68 research outputs found
Kinetics and mechanism of the reduction of colloidal MnO2 by glycyl-leucine in the absence and presence of surfactants
AbstractThe kinetics of the reduction of water-soluble colloidal manganese dioxide by glycyl-leucine (Gly-Leu) has been investigated in the presence of perchloric acid both in aqueous as well as micellar media at 35°C. The study was carried out as functions of [MnO2], [Gly-Leu] and [HClO4]. The first-order-rate is observed with respect to [MnO2], whereas fractional-order-rates are determined in both [Gly-Leu] and [HClO4]. Addition of sodium pyrophosphate and sodium fluoride enhanced the rate of the reaction. Further, the use of surfactant micelles is highlighted as, in favourable cases, the micelles help the redox reactions by bringing the reactants into a close proximity due to hydrogen bonding. While the ionic surfactants SDS and CTAB have not shown any effect on the reaction rate, the nonionic surfactant TX-100 has catalytic effect which is explained in terms of the mathematical model proposed by Tuncay et al. (1999). The Arrhenius and Eyring equations are valid for the reaction over the range of temperatures used and different activation parameters (Ea, ÎH#, ÎS# and ÎG#) have been evaluated. Kinetic studies show that the redox reaction between MnO2 and Gly-Leu proceeds through a mechanism combining one- and two-electron pathways: Mn(IV)âMn(III)âMn(II) and Mn(IV)âMn(II). On the basis of the observed results, a possible mechanism has been proposed and discussed
Preparation and characterization of silver nanoparticles using aniline
AbstractUVâVis spectroscopy, transmission electron microscopy (TEM) and selected area electron diffraction (SAED) have been employed to characterize silver nanoparticles (AgNPs) using aniline and silver nitrate as reductant and oxidant, respectively. A broad surface resonance plasmon (SRP) band appears at 400nm, indicating that the AgNPs are spherical. The TEM images show that AgNPs aggregated in an unsymmetrical manner, leading to the formation of beautiful silver nanocrystals. Aniline adsorbed onto the surface of Ag-nanocrystals through electrostatic, van der Walls forces and hydrogen bonding. Cetyltrimethylammonium bromide (CTAB) acted as a stabilizer and/or capping agent
2-[(1-Methyl-1H-pyrrol-2-yl)methylÂidene]propaneÂdinitrile
In the title compound, C9H7N3, the N-bound methyl group and vinyl H atom are syn. The 12 non-H atoms comprising the molÂecule are essentially coplanar (r.m.s. deviation = 0.071â
Ă
). SupraÂmolecular tapes feature in the crystal packing, orientated perpendicular to [10-1], and are formed by CâHâŻN interÂactions involving each cyano N atom. The tapes are connected into layers via ÏâÏ interÂactions occurring between translationally related pyrrole rings [ring centroidâcentroid distance = 3.8754â
(10)â
Ă
]; the layers stack along the b axis
Self-decoration of Pt metal particles on TiO2 nanotubes used for highly efficient photocatalytic H2 production
Pt decorated TiO2 has, over the past decades, been a key material for photocatalytic hydrogen production. The present work shows that growing anodic self-organized TiO2 nanotubes from TiâPt alloy with a low Pt content of 0.2 at% leads to oxide nanotube layers that are self-decorated with Pt nanoparticles of 4â5 nm in diameter. The average particle spacing is in the range of ~50 nm and is partially adjustable by the anodization conditions. This intrinsic decoration of TiO2 nanotubes with Pt leads to a highly active photocatalyst for the production of H2 under UV or visible light conditions
Solvent-Free Biginelli Reactions Catalyzed by Hierarchical Zeolite Utilizing a Ball Mill Technique: A Green Sustainable Process
A sustainable, green one-pot process for the synthesis of dihydropyrimidinones (DHPMs) derivatives by a three-component reaction of ÎČ-ketoester derivatives, aldehyde and urea or thiourea over the alkali-treated H-ZSM-5 zeolite under ball-milling was developed. Isolation of the product with ethyl acetate shadowed by vanishing of solvent was applied. The hierachical zeolite catalyst (MFI27_6) showed high yield (86%â96%) of DHPMs in a very short time (10â30 min). The recyclability of the catalyst for the subsequent reactions was examined in four subsequent runs. The catalyst was shown to be robust without a detectable reduction in catalytic activity, and high yields of products showed the efficient protocol of the Biginelli reactions
NH3 treatment of TiO2 nanotubes: from N-doping to semimetallic conductivity
In the present work we show that a suitable high temperature ammonia treatment allows for the conversion of single-walled TiO2 nanotube arrays not only to a N-doped photoactive anatase material (which is already well established), but even further into fully functional titanium nitride (TiN) tubular structures that exhibit semimetallic conductivity
Two polymeric 36-metal pure lanthanide nanosize clusters
973 Program [2011CBA00507, 2011CB932504]; National Natural Science Foundation of China [21131006]; Natural Science Foundation of Fujian ProvinceTwo rarely seen 2D coordination polymers based on huge 36-metal pure lanthanide clusters, {[Gd-36(NA)(36)(OH)(49)(O)(6)(NO3)(6)(N-3)(3)(H2O)(20)]Cl-2 center dot 28H(2)O}(n) (1) and {[Dy-36(NA)(36)(OH)(49)(O)(6)(NO3)(6)(N-3)(3-)(H2O)(20)]Cl-2 center dot 28H(2)O}(n) (2) (HNA = nicotinic acid), were synthesized and structurally characterized. The spherical Ln(36) skeleton can be viewed as the aggregation of one cyclohexane chair-like Ln(24) wheel and two identical tripod-like Ln(6) units. The coordination of the carboxylic groups of the NA ligands with the Ln(III) cations results in a square layer. Additionally, compound 1 possesses a large MCE of 39.66 J kg(-1) K-1 and compound 2 exhibits slow relaxation of the magnetization
Synthesis, Structure Optimization and Antifungal Screening of Novel Tetrazole Ring Bearing Acyl-Hydrazones
Azoles are generally fungistatic, and resistance to fluconazole is emerging in several fungal pathogens. In an attempt to find novel azole antifungal agents with improved activity, a series of tetrazole ring bearing acylhydrazone derivatives were synthesized and screened for their in vitro antifungal activity. The mechanism of their antifungal activity was assessed by studying their effect on the plasma membrane using flow cytometry and determination of the levels of ergosterol, a fungal-specific sterol. Propidium iodide rapidly penetrated a majority of yeast cells when they were treated with the synthesized compounds at concentrations just above MIC, implying that fungicidal activity resulted from extensive lesions of the plasma membrane. Target compounds also caused a considerable reduction in the amount of ergosterol. The results also showed that the presence and position of different substituents on the phenyl ring of the acylhydrazone pendant seem to play a role on the antifungal activity as well as in deciding the fungistatic and fungicidal nature of the compounds
Synthesis, Structure Optimization and Antifungal Screening of Novel Tetrazole Ring Bearing Acyl-Hydrazones
Azoles are generally fungistatic, and resistance to fluconazole is emerging in several fungal pathogens. In an attempt to find novel azole antifungal agents with improved activity, a series of tetrazole ring bearing acylhydrazone derivatives were synthesized and screened for their <em>in vitro</em> antifungal activity. The mechanism of their antifungal activity was assessed by studying their effect on the plasma membrane using flow cytometry and determination of the levels of ergosterol, a fungal-specific sterol. Propidium iodide rapidly penetrated a majority of yeast cells when they were treated with the synthesized compounds at concentrations just above MIC, implying that fungicidal activity resulted from extensive lesions of the plasma membrane. Target compounds also caused a considerable reduction in the amount of ergosterol. The results also showed that the presence and position of different substituents on the phenyl ring of the acylhydrazone pendant seem to play a role on the antifungal activity as well as in deciding the fungistatic and fungicidal nature of the compounds
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