Interaction of dimethyltin(IV)dichloride with 5′-AMP and 5′-GMP

2006 ◽  
Vol 84 (11) ◽  
pp. 1534-1540 ◽  
Author(s):  
Farrokh Gharib ◽  
Elnaz Farzad ◽  
Mostafa Mohammadpour Amini
Keyword(s):  
Aqueous Solution ◽  
Ionic Strength ◽  
Ftir Spectroscopy ◽  
Constant Temperature ◽  
Elemental Analysis ◽  
Formation Constants ◽  
Low Ph ◽  
Ph Values ◽  
Species Formation ◽  
Ph Range

The formation constants of the species formed in the systems H+ + dimethyltin(IV) + 5′-AMP and 5′-GMP, H+ + 5′-AMP, and H+ + 5′-GMP have been determined in aqueous solution in the pH range of 1.5–9 at constant temperature (25 °C) and constant ionic strength (0.1 mol dm–3, NaClO4) using spectrophotometric and potentiometric techniques. 1H and 31P NMR investigations in aqueous solution confirmed the species formation and led us to propose their structures. The precipitated complexes of AMP and GMP by Me2Sn(IV)2+ at low pH values were characterized by elemental analysis and FTIR spectroscopy, which ruled out purine moiety (N-1 and N-7) coordination and a bidentated coordination of the phosphate group is concluded in both cases.Key words: dimethyltin(IV)dichloride, guanosine 5′-monophosphate, adenosine 5′-monophosphate, stability and protonation constants.

scholarly journals Chemoenzymatic synthesis of the pH responsive surfactant octyl β-D-glucopyranoside uronic acid

2019 ◽  
Vol 104 (3) ◽  
pp. 1055-1062 ◽  
Author(s):  
Ngoc T. N. Ngo ◽  
Carl Grey ◽  
Patrick Adlercreutz
Keyword(s):  
Substrate Concentration ◽  
Uronic Acid ◽  
Catalyst System ◽  
Low Ph ◽  
Chemoenzymatic Synthesis ◽  
Ph Responsive ◽  
Ph Values ◽  
Wide Ph Range ◽  
Carboxyl Derivative ◽  
Ph Range

AbstractMethodology was developed to expand the range of benign alkyl glycoside surfactants to include also anionic types. This was demonstrated possible through conversion of the glycoside to its carboxyl derivative. Specifically, octyl β-D-glucopyranoside (OG) was oxidised to the corresponding uronic acid (octyl β-D-glucopyranoside uronic acid, OG-COOH) using the catalyst system T. versicolor laccase/2,2,6,6-tetramethylpiperidinyloxy (TEMPO) and oxygen from air as oxidant. The effects of oxygen supply methodology, concentrations of laccase, TEMPO and OG as well as reaction temperature were evaluated. At 10 mM substrate concentration, the substrate was almost quantitatively converted into product, and even at a substrate concentration of 60 mM, 85% conversion was reached within 24 h. The surfactant properties of OG-COOH were markedly dependent on pH. Foaming was only observed at low pH, while no foam was formed at pH values above 5.0. Thus, OG-COOH can be an attractive low-foaming surfactant, for example for cleaning applications and emulsification, in a wide pH range (pH 1.5–10.0).

Formation et stabilité de complexes hydroxo–ammonio en solution aqueuse. I. Complexes de zinc

1968 ◽  
Vol 46 (10) ◽  
pp. 1707-1714 ◽  
Author(s):  
A. O. Gubeli ◽  
J. Ste-Marie
Keyword(s):  
Aqueous Solution ◽  
Ionic Strength ◽  
Formation Constants ◽  
New Method ◽  
Hydroxo Complexes ◽  
Solution Aqueuse

A new method has been developed for the calculation of the formation constants of complexes in equilibrium with a precipitate in aqueous solution. This has been applied to the study of ammonio and ammonio–hydroxo complexes of zinc in the presence of the hydroxide. The curves of solubility vs. pH and pNH3 tot have been established by means of 65Zn at 25 °C and ionic strength 1.0 with NaClO4.

Coordinating Properties of Aromatic and Aliphatic Sulfur with Bivalent Metals in Aqueous Solution. A Calorimetric Study

1979 ◽  
Vol 32 (4) ◽  
pp. 709 ◽  
Author(s):  
R Aruga
Keyword(s):  
Aqueous Solution ◽  
Ionic Strength ◽  
Complex Formation ◽  
Aqueous Medium ◽  
Formation Constants ◽  
Calorimetric Study ◽  
Thermodynamic Quantities ◽  
Direct Calorimetry ◽  
Bivalent Metals

Heats and entropies of complex formation of the thiophen-2-carboxylate ion with Ni2+, Cu2+, Zn2+ and Cd2+ have been determined by direct calorimetry, the formation constants being known from the literature. The measurements were carried out in aqueous medium at 25�C and an ionic strength of 1. The values of the thermodynamic quantities for thiophen-2-carboxylate, compared with those for (ethylthio)acetate and (phenylthio)acetate obtained previously, indicate a greater tendency for aromatic sulfur to form bonds with the above metals than for aliphatic sulfur. The causes of this behaviour are discussed.

scholarly journals Zinc adsorption in highly weathered soils

2008 ◽  
Vol 43 (1) ◽  
pp. 131-139 ◽  
Author(s):  
José Carlos Casagrande ◽  
Marcio Roberto Soares ◽  
Ernesto Rinaldi Mouta
Keyword(s):  
Ionic Strength ◽  
Ph Value ◽  
Batch Adsorption ◽  
Adsorption Mechanisms ◽  
Ionic Strength Effect ◽  
Ph Values ◽  
Effects Of Ph ◽  
Ph Range ◽  
Highly Weathered Soils ◽  
Zinc Adsorption

The objective of this work was to assess the effects of pH and ionic strength upon zinc adsorption, in three highly weathered variable charge soils. Adsorption isotherms were elaborated from batch adsorption experiments, with increasing Zn concentrations (0-80 mg L-1), and adsorption envelopes were constructed through soil samples reactions with 0.01, 0.1 and 1 mol L-1 Ca(NO3)2 solutions containing 5 mg L-1 of Zn, with an increasing pH value from 3 to 8. Driving force of reaction was quantified by Gibbs free energy and separation factor. Isotherms were C-, H- and L-type and experimental results were fitted to nonlinear Langmuir model. Maximum adsorption ranged from 59-810 mg kg-1, and Zn affinity was greater in subsoil (0.13-0.81 L kg-1) than in the topsoil samples (0.01-0.34 L kg-1). Zinc adsorption was favorable and spontaneous, and showed sharply increase (20-90%) in the 4-6 pH range. No effect of ionic strength was observed at pH values below 5, because specific adsorption mechanisms predominated in the 3-5 pH range. Above pH 5, and in subsoil samples, Zn was adsorbed by electrostatic mechanisms, since ionic strength effect was observed. Despite depth and ionic strength effects, Zn adsorption depends mainly on the pH.

scholarly journals Kinetics and Mechanism of the Decarboxylation of Pyrrole-2-carboxylic Acid in Aqueous Solution

1971 ◽  
Vol 49 (7) ◽  
pp. 1032-1035 ◽  
Author(s):  
G. E. Dunn ◽  
Gordon K. J . Lee
Keyword(s):  
Aqueous Solution ◽  
Ionic Strength ◽  
Carboxylic Acid ◽  
Isotope Effect ◽  
Anthranilic Acid ◽  
Kinetic Isotope Effect ◽  
Pyrrole Ring ◽  
First Order ◽  
Kinetic Isotope ◽  
Ph Range

The decarboxylation of pyrrole-2-carboxylic acid in aqueous buffers at 50° and ionic strength 1.0 has been found to be first order with respect to substrate at a fixed pH. As the pH is decreased, the rate constant increases slightly in the pH range 3–1, then rises rapidly from pH 1 to 10 M HCl. The 13C-carboxyl kinetic isotope effect is 2.8% in 4 M HClO4 and negligible at pH ~ 3. These observations can be accounted for by a mechanism, previously proposed for the decarboxylation of anthranilic acid, in which the species undergoing decarboxylation is the carboxylate ion protonated at the 2-position of the pyrrole ring. This intermediate can be formed both by ring-protonation of the carboxylate anion and by ionization of the ring-protonated acid. At low acidities ring-protonation is rate determining, but at higher acidities the rate of protonation exceeds that of decarboxylation.

scholarly journals Metallation of tetradentate N2O2 Schiff base with Mn(II), Co(II), Cu(II) and Zn(II): synthesis, characterization and formation constants measurement

2010 ◽  
Vol 8 (2) ◽  
pp. 291-299 ◽  
Author(s):  
Mozaffar Asadi ◽  
Maryam Mohammadikish ◽  
Khosro Mohammadi
Keyword(s):  
Mass Spectrometry ◽  
Schiff Base ◽  
Ionic Strength ◽  
Nmr Spectroscopy ◽  
Elemental Analysis ◽  
1H Nmr Spectroscopy ◽  
Formation Constants ◽  
Free Energies ◽  
Schiff Base Ligands ◽  
Ft Ir

AbstractFour Schiff base ligands, salabza-H2 = N,N′-bis(salicylidene)-2-aminobenzylamine, were synthesized by condensation of one mole of 2-aminobenzylamine and two moles of salicylaldehyde and/or two moles of substituted salicylaldehyde (5-OMe, 5-Br, 5-NO2). All the four Schiff bases and their Mn(II), Co(II), Cu(II) and Zn(II) complexes are characterized by UV-Vis, FT-IR, 1H NMR spectroscopy, mass spectrometry and elemental analysis. The formation constants and the Gibbs free energies were measured spectrophotometrically for 1:1 complexes in methanol in constant ionic strength (I = 0.1 mol dm−3 NaClO4) and at 25°C. The data refinement was carried out with the SQUAD program. The trend of formation constants of H2L1 with M(II) follows the order: Mn(II) (3.97) Also, the trend of formation constants of ligand toward a given metal (for example Mn) is as follows: H2L1 (p-OMe) (3.97) > H2L2 (p-H) (3.65) > H2L3 (p-Br) (3.37) > H2L4 (p-NO2) (3.04)

Triggered Cell Release from Shellac-Cells Composite Microcapsules

2013 ◽  
Vol 1498 ◽  
pp. 177-182
Author(s):  
Shwan A. Hamad ◽  
Simeon D. Stoyanov ◽  
Vesselin N. Paunov
Keyword(s):  
Aqueous Solution ◽  
Shear Stress ◽  
Aqueous Solutions ◽  
Slow Release ◽  
Culture Media ◽  
Low Ph ◽  
Yeast Cells ◽  
Triggered Release ◽  
Cell Release ◽  
Ph Range

ABSTRACTWe have fabricated novel shellac-cells composite microcapsules capable of pH-stimulus induced release of cells in a narrow pH range. The microcapsules were produced with yeast cells as a model for probiotics which were co-precipitated from an aqueous solution of ammonium shellac doped with pH-sensitive polyelectrolytes. The yeast cells in the composite shellac-cell microcapsules retained their viability even when treated with aqueous solutions of very low pH and subjected to shear stress. We studied the pH triggered release of cells from these microcapsules and measured their disintegration times. These microcapsules showed versatile responses ranging from slow release to explosive swelling at higher pH depending on the type and concentration of the polyelectrolyte integrated in the shellac microcapsules. We also observed growth-triggered release of cells from these microcapsules upon exposure to culture media. In both cases the cells retained their viability following their release from the microcapsules into the aqueous solution.

THE DECOMPOSITION OF 2-METHYL-Δ2-OXAZOLINE IN AQUEOUS SOLUTION

1963 ◽  
Vol 41 (7) ◽  
pp. 1662-1670 ◽  
Author(s):  
R. Greenhalgh ◽  
R. M. Heggie ◽  
M. A. Weinberger
Keyword(s):  
Aqueous Solution ◽  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Water Concentration ◽  
Acidity Function ◽  
First Order ◽  
Ph Values ◽  
Constant Ph ◽  
Kinetic Expression ◽  
Ph Range

Nuclear magnetic resonance has been used to follow the decomposition of aqueous solutions of 2-methyl-Δ2-oxazoline (0.29 M) at constant pH values in the range −1 to 14. The decomposition is first order with respect to total oxazoline at any specific pH, but deviates from the simple reaction of water with the protonated species above pH 5. At neutral pH values this is shown to be partially due to a second reaction involving 2-methyl-Δ2-oxazoline and O-acetylethanolamine which yields N-2-acetoxyethyl N′-2-hydroxyethyl acetamidate. The decrease in rate constant at pH < 2 is accounted for by variation in the water concentration, which is related to the acidity function. A kinetic expression is derived for the decomposition over the whole pH range studied. The decomposition of the amidate is also discussed.

scholarly journals Determination of Chromium in Tannery Effluent and Study of Adsorption of Cr (VI) on Saw dust and Charcoal from Sugarcane Bagasses

1970 ◽  
Vol 23 ◽  
pp. 93-101 ◽  
Author(s):  
T. P. Dhungana ◽  
P. N. Yadav
Keyword(s):  
Waste Water ◽  
Aqueous Solution ◽  
Spectrophotometric Method ◽  
Chromium Content ◽  
Chemical Society ◽  
Tannery Effluent ◽  
Saw Dust ◽  
Ph Values ◽  
Ph Range

Spectrophotometric method using diphenylcarbazide as a colour developing reagent has been used to analyze the chromium content in tannery effluent located in Bara and Parsa districts of Nepal and Sirsiya River which is an ultimate drainage of these waste water streams. The adsorption of hexavalent chromium from aqueous solution onto formaldehyde treated sawdust and charcoal of sugarcane begasses has been investigated at various Cr(VI) concentrations of 5-40 mg/L and pH values. From the experimental observations, it has been found that chromium can be removed quantitatively at the equilibrium pH range of around 1 and the adsorption behavior revealed to follow Langmuir and Freundlich adsorption isotherms.Keywords : chromium, diphenylcarbazide, adsorption.DOI: 10.3126/jncs.v23i0.2102Journal of Nepal Chemical Society, Vol. 23, 2008/2009 Page; 93-101

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