Sharif Digital Repository

Incorporation of calcium(ii), zinc(ii) and aluminium(iii) to manganese oxides greatly improved the activity of manganese oxide towards the epoxidation of olefins in the presence of anhydrous tert-butyl hydroperoxide as an oxidant  

Three newly synthesized room temperature ionic liquids containing molybdate anion, [DMIm][MoO 2(NCS) 4], [RPy][MoO 2(NCS) 4] (R = butyl or decyl), and previously reported [BMIm][MoO 2(NCS) 4] were used as catalysts for the reduction of sulfoxides. For facilitating the recyclability of the catalysts, the ionic liquids [RMIm][PF 6] and [RPy][PF 6] (RMIm = 1-n-alkyl-3-methylimidazolium, RPy = 1-n-alkylpyridinium) were applied as ionic solvents and toluene is used as solvent for the organic phase. Molybdenum salts immobilized in RTILs constituted a reusable and efficient heterogeneous catalyst system. A maximum conversion (>99%) was achieved for reduction of diphenyl sulfoxide to diphenyl... 

Some cis-dioxomolybdenum (VI) complexes with tridentate Schiff base ligands derived from salicylaldehyde and aminophenols, aminoalcohol or o-aminobenzenethiol were examined as catalysts for epoxidation of different aliphatic and aromatic olefins, with tert-butyl hydroperoxide as oxidant. All complexes exhibited high activity and selectivity for epoxidation of aliphatic substrates during a short time period (95% conversion of cyclooctene after 30 min). The epoxide yield increased with the nucleophilic character of olefin. The catalysts activation strongly depends on the reaction temperature and nature of the solvent. Epoxidation of olefins by these catalysts is inhibited by ligands or... 

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  

In this paper, CdS nanoparticles as a visible light active photocatalyst were coupled by NiFe2O4 and reduced graphene oxide (rGO) to form CdS–NiFe2O4/rGO nanocomposite by facile hydrothermal methods. The CdS–NiFe2O4/rGO nanocomposite shows enhanced photocatalytic activity for the degradation of methylene blue (MB) under visible light illumination. In addition to improved photocatalytic performance, this prepared nanocomposite shows increased photostability and is magnetically separable from the aqueous media. The degradation rate constant (kapp) of the optimized photocatalyst, i.e. CdS–NiFe2O4 (0.05)/rGO 25 wt% nanocomposite, was higher than the corresponding CdS and NiFe2O4 nanoparticles by... 

A heterogeneous nanocatalyst containing polyoxomolybdate immobilized on the internal surface of amino-functionalized SBA-15 pores was prepared and fully characterized by several analytical techniques. The textural property of supported material was found to retain important mesoporous features, compatible with its potential use as heterogeneous catalysts. The catalyst SBA-15-NH3+•{Mo36}–shows excellent catalytic activity for the epoxidation of alkenes as compared to POM, which is attributed to the large specific surface area and highly ordered pore structure of SBA-15, allowing for easy access of reactants to the active sites and removal of products. The prepared catalyst has high... 

A manganese(III) complex, [Mn(phox)2(CH3OH) 2]ClO4 (phox = 2-(2′-hydroxyphenyl)oxazoline), was immobilized on silica-coated magnetic Fe3O4 nanoparticles through the amino propyl linkage using a grafting process in dichloromethane. The resulting Fe3O4@SiO2-NH2@Mn(III) nanoparticles are used as efficient and recyclable catalysts for selective oxidation of thiols to disulfides using urea-hydrogen peroxide as the oxidant. The nanocatalyst was recycled several times. Leaching and recycling experiments revealed that the nanocatalyst can be recovered, recycled, and reused more than five times, without the loss of catalytic activity and magnetic properties. The recycling of the nanocatalyst in six... 

We propose a lightweight scheme where the formation of a data block is changed in such a way that it can tolerate soft errors significantly better than the baseline. The key insight behind our work is that CNN weights are normalized between -1 and 1 after each convolutional layer, and this leaves one bit unused in half-precision floating-point representation. By taking advantage of the unused bit, we create a backup for the most significant bit to protect it against the soft errors. Also, considering the fact that in MLC STT-RAMs the cost of memory operations (read and write), and reliability of a cell are content-dependent (some patterns take larger current and longer time, while they are... 

The use of 1,3-bis(N-heterocyclic)carbene ligands with different alkyl wingtip groups (alkyl = methyl, isopropyl and tert-butyl) is an effective method for the palladium-catalysed direct S-arylation of methylphenyl sulfoxide and C-C coupling of various of aryl halides with alkenes. The reactions proceed in moderate to good yields. Interestingly, it is shown experimentally that, by using bulkier bidentate N-heterocyclic carbene ligands, more selective catalytic systems towards cis products in Heck coupling reactions can be achieved  

An efficient and reliable Multi-Level Cell (MLC) Spin-Transfer Torque Random Access Memory (STT-RAM) is proposed based on a Drop-And-Rearrange Approach, called DARA. Since CNN models are rather robust, less important bits are dropped, allowing important bits to be written in safe and reliable Single-Level Cell mode. Also, bits are rearranged to make the representation better aligned with memory cell characteristics. Bits with higher impact on the features value are stored in safer bit positions reducing the chance of read/write circuits to malfunction. Experimental results show that our approach provides comparable to error-free scenario reliability level, while doubling the bandwidth and... 

The use of 1,3-bis(N-heterocyclic)carbene ligands with different alkyl wingtip groups (alkyl = methyl, isopropyl and tert-butyl) is an effective method for the palladium-catalysed direct S-arylation of methylphenyl sulfoxide and C–C coupling of various of aryl halides with alkenes. The reactions proceed in moderate to good yields. Interestingly, it is shown experimentally that, by using bulkier bidentate N-heterocyclic carbene ligands, more selective catalytic systems towards cis products in Heck coupling reactions can be achieved. Copyright © 2016 John Wiley & Sons, Ltd  

A novel organic-inorganic hybrid heterogeneous catalyst system was obtained from the reaction of the molybdenum(VI) complex of salicylidene 2-picoloyl hydrazone with mesoporous silica containing 3-chloropropyl groups prepared by a direct synthetic approach involving hydrolysis and co-condensation of tetraethylorthosilicate (TEOS) and 3-chloropropyltrimethoxysilane in the presence of the triblock copolymer P123 as template under acidic conditions. Characterization of the functionalized materials by X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), N2 adsorption/desorption, FT-IR and UV-Vis spectroscopy, and thermogravimetric... 

A heterogeneous nanocatalyst was prepared via covalent anchoring of dioxomolybdenum(VI) Schiff base complex on core-shell structured Fe3O4@SiO2. The properties and the nature of the surface-fixed complex have been identified by a series of characterization techniques such as SEM, EDX, XRD, TGA, FT-IR, and VSM. The synthesized hybrid material was an efficient nanocatalyst for selective oxidation of olefins to corresponding epoxides with t-BuOOH in high yields and selectivity. The catalyst could be conveniently recovered by applying an external magnetic field and reused several times without significant loss of efficiency. © 2016 Taylor and Francis  

In this research, cobalt ferrite (CoFe2O4) magnetic nanoparticles as well as MIL-53(Fe) structure were synthesized by the hydrothermal and solvothermal methods, respectively. Moreover, magnetic composites of MIL-53(Fe)/CoFe2O4 nanoparticles with different cobalt ferrite loadings (i.e.; 0.05, 0.1 and 0.2 g) were prepared via the solvothermal method. The main novelty of the present research was to synthesize a magnetic composite of MIL-53(Fe)/CoFe2O4 nanoparticles in order to perform rapid photodegradation of Direct Red 23 (DR23) dye under the LED visible light irradiation. Good magnetic properties of the fabricated composite led to easy separation and rapid retrieval of the catalyst from the... 

The reaction between [MoO2(acac)2] and an ONO type Schiff-base ligand (L = 4-bromo-2-((2-hydroxy-5-methylphenylimino)methyl)phenol) resulted a new oligomer molybdenum complex ([MoO2(L)]n). The oligomer complex was characterized by elemental analysis, FT-IR, 1H and 13C NMR spectroscopies. A suitable single crystal of the complex was grown in DMSO and characterized by X-ray single crystal diffraction as monomer stabilized by one DMSO molecule, [MoO2L(DMSO)]. The [MoO2(L)]n complex was used as a catalyst in epoxidation of olefins. Besides the high activity and selectivity, very high turnover numbers were a remarkable advantage of the catalytic system. © 2017  

Metal–organic frameworks (MOFs) are best known for their great structural diversity. The uniformity in the properties of MOFs is mainly governed by the size and morphology of the particles. In the present research, iron-MIL-88A was prepared by a modulator-assisted solvothermal method, and the role of modulating agents in the formation process of MOF particles was investigated. Acetic acid and formic acid were chosen as monoligand modulating agents. The changes in morphology and size distribution of the products were scrutinized by using SEM micrographs. Both modulators clearly interfered with the crystallization process through their attachment to the reactive sites. At low modulator... 

The potentiometric response characteristics with respect to salicylate anion of several membrane electrodes based on iron(II) tetraphenylporphyrin chloride (FeTPPCl) and derivatives with electrophilic and nucleophilic substituents, incorporated into plasticized polyvinylchloride (PVC) membranes were investigated. Complexes tetraphenyl porphyrin iron(III) chloride (FeTPPCl; A), tetrakis (4-methoxyphenyl) porphyrin iron(III) chloride (Fe(TOCH 3PP)Cl; B), tetrakis (2,6-dichlorophenyl) porphyrin iron(III) chloride (Fe(TDClPP)Cl; C), tetrakis (4-nitrophenyl) porphyrin iron(III) chloride (Fe(TNO2PP)Cl; D), and tetrakis (pentafluorophenyl) porphyrin iron(III) chloride (Fe(TPFPP)Cl; E) were used as... 

Two new potentially heptadentate N4O3 Schiff base ligands {N[(CH2)3NCH(2-OH-3,5-t-Bu2C 6H2)]3} (H3L1) and {N[(CH2)3NCH(2-OH-3,5-t-Bu2C6H 2)]2 [(CH2)2-NCH(2-OH-3,5-t-Bu 2C6H2)]} (H3L2) were synthesized and characterized by various spectroscopic methods. The heptadentate N4O3 Schiff bases, H3L1 and H 3L2, were derived from the condensation reaction of two tripodal tetraamine ligands, tris(3-aminopropyl)amine and (2-aminoethyl)-bis(3- aminopropyl)amine with 3 equiv. of 3,5-di-tert-butylsalicylaldehyde, respectively. The neutral gadolinium(III) and samarium(III) complexes, [Ln(L)], of these bulky ligands and also a gadolinium(III) complex of a previously known ligand,... 

Astaxanthin (AXT) is one of the most important fat-soluble carotenoids that have abundant and diverse therapeutic applications namely in liver disease, cardiovascular disease, cancer treatment, protection of the nervous system, protection of the skin and eyes against UV radiation, and boosting the immune system. However, due to its intrinsic reactivity, it is chemically unstable, and therefore, the design and production processes for this compound need to be precisely formulated. Nanoencapsulation is widely applied to protect AXT against degradation during digestion and storage, thus improving its physicochemical properties and therapeutic effects. Nanocarriers are delivery systems with many... 

Astaxanthin (AXT) is one of the most important fat-soluble carotenoids that have abundant and diverse therapeutic applications namely in liver disease, cardiovascular disease, cancer treatment, protection of the nervous system, protection of the skin and eyes against UV radiation, and boosting the immune system. However, due to its intrinsic reactivity, it is chemically unstable, and therefore, the design and production processes for this compound need to be precisely formulated. Nanoencapsulation is widely applied to protect AXT against degradation during digestion and storage, thus improving its physicochemical properties and therapeutic effects. Nanocarriers are delivery systems with many...