulfuric acid:A versatile reagent for oxathioacetalyzation of carbonyl compounds and deprotection of 1,3-oxathiolanes

Oxathioacetalyzation of carbonyl compounds with 2-mercaptoethanol and deprotection of the obtained 1,3-oxathiolanes is easily performed in the presence of silica sulfuric acid (SSA). All reactions were performed under mild and completely heterogeneous reaction conditions in good to high yields.     

A Unique Example of a Co-crystal of [Co(AMTTO)2(H2O)2](NO3)2 and [Co(AMTTO)2(CH3CN)2](NO3)2 (AMTTO = 4-amino-5-methyl-1,2,4-triazol-3(2H)-thione)

A co-crystal of cobalt(II) complexes, Co(AMTTO)₂(CH₃CN)₂]²⁺(NO₃)₂. [Co(AMTTO)₂(H₂O)₂]²⁺(NO₃)₂, compound (1) was isolated from the reaction of Co(NO₃)₂?6H₂O and 4-amino-3-mercapto-6-methyl-5-oxo-1,2,4-triazine (AMTTO) in acetonitrile as solvent. Isolated crystals were characterized by elemental analyses, IR spectroscopy as well as X-ray diffraction studies. Crystal data for 1 at 95 K revealed a monoclinic space group P2₁/n, a?=?11.7903(5), b?=?12.1279(5), c?=?14.1443(6) Å, β?=?99.244(4)°, Z?=?2, R₁?=?0.0339. Compound 1 consists of two co-crystallized Co(II) complexes [Co(AMTTO)₂(CH₃CN)₂]²⁺ and [Co(AMTTO)₂(H₂O)₂]²⁺ and four nitrate counter anions In both complexes, cobalt(II) ions are in an octahedral arrangement. Two S, N bidentate AMTTO ligands are coordinated to both Co(II) ions. The coordination sphere of Co1 is completed by two acetonitrile molecules, and these positions are occupied by water molecules for Co2.

Graphic Abstract

A co-crystal of cobalt(II) compound was isolated from the reaction of Co(NO₃)₂?6H₂O and 4-amino-3-mercapto-6-methyl-5-oxo-1,2,4-triazine in acetonitrile as solvent.

     

Tandem and transition metal-free synthesis of novel benzoimidazo-quinazoline as highly selective Hg<Superscript>2+</Superscript> sensors

A one-pot procedure for the synthesis of novel planar aza-heterocycles possessing good fluorescence potencies was described. These benzo-imidazopyrimido[4,5-b]quinolone derivatives came from the reaction of 2-chloroquinoline-3-carboxaldehydes and 2-aminobenzimidazole using K₂CO₃ in DMF. The fluorescence study of these conjugated systems was also considered, which revealed that they have highly selective sensing of mercury. Consequently, to investigate another aspect of the reaction, a three-component reaction was developed by adding malononitrile to the aforementioned starting materials in the presence of l-proline under reflux condition in H₂O/EtOH to provide amino-quinolin-3-yl-dihydrobenzo-imidazo-pyrimidine-3-carbonitriles in good yields.     

Synthesis and photocatalytic activity of V-doped mesoporous TiO2 photosensitized with porphyrin supported by SBA-15

Research on Chemical Intermediates - A highly efficient photocatalyst was produced by immobilizing V-doped mesoporous TiO2/tetrakis(4-carboxyphenyl)porphyrin (V-TiO2/TCPP) onto SBA-15 walls, and...     

Toward efficient functionalization of polystyrene backbone through ketene chemistry: Synthesis,characterization, and DFT study

In this study, polystyrene was functionalized with Meldrum's acid toward the introduction of the ketenes (CCO) system to its backbone for producing a dramatically reactive intermediate. Meldrum's acid, as a ketene source, was reacted by poly(styrene-co-p-chloromethyl styrene) through a simple nucleophilic reaction to synthesize poly(styrene-co-styryl Meldrum's acid). Then, the pendant Meldrum's acid under thermal treatment converted to ketene intermediate resulting in highly reactive polystyrenes derivatives, which rapidly reacted by nucleophilic reagents to afford ultimate organic building blocks. The polystyrene derivatives were characterized using elemental analysis, FT-IR, high-resolution solid-state NMR, thermogravimetric analysis (TGA), and differential thermogravimetric analysis (DTG). To clarify the evolutionary mechanisms of polystyrene products, density functional theory (DFT) method B3LYP with the 6–311++G(2d,p) basis set was used. We studied the preparation of polystyrene model compounds through Meldrum's acid thermolysis and nucleophilic substitution. The kinetic and thermodynamic parameters in all reactions and the structural and electronic properties of all molecules were calculated. These data exhibited that based on Gibbs Free energy values, the structure of syndiotactic polystyrene is more stable than that of isotactic polystyrene. Furthermore, it was found that the presence of an electron donor or acceptor substituent on the polystyrene structure affects the electronic bandgap.     

Nonlinear optical characterization of phosphate glasses based on ZnO using the Z-scan technique

The nonlinear optical properties of a phosphate vitreous system [(ZnO)_x-(MgO)_30-x-(P₂ O₅)₇₀], where x=8, 10, 15, 18, and 20 mol% synthesized through the melt-quenching technique have been investigated by using the Z-scan technique. In the experiment, a continuous-wave laser with a wavelength of 405 nm was utilized to determine the sign and value of the nonlinear refractive (NLR) index and the absorption coefficient with closed and opened apertures of the Z-scan setup. The NLR index was found to increase with the ZnO concentration in the glass samples by an order of 10^-10 cm²·W^-1. The real and imaginary parts of the third-order nonlinear susceptibility were calculated by referring to the NLR index (n₂) and absorption coefficient (β) of the samples. The value of the third-order nonlinear susceptibility was presented by nonlinear refractive or absorptive behavior of phosphate glasses for proper utilization in nonlinear optical devices. Based on the measurement, the positive sign of the NLR index shows a self-focusing phenomenon. The figures of merit for each sample were calculated to judge the potential of phosphate glasses for application in optical switching.     

A note on supercyclic vectors of Hilbert space operators

Let H be an infinite dimensional complex Hilbert space and T be a bounded linear operator on H. We show that if there exists $x\in H$ such that the closure of $\{\alpha T^{n}x:\alpha \in \mathbb{C},n?0\}$ is H, then there is a subsequence ${(n_k)}_{k=1}^{\infty }$ such that the closed linear span of $\{T^{n_k}x:k?1\}$ is not the whole space H.