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  • Articles  (104)
  • Physical Chemistry  (104)
  • Wiley-Blackwell  (104)
  • 1995-1999  (61)
  • 1975-1979  (43)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 23-24 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 175-185 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Relaxation rates for O2(1Σg+) by nonradiative pathways have been determined using the fast-flow technique. O2(1Σg+) is formed from O2(1Δg) by an energy pooling process. O2(1Δg) is generated by passing purified oxygen through a microwave discharge. Oxygen atoms are removed by distilling mercury vapor through the discharge zone. It has been observed that the wall loss rate for O2(1Σg+) decreases with increasing pressure of oxygen and thus appears to be diffusion controlled. Quenching rate constants for O2, N2, and He have been determined and found to be (1.5 ± 0.1) × 104, (1.0 ± 0.05) × 106 and (1.2 ± 0.1) × 105 l./mol·sec, respectively.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 27 (1995), S. 369-377 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A laser flash photolysis-resonance fluorescence technique has been employed to study the kinetics of the reaction of O(3P) with CF3NO (k2) as a function of temperature. Our results are described by the Arrhenius expression k2(T) = (4.54 ± 0.70) × 10-12 exp[(-560± 46)/T] cm3molecule-1 s-1 (243 K ≤ T ≤ 424 K); errors are 2σ and represent precision only. The O(3P) + CF3NO reaction is sufficiently rapid that CF3NO cannot be employed as a selective quencher for O2(a1Δg) in laboratory systems where O(3P) and O2(a1Δg) coexist, and where O(3P) kinetics are being investigated. © 1995 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 357-374 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate, equilibrium, and thermodynamic data for reaction (1) of 2,6-diphenyl-4R-phenoxyl radicals, where R==OCH3 (I), Ph (II), OC2H5 (III), O-n-C18H37 (IV), and 2,6-dicyclohexyl-4-phenylphenoxyl radical (V), in various solvents are obtained. The k1 values of radicals I to V are within (5.5 ± 1.0) × 107-(1.4 ± 0.3) × 109M-1·sec-1 in propanol. The solvent effect on k1 for radicals I and II was studied. The dimerization of radical I is diffusion-controlled in all solvent studies. The dimerization of radical II is viscosity-dependent but not diffusion-controlled. Plots of k1 against ET have a V shape. Specific solvent-solute interactions are seeming to be responsible for numerical k1 values of radicals I and II. The solvent effect is more pronounced for “slow” dimerization of radicals II than for “fast” dimerization of radicals I. The minimum k1 values correspond to pyridine and chloroform. The reaction (1) rate strongly depends upon the composition of a chloroform (S)-cosolvent binary mixture. Besides reaction (1) the following reactions proceed in binary mixture: \documentclass{article}\pagestyle{empty}\begin{document}$$ K_{14} = 0.18 \pm 0.05M^{ - 1},k_{15} = (2.0 \pm 1.0) \times 10^8 M^{ - 1} \cdot \sec ^{ - 1} $$\end{document} (radical I, S-CCL4 mixture) \documentclass{article}\pagestyle{empty}\begin{document}$$ K_{14} = 0.9 \pm 0.2M^{ - 1},k_{15} = (1.2 \pm 0.5) \times 10^7 M^{ - 1} \cdot \sec ^{ - 1} $$\end{document}(radical II, S-C6H14 mixture) \documentclass{article}\pagestyle{empty}\begin{document}$$ K_{14} = 0.45 \pm 0.10M^{ - 1},k_{15} = (9.0 \pm 2.0) \times 10^6 M^{ - 1} \cdot \sec ^{ - 1} $$\end{document}(radical II, S-CCL4 mixture)In all cases k16 ≪ k15. Factors influencing dimerization rates in strongly nonideal mixtures CH3OH-CCL4 and CH3OH-CHCl3 are discussed.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 8 (1995), S. 5-14 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new approach to the long-standing problem of interrelating meta and para substituent constants is presented. An analysis of the unified σ0-scale shows that the interrelation between σ40 and σ40/σ30 can be modelled by a pair of conjugate rectangular hyperbolae, one for normal (n) and the other for special (s) substituents. The latter are characterized by a lone electron pair in the first atom. The equations σ4n0 (σ4n0 - γ0)/(σ4n0 - 2γ0) = λ0 σ3n0 and σ4s0 = γ0 + λ0 σ3s0 are derived and discussed in terms of Taft's separation of mesomeric and non-mesomeric effects. Asymptotic values λ = 0.960 γ = -0.225 were obtained by non-linear least rectangles fitting. A nonnegligible mesomeric contribution to σ0 constants for normal substituents is predicted by the hyperbolic model. The present results are at variance with Exner's analysis of the meta-para interrelationship in benzene compounds with normal substituents. This divergence is ascribed to opposite views concerning the role of the π-inductive effect.
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  • 6
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystal and molecular structues of six quasi-phosphonium salts containing phosphorus-heteroatom heteroatom=oxygen, sulphur or nitrogen0 bonds were determined. Comparison of the molecular parameters obtained with those available for reference structures demonstrated that the ‘double bond’ character for the P+ — Y bond decreases in the order Y = N ≫ O 〉 S.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 8 (1995), S. 77-83 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The hydrogen bond complexes between metyrapone [methyl-1,2-di(3-pyridyl)propan-1-one] and hydroxylic proton donors (phenols, water) were investigated by infrared spectroscopy. The thermodynamic and spectroscopic data determined in carbon tetrachloride suggest that the nitrogen atom of the pyridine ring A [bonded to the C(CH3)2 group] is the main hydrogen bond interaction site. The data are compared with di-2-pyridylglyoxal complexes where the hydrogen bonds are formed on the oxygen atom of the carbonyl function. In the solid adduct of metyrapone with HCl, protonation takes place on the two nitrogen atoms of the pyridine rings. The data from this work are compared with those from chemical oxidation, which leads predominantly to the formation of mono-N-oxide A and di-N-oxide.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 8 (1995), S. 605-609 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Interactions between compounds containing phosphoryl, carbonyl, or hydroxyl groups (or combinations of these groups) with metal ions (Na+, Mg2+) were probed in CD3CN solutions by 17O NMR spectroscopy. For all phosphoryl and carbonyl substrates a strong high - field shift of the P=O and C=O signals was observed on the addition of a salt; no shift was observed, however, for the OH group signal, indicating that no chelation takes place in the hydroxyphosphoryl (or hydroxycarbonyl) derivatives. For 2-hydroxy-3-benzoylpropylphosphonic diester the 17O NMR studies, together with conformational analysis based on the 1H spectroscopy, demonstrated the chelation of a metal ion by the P=O and C=O functions (fermation of an eight-membered cyclic structure) with the OH group involved in the intramolecular hydrogen bonding, but not in the complexation to the metal ion.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 8 (1995), S. 671-688 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The original Hammett equation, Δ = ρσ, is transformed in a constrained tetralinear relationship where each straight line with variable intercept term correlates one of the following four groups or subsets of dipolar substituents: normal and special substituents (depending on the absence or the presence of a lone electron pair in their atom next to the aromatic ring) and, in each of these classes, separating meta and para derivatives. There are a total of four fitting parameters in the resulting plurilinear Hammettian transformation (PHT) from which the statistically corrected parameters λ and γ are derived; λ and γ are the asymptotic values in a hyperbolic model for the representation of Δ4 vs Δ4/Δ3. This meta-para interrelationship is assumed to hold in the absence of through-resonance effects which, in turn, are allowed for by the use of alternative sigma scales of substituent constants. By applying the PHT to a large number of selected literature data, parameters λ and γ are determined for the ionization equilibria of 3- and 4-monosubstituted benzoic acids, anilinium ions, phenols and pyridinium ions. In these reactions series, parameter λ, which measures the para/meta ratio of field/inductive effects, is lower than unity and shows a marked dependence on the basic molecular framework. It is best modelled in terms of a through-space field effect approach. The ratio γ/γ0, where γ0 is referred to the unified sigma-zero scale, is shown to correspond to the original Hammett's reaction constant ρ. It is concluded that the PHT constitutes an improved Hammett equation for the analysis of substituent effects in benzene derivatives taking into account statistical errors and making allowance for different transmission coefficients for the field/inductive effect from meta and para positions in different reaction series.
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  • 10
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The synthesis of symmetrical blocked pyrylium derivatives by reaction of a cyclic aromatic ketone with ethyl orthoformate goes through an intermediate which can be isolated under certain conditions. This intermediate is unstable when starting from 1-tetralone derivatives but, surprisingly, it can be isolated easily when the synthesis is performed with 1-indanone derivatives. Further, in the latter case, this intermediate cyclizes hardly into the expected blocked pyrylium derivative. Its ionic structure was demonstrated by mass spectrometry and by 500 MHz 1H and 13C NMR techniques including heteronuclear H-C COSY and DEPT polarization transfer experiments. Hydrolysis of this intermediate in aqueous ethanol solution forms, in acidic or basic media, a pseudo-base, which in the latter case presents strong similarities with that obtained by the base-catalysed ring-opening of a blocked pyrylium ion. In both acidic and basic solutions, the pseudo-base obtained by the two sources shows identical UV-visible absorption spectra. The difficulty of the intermediate (g) originating from 1-indanone derivatives in cyclizing into the blocked pyrylium structure, in contrast to the intermediate formed from 1-tetralone derivatives, is tentatively explained.
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