- Fabrication of La (III) supported on CoFe2O4 MNPs: a novel and efficient heterogeneous catalyst for selective oxidation of sulfides and synthesis of symmetrical disulfides
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Abstract: This paper reports the fabrication of La supported on CoFe2O4 nanoparticles through tryptophan (Trp) post-functionalization modification of CoFe2O4 which can be used as an efficient recyclable nanocata
- Molaei, Somayeh,Ghadermazi, Mohammad,Moeini, Nazanin
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p. 771 - 793
(2021/12/02)
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- Synthesis and characterization of magnetic Fe3O4@Creatinine@Zr nanoparticles as novel catalyst for the synthesis of 5-substituted 1H-tetrazoles in water and the selective oxidation of sulfides with classical and ultrasonic methods
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Tetrazoles and sulfoxide compounds have a wide range of applications in industries and are of great expectation to be environmentally friendly and cost-effective. This paper reports the introduction of zirconium supported on Fe3O4 na
- Ghadermazi, Mohammad,Moeini, Nazanin,Molaei, Somayeh
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- Copper based on diaminonaphthalene-coated magnetic nanoparticles as robust catalysts for catalytic oxidation reactions and C-S cross-coupling reactions
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In this work, the immobilization of copper(ii) on the surface of 1,8-diaminonaphthalene (DAN)-coated magnetic nanoparticles provides a highly active catalyst for the oxidation reaction of sulfides to sulfoxides and the oxidative coupling of thiols to disulfides using hydrogen peroxide (H2O2). This catalyst was also applied for the one-pot synthesis of symmetrical sulfidesviathe reaction of aryl halides with thiourea as the sulfur source in the presence of NaOH instead of former strongly basic and harsh reaction conditions. Under optimum conditions, the synthesis yields of sulfoxides, symmetrical sulfides, and disulfides were about 99%, 95%, and 96% respectively with highest selectivity. The heterogeneous copper-based catalyst has advantages such as the easy recyclability of the catalyst, the easy separation of the product and the less wastage of products during the separation of the catalyst. This heterogeneous nanocatalyst was characterized by FESEM, FT-IR, VSM, XRD, EDX, ICP and TGA. Furthermore, the recycled catalyst can be reused for several runs and is economically effective.
- Yarmohammadi, Nasrin,Ghadermazi, Mohammad,Mozafari, Roya
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p. 9366 - 9380
(2021/03/16)
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- A nickel nanoparticle engineered CoFe2O4/SiO2-NH2@carboxamide composite as a novel scaffold for the oxidation of sulfides and oxidative coupling of thiols
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The purpose of this work was to prepare a new Ni-carboxamide complex supported on CoFe2O4 nanoparticles (CoFe2O4/SiO2-NH2@carboxamide-Ni). The carboxamide host material unit generated cavities that stabilized the nickel nanoparticles effectively and preve
- Zohrevandi, Mina,Mozafari, Roya,Ghadermazi, Mohammad
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p. 14717 - 14729
(2021/05/19)
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- Ordered mesoporous SBA-15 functionalized with yttrium(III) and cerium(III) complexes: Towards active heterogeneous catalysts for oxidation of sulfides and preparation of 5-substituted 1H-tetrazoles
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Mesoporous SBA-15 was synthesized and modified with 3-chloropropyltrimethoxysilane and then used in immobilization of creatinine groups, which were employed to introduce Y3+ and Ce3+ to give rise to two novel yttrium and cerium catalysts: SBA-15@Creatinine@M (M?=?Y and Ce). The structures of the SBA-15@Creatinine@M catalysts were determined using various techniques. These catalysts offered outstanding catalytic performances in the oxidation of sulfides to sulfoxides and in the preparation of 5-substituted 1H-tetrazoles. An important characteristic of the SBA-15@Creatinine@M catalysts is that they are very stable without a considerable decrease in their catalytic performance lasting seven cycles.
- Molaei, Somayeh,Tamoradi, Taiebeh,Ghadermazi, Mohammad,Ghorbani-Choghamarani, Arash
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- Immobilization of cerium (IV) and erbium (III) in mesoporous MCM-41: Two novel and highly active heterogeneous catalysts for the synthesis of 5-substituted tetrazoles, and chemo- and homoselective oxidation of sulfides
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Two well-ordered 2D-hexagonal cerium (IV) and erbium (III) embedded functionalized mesoporous MCM-41(MCM-41@Serine/Ce and MCM-41@Serine/Er) have been developed via functionalization of mesoporous MCM-41. The surface modification method has been used in the preparation of serine-grafted MCM-41 and led to the development of MCM-41@Serine. The reaction of MCM-41@Serine with Ce (NH4)2(NO3)6·2H2O or ErCl3·6H2O in ethanol under reflux led to the organization of MCM-41@Serine/Ce and MCM-41@Serine/Er catalysts. The structures of these catalysts were determined using scanning electron microscopy, mapping, energy-dispersive X-ray spectroscopy, Fourier transform-infrared, thermogravimetric analysis, X-ray diffraction, inductively coupled plasma, and Brunauer–Emmett–Teller analysis. These MCM-41@Serine/Ce and MCM-41@Serine/Er catalysts show outstanding catalytic performance in sulfides oxidation and synthesis of 5-substituted tetrazoles. These catalysts can be recycled for seven repeated reaction runs without showing a considerable decrease in catalytic performance.
- Molaei, Somayeh,Ghadermazi, Mohammad
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- Synthesis and characterization of indium and thallium immobilized on isonicotinamide-functionalized mesoporous MCM-41: Two novel and highly active heterogeneous catalysts for selective oxidation of sulfides and thiols to their corresponding sulfoxides and disulfides
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Two highly ordered isonicotinamide (INA)-functionalized mesoporous MCM-41 materials supporting indium and thallium (MCM-41-INA-In and MCM-41-INA-Tl) have been developed using a covalent grafting method. A surface functionalization method has been applied to prepare Cl-modified mesoporous MCM-41 material. Condensation of this Cl-functionalized MCM-41 with INA leads to the formation of MCM-41-INA. The reaction of MCM-41-INA with In(NO3)3 or Tl(NO3)3 leads to the formation of MCM-41-INA-In and MCM-41-INA-Tl catalysts. The resulting materials were characterized using various techniques. These MCM-41-INA-In and MCM-41-INA-Tl catalysts show excellent catalytic performance in the selective oxidation of sulfides and thiols to their corresponding sulfoxides and disulfides. Finally, it is found that the anchored indium and thallium do not leach out from the surface of the mesoporous catalysts during reaction and the catalysts can be reused for seven repeat reaction runs without considerable loss of catalytic performance.
- Molaei, Somayeh,Ghadermazi, Mohammad
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- A synthesis of sulfoxides and disulfides under classical and ultrasonic conditions in presence of recoverable inorganic–organic hybrid magnetism nanocatalysts Fe3O4@Tryptophan-M (M: Cu, Co and Fe)
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Three inorganic–organic hybrid magnetic nanocatalysts have been reported as new catalysts for the synthesis of sulfoxides and disulfides. Also, the effect of ultrasound irradiation on the synthesis of sulfoxides and disulfides was checked. The time of rea
- Moeini, Nazanin,Ghadermazi, Mohammad,Ghorbani-Choghamarani, Arash
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p. 278 - 286
(2019/06/25)
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- Anchoring Ni (II) on Fe3O4@tryptophan: A recyclable, green and extremely efficient magnetic nanocatalyst for one-pot synthesis of 5-substituted 1H-tetrazoles and chemoselective oxidation of sulfides and thiols
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A green, novel and extremely efficient nanocatalyst was successfully synthesized by the immobilization of Ni as a transition metal on Fe3O4 nanoparticles coated with tryptophan. This nanostructured material was characterized using Fourier transform infrared spectroscopy, transmission electron microscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, thermogravimetric analysis, inductively coupled plasma optical emission spectroscopy, vibrating sample magnetometry and X-ray diffraction. The prepared nanocatalyst was applied for the oxidation of sulfides, oxidative coupling of thiols and synthesis of 5-substituted 1H-tetrazoles. The use of non-toxic, green and inexpensive materials, easy separation of magnetic nanoparticles from a reaction mixture using a magnetic field, efficient and one-pot synthesis, and high yields of products are the most important advantages of this nanocatalyst.
- Moeini, Nazanin,Tamoradi, Taiebeh,Ghadermazi, Mohammad,Ghorbani-Choghamarani, Arash
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- Influence of sulfur groups on carboxylic acid strengths
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The relative acid strength for a series of monocarboxylic acids of the general formula R–X–(CH2)n–COOH and related dicarboxylic acids of the general formula HOOC–(CH2)n–X–(CH2)n–COOH, where R = Ph or Me, X = CH2, –S– –SO– or –SO2–; and n = 1 or 2 as appropriate; have been studied as a function of X. It is found that sulfur containing acids have lower pKa values than the corresponding carbon analogues, that the pKa is highest for the thioacids and lowest for the sulfonyl acids, that the pKas increase as n increases, and that for the dicarboxylic acid systems only the thio members show a significant reduction in pKa (2) – pKa (1) differences upon changing n from 1 to 2.
- Boschmann, Erwin,Miller, Roger D.
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p. 2617 - 2619
(2018/04/30)
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- Spectroscopic investigation on kinetics, thermodynamics and mechanism for electron transfer reaction of iron(III) complex with sulphur centered radical in stimulated biological system
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Electron transfer reactions of biological organic sulphides with several metal ions to generate sulphide radical cations are a great concern in biochemical process. To understand the mechanism, a stimulated biological system having model compounds, iron(III)-bipyridyl complex with thio-diglycolic acid (TDGA) was investigated. Spectroscopic study reveals the kinetics and thermodynamics of the reaction in aqueous perchloric acid medium. The reaction follows first and fractional order of 0.412 with respect to [Fe(bpy) 3]3+ and TDGA, respectively. The oxidation is insensitive to variation in [H+] but slightly decreases with increase in ionic strength ([I]). Addition of acrylamide, a radical scavenger has no effect on the rate of the reaction. The high negative value of ΔS# (-74.3 ± 1.09 J K-1 mol-1) indicates the complex formed has a definite orientation higher than the reactants. Based on the above results, a suitable reaction mechanism for this reactionis proposed.
- Deepalakshmi,Sivalingam,Kannadasan,Subramaniam,Sivakumar,Brahadeesh
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p. 315 - 321
(2014/03/21)
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- Sulfur-containing carboxylic acids: 6.* The syntheses of 3,3′-sulfinyldipropionic and 2,2′-sulfinyldiacetic acids
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Pure sulfoxides of thiodialiphatic acids were obtained in high yields by oxidation of the corresponding sulfides in organic solvents. 3,3′-Sulfinyldipropionic acid was obtained by the reaction of hydrogen peroxide with thiodipropionic acid in acetone. 2,2′-Sulfinyldiacetic acid was synthesized by the reaction of thiodiglycolic acid with H2O 2 in acetone containing acetic acid (26 mol %). Pure 2,2′-sulfinyldiacetic acid was found to be stable in storage rather than labile as reported previously.
- Vasil'eva
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p. 958 - 960
(2007/10/03)
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- Cathodic oxidation of sulfoxides to sulfones using a tungstate/pertungstate redox mediator
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A new cathodic oxidation system for the oxidation of sulfoxides was developed. The system involves the cathodic reduction of dioxygen to hydrogen peroxide which oxidizes tungstate to pertungstate in the solution, and sulfoxides arc oxidized to the corresponding sulfones with the resulting tungstate/ pertungstate redox mediator in high cfficncy and selectivity.
- Li, Wei,Nonaka, Tsutomu
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p. 387 - 388
(2007/10/03)
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