Sharif Digital Repository

Condensation of pyrrole with various aldehydes in the presence of BF3•etherate as an acid catalyst in water provides good yield of some dipyrromethanes. Prolongation of the reaction time with aldehydes substituted by electron-donating (mesityl) or electron-withdrawing (2,6-dichlorophenyl) groups on the ortho positions of the phenyl did not lead to decomposition or scrambling. Manganese trans disubstituted porphyrin complexes which derive from various dipyrromethanes and manganese tetraaryl porphyrin complexes including various substituents with different steric and electronic properties show good catalytic activity in epoxidation of alkenes by NaIO4 in the presence of imidazole (ImH). The... 

The objective of this work was to study the influence of titanium variations on the API 5L-X70 steel weld metal properties. The relationship between microstructure and toughness of the weld deposit was studied by means of full metallographic, longitudinal tensile and Charpy-V notch tests on the specimens cut transversely to the weld beads. The best combination of microstructure and impact properties was obtained in the range of 0.02-0.05% titanium. By further increasing of titanium content, the microstructure was changed from a mixture of acicular ferrite, grain-boundary ferrite, Widmanstätten ferrite to a mixture of acicular ferrite, grain-boundary ferrite, bainite and ferrite with M/A... 

Montmorillonite K10-supported manganese(II) chloride was found to be an efficient and convenient catalyst for the oxidative cleavage of oximes, phenylhydrazones and semicarbazones to the corresponding carbonyl compounds with molecular oxygen. © 2006 Bentham Science Publishers Ltd  

A mixture of cobalt(II) and manganese(II) salts of 4-aminobenzoic acid supported on silica gel catalyses the oxidation of thiols to disulfides in the presence of oxygen or air  

A 1:1 molar ratio of the cobalt and manganese salts of p-amino benzoic acid supported on silica gel is an effective catalyst for the oxidation of various organic compounds in reasonable yields using molecular oxygen. The catalyst can be reused several times  

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  

Magnetic nanoparticles (MNPs), Fe3O4@SiO2, have been prepared and functionalized by 3-(chloropropyl)trimethoxysilane and then by imidazole to synthesize Fe3O4@SiO2-Im. The functionalized Fe3O4 nanoparticles were used as a support to anchor manganese porphyrin via axial ligation. The prepared catalyst was characterized by elemental analysis, FT-IR spectroscopy, X-ray powder diffraction, UV-vis spectroscopy, and scanning electron microscopy. Application of immobilized manganese porphyrin as a heterogeneous catalyst in oxidation of alkenes and sulfides was explored. To find suitable reaction conditions,... 

Oxidation of a variety of organic compounds, using Mn-porphyrin, mesotetrakis(4-hydroxyphenyl)porphyrinatomanganese(III), supported onto functionalized silica-coated magnetic nanoparticles via “Click” reaction has been investigated. The heterogeneous catalyst was characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), FT-IR spectroscopy, inductively coupled plasma optical emission spectroscopy (ICP/OES) and energy-dispersive X-ray spectroscopy (EDX). Thermogravimetric analysis (TGA) demonstrated that the prepared catalyst was thermally stable to almost 300 °C, exhibiting high thermostability of the nanocatalyst over a broad range of temperatures. This... 

Manganeses(II) chloride supported on montmorillonite K10 was found to be an efficient catalysts for the oxidation of alcohols to carbonyl compounds with hydrogen peroxide as oxidant  

A mixture of cobalt and manganese salts of p-aminobenzoic acid supported on silica gel catalyses the epoxidation of terminal olefins to the corresponding 1,2-epoxy compounds in the presence of oxygen  

We report a novel method of growing red luminescent (635 nm) Mn-doped CdS (CdS:Mn) nanoparticles capped by an inorganic shell of Mn(OH)2. CdSO4, Na2S2O3 and Mn(NO3)2 were used as the precursors, and thioglycerol (C3H8O2S) was employed as the capping agent and also the catalyst of the reaction. Using these materials resulted in very slow rate of the reaction and particles growth. The self-assembled one-pot process was performed at pH of 8 and Mn:Cd ratio of 10, and took about 10 days for completion. CdS:Mn nanoparticles are slowly formed in the first day of the process; however, the luminescence is weak. After 7 days, the solution turns white turbid through the formation of additional... 

Catalytic studies were performed to develop a simple oxidation system for olefins and sulfides using manganese(III)-tridentate Schiff base complex, Mn(N-OPh-sal)(acac)(EtOH) (N-HOPh-Hsal = N-hydroxyphenyl-salicyldienamine, Hacac = acetylacetone), and urea-hydrogen peroxide (UHP) as terminal oxidant. Conversions up to 90% for olefins at 0 °C and 96% for sulfides at room temperature as well as sulfoxide selectivity up to 73% were achieved in short reaction times. Also this study confirms the accelerating effect of strong π-donor axial ligands such as imidazole (ImH) on the oxidation reactions. © 2008 Elsevier B.V. All rights reserved  

The catalytic activity of two manganese(III)-oxazoline complexes [Mn(phox)2(CH3OH)2]ClO4 and Mn(phox)3 (Hphox = 2-(2′-hydroxylphenyl)oxazoline), was studied in the epoxidation of various olefins. All of epoxidation reactions were carried out in (1:1) mixture of methanol:dichloromethane at room temperature using urea hydrogen peroxide (UHP) as oxidant and imidazole as co-catalyst. The epoxide yields clearly demonstrate the influence of steric and electronic properties of olefins, the catalysts and nitrogenous bases as axial ligand. [Mn(phox)2(CH3OH)2]ClO4 catalyst with low steric properties has higher catalytic activity than Mn(phox)3. The highest epoxide yield (95%) was achieved for indene... 

The mononuclear complex [Mn(tptz)(CH3COO)(OH2)2]NO3 (1) was investigated by electrospray ionization mass spectrometry in aqueous solution at pH 4.5. Electrospray ionization mass spectrometry shows that mononuclear and dinuclear manganese cationic species are present in solution, probably in equilibrium with neutral 1. An experiment showed that the most important reaction in the presence of oxone (2KHSO5·KHSO4·K2SO4) is decoordination  

Activated layered manganese oxides with deposited nano-sized gold or silver were synthesized and characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction spectrometry, atomic absorption spectroscopy and energy-dispersive X-ray mapping. Here, we report that Au or Ag nanoparticles deposited on layered Mn oxides improve the catalytic activity of the Mn oxides toward the epoxidation of olefins in the presence of H2O2 and NaHCO3  

Nano-sized particles of manganese oxides have been prepared by a very simple and cheap process using a decomposing aqueous solution of manganese nitrate at 100 °C. Scanning electron microscopy, transmission electron microscopy and X-ray diffraction spectrometry have been used to characterize the phase and the morphology of the manganese oxide. The nano-sized manganese oxide shows efficient catalytic activity toward water oxidation and the epoxidation of olefins in the presence of cerium(iv) ammonium nitrate and hydrogen peroxide, respectively  

Oxygen evolution was observed upon mixing solid manganese(III) bidentate Schiff base complexes with aqueous solutions of cerium(IV) ammonium nitrate. However, oxygen evolution was not observed upon mixing solutions of the complexes (in acetonitrile) with Ce(IV). Electron-withdrawing substituents on the Schiff base ligands (NO2, Br) enhanced the reactivity of the manganese complexes toward oxygen evolution. Oxygen evolution was also affected by R groups on the ligands, in the order Me > Et Bz. © 2009 Springer Science+Business Media B.V  

Manganese Peroxidase (MnP), is one of the most promising lignin depolymerization enzymes, which has been widely used for degradation purposes. Nevertheless, MnP tends to lose activity rapidly during its maintenance phase and degradation process, especially in the inevitable presence of hydrogen peroxide. This study aimed to improve MnP efficiency produced by Phanerochaete chrysosporium, via enhancing its sustainability. In this context, the effects of MnO2, Fe3O4, PEG, Veratryl Alcohol (VA), and DMSO as stabilizing agents on MnP activity were explored both in vivo and in vitro. During in vivo experiments, heterogeneous Fe3O4 was found to be the desirable choice to enhance MnP production,...