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61.
Ahmad Rouhollahi Mohammad Kazem Amini Mojtaba Shamsipur 《Journal of solution chemistry》1994,23(1):63-74
Proton NMR was used to study the complexation reaction between lead ion and 18-crown-6 in a number of binary acetonitrile-water mixtures. Formation constant for the resulting 11 complexes in different solvent mixtures was determined by computer fitting of the chemical shift-mole ratio data. There is an inverse relationship between the complex stability and amount of water in the mixed solvent. The dissociative kinetics of the complex was studied by proton line-shape analysis. The Arrhenius plots showed a distinct isokinetic temperature at about 25°C at which the decomplexation rate is more or less independent of the solvent composition. the complexation rate and the activation parameters E
a
, H and S, for the exchange have been determined and found to be strongly solvent dependent. There is actually a linear relationship between the mole fraction of acetonitrile in the mixed solvent and logarithm of the stability constant as well as activation parameters. 相似文献
62.
Lopez-Martens A Hannachi F Dossing T Schück C Collatz R Gueorguieva E Vieu C Leoni S Herskind B Khoo TL Lauritsen T Ahmad I Blumenthal DJ Carpenter MP Gassmann D Janssens RV Nisius D Korichi A Bourgeois C Astier A Ducroux L Le Coz Y Meyer M Redon N Sharpey-Schafer JF Wilson AN Korten W Bracco A Lucas R 《Physical review letters》1996,77(9):1707-1710
63.
64.
Ahmad Al-Alousy Saad Alshehri John Burgess Maria del Mar Graciani Maria-Luisa Moya Ernestina Muñoz Amalia Rodriguez Francisco Sanchez 《Transition Metal Chemistry》1993,18(2):179-181
Summary Dependences of rate constants on pressure (up to 1 kbar) and on added salt concentration (up to 6.0 mol dm–3 LiNO3, NaNO3, NaCl, Na2SO4 or KNO3) have been established for dissociative substitution of pentacyanoferrates(II), [Fe(CN)5L]3– with L = 4-cyanopyridine, 4,4-bipyridyl, 4-phenylpyridine and 4-t-butylpyridine. Activation volumes derived directly from pressure effects, and indirectly from salt effects via surface tension dependences and derived surfaces of activation, are reported, compared and discussed. 相似文献
65.
The kinetics and mechanism of glutamic acid (GCO2H) oxidation by acid permanganate has been carried out in the absence and presence of sodium dodecyl sulphate (SDS). The surfactant enhances the reaction rate without changing the reaction mechanism. The overall rate expression for the reduction of MnVII may be written:
相似文献
66.
67.
JPC – Journal of Planar Chromatography – Modern TLC - 相似文献
68.
The effect of addition of sodium anthranilate to 5 mM micellar solutions of gemini surfactant 1,4-bis(N-hexadecyl-N,N-dimethylammonium)butane dibromide is investigated by 1H NMR. The solubilization site of anthranilate anion near the micellar surface is inferred. In the micelles, the An− ions intercalate among the surfactant headgroups producing morphological changes. 相似文献
69.
Ahmad Shaabani Abbas Rahmati Soheila Naderi 《Monatshefte für Chemie / Chemical Monthly》2007,138(6):553-557
Summary. Reaction of triphenylphosphine and an electron deficient acetylenic ester in the presence of strong N–H acid such as alkyl
and aryl sulfamides or acetamide produces phosphorous ylides at room temperature in CH2Cl2. The aryl sulfamide phosphoranes undergo a smooth transformation reaction in boiling toluene and produce iminophosphoranes. 相似文献
70.
F. Ahmad 《Journal of the Iranian Chemical Society》2004,1(2):99-105
A method is suggested to determine valid and authentic values of thermodynamic stability parameters of proteins from their heat-induced conformational transition curves. We show (a) that the estimate of ΔHm van, the enthalpy change on denaturation at Tm, the midpoint of denaturation, is significantly less than ΔHm cal, the value obtained by the calorimetric measurements, if the analysis of the conformational transition curve uses the conventional method which assumes a linear temperature-dependence of the pre- and post-transition baselines; and (b) that there exists an excellent agreement between ΔHm van and ΔHm cal values of proteins, if the analysis of thermal denaturation curves assumes that the temperature-dependence of pre- and post-transition baselines is described by a parabolic function. The latter analysis is supported by our observations that the temperaturedependencies of the absorption and circular dichroism properties of protein groups are indeed nonlinear. It is observed that the estimate of ΔCp, the constant-pressure heat capacity change is independent of the model used to describe the temperaturedependence of the pre- and post-transition baselines. An important conclusion is that for proteins which exhibit a two-state character, all stability parameters are measured with the same error as that observed with a calorimeter. 相似文献
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