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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 4 (1991), S. 141-148 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The influence of solvation on the Z - E isomerization process of three representative molecules of simple push-pull ethylenes [H2N(H)C1=C2(H)R = NO2, COH and CN] derived from aminoethylene was investigated by means of RHF-SCF ab initio calculations at the 3-21 + G level. Solute-solvent interactions were modelled by a cavity model. The shape of the cavity is based on electronic isodensity surfaces. By using an ellipsoidal cavity very close to the isodensity surface, the perturbation due to the solvent takes an analytical form which is incorporated into the Hartree-Fock equations and leads to efficient quantum chemical computations. The polarization of the solutes under the influence of the solvent is noticeable and was analysed in detail. Similarly, the barriers to internal rotations are substantially modified by the solvent: the barrier around the C=C double bond is appreciably decreased in the thermal mechanism whereas its lowering is less important in the anionic mechanism; in contrast, the barrier around the C-1—N bond is slightly increased. The variation of the barriers with the nature of the acceptor group is fairly well reproduced by the computations. The electronic structure of the push-pull ethylene molecules and the modifications of this structure under the influence of the solvent are analysed in detail.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 21 (1989), S. 51-61 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have carried out a kinetic study of the 4-pyridinecarboxaldehyde plus n-hexylamine system, at 25°C, in water-dioxan mixtures (0-60% v/v) and in the pH range pKa + 1.5 〉 pH 〉 pKa - 1.5, where pKa is the pK value of the conjugate acid of the amine. The results obtained could be interpreted in terms of a rate constant for Schiff's base hydrolysis and a rate constant for the reaction between the nonprotonated n-hexylamine and the nonhydrated form of 4-pyridinecarboxaldehyde. Both constants decrease sharply as the dioxan content of the solvent increases, in a manner consistent with Marshall's model [J. Phys. Chem., 74, 346 (1970)]. It is suggested that the transition state of the rate-limiting step (carbinolamine dehydration) is highly solvated by water molecules and has a high separation of charges.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 24 (1992), S. 359-368 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics and mechanism of the reaction of Ni(II) with heptane-,5-dione (Hhptd) have been investigated in concentrated sodium perchlorate aqueous solutions at 298 K. The kinetic data in the different media are consistent with a mechanism in which Ni(II) reacts with the enol form of the ligand. The observed positive salt effect on the rate of the reaction of formation of the complex Nihptd+ is rationalized taking into account the increase of the rate of water exchange from the first solvation sphere of the metal ion to the bulk solvent when increasing salt concentration.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 18 (1986), S. 1249-1258 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The decomposition reactions of N-bromodiethanolamine, N-bromoethylethanolamine, and N-bromomethylethanolamine in aqueous solution have been studied kinetically under various experimental conditions. The results support a proposed reaction mechanism in which the rate controlling step is assumed to be the formation of an imine which is then hydrolyzed to the final decomposition products.
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 28 (1996), S. 57-60 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electron transfer reaction [(NH3)4COIII(μ-pzCO2)FeII(CN)5]- → [(NH3)4COII(μ-pzCO2)FeIII(CN)5]- has been studied in water-cosolvent mixtures at ionic strength of I = 0.5 mol dm-3 (NaClO4). A multiparameter regression coefficients have been compared to those obtained for the same reaction to a different ionic strength (I = 2.8 10-3 mol dm-3). The magnitude of these coefficients changes with the ionic strength. An explanation is given for this behavior. © 1996 John Wiley & Sons, Inc.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 24 (1992), S. 1083-1091 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study is made of the kinetic salt effects upon the outer-sphere electron transfer reaction between hexacyanoferrate(II) and 4-pyridinecarboxylatopentaamminecobalt(III). The observed salts effects are analyzed, taking into account the possible association of the reactants with the ions of the supporting electrolyte, though no conclusive results could be obtained. A correlation has been established between the logarithm of the observed second-order rate constants and the logarithm of the rate constants for a related innersphere electron transfer reaction. From this correlation the conclusion can be drawn that the observed salt effects in concentrated electrolyte solutions are mainly due to the effects on the electron transfer step. © John Wiley & Sons, Inc.
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  • 7
    ISSN: 0749-1581
    Keywords: Indirect heteronuclear NOEs ; 1H-19F-1H and 1H-19F-13C systems ; Three-spin effects ; Anomalous intensity effects ; Conformational analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Indirect nuclear Overhauser enhancements through 19F have been determined for the three-spin systems 1H-19F-1H and 1H-19F-13C by steady-state presaturation of the appropriate proton, and applied to the conformational analysis of 5-bromo-2-fluoro-4-nitroacetanilide. The 1H NOE difference spectra at 400 MHz showed antiphase doublets for protons undergoing simultaneous dipolar relaxation with, and scalar coupling to, 19F. Similarly, in the 13C selective NOE difference spectrum at 100 MHz, the two lines of the fluorine-bearing carbon showed negative enhancement factors of different magnitude on presaturation of the appropriate proton. The use of these anomalous intensity effects in conformational analysis is illustrated.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 397-409 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chlorinations of dimethylamine, diethylamine, methylethanolamine, ethylethanolamine and diethanolamine by N-chlorosuccinimide have been found to be equilibrium reactions of order one with respect to both N-chlorosuccinimide and amine in the forward direction and of order one with respect to succinimide and the resulting N-chloramine in the other. These results are explained by postulating a mechanism in which the rate controlling step consists in direct exchange of positive chlorine between the N-chlorosuccinimide and the amine.
    Additional Material: 5 Ill.
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  • 9
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction between Co(en)2(2-pzCO2)2+ (bis-ethylenediamine (2-pyrazinecarboxylato)cobalt(III)) and Fe(CN)5H2O3- (aquopentacyanoferrate(II)) to form the binuclear complex [(en)2Co( μ-pzCO2)Fe(CN)5]- has been studied in several isodielectric binary mixtures at 298.2 K (cosolvents: methanol, ethanol, tertbutyl alcohol, ethyleneglycol, and glycerol). Results were rationalized by using a free energy relationship. The importance of correcting the rate constants obtained in the different mixtures from the ionic strength influence has been shown. © 1995 John Wiley & Sons, Inc.
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  • 10
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Time-resolved investigations of the atomic resonance fluorescence Sr(53P1 → 51S0) and the molecular chemiluminescence from SrCl(A2Π1/2,3/2, B2Σ+ → X2Σ+) are reported following the reaction of the electronically excited strontium atom, Sr(5s5p(3PJ)), 1.807 eV above its 5s2(1S0) electronic ground state, with CH2Cl2. The optically metastable strontium atom was generated by pulsed dye-laser excitation of ground state strontium vapor to the Sr(53P1) state at λ = 689.3 nm (Sr(53P1 ← 51S0)) at elevated temperature (850 K) in the presence of excess helium buffer gas in which rapid Boltzmann equilibration within the 53PJ manifold takes place. Sr(53PJ) was then monitored by time-resolved atomic fluorescence from Sr(53P1) at the resonance wavelength together with chemiluminescence from electronically excited SrCl resulting from reaction of the excited atom with CH2Cl2. The molecular systems recorded in the time-domain were SrCl(A2Π1/2 → X2Σ+) (Δν = 0, λ = 674 nm), SrCl(A2Π3/2 → X2Σ+) (Δν = 0, λ = 660 nm), and SrCl(B2Σ+ → X2Σ+) (Δν = 0, λ = 636 nm). Both the A2Π (179.0 kJ mol-1) and (B2Σ+(188.0) kJ mol-1) states of SrCl are energetically accessible on collision between Sr(3P) and CH2Cl2. Exponential decay profiles for both the atomic and molecular (A,B - X) chemiluminescence emission are observed and the first-order decay coefficients characterized in each case. These are found to be equal under identical conditions and hence SrCl(A2Π, B2Σ+) are shown to arise from direct Cl-atom abstractions on reaction with this halogenated species. The combination of integrated molecular and atomic intensity measurements, coupled with optical sensitivity calibration, yields estimations of the branching ratios into the A1/2,3/2, B, and X states arising from Sr(53 PJ) + CH2Cl2 which are found to be as follows: A1/2, 3.0 × 10-3; A3/2, 1.7 × 10-3; B, 4.4 × 10-4 yielding ΣSrCl(A1/2 + A3/2 + B) = 5.1 × 10-3. As only the X, A and B states of SrCl are accessible on reaction, this indicates an upper limit for the branching ratio into the ground state of 0.995. The present results are compared with previous time-resolved measurements on SrF, Cl, Br(A2Π,B2Σ+ - X2Σ+) that we have reported on various halogenated species and with analogous chemiluminescence studies on Sr(3P) with other halides obtained from molecular beam measurements. The results are further compared with those from a series of previous analogous investigations in the time-domain we have presented of molecular emissions from CaF, Cl, Br, I (A,B - X) arising from the collisions of Ca(43PJ) with appropriate halides and with branching ratio data for Ca(43PJ) obtained in beam measurements. © 1995 John Wiley & Sons, Inc.
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