Search results for "aqueous solution"
showing 10 items of 1610 documents
New Multidimensional Coordination Polymers with μ 2 ‐ and μ 3 ‐dcno Cyano Carbanion Ligand {dcno – = [(NC) 2 CC(O)O(CH 2 ) 2 OH] – }
2006
New polymeric materials [M(dcno)2(H2O)2] [M = FeII (1), CoII (2)] and [M(dcno)2] [M = CuII (3), MnII (4)] with dcno– =[(NC)2CC(O)O(CH2)2OH]– = 2,2-dicyano-1-(2-hydroxyethoxy)ethenolate anion have been synthesised and characterised by IR spectroscopy, X-ray crystallography and magnetic measurements. In compounds 1 and 2, each organic ligand acts in a bridging mode with its two nitrogen atoms bound to two different metal ions, while in compounds 3 and 4, each organic anion acts as a μ3-bridging ligand through its two nitrogen atoms and the oxygen atom of the OH group. Each metal ion has a pseudo-octahedral trans-MN4O2 environment with four nitrogen atoms from four different organic ligands an…
Homo- and Heterobinuclear Cu2+ and Zn2+ Complexes of Ditopic Aza Scorpiand Ligands as Superoxide Dismutase Mimics
2017
Two polytopic aza-scorpiand-like ligands, 6-[7-(diaminoethyl)-3,7-diazaheptyl]-3,6,9-triaza-1-(2,6-pyridina)cyclodecaphane (L1) and 6-[6′-[3,6,9-triaza-1-(2,6-pyridina)cyclodecaphan-6-yl]-3-azahexyl]-3,6,9-triaza-1-(2,6-pyridina)cyclodecaphane (L2), have been synthesized. The acid–base behavior and Cu2+, Zn2+, and Cu2+/Zn2+ mixed coordination have been analyzed by potentiometry, cyclic voltammetry, and UV–vis spectroscopy. The resolution of the crystal structures of [Cu2L2Cl2](ClO4)2·1.67H2O (1), [Cu2HL2Br2](ClO4)3·1.5H2O (2), and [CuZnL2Cl2](ClO4)2·1.64H2O (3) shows, in agreement with the solution data, the formation of homobinuclear Cu2+/Cu2+ and heterobinuclear Cu2+/Zn2+ complexes. The m…
Low temperature optical spectroscopy of cobalt-substituted hemocyanin from Carcinus maenas
1993
In this work we report the optical absorption spectra of three cobalt-substituted derivatives of hemocyanin (He) from Carcinus maenas, in the temperature range 300–20 K. The derivatives studied are the mononuclear (Co2+)-He with a single cobalt ion in the “CuA” site, the binuclear (Co2+)2-He and the binuclear mixed metal (Co2+-Cu1+)-He. At low temperature three main bands are clearly resolved; the temperature dependence of their zeroth, first and second moments sheds light on the stereodynamic properties in the surroundings of the chromophore. Within the limits of the reported analysis, in the binuclear derivatives the motions coupled to the chromophore appear to be “essentially harmonic” i…
Removal of Pesticide Oxadixyl from an Aqueous Solution
2007
ABSTRACT The mycelium of Phomopsis helianthi (Ascomycete) was hydrolyzed with boiling NaOH to give an insoluble fraction composed of chitosan and glucans. The biomass obtained was tested as an agent for the removal of pesticides from an aqueous solution. Oxadixyl, which has a solubility in water of 3400 mg L−1, has been chosen as a hydrophilic organic contaminant model. The new, cheap material was demonstrated to recover up to 6 mg of oxadixyl per gram of adsorbent. The experimental data show an excellent correlation with the Langmuir isotherm model.
2-Aminopurine non-radiative decay and emission in aqueous solution: A theoretical study
2008
Abstract The minimum energy path along the lowest-lying ππ ∗ excited state of 2-aminopurine was calculated to elucidate the mechanisms of radiationless decay and emission in water. The sequential Monte Carlo quantum mechanics approach with a multiconfigurational and perturbative description of the wave function was employed to compute the minimum, transition state, and conical intersection. It was found that the barrier in the potential energy surface to access the conical intersection funnel increases in aqueous environment, making the system prone to enlarge the emission yield. These results rationalize the observed enhancement of emission in 2-aminopurine upon increasing of the solvent p…
Aggregation of Free-Base Octacarboxyphthalocyanine in Aqueous Solutions
1999
Results of spectral (UV-VIS) investigations on the aggregation phenomena of the freebase 2,3,9,10,16,17,23,24-octacarboxypthalocyanine are reported. Phthalocyanine exists mainly in associated (aggregated) froms in water. The aggregates are present even in very diluted (10-7 -10-6 mol/dm-3) solutions. The hydrogen bonding between the carboxyl groups of the adjacent molecules in considered. The increase in pH and temperature, as well as the presence of the cationic surfactant and alcohols (in an appropriate quantity) cause a prtial or full disaggregation. The spectrum of the monomeric phthalocyanine from has been observed. The increase in H2Pc(COOH)8 concentration, the decrease in pH, as well…
Influence of Anion and Cation Structure of Ionic Liquids on Carboxylic Acids Extraction
2019
A recently proposed new mechanism and a model of reactive extraction of carboxylic acids by hydrophobic ionic liquids (ILs) was tested on five systems from published as well as from new equilibrium data on liquid-liquid extraction of butyric and lactic acids (BA and LA) from aqueous solutions. Two phosphonium and one ammonium ILs were used. The model describes experimental data for all systems with a good fit. The mechanism of acid extraction by ILs is very similar for all tested systems. This indicates a more general validity of the developed model. The model allows deeper understanding of regularities in carboxylic acid extraction by hydrophobic ILs. Stability constants of the first acid-…
Solubilization by polysoaps
1994
The aqueous solubilization power of several series of micellar homopolymers and copolymers (''polysoaps'') is investigated. Using five insoluble or poorly water-soluble dyes, comparisons of the capacities are made with respect to the influence of structural variables such as the polymer backbone, the polymer geometry, the comonomer content, and the charge of the hydrophilic group. Some guidelines for polysoap structures suited for efficient solubilization are established. Noteworthy is that the solubilization capacities of the polysoaps are neither linked to the ability to reduce the surface tension of water, nor to the polarity of the solubilization sites deduced from spectroscopic probes.
Cyclodextrins in Polymer Synthesis: Influence of Acrylate Side Groups on the Initial Rate of Radical Polymerization of Various Acrylate/Methylated β…
2001
Methylated β-cyclodextrin was used to complex the hydrophobic monomers n-propyl acrylate (1), n-butyl acrylate (2), n-pentyl acrylate (3), n-hexyl acrylate (4), and cyclohexyl acrylate (5) respectively yielding the corresponding water-soluble host/guest-complexes 1a−5a. The complexes were polymerized in water by free radical mechanism and the initial polymerization rates (v0) determined. We found that v0 increases as follows: 1a (12.5), 2a (27.5), 3a (44.2), 5a (49.4), 4a (75.8 × 10-6 mol·L-1·s-1). To investigate the influence of the hydrophobic character of the guest monomers on the reaction rate, the water solubilities of the uncomplexed monomers 1−5 were determined by HPLC measurements.…
Thermodynamic studies of octyltrimethylammonium chloride in water
1992
Densities, heat capacities, enthalpies of dilution at 298 K and osmotic coefficients at 310 K of octyltrimethylammonium chloride were measured as functions of concentration. From the experimental data, the partial molar volumes, heat capacities, relative enthalpies, nonideal free energies and entropies at 298 K were derived as functions of concentration. A comparison between the above data and those of dodecyltrimethylammonium chloride reported in the literature shows that the increase of the alkyl chain length shifts the apparent molar volumevs. concentration curves towards greater values and the heat capacity, relative enthalpy and free energyvs. concentration curves towards smaller value…