Sharif Digital Repository

A five-coordinated Fe(III) complex with the distorted trigonal bipyramidal configuration was synthesized by reactions of FeCl36H2O and 2-(2′-hydroxyphenyl)oxazoline (Hphox) as a bidentate ON donor oxazoline ligand. Complex [Fe(phox)2Cl] was fully characterized, including by single-crystal X-ray structure analysis. DFT calculations were accompanied with experimental results in order to obtain a deeper insight into the electronic structure and vibrational normal modes of complex. Oxidation of sulfides to sulfoxides in one-step was conducted by this complex as catalyst using urea hydrogen peroxide (UHP) in mixture of CH2Cl 2/CH3OH (1:1) under air at room temperature. The results show that using... 

A high silica CHA-type membrane was synthesized by the in-situ crystallization method on a disk like α-alumina porous support to separate both acid (H2S, CO2) gases from methane. The membrane showed a permeance of 3.39×10-8mol/m2sPa for pure CO2with CO2/CH4 ideal selectivity of 21.6 at 303K and 100kPa pressure difference across the membrane. The membrane was also tested with N2 and O2 pure gases indicating a small O2/N2 selectivity of 1.2-1.4, which shows that this type of membrane is not suitable for O2/N2 separation. The membrane performance was also analyzed by binary (CO2-CH4) and ternary (H2S-CO2-CH4) gas mixtures, with compositions near the real sour natural gas (CO2: 2.13mol%, H2S:... 

The reaction of a solution of MoO2(acac)2 in CH3OH and salicylidene 2-picoloyl hydrazone as a tridentate ONO donor Schiff base (ONO) afford a six-coordinated Mo(VI) complex [MoO2(ONO)(CH3OH)], with a distorted octahedral configuration. [MoO2(ONO)(CH3OH)] was isolated as an air-stable crystalline solid and fully characterized by single-crystal X-ray structure analysis. [MoO2(ONO)(CH3OH)] shows reactivity in the oxidation of sulfides to their corresponding sulfoxides using urea hydrogen peroxide as the oxidant at room temperature under air  

PbS nanoparticles were in situ deposited on graphene sheets by a successive ionic liquid adsorption and reaction method to prepare a graphene/PbS composite counter electrode for CdS/CdSe quantum dot sensitized solar cells (QDSCs). Under 1 sun illumination, the cells with graphene/PbS counter electrodes (CEs) show a maximum energy conversion efficiency of 2.63%, which is remarkably higher than that of those employing PbS (1.28%) or graphene (0.23%) CEs. Electrochemical impedance spectroscopy analysis shows that graphene/PbS composite counter electrodes have lower charge-transfer resistance at the interface of the CE and the polysulfide redox electrolyte, compared to those cells with PbS and... 

CdS nanocrystals were thermochemically (thermally activated) synthesized thorough the reaction between CdSO4 and Na2S 2O3 in an aqueous solution. Thioglycolic Acid (TGA) was used as the capping agent and catalyst of the reaction. The method was based on heat activated dissociation of Na2S2O3 and controllable release of S and free electrons in the solution. CdS NCs were formed by heating the sample solution at 96 C for 1 h. The results of optical spectroscopy and transmission electron microscopy demonstrated round shape NCs with sizes about 3.0 nm. The nanocrystals were also luminescent and represented a broad emission with a peak located at 515 nm and FWHM of 160 nm. Several samples were... 

Vertically aligned ZnO@CdS nanorod heterostructure films with various loadings of CdS nanoparticle shell were synthesized and applied in photoinactivation of Escherichia coli bacteria under visible light irradiation. While neither the bare ZnO nanorods (with band-gap energy (Eg) of ∼3.28 eV) under visible light irradiation nor the nanorod heterostructures in dark exhibited any significant antibacterial activity, the ZnO@CdS nanorod heterostructures (with Eg ∼2.5-2.6 eV) could successfully inactivate the bacteria under visible light irradiation. Furthermore, it was found that an optimum loading of the CdS shell (corresponding to the effective thickness less than ∼15 nm) is required to achieve... 

The leaching kinetics of stibnite in basic solution has been investigated. Spherical pellets of antimony sulphide were dissolved in 1 molar sodium hydroxide solutions at different temperatures. It was found that the shrinking core with ash layer model could satisfactorily explain the dissolution process. Using this model, it was found that initially the rate controlling step was a chemical reaction with activation energy of 10.2 kJ/mol. As the ash layer built up, diffusion through the ash layer became the rate controlling step. The activation energy for this step was found to be 33.4 kJ/mol. It was also observed that smaller particle size, larger solid to liquid ratio, and higher NaOH... 

CuMS2 (M=A1, In, Fe) ternary compounds were synthesized via the facile polyol method in autoclave. Depending on the functional groups of solvent and surfactant, the structure of the nanocrystals can be controlled in the form of wurtzite or chalcopyrite. The chalcopyrite structure was obtained when the precursors solved in the mixture of diethylene glycol, polyethylene glycol 600 and ammonium hydroxide. When the solvent was replaced by ethylene diamine, the wurtzite was obtained along with chalcopyrite (polytypism). The products were characterized by X-Ray Diffraction (XRD) for analysis of structural properties, Transmission Electron Microscopy (TEM) for studying morphological... 

CdS/TiO2/graphene (CTG) nanocomposite thin films were synthesized by a facile production route. The TiO2/graphene (TG) nanocomposite was initially fabricated by sol-gel method in such a way that TiO2 nanoparticles loaded on graphene oxide (GO) sheet via photocatalytic process. Then, CdS nanoparticles were deposited on the TG thin film by successive ion layer adsorption and reaction process (SILAR) approach. Based on atomic force microscopy (AFM), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses, the TG thin film possessed a larger surface area as compared with the pure TiO2 thin film due to presence of graphene sheet. UV/visible spectroscopy exhibited... 

In this paper, we report that a known dinuclear Fe complex, [tpa(H2O)FeOFe(H2O)tpa](ClO4)4 (tpa: tris(2-pyridylmethyl)amine), is an efficient catalyst toward organic sulfide oxidation in the presence of urea-hydrogen peroxide  

We report a new design of solar cells based on semiconductor quantum dots (QDs), monolithic quantum dot sensitized solar cells (MQDSCs). MQDSCs offer the prospect of having lower cost and a simpler manufacturing process in comparison to conventional double substrate QDSCs. Our proposed monolithic QDSCs have a triple-layer structure, composed of a CdS sensitized mesoporous TiO2 photoanode, a scattering layer made by a core-shell structure of TiO 2/SiO2, and a carbon active/graphite counter electrode layer, which are all deposited on a single fluorine doped tin oxide (FTO) glass substrate. Mesoporous TiO2 was sensitized with CdS QDs by successive ionic layer adsorption and reaction. Here,... 

In the present work a new strategy for straightforward fabrication of CdS/CdTe solar cells, containing CdS nanowires and nanoparticles as a window layer and CdTe nanoparticles and microparticles as an absorber layer, are reported. CdS and CdTe nanostructures were synthesized by solvothermal method. X-ray diffraction analysis revealed that highly pure and crystallized CdS nanowires and nanoparticles with hexagonal structure and CdTe nanoparticles with cubic structure were obtained. Atomic force microscope and field emission scanning electron microscope images showed that CdS nanowires with length of several μm and average diameter of 35 nm, CdS nanoparticles with average particle size of 32... 

Novel ZnO-carbon and ZnO nanofibers were fabricated by electrospinning of polymer precursor followed by subsequent annealing in nitrogen and air, respectively. Field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD) indicated the smooth and beadless nanofibers with wurtzite crystal structure. X-ray photoelectron spectroscopy (XPS) showed the presence of oxygen vacancies (VO) and chemisorbed O2 on the surface of the samples. Band gap narrowing of the ZnO-carbon nanofibers in comparison to ZnO were measured by diffuse reflectance spectroscopy (DRS). Photo-degradation of azo dye under the UV and visible light was evaluated and ZnO-carbon showed an enhancement in... 

New experimental results are presented for the solubility of carbon dioxide, hydrogen sulfide in the ionic liquid 1-octyl-3-methylimidazolium hexafluorophosphate ([C8mim][PF6]) at temperatures range from (303.15 to 353.15) K and pressures up to about 2 MPa. The solubility of the mixture of CO2/H2S in [C8mim][PF6] under various feed compositions were also measured at temperatures of (303.15, 323.15 and 343.15) K and the pressure up to 1 MPa. The solubility of carbon dioxide and hydrogen sulfide increased with increasing pressure and decreased with increasing temperature and the solubility of H2S is about three times that of CO2 in the particular ionic liquid studied. The measured data were... 

Two room temperature liquid salts containing molybdenum(VI), [BMIM] 2[MoO2(NCS)4] (1) and [DMIM] 2[MoO2(NCS)4] (2), were immobilized on ionic liquid-modified silica leading to materials which showed notable catalytic activity for the reduction of sulfoxides into sulfides with triphenylphosphine (PPh3). The molybdenum liquid salts immobilized on the supported ionic liquid phase could be reused at least for three catalytic cycles without significant loss of activity  

The reactions of FeCl3·3H2O and 2-(2′-hydroxyphenyl)-5,6-dihydro-1,3-oxazine (N-O) as a bidentate O, N donor ligand afforded a five-coordinated iron(III) complex, [Fe(N-O) 2Cl], with a distorted trigonal bipyramidal configuration. The complex [Fe(N-O)2Cl] was isolated as an air-stable crystalline solid and was fully characterized, including by single-crystal X-ray structure analysis. The complex [Fe(N-O)2Cl] shows very efficient reactivity in the oxidation of sulfides to their corresponding sulfoxides using urea hydrogen peroxide (UHP) as the oxidant at room temperature under air. To get an insight into the electronic structure of the complex, the experimental studies have been accompanied... 

An oxido-peroxido tungsten(VI) complex [WO(O2)L(CH 30H)] using salicylidene benzoyl hydrazine as a tridentate ONO donor Schiff base (H2L) has been synthesized and characterized by elemental analysis, IR, 1H NMR, molar conductance data, and single-crystal X-ray analysis. The complex was used as a catalyst for epoxidation of olefins and oxidation of sulfides. The results show that epoxides and sulfoxides were produced in high yield, turnover number, and selectivity  

We have studied systematically photocatalytic properties of the vertically aligned ZnO@CdS core-shell nanorods where the features were grown through a multistep procedure including sol-gel for the formation of ZnO seed layer, hydrothermal process to grow ZnO nanorods, and successive ion layer adsorption and reaction (SILAR) process to deposit CdS nanoshells onto the ZnO nanorods. Formation of the ZnO seed layer and vertically aligned ZnO nanorods (d ∼ 40 nm) with a hexagonal cross-section was confirmed by AFM and SEM imaging. Successful capping of ZnO nanorods with homogeneous CdS nanocrystallites (∼5 nm) was ascertained by HRTEM diffraction and imaging. Optical properties of the samples... 

This paper presents a new method for spectrophotometirc detection of sulfide applying fungal peroxidase immobilized on sodium alginate. The sensing scheme was based on decrease of the absorbance of the orange compound, purpurogallin produced from pyrogallol and H2O2 as substrates, due to the inhibition of peroxidase by sulfide. Absorbance of purpurogallin was detected at 420nm by using a spectrophotometer. The proposed method could successfully detect the sulfide in the concentration range of 0.6-7.0μM with a detection limit of 0.4μM. The kinetic parameters of Michaelis-Menten with and without sulfide were also calculated. Possible inhibition mechanism of peroxidase by sulfide was deduced... 

A new manganese(III) complex [(N-O)2Mn(OAc)] was synthesized using 2-(2'-hydroxyphenyl)-5,6-dihydro-1,3-oxazine (N-O) as a bidentate O, N donor. The complex has been characterized by elemental analysis, IR, UV-vis spectroscopy, and X-ray structure analysis. Oxidation of sulfides and epoxidation of olefins, respectively, to their corresponding sulfoxides and epoxides were conducted by this catalyst using urea hydrogen peroxide as oxidant at room temperature under air. The catalyst is efficient in oxidation reactions giving high yields and selectivities