Search results for "Chloride"
showing 10 items of 1691 documents
Speciation of tin(II) in aqueous solution: thermodynamic and spectroscopic study of simple and mixed hydroxocarboxylate complexes
2013
This contribution reports the results of potentiometric and Mossbauer investigations on the formation, stability, and structure of binary and ternary mono- and binuclear complexes of Sn2+ with three hydroxocarboxylic ligands (namely L = tartrate, malate, and citrate) and chloride at T = 298.15 K in different ionic media and ionic strengths (0.15 and 1.00 mol dm−3 in NaCl(aq) and 1.00 mol dm−3 in NaNO3(aq)). The stability constants of various simple Sn i H j L (2+−) and mixed Sn i H j L k Cl (2+−−) species obtained in the different experimental conditions are reported, and various speciation diagrams of the simple and mixed systems are shown in different conditions. The sequestering ability …
Intrinsic viscosities of polyelectrolytes: specific salt effects and viscometric master curves.
2013
Dilute solutions of the sodium salt of polystyrene sulfonic acid (PSS-Na) were measured viscometrically as a function of composition in aqueous solvents of different salinity, where the extra salt was either NaCl or CaCl2. Such experiments yield {η}, the generalized intrinsic viscosities (hydrodynamic specific volume) of the polyelectrolyte for arbitrary polymer concentrations, c. In the limit of infinite dilution {η} becomes identical to the intrinsic viscosity [η]. For NaCl {η} decreases monotonously with rising c, whereas maxima are passed in the case of CaCl2. Condensing c and the concentration of extra salt in the mixed solvent into a single variable enables the establishment of predic…
Uranyl ion complexes with aminoalcoholbis(phenolate) [O,N,O,O′] donor ligands
2006
Abstract The reaction between uranyl nitrate hexahydrate and phenolic ligand precursor N,N-bis(2-hydroxy-3,5-dimethylbenzyl)-2-aminoethanol (H3L1) in acetonitrile without base affords the dinuclear uranyl complex [(UO2)2(H2L1)2(NO3)2] (1); in the presence of base, the mononuclear complex [UO2(H2L1)2] · 2H2O (2) is formed. Ligand N,N-bis(2-hydroxy-5-t-butyl-3-methylbenzyl)-2-aminoethanol (H3L2) affords a uranyl complex of formula [UO2(H2L2)2] · 2CH3CN (3); ligand N,N-bis(2-hydroxy-3,5-dimethylbenzyl)-3-amino-1-propanol (H3L3) affords a uranyl complex of formula [UO2(H2L3)2] (4); whilst ligand N,N-bis(2-hydroxy-5-t-butyl-3-methylbenzyl)-3-amino-1-propanol (H3L4), used as the hydrochloride, af…
Evidence of a 1,4-dipole intermediate in the reaction of 1-phenyl-4-vinylpyrazole with ptad
1985
Abstract 1-Phenyl-4-vinylpyrazole reacts with 1-phenyl-1,2,4-triazoline-3,5-dione in methylene chloride to form an unstable azetidine (4). An intermediate 1,4-dipole is probably involved since, when the reaction is conducted in acetone, a 1:1:1 adduct (3) is isolated.
A non-catalyzed ring-opening aminolysis reaction of sesquiterpene lactones
1994
Abstract Santonin (1) and other sesquiterpene lactones (6–10) react cleanly with pyrrolidine at room temperature to afford γ-hydroxyalkylamides, which by elimination with mesyl chloride in pyridine-benzene at 80°C give unsaturated alkylamides.
Cell Adhesive and Antifouling Polyvinyl Chloride Surfaces Via Wet Chemical Modification
2012
Polyvinyl chloride (PVC) is one of the most frequently used polymers for the manufacturing of medical devices. Limitations for its usage are based upon unfavorable surface properties of the polymer including its hydrophobicity and lack of functionalities in order to increase its versatility. To address this issue, wet chemical modification of PVC was performed through surface amination using the bifunctional compound ethylene diamine. The reaction was conducted in order to achieve maximum surface amination while leaving the bulk material unaffected. The initial activation step was characterized by means of various methods including contact angle measurements, colorimetric amine quantificati…
From ceria nanotubes to nanowires through electrogeneration of base
2009
The preparation of Ce(OH)3/CeO2 nanostructures (NSs) through electrogeneration of base into anodic alumina membranes was studied. The effects of solvent (alcohol and/or water), Ce3? partner anion nature (chloride or nitrate) and concentration, applied potential or current density in driving the morphology toward nanowires (NWs) and/or nanotubes (NTs) was described. The structural analysis performed by X-Ray Diffraction and Raman Spectroscopy allowed to evidence that the presence of Ce(IV) into the nanostructures strongly depends on the oxygen content in the growing environment.
Antidiabetic Behavior of Biguanides
1983
The existence of active electron pairs on some nitrogen atoms in phenformin hydrochloride is inferred from the presence of a hydrogen catalytic polarographic wave. This finding emphasizes the ability of biguanides to form hydrogen bridges with other molecular species such as amino acids and proteins, as well as to form coordination complexes with zinc and other metallic cations by means of these electron pairs. The antidiabetic action of phenformin and other related biguanides can be explained in terms of competition between these molecules and insulin to coordinate cationic oligoelements together with their ability to form hydrogen bonds between the biguanide moiety and insulin itself.
Electrochemical carboxylation of benzal chloride
1984
Abstract The clectrocarboxylation of benzal chloride to -chlorophenylacetic and phenylmalonic acids is realized in diaphragmless cells with aluminium sacrificial anodes. Yields respectively up to 50% and 30% can be obtained. Phenylacetic acid is always present among the products.
FT-IR investigation of the state of iron (III) chloride clusters confined in AOT reverse micelles dispersed in carbon tetrachloride
2007
The state of the water-soluble salt iron(III) chloride in AOT reverse micelles dispersed in carbon tetrachloride has been investigated by FT-IR spectroscopy. Interestingly, while the entrapment of a lot of water-soluble inorganic salts in AOT reverse micelles requires preliminarily the presence of significant amounts of water within the micellar core, solubilization of FeCl3 occurs without the need to add water in the micellar solution reaching the very high solubility value, expressed as the maximum salt-to-surfactant molar ratio, of 1.30. The analysis of the spectral features of the investigated samples leads to hypothesize that iron(III) chloride is confined within the reverse micellar c…