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This study reports synthesis and characterization of polymeric [MoO2(Salen)] complexes that combine MoO2(acac)2 and polymeric ligands bearing N2O2 coordination sites, abbreviated herein as [piperazinCH2{MoO2(Salen)}]n (6), [piperazinCH2{MoO2(Salophen)}]n (7), and [piperazinCH2{MoO2(Salpn)}]n (8). The epoxidation of alkenes using tert-butyl hydroperoxide and oxidation of sulfides to sulfoxides by urea hydrogen peroxide were enhanced with excellent selectivity under the catalytic influence of these coordination polymers. No relevant difference in activity was found due to change in the diamine in the Schiffs base ligands. The stability of polymeric catalysts was assessed by recycling a sample... 

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  

The Mn-hydrazone Schiff base has been prepared, characterized, and encapsulated into NaY to prepare a new heterogeneous catalyst. Elemental analysis, UV-Vis, infrared spectroscopic analysis, diffuse reflectance spectroscopy, thermal analysis, small angle X-ray diffraction, and N2 sorption indicate the presence of Mn-hydrazone Schiff base within the nanocavity pores of zeolite-Y. The catalysts showed excellent catalytic efficiency in epoxidation with various olefinic compounds including cyclooctene, using tert-BuOOH as oxidant. Cyclooctene showed high conversion (97%) as well as epoxide selectivity (89%) with tert-BuOOH. Moreover, the encapsulated complex showed good recoverability without... 

The monoanionic bidentate Schiff base, N-(phenolyl)-benzaldimine (HL), has been employed to synthesize a new vanadium(IV) complex of general composition [VO(L)2] (where L = O, N donor of Schiff base). The ligand and complex have been fully characterized by elemental analyses, molar conductance data, FT-IR, 1H- and 13C-NMR, and UV-Vis spectroscopies. Oxidation of alcohols to their corresponding aldehydes and ketones was conducted by this complex catalyst using Oxone as oxidant under biphasic reaction conditions (CH2Cl2/H2O) and tetra-n-butylammonium bromide as phase transfer agent under air at room temperature  

An hydrazone Schiff base-iron(III) complex using salicylidene benzoyl hydrazine (L) as ligand has been synthesized and characterized by elemental analyses, IR, 1H and 13C NMR and UV-Vis spectroscopy. Oxidation of sulfides to sulfoxides in one-step was conducted by this complex catalyst using urea hydrogen peroxide (UHP) in mixture of CH2Cl2/CH3OH (1:1) under air at room temperature. The effect of the reaction conditions on the oxidation of methylphenylsulfide was studied by varying the amount of the catalyst, reaction temperature, reaction time and the amount of UHP. The results showed that using this system in the oxidation of sulfides, sulfoxides were obtained as the main products,... 

Epoxides are important materials in the production of fine chemicals. Selective oxidation of alkenes to epoxides remains a challenge in synthetic chemistry. There has been considerable progress in tungsten-catalyzed epoxidation of alkenes in recent years. This review highlights the use of monomeric and dimeric oxido-peroxido tungsten(VI) complexes as catalysts or oxidants in homogeneous or heterogeneous catalytic systems for epoxidation of olefins  

This review mainly discusses the application of oxido-peroxido Molybdenum(VI) complexes as catalysts or mediators in homogeneous or heterogeneous catalytic systems for oxidations of olefins, sulfides, alcohols, alkanes, and amines toward the synthesis of a variety of organic compounds, such as epoxides, sulfoxides, aldehydes and ketones, carboxylic acids, alcohols and nitroso compounds  

Palladium nanoparticles (Pd-NPs) were supported on functional and nonfunctional Co-coordination polymers (Pd/CoBDCNH2 and Pd/CoBDC). Advanced analytical techniques revealed that Pd-NPs are supported on the external surface of the polymer framework and the functionalized framework possesses effective influence to prevent Pd-NP aggregation. Supported Pd-NPs were effectively applied as heterogeneous recyclable catalysts in the Mizoroki–Heck C–C cross coupling reactions of iodobenzene and either aromatic or aliphatic terminal alkenes. Catalytic results exhibited that highly dispersed Pd-NPs with low loading (1%) on the functional polymer (Pd/CoBDCNH2) are more effective than aggregated Pd-NPs... 

A molybdenum complex, [MoO2Cl2(DMSO)2], was immobilized on amino propyl and Schiff base modified magnetic Fe3O4@SiO2 nanoparticles by covalent linkage. The resulting nanoparticles were used as efficient and recyclable catalysts for the selective oxidation of sulfides to sulfoxides using urea hydrogen peroxide as the oxidant. The complete characterization of catalysts was carried out by means of thermogravimetric analysis (TGA), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), X-ray photoelectron spectroscopy (XPS), elemental analysis, FT-IR and Raman microprobe... 

A magnetically recyclable vanadium(V) catalyst was synthesized by covalent anchoring of VO(salen)Cl on silica-coated Fe 3O 4 nanoparticles. This straightforward preparation yields magnetically separable Fe 3O 4@SiO 2@VO(salen) nanoparticles with high vanadium loading. These nanoparticles were efficient catalysts for selective oxidation of sulfides to corresponding sulfoxides with urea hydrogen peroxide in excellent yields. Leaching and recycling experiments revealed that the nanocatalyst can be applied for nearly complete oxidation of sulfides for at least five successive cycles  

Abstract: Polyoxometalate-functionalized magnetic nanoparticles (Fe3O4@SiO2–MnPOW) were successfully synthesized via covalent anchoring of Mn(II)-substituted phosphotungstate on ammonium-modified Fe3O4@SiO2 nanoparticles. The complete characterization of nanoparticles has been carried out by scanning electron microscope, energy-dispersive X-ray, X-ray diffraction, Fourier transform infrared and elemental analysis. The resulting nanocomposites were efficient catalysts for the selective oxidation of sulfides with different green oxidants in good to excellent yields and also high selectivity. Leaching and recycling tests showed that the nanocatalyst can be reused several times without... 

Herein, MIL-101(Fe), CoFe2O4, novel binary (MIL-101(Fe)/CoFe2O4, MIL-101(Fe)/GO and CoFe2O4/GO), and ternary (MIL-101(Fe)/CoFe2O4/(3%)GO and MIL-101(Fe)/CoFe2O4/(7%)GO) magnetic composites based upon the MIL-101(Fe) were synthesized. The XRD, FESEM, TEM, EDX, BET-BJH, FTIR, VSM, DRS, PL, EIS and other electrochemical analyses were applied to characterize samples. The MIL/CoFe2O4/(3%)GO demonstrated the best performance compared to other samples for visible light photocatalytic and photo-Fenton-like degradation of Direct Red 23 (DtR-23), Reactive Red 198 (ReR-198) dyes as well as Tetracycline Hydrochloride (TC-H) antibiotic. Degradation of dyes using the ternary composite after 70 min of... 

A molybdenum complex was immobilized on Schiff-base-modified magnetic and non-magnetic particles by covalent linkage. The characterizations of the obtained materials were carried out by means of TG–DTG, SEM, TEM, VSM, XPS, IR, and Raman microprobe techniques. All of them exhibited efficient activities in the oxidation of sulfides to sulfoxides by urea hydrogen peroxide oxidant. The advantages and disadvantages of these catalysts are discussed in detail. Molybdenum complex immobilized on silica bead can be recycled and recovered by simple filtration, but it demonstrated low activity in catalytic oxidation reaction. Immobilization on nano-SiO 2 leads to the formation of nanocatalyst having... 

A copper catalyst has been explored as an efficient and recyclable catalyst to effect Sonogashira and Suzuki cross-coupling reactions. After modification of 2-(((piperazin-1-ylmethyl)imino)methyl)phenol (PP) on the surface of amorphous silica-coated iron oxide (Fe3O4@SiO2@Cl) magnetic core-shell nanocomposite, copper(II) chloride was employed to synthesize the Fe3O4@SiO2@PP-Cu catalyst, affording a copper loading of 1.52 mmol g-1. High yield, low reaction times, non-toxicity and recyclability of the catalyst are the main merits of this protocol. The catalyst was characterized using Fourier transform infrared, X-ray photoelectron, energy-dispersive X-ray and inductively coupled plasma optical... 

Vanadium supported on spinel cobalt ferrite nanoparticles was synthesized and characterized using Fourier transform infrared spectroscopy, X-ray diffraction, energy-dispersive X-ray analysis and transmission electron microscopy. For the first time, the prepared material was used for the catalytic degradation of methylene blue as an organic dye in the presence of hydrogen peroxide as a green oxidant and NaHCO3 as a co-reagent at room temperature. The dependency of removal percentage on various parameters such as amount of catalyst, pH, reaction time and temperature and the effect of radical scavenging agents were studied. Finally, recoverability and reusability of the vanadium supported on... 

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... 

A copper catalyst has been explored as an efficient and recyclable catalyst to effect Sonogashira and Suzuki cross-coupling reactions. After modification of 2-(((piperazin-1-ylmethyl)imino)methyl)phenol (PP) on the surface of amorphous silica-coated iron oxide (Fe3O4@SiO2@Cl) magnetic core–shell nanocomposite, copper(II) chloride was employed to synthesize the Fe3O4@SiO2@PP-Cu catalyst, affording a copper loading of 1.52 mmol g−1. High yield, low reaction times, non-toxicity and recyclability of the catalyst are the main merits of this protocol. The catalyst was characterized using Fourier transform infrared, X-ray photoelectron, energy-dispersive X-ray and inductively coupled plasma optical... 

Humanity's challenges are becoming increasingly difficult, and as these challenges become more advanced, the need for effective and intelligent action becomes more apparent. Meanwhile, the novel coronavirus disease (COVID-19) pandemic, which has plagued the world, could be considered as an opportunity to take a step toward the need for atomic engineering, compared to molecular engineering, as well as to accelerate this type of research. This approach, which can be expressed in terms of picotechnology, makes it possible to identify living cell types or in general, chemical and biological surfaces using their atomic arrays, and applied for early diagnosis even treatment of the disease. © 2020... 

The mild and efficient oxidation of a variety of organic functional groups with a twin catalyst/oxidant, bis(phenanthroline)silver(II) peroxydisulfate, [Ag(phen)2]S2O8, is reported. This reagent shows high selectivity and the type of obtained products and the extent of oxidation are strongly dependent to the type of the functional groups and oxidant/substrate molar ratios  

A metal-organic framework [Co3(BDC)3(DMF)2(H2O)2] was synthesized and structurally characterized. X-ray single crystal analysis revealed that the framework contains a 2D polymeric chain through coordination of 1,4-benzenedicarboxylic acid linker ligand to cobalt centers. The polymer crystallize in monoclinic P21 /n space group with a=13.989(3) Å, b=9.6728(17) Å, c=16.707(3) Å, and Z=2. The polymer features a framework based on the perfect octahedral Co-O6 secondary building units. The catalytic activities of [Co3(BDC)3(DMF)2(H2O)2]n for olefins oxidation was conducted. The heterogeneous catalyst could be facilely separated from the reaction mixture, and reused three times without significant...