Sharif Digital Repository

Horseradish peroxidase (HRP) was successfully immobilized on amine functionalized TiO2-coated multiwalled carbon nanotubes (NH2 – TiO2 – CNTs) by a convenient and efficient method. Electrochemical impedance spectroscopy, cyclic voltammetry and amperometry were applied to characterize the HRP/NH2 – TiO2 – CNT nano-composite. These techniques showed that the NH2 – TiO2 – CNTs greatly enhance the electron transfer between HRP and the modified electrode. Owing to the redox reaction of the electroactive centre of HRP, the HRP = NH2 – TiO2 – CNTs modified electrode exhibited a pair of quasi-reversible peaks with a peak-to-peak separation (ΔEp) of 70.6 mV and a formal potential (E 0′) of 367.65 mV... 

Alcohols have been successfully converted into their corresponding carbonyl compounds using hydrogen peroxide catalyzed by lithium chloride on montmorillonite K10. Clay supported lithium chloride can be recovered after using as catalyst for oxidation of alcohols. The future runs according to this procedure showed no considerable decrease in the reaction yield and catalyst effect  

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  

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 oxidation of sulfides to sulfoxides with hydrogen peroxide in good yield and high selectivity has been catalyzed very effectively by a series of Schiff base salen-type iron complexes in a monophasic medium (CH 2Cl2/CH3OH) at ambient temperature. The results of the present study show that the reaction rate strongly depends on both catalyst steric effects and steric and electronic properties of sulfides. In the system, the electronic spectral studies are applied to explain the formation of a reactive (salen) Fe=O intermediate  

A mononuclear mixed ligand complex of iron, [FeIII(N-OPh-sal)(acac)EtOH], where Hacac and N-HOPh-Hsal denote acetylacetone and N-hydroxyphenyl-salicylideneamine, respectively, has been synthesized and characterized by elemental analysis, spectral studies and X-ray crystallography. The catalytic system containing this complex and urea hydrogen peroxide as oxidizing agent was used to selectively oxidize a range of sulfides to the corresponding sulfoxides in good yields under mild conditions. The electronic spectra of the catalytic system were applied to explore reactivity and stability of the catalyst during sulfide oxidation reactions and to examine the nature of active species, as well. ©... 

A novel binuclear iron(III)-salicylaldazine complex has been synthesized and characterized by various techniques such as IR and UV–Vis spectroscopy and X-ray crystallography. The catalytic oxidation of sulfides in the presence of the aforementioned complex was explored at room temperature using urea hydrogen peroxide (UHP) as an oxidant. Effects of different reaction conditions consisting catalyst and oxidant amount, solvent effect and reaction time on the catalytic activity and selectivity in the reaction of methylphenylsulfide oxidation has been surveyed. Perfect selectivity toward sulfoxide was achieved after 15 min in CH3CN by choice of a properly optimized reaction condition. © 2020... 

Oximes were oxidized to the corresponding carbonyl compounds in good to high yields by environmentally friendly and green oxidant, H2O2 catalyzed by montmorillonite K-10 supported cobalt(II) chloride. © 2007 Ali Ezabadi  

Gelatin is a denatured protein derived from collagen by thermohydrolysis and has a rheological property of thermo reversible transformation between sol & gel. Gelatin is one of the most important biopolymers, with widespread applications in the food, pharmaceutical, cosmetic and photographic industries. Gelatin is commercially made from skins and skeletons of bovine and porcine and mammalian gelatin has been intensively studied. However, mammalian gelatin is at risk for contamination with bovine spongiform encephalopathy and increase in demand for kosher and halal foods have created a demand for fish gelatin for food applications. Therefore, the objective of this study was to extract gelatin... 

Hydrogen peroxide readily oxidizes phenols to the corresponding quinones in the presence of cobalt(II) acetate or manganese(II) acetate as catalyst  

Hydrogen peroxide readily oxidizes Hantzsch type 1,4-dihydropyridines in the presence of cobalt(II) acetate as catalyst at room temperature. No evidence of a dealkylation process for 4-alkyl 1,4-dihydropyridines has been observed  

Novel molybdenum complex, cis-[MoO2(phox)2] has been synthesized and characterized by IR, 1H NMR, elemental analyses (CHN), and X-ray molecular structure determination methods. This complex was found to be an efficient, selective catalyst for the oxidation of various sulfides to sulfoxides with urea hydrogen peroxide (UHP) in excellent yields (100% for diallylsulfide) and short reaction times (20 min) at room temperature. The catalytic system oxidizes diallylsulfide chemoselectively to its corresponding sulfoxide without any over oxidation in double bond. © 2007 Elsevier B.V. All rights reserved  

Photo-oxidation of dyes is a new concern among researchers since it offers an attractive method for decoloration of dyes and breaks them into simple mineral forms. An advanced oxidation process, UV/H2O2, was investigated in a laboratory scale photoreactor for decolorization of the Reactive blue 19 (RB19 dye from synthetic textile wastewater. The effects of operating parameters such as hydrogen peroxide dosage, pH, initial dye concentration and UV dosage, on decolorization have been evaluated. The RB19 solution was completely decolorized under optimal hydrogen peroxide dosage of 2.5 mmol L-1 and low-pressure mercury UV-C lamps (55 w) in less than 30 min. The decolorization rate followed...