Spectrophotometric study of interaction of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone with diaza-18-crown-6 and diaza-15-crown-5 in acetonitrile and chloroform solutions

Interactions of diaza-18-crown-6 and diaza-15-crown-5, as electron donors, with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), as an electron acceptor, have been investigated spectrophotometrically in acetonitrile and chloroform solutions. The results indicated immediate formation of an electron donor-electron acceptor complex DA: [reaction in text] which is followed by two relatively slow consecutive reactions: [reaction in text]. The pseudo-first-order rate constants for the formation of the ionic intermediate and the final product have been evaluated at various temperatures by computer fitting of the absorbance time data to appropriate equations. The formation constants of the resulting DA complexes have also been determined. The influences of both the azacrown's structure and the solvent properties on the formation of DA complexes and the rates of subsequent reactions are discussed.     

Conductance study of ammonium complexes with several crown ethers and cryptands in nitrobenzene,acetonitrile and dimethylformamide solutions

The formation of ammonium complexes with several crown ethers and cryptands in nitrobenzene, acetonitrile and dimethylformamide solutions was investigated by conductometry at 25°C. Stability constants of the resulting 1:1 complexes sere determined from the molar conductance-mole ratio data and found to vary in the order DC18C6>18C6>DB30C10>DB21C7>DB24C8>DB18C6>15C5>B15C5>12C4, in the case of crown complexes, and in the order C222>C221>C211>C22>C21 for the ammonium cryptates. The stabilities of the complexes varied inversely with the Gutmann donicity of the solvents. Influences of the number of members in the macrocycle, nature of the substituents in the polyether ring, cavity size and dimensionality, conformations of the free and complexed ligands and number of N⁺–H bonds available for hydrogen bonding are discussed.     

Design and characterization of [(Et)3 N-H]FeCl4 as a nanomagnetic ionic liquid catalyst for the synthesis of xanthene derivatives under solvent-free conditions

The triethylamine-based nanomagnetic ionic liquid, [(Et)₃ N-H]FeCl₄, was synthesized, and its structural and chemical characteristics were detected. The thermogravimetric analysis indicated its high thermal stability with a decomposition temperature higher than 300 °C. Additionally, [(Et)₃ N-H]FeCl₄ was used to efficiently catalyze the synthesis of xanthene derivatives under solvent-free conditions at 120 °C. [(Et)₃ N-H]FeCl₄ was recycled and reused at least five times.

Graphical abstract

     

Degrees of Freedom of a K-User Interference Channel in the Presence of an Instantaneous Relay

In this paper, we study the degrees of freedom (DoF) of a frequency-selective K-user interference channel in the presence of an instantaneous relay (IR) with multiple receiving and transmitting antennas. We investigate two scenarios based on the IR antennas’ cooperation ability. First, we assume that the IR receiving and transmitting antennas can coordinate with each other and that the transmitted signal of each transmitting antenna can depend on the received signals of all receiving antennas, and we derive lower and upper bounds for the sum DoF of this model. In an interference alignment scheme, we divide receivers into two groups called clean and dirty receivers. We design our scheme such that a part of the messages of clean receivers can be de-multiplexed at the IR. Thus, the IR can use these message streams for an interference cancellation at the clean receivers. Next, we consider an IR, the antennas of which do not have coordination with each other and where the transmitted signal of each transmitting antenna depends only on the received signal of its corresponding receiving antenna. We also derive lower and upper bounds for the sum DoF for this model of IR. We show that the achievable sum DoF decreases considerably compared with the coordinated case. In both of these models, our schemes achieve the maximum K sum DoF if the number of transmitting and receiving antennas is more than a finite threshold.     

Fluorine extraction from organofluorine molecules to make fluorinated clusters in yttrium MOFs

A new rare earth based two-dimensional coordination network and a three-dimensional metal–organic framework (MOF) have been synthesized using bicinchoninic acid (BCA) and yttrium(iii) ions. Yttrium dimer nodes are formed in the absence of a modulator, resulting in a 2D layered coordination network (Y–BCA-2D). The presence of fluorinating agents, e.g., 2-fluorobenzoic acid (2-FBA), 2,6-difluorobenzoic acid (2,6-DFBA), and perfluorohexanoic acid (PFHxA) result in μ₃-F bridged metal hexaclusters (Y₆F₈) that form a three-dimensional MOF (Y–BCA-3D). It was found that Y³⁺ can break highly stable C–F bonds in aromatic and aliphatic fluorinated compounds. Single-crystal X-ray diffraction (SC-XRD) shows the presence of fluorine in the metal cluster which was confirmed by energy dispersive X-ray spectroscopy (EDS). High resolution X-ray photoelectron spectroscopy (XPS) and ¹⁹F Nuclear Magnetic Resonance (NMR) also verify the presence of metal–fluorine bonds in the cluster. The Y–BCA-3D MOF selectively adsorbs CO₂ but not N₂.

The reaction of yttrium(iii) and linker makes a 2D metal–organic framework. The addition of fluorinated modulators result in fluorine extraction from modulators and makes a 3D-MOF.     

Two-phase simulation of nanofluid flow in a heat exchanger with grooved wall

Journal of Thermal Analysis and Calorimetry - The aim of this paper is to achieve a smaller and cheaper heat exchanger with similar performance. To fulfill this demand, ANSYS-Fluent software and...     

Reducing Occupational Noise Propagated from Centrifugal Fan through Dissipative Silencers: A Field Study

Acoustic performance of dissipative silencer was evaluated to determine the effectiveness of perforated duct porosity and absorbent material density in reducing occupational noise exposure propagated from centrifugal fan. Design charts were applied to predict noise reduction and length of a dissipative silencer. Dissipative silencers with various punched duct porosity (14%, 30% and 40%) and sound absorbent density (80 Kg/m³, 120 Kg/m³, and 140 Kg/m³) were designed and fabricated. According to ISO9612 and ISO11820, noise level was measured before and after installing all nine test silencers at fixed workstations around the discharge side of a centrifugal fan in a manufacturing plant. On average, the noise level at the discharge side of a fan without silencer was measured to be 93.6 dBA, whereas it was significantly mitigated by 67.4 dBA to 70.1 dBA after installing all silencers. Dynamic insertion loss for a dissipative silencer with 100 cm length was predicted to be 27.9 dB, which was in agreement with experimental ones. Although, there was no significant differences between insertion loss of silencers, the one with 30% porosity and 120 Kg/m³ rock wool density had the highest insertion loss of 26.2 dBA. Dissipative silencers noticeably reduced centrifugal fan noise exposures. Increasing sound absorbent density and duct porosity up to a certain limit could probably be effective in noise reduction of dissipative silencers.     

Chemoselective trimethylsilylation of alcohols catalyzed by saccharin sulfonic acid

Abstract  

Saccharin sulfonic acid was easily prepared by the reaction of saccharin with neat chlorosulfonic acid at room temperature. This reagent is efficiently able to catalyze the chemoselective trimethylsilylation of alcohols with hexamethyldisilazane in the presence of amines and thiols.     

Simultaneous spectrofluorimetric determination of levodopa and propranolol in urine using feed-forward neural networks assisted by principal component analysis

The simultaneous determination of levodopa (LD) and propranolol (PRO) using fluorescence spectrometric technique is described. The method involves measuring the natural fluorescence of these drugs in the micellar media of sodium dodecyl sulfate (SDS) using principal component analysis-feed-forward neural networks (PC-FFNNs). Experimental conditions such as effect of pH and SDS concentration were optimized. Under the optimum conditions, the linear determination ranges of LD and PRO are 2.0 × 10⁻⁸ to 1.0 × 10⁻⁵ mol L⁻¹ and 3.6 × 10⁻⁹ to 1.8 × 10⁻⁶ mol L⁻¹, respectively. A set of synthetic binary mixtures of LD and PRO was prepared and their concentrations were predicted by the proposed method. Satisfactory results were obtained by the combination of fluorescence technique with chemometrics methods. The method was successfully applied to the determination of LD and PRO in tap water and in urine samples.     

Catalytic effect of lucunary heteropolyanion containing molybdenum and tungsten atoms on decolorization of direct blue 71

In this research,a lucunary Keggin structure,[PMo₂W₉O₃₉]^7- was selected as an efficient homogenous catalyst for degradation of an azo dye（direct blue 71） and a simple method was developed for degradation of DB71.The method is based on the oxidation of azo dye in the presence of a lucunary Keggin form of polyoxometalates,K₇[PMo₂W₉O₃₉]? 19H₂O,as a homogenous catalyst at room temperature.The reaction is monitored spectrophotometrically by measuring the absorbance of dye atλ=585 nm.Some parameters including concentration of catalyst,concentration of H₂O₂,pH and reaction time were investigated and optimized. Results show that K₇[PMo₂W₉O₃₉]? 19H₂O is more efficient in the presence of hydrogen peroxide.Degradation of dye in the presence of the catalyst and H₂O₂ could lead to the disappearance approximately 65%of dye after 60 min.But degradation for the same experiment performed in the absence of catalyst or in the absence of H₂O₂ was 22%or 5%respectively.Approximately 87% azo dyes has been eliminated after 90 min in the presence of catalyst,H₂O₂ and optimize conditions(0.6 g/L of K₇[PMo_2- W₉O₃₉H₉H₂O,0.08 mol/L hydrogen peroxide and room temperature).