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  • 201
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 33-38 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Several Cotton effects are developed within absorption bands of trinuclear organotransitionmetal complexes in the presence of acids, diols, amines and aminoalcohols even in the case of bulky substituents on nitrogen; with monohydroxy compounds no circular dichroism could be detected.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 202
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 29-31 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The Disparity reaction proposed in a recent application of Marcus-Grunwald theory to nitroalkane ionization is shown to put the reaction's transition state in an energy-diagram region where electronic rearrangement leads proton transfer, contrary to experimental evidence; it is suggested that addition of solvent reorganization to electronic rearrangement as the second reaction progress variable would remedy this situation.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 203
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 39-46 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Triethylsilyl radical was generated by laser flash photolysis of a 1:1 (v/v) solution of triethylsilane and di-tert-butyl peroxide. The silicon centered radical was reacted with sulfides to give carbon centered radicals by displacement at sulfur. The carbon radicals were readily detected by their transient absorption spectra. The absolute rate of reaction of triethylsilyl radical with 9-fluorenylphenylsulfide, di-n-butylsulfide, di-sec-butyl sulfide, di-tert-butyl sulfide and di-n-butyl disulfide are 2.40 ± 0.12 × 108 M-1S-1, 1.1 × 107±0.89×106M-1S-1, 8.79± 0.73×106M-1S-1, 3.29±0.18×106 M-1S-1, and 3.41±0.09×108 M-1S-1, respectively.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 204
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 59-61 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Treatment of α, α′ -diketo selenides, which recently became readily obtainable, with base affords α-oxo selenoaldehydes and ketones. The seleno-carbonyl compounds thus formed are reactive transient species, but can be trapped by Diels-Alder reaction to give 3,6-dihydro-2H-selenapyran derivatives in moderate to good yields.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 205
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 47-51 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: This paper describes the synthesis and electrochemical behavior of dicationic salts of ethenediylidene-2,2′ -bis(1,3-dithiole) (3) and butatriene-1,4-diylidene-2,2′ -bis(1,3-dithiole) (4). These are expected as donor components for developing organic conducting and superconducting materials, on the grounds of high electron donating ability and of rigid skeletal structure with two and four cumulenic carbons inserted between two 1,3-dithioles. These salts were obtained in good overall yields by several steps starting from (2-morpholino-4,5-dimethyl or -diphenyl)-1,3-dithiolylium salt. From the 1H and 13C NMR, and electronic spectra it is suggested that the π conjugation between two 1,3-dithiolylium ions through an acetylenic bond is less effective than that through an olefinic bond of the corresponding salts of ethanediylidene-2,2′ -bis(1,3-dithiole) (1) and 2-butene-1,4-diylidene-2,2′-bis(1,3-dithiole) (2). The cyclic voltammetric study shows that the corresponding radical cations, and in particular 3 and 4, are less stable even at -40°C, thus providing reasons for our current lack of success in isolation of 3 and 4. From comparison of the first redox potentials of neutral species, it is deduced that the donating ability increases in the order of TTF 〈 1 ⋍ 2 ≲ 3 ≪ 4.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 206
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988) 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 207
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 63-73 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Novel structural features of 5, 15-dialkylporphyrins in solution are described. The 1H-NMR spectra of these compounds showed broad signals at room temperature, which split into two sets of signals at lower temperatures. This unusual phenomenon was ascribed to a dynamic interconversion between tow distorted structures. The 5, 15-dialkylporphyrin has a distorted ring due to the steric hindrance between the 5(or 15)-alkyl group and the 3, 7(or 13, 17)-alkyl groups and, depending on the position of the 5, 15-alkyl groups relative to the average ring plane, can exist in two conformations; syn (where the two alkyl groups are on the same side of the ring plane) and anti (on the opposite sides). Preliminary kinetic study of this interconversion using the NMR line shape analyses is also reported.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 208
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 75-81 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Highly sterically demanding 2,4,6-tri-t-butylphenyllithium (1) reacts with carbon disulfide to give 1,2-dibutylthio-1,2-bis(2,4,6-tri-t-butylphenylthio) ethene (3), l-butylthio-1-(2,4,6-tri-t-butylphenylthio)pent-l-ene (4), and 2-butylthio-3-(2,4,6-tri-t-butylphenylthio)-1,3-dithiole-2-thione (5) when 1 is prepared by the reaction of 1-bromo-2,4,6-tri-t-butylbenzene with n-butyllithium. When the reaction is carried out using 1 prepared from 2 and t-butyllithium and then quenched with l-iodoethane, 2-ethylthio-3-(2,4,6-tri-butylphenylthio)-1,3-dithiole-2-thione and 1,2-diethylthio-1,2-bis(2,4,6-tri-t-butylphenylthio) ethene are produced. The formation of all these products can be explained in terms of initial thiophilic attack of 1 on the sulfur of carbon disulfide and an intermediate with a dual property of carbanion and carbene (i.e., ArSC(Li)(=S) ⇌ ArSC̈SLi) is suggested. The reaction of 1 with thiophosgene affords 1,2-dichloro-1,2-bis(2,4,6-tri-t-butylphenylthio) ethene, bis(2,4,6-tri-t-butylphenylthio)acetylene, and 1-chloro 2,4,6-tri-t-butylbenzene, the first two of which are explained to be formed by thiophilic attack of 1 with thiophosgene.
    Materialart: Digitale Medien
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  • 209
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 91-102 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The photolysis of benzoinalkylethers 1-5 solubilized in detergents show a significant deviation from the course of reaction in isotropic organic solvents. Remarkable difference in photobehaviour is noticed between the short chain (1-3) and the long chain (4 and 5) benzoinalkylethers in the micellar media. However, the influence of the micellar media on the photobehaviour of alkyldeoxybenzoins 6 and 7 was small. The importance of ‘cage effect’ in controlling the product distribution was evident from its dependence on the micellar size and on the occupancy number. More importantly, a comparative analysis of the photobehaviour of the ketone 1-7 reveals that the micellar interface can be used to control the conformations of organic molecules.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 210
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 83-90 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Theoretical studies on the reactions of ammonia with ketene and dimethylketene using the MNDO method are reported. The single step addition of ammonia to the olefinic bond of ketenes was found to provide a lower energy-barrier path than the two step carbonyl addition mechanism. The barrier height was lower in the reaction of keten compared with that of dimethylketene in support of the faster rate of solution phase reactions of aniline and ketenes. The deformation energies of reactants had an overwhelming influence in determining the activation barriers in all the reactions investigated.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 211
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. ii 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 212
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988) 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 213
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 1-20 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Substrates with neutral leaving groups undergo unimolecular solvolysis in nonpolar solvents. Whereas t-alkyl substrates invariably solvolyze by a unimolecular mechanism, s-alkyl and primary alkyl substrates can undergo both uni and bimolecular reactions, and the bimolecular step can take place on either the substrate itself or on an intimate ion-molecule pair formed in either a pre-equilibrium or in a rate determining step. Study of reactions at borderlines indicates that the individual reaction types remain distinct and do not merge.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 214
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 21-27 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The structure of radical intermediates appearing in the reactions of MeMgBr with aromatic monoketones was investigated by using ESR and visible spectroscopy. Stable radical intermediates in the reacting solutions were assigned to the dimeric radical ion pairs.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 215
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 1 (1988), S. 53-57 
    ISSN: 0894-3230
    Schlagwort(e): Organic Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The reaction of sulfur ylides with elemental sulfur or selenium initially affords thio- or seleno-carbonyl compounds, which then react with starting ylides to give episulfides or episelenides from which the heteroatom (sulfur or selenium) is extruded to give olefins as the final product. In the case of carbonyl-stabilized ylides, the resulting thio- or seleno-carbonyl compounds react with starting ylides to afford 1,3-oxathioles or 1,3-oxaselenoles as previously reported. Supporting evidence for the intermediacy of thio(seleno)-carbonyl compounds and episulfides (episelenides) is presented.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 216
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: We present a kinetic study of atomic potassium in its electronic ground state, K(42S½), generated in the “single-shot mode” by pulsed irradiation at elevated temperatures and monitored by time-resolved atomic resonance absorption spectroscopy using the Rydberg doublet at λ = 404 nm (K[52PJ]←K[42S½]). Profiles for the decay of atomic potassium in the presence of various halogenated reactants were recorded at different temperatures, yielding the following Arrhenius parameters (kR = A exp(-E/RT), errors 1σ): TextRA/10-10 cm3 molecule-1s-1E/kJ mol-1Temp. RangeCH3F1.93+1.1-0.759±3.3822-922 KC2H5F1.40+2.5-0.962±6.6694-807 KC6H5F2.0+1.6-0.941±3.9705-812 KCH3Br1.7+0.3-0.215.9±1.2798-903 KHCl5.6+3.5-2.134.7±3.5828-902 KHBr1.9+0.3-0.334±1.2836-925 KA limited body of data is reported for k(K + C2H5Br) = 3.6 × 10-11 cm3 molecule-1 s-1 for the temperature range 704-733 K. These results for atomic potassium constitute a new body of absolute rate data which are compared with some previous results for reactions of atomic potassium with other reactants, and for reactions of atomic sodium, also determined by time-resolved atomic resonance absorption spectroscopy. The data for HCl and HBr are finally compared with early estimates reported using diffusion flames.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 217
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 297-306 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Studies of the reaction of Br + propylene to produce HBr and allyl radical were made using VLPR (Very Low Pressure Reactor) over the range 263-363 K. Apparent bimolecular rate constants k1app were found to vary in an inverse manner with the initial concentration of bromine atoms introduced into the reactor. Plots of k1app against [Br]0-1 give straight lines whose intercepts were taken to be the true bimolecular, metathesis rate constant k1. The reaction scheme is \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{rcl} {\rm Br} + {\rm C}_{\rm 3} {\rm H}_6& \stackrel{1} {\rightleftharpoons}& {\rm HBr} + {\rm allyl}\\ {\rm Br} + {\rm allyl} & \stackrel{2} {\longrightarrow}& {\rm HBr} + {\rm allene}\\ \end{array} $$\end{document} where k2 ≫ k1 and k-1 [HBr] is negligibly small under our conditions.Arrhenius parameters for k1 were assigned for linear and bent transition states and shown to give excellent fits to the observed intercepts. \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{rcl} {{\rm linear:}}\quad \log {(k_1 /{\rm cm}^3\, {\rm mol}^{{\rm - 1}}\,{\rm s}^{{\rm - 1}})} &=& 12.1 - 3.5/\theta\\ {{\rm bent:}}\quad \log {(k_1 /{\rm cm}^3\, {\rm mol}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}})} &=& 12.7 - 4.4/\theta \end{array} $$\end{document} where θ = 2.303 RT (kcal mol-1).The dependence of k1app on [Br]0-1 is accounted for in terms of the reactivity of Br* (2P1/2) produced in the microwave discharge. The activation energy for the metathesis reaction of Br* with propylene is shown to be very small.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 218
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 331-338 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The temperature dependencies of the rate constants for the gas phase reactions of OH radicals with a series of carboxylic acids were measured in a flash photolysis resonance fluorescence apparatus over the temperature range 240-440 K. The data at total pressures (using Ar diluent gas) between 25-50 torr for acetic acid (k1), propionic acid (k2), and i-butyric acid (k3) were used to derive the Arrhenius expressions \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{rcl} k_1 &=& (1.3\, \pm \,0.1)\, \times \,10^{- 12} {\rm \,exp[- (170}\, \pm \,2{\rm 0)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm \,s}^{{\rm -1}}\\ k_2 &=& (1.8\, \pm \,0.2)\, \times \,10^{- 12} {\rm \,exp[- (120}\, \pm \,3{\rm 0)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm \,s}^{{\rm - 1}} \end{array} $$\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$$k_3 = (2.6 \pm 0.2) \times 10^{- 12}\, {\rm exp[- (70} \pm 25{\rm)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}$$\end{document} At 298 K, the measured rate constants (in units of 10-12 cm3 molecule-1 s-1) were: k1 = (0.74 ± 0.06), k2 = (1.22 ± 0.12), and k3 = (2.00 ± 0.20). In addition a rate constant of (0.37 ± 0.04), in the above units, was determined for the reaction of OH with formic acid. The error limits cited above are 2σ from the linear least squares analyses. These results are discussed in terms of the mechanisms for these reactions and are compared to literature data.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 219
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 609-620 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Rate constants for the recombination reaction OD + NO2 + M → DNO3 + M have been determined in the falloff region (5-500 torr) and at 297 ± 2 K, in the presence of He, N2, and SF6 as third bodies, by using a pulsed laser photolysis-resonance absorption technique. Values of k0, kx and the falloff parameter Fc have been estimated. Our rate constants were, within the experimental uncertainty, the same as those reported for the reaction of OH radicals with NO2.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 220
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 221
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 699-712 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The kinetics of the interactions of the Keggin type heteropolyanion [CoW12O40]5-, with all the molecular and anionic forms of citric acid have been investigated spectrophotometrically in the pH range 0.60-5.45 at 60°C. With the exception of the molecular form of the acid (H3L), all the other species (H2L-, HL2-, and L3-) undergo oxidation through an alkali metal ion catalyzed path in addition to the uncatalyzed one. The catalytic power increases with increasing size of the alkali metal ion. The contributions of each path have been evaluated from the kinetic data with the help of the measured dissociation constant values of citric acid. A plausible mechanism involving the formation of a bridged outer-sphere complex of the reacting species with the alkali cation, has been suggested. The observed limiting dependence of kobs on [citrate] at high concentrations owing to an equilibrium between the reactants preceeding the electron transfer step supports the proposed mechanism. The pH-rate profile gives an excellent fit with the evaluated kinetic parameters.
    Zusätzliches Material: 3 Ill.
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  • 222
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 827-827 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 223
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 867-875 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The relative rate technique has been used to determine the rate constants for the reaction of chlorine atoms with a series of oxygenated organic species. Experiments were performed at 295 ± 2 K and atmospheric pressure of synthetic air or nitrogen. The decay rates of the organic species were measured relative to that of ethane or n-butane. Using rate constants of 5.7 × 10-11 cm3 molecule-1 s-1, and 2.25 × 10-10 cm3 molecule-1 s-1 for the reaction of Cl with ethane and n-butane respectively the following rate constants were derived, in units of 10-11 cm3 molecule-1 s-1: propane, (16.0 ± 0.4);i-butane, (15.1 ± 0.9) n-pentane, (31.0 ± 1.6); n-hexane, (34.5 ± 2.3); cyclohexane, (36.1 ± 1.5); methanol, (4.57 ± 0.40); ethanol, (8.45 ± 0.91); n-propanol, (14.4 ± 1.2); t-butylalcohol, (3.26 ± 0.19); acetaldehyde, (8.45 ± 0.79); propionaldehyde, (11.3 ± 0.9); dimethylether, (20.5 ± 0.8); diethylether, (35.6 ± 2.8); and methyl-t-butylether, (16.6 ± 1.2). Quoted errors represent 2σ, and do not include any errors due to uncertainties in the rate constants used to place our relative measurements on an absolute basis. The results are discussed with respect to the mechanisms of these reactions and to previous literature data.
    Zusätzliches Material: 5 Ill.
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  • 224
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 897-907 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A kinetic study of the reactions of H atoms with CH3SH and C2H5SH has been carried out at 298 K by the discharge flow technique with EPR and mass spectrometric analysis of the species. The pressure was 1 torr. It was found: k1 = (2.20 ± 0.20) × 10-12 for the reaction H + CH3SH (1) and k2 = (2.40 ± 0.16) × 10-12 for the reaction H + C2H5SH (2). Units are cm3 molecule-1 s-1. A mass spectrometric analysis of the reaction products and a computer simulation of the reacting systems have shown that reaction (1) proceeds through two mechanisms leading to the formation of CH3S + H2 (1a) and CH3 + H2S (1b).
    Zusätzliches Material: 5 Ill.
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  • 225
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 226
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 915-938 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The generation of metastable O2(1Σg+) and O2(1Δg) in the H + O2 system of reactions was studied by the flow discharge chemiluminescence detection method. In addition to the O2(1Σg+) and O2(1Δg) emissions, strong OH(v = 2) → OH(v = 0), OH(v = 3) → OH(v = 1), HO2(2A′000) → HO2(2A″000), HO2(2A′001) → HO2(2A″000), and H O2(2A″200) → HO2(2A″000) emissions were detected in the H + O2 system. The rate constants for the quenching of O2(1Σg+) by H and H2 were determined to be (5.1 ± 1.4) × 10-13 and (7.1 ± 0.1) × 10-13 cm3 s-1, respectively. An upper limit for the branching ratio to produce O2(1Σg+) by the H + HO2 reaction was calculated to be 2.1%. The contributions from other reactions producing singlet oxygen were investigated.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 227
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 939-955 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A flow system has been developed to study relative rate coefficients of hydroxyl radicals reacting with alkanes under conditions relating to tropospheric chemistry. Relative Arrhenius parameters have been measured over the temperature range 243-328 K for pairs of alkanes from a list consisting of n-butane, 2-methylpropane, n-pentane, n-hexane, 2,2- and 2,3-dimethylbutane, 2,3,3-trimethylbutane, and 2,3,4-trimethylpentane.The results have been incorporated into a Structure-Activity Relation for hydroxylalkane reactions which leads to the following group rate coefficients for a temperature range of 240-500 K. \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{rcl} k_{{\rm prime}}^0 &=& 3.13 \times 10^{ - 12}\, {\rm exp(} - 904/T)\,{\rm cm}^{\rm 3}\, {\rm molecule}^{ - 1}\, {\rm s}^{ - 1} \\ k_{{\rm sec}}^0 &=& 2.45 \times 10^{ - 12} \,{\rm exp(} - 320/T)\,{\rm cm}^{\rm 3}\, {\rm molecule}^{ - 1}\, {\rm s}^{ - 1} \\ k_{{\rm tert}}^0 &=& 1.88 \times 10^{ - 12} \,{\rm cm}^{\rm 3}\, {\rm molecule}^{ - 1}\, {\rm s}^{ - 1} \end{array}$$\end{document}
    Zusätzliches Material: 3 Ill.
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  • 228
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 673-685 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The slow gas-phase oxidation of tetrahydrofuran was studied under static conditions at 220°C. The relative amounts of each product, if extrapolated to zero reaction time, show which are the primary reaction products, and the reaction stoichiometry was thus established. Rate constants for hydroperoxides production and consumption were calculated; these hydroperoxides are responsible for chain branching. Carbon monoxide and carbon dioxide have been shown to be formed in the early stages of the reaction and not simply as end products of oxidative degradation processes. It has been found that at reaction times close to zero one tetrahydrofuran molecule may be attacked in one or several carbon atoms. 65.9% of tetrahydrofuran consumed in the first stages of the reaction forms succinic acid through a mechanism in which one molecule of fuel is attacked by two molecules of oxygen. More than 20% of the tetrahydrofuran molecules are attacked at least by three molecules of oxygen.
    Zusätzliches Material: 3 Ill.
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  • 229
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 230
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 749-752 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: ESR equilibrium measurements in radical buffer systems yield a value of 76.0 kcal/mol for the O—H bond energy in α-tocopherol.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 231
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 957-965 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Direct kinetic measurements have been made on the reaction: 2NO2 = N2O4. Equilibrium mixtures of NO2 and N2O4 at (224 ± 2) K were perturbed by flash photolysis of a fraction of the N2O4. The rate of relaxation back to equilibrium was monitored by observing the transmittance of the 14P(11) line from a cw CO laser selected to coincide with the v9 band of N2O4. Measurements were made in the presence of 350-750 torr of He, N2, or CF4. Within this limited pressure range, the kinetics were consistent with third-order behavior with the following rate constants (cm3 molecule-1 s-1): k0 = (2.4 ± 0.5) × 10-34 [He]; (1.0 ± 0.1) × 10-33 [N2]; (1.8 ± 0.3) × 10-33 [CF4].
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 232
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 967-978 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Heterogeneous recombination of O + CO → CO2 over a solid CO2 surface at 77 K was investigated. A modified discharge flow setup was used to generate low O atom concentrations by the reaction N + NO → N2 + O(3P). The O atom concentrations were measured upstream and downstream of the solid CO2 substrate using resonance fluorescence by monitoring the unresolved 130.3 nm triplet transition 3S1 - 3P2,1,0 at the two fixed points. CO2 formed was determined by measuring the β activity from C14O2 produced from CO containing C14O as a reactant gas. The CO2 formation was found to be first order in CO and independent of O atom concentration over the entire range of 4.3 × 1012 to 1.9 × 1014 cm-3 and 1.2 × 1011 to 5.6 × 1012 cm-3 for CO and O respectively. The first order recombination coefficient, λCO was found to be 1.4 (±.38) × 10-5.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 233
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 177-186 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Absolute rate constants were determined for the gas phase reactions of OH radicals with a series of esters using the flash photolysis resonance fluorescence technique. Experiments were performed over the temperature range 240-440 K at total pressures (using Ar diluent gas) between 25-50 torr. The kinetic data for methyltrifluoroacetate (k1) over the complete temperature range, and for methylacetate (k2), and ethylacetate (k3) over the range 296-440 K were used to derive the Arrhenius expressions; \documentclass{article}\pagestyle{empty}\begin{document}$$k_1 = (3.0 \pm 0.7) \times 10^{- 13} {\rm \,exp[- (512} \pm {\rm 78)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$k_2 = (8.3 \pm 3.5) \times 10^{- 13} {\rm \,exp[- (260} \pm 150{\rm)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$k_3 = (2.3 \pm 0.2) \times 10^{- 12} {\rm \,exp[- (131} \pm 28{\rm)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}$$\end{document} At 296 K, the measured rate constants (in units of 10-13 cm3 molecule-1 s-1) were: k1 = (0.52 ± 0.08), k2 = (3.41 ± 0.29), and k3 = (15.1 ± 1.4). Room temperature rate constants for the OH reactions with several other aliphatic esters were also measured. These were (in the above units): methylformate, (2.27 ± 0.34); ethylformate, (10.2 ± 1.4); n-propylformate, (23.8 ± 2.7); n-butylformate, (31.2 ± 3.3); n-propylacetate, (34.5 ± 3.4); i-propylacetate, (37.2 ± 2.9); n-butylacetate, (41.5 ± 3.0); s-butylacetate, (56.5 ± 5.9); methylpropionate, (10.3 ± 0.4); ethylpropionate, (21.4 ± 3.0); n-propylpropionate, (40.2 ± 3.2); methylbutyrate, (30.4 ± 3.3); ethylbutyrate, (49.4 ± 3.8); n-propylbutyrate, (74.1 ± 3.2), and n-butylbutyrate, (106 ± 13), error limits represent 2σ from linear least-squares analyses. The results are discussed in terms of the reaction mechanisms and are compared to previous literature data.
    Zusätzliches Material: 4 Ill.
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  • 234
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 273-281 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The kinetics of the gas-phase reactions of the OH radical with (C2H5O)3PO and (CH3O)2P(S)Cl and of the reactions of NO3 radicals and O3 with (CH3O)2P(S)Cl have been studied at room temperature. Using a relative rate technique, the rate constants determined for the reactions of the OH radical with (C2H5O)3PO and (CH3O)2P(S)Cl at 296 ± 2 K and 740 torr total pressure of air were (5.53 ± 0.35) × 10-11 and (5.96 ± 0.38) × 10-11 cm3 molecule-1 s-1, respectively. Upper limits to the rate constants for the NO3 radical and O3 reactions with (CH3O)2P(S)Cl of 〈3 × 10-14 cm3 molecule-1 s-1 and 〈2 × 10-19 cm3 molecule-1 s-1, respectively, were obtained. These data are compared and discussed with previous literature data for organophosphorus compounds.
    Zusätzliches Material: 2 Ill.
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  • 235
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 307-329 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: It is shown that the master equation describing fall-off effects in unimolecular and recombination reactions, with angular momentum (J) conservation taken into account, can be solved exactly if the assumption is made that the probability of collisional energy transfer in J is independent of initial state; this assumption is shown to be physically acceptable (from general conservation considerations and from trajectory calculations) for typical neutral radical recombination and decomposition reactions. This leads to a J-averaged master equation which can be readily solved by standard means. Illustrative computations using this treatment are presented.
    Zusätzliches Material: 3 Ill.
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  • 236
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 379-386 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The thermal isomerization of azulene was studied in shock waves over the range 1300-1900 K. Monitoring azulene and naphthalene light absorptions in the UV, a complete conversion azulene → naphthalene was observed. After correction for some falloff effects, a limiting high pressure rate constant kx = 1012.93 exp(-263 kJ mol-1/RT) s-1 was derived. Based on this kx, specific rate constants k(E) for photoexcitation experiments were constructed.
    Zusätzliches Material: 6 Ill.
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  • 237
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 238
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 455-466 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A new estimate is derived for the group additivity contribution ΔHƒ∘[O - (O)2] = 55 ± 6 kJ mol-1, based upon recent experimental data, which enables heats of formation and bond dissociation energies to be estimated for species ROnR and ROn¨(R = H, CH3, and CF3). Semi-empirical MNDO calculated heats of formation, for these species, provide independent support for the new thermochemical estimates. The results are also consistent with other theoretical and experimental evidence.
    Zusätzliches Material: 3 Tab.
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  • 239
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 494-494 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 240
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 513-539 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The kinetics of the atmospherically important gas-phase reactions of acenaphthene and acenaphthylene with OH and NO3 radicals, O3 and N2O5 have been investigated at 296 ± 2 K. In addition, rate constants have been determined for the reactions of OH and NO3 radicals with tetralin and styrene, and for the reactions of NO3 radicals and/or N2O5 with naphthalene, 1- and 2-methylnaphthalene, 2,3-dimethylnaphthalene, toluene, toluene-α,α,α-d3 and toluene-d8. The rate constants obtained (in cm3 molecule-1 s-1 units) at 296 ± 2 K were: for the reactions of O3; acenaphthene, 〈5 × 10-19 and acenaphthylene, ca. 5.5 × 10-16; for the OH radical reactions (determined using a relative rate method); acenaphthene, (1.03 ± 0.13) × 10-10; acenaphthylene, (1.10 ± 0.11) × 10-10; tetralin, (3.43 ± 0.06) × 10-11 and styrene, (5.87 ± 0.15) × 10-11; for the reactions of NO3 (also determined using a relative rate method); acenaphthene, (4.6 ± 2.6) × 10-13; acenaphthylene, (5.4 ± 0.8) × 10-12; tetralin, (8.6 ± 1.3) × 10-15; styrene, (1.51 ± 0.20) × 10-13; toluene, (7.8 ± 1.5) × 10-17; toluene-α,α,α-d3, (3.8 ± 0.9) × 10-17 and toluene-d8, (3.4 ± 1.9) × 10-17. The aromatic compounds which were observed to react with N2O5 and the rate constants derived were (in cm3 molecule-1 s-1 units): acenaphthene, 5.5 × 10-17; naphthalene, 1.1 × 10-17; 1-methylnaphthalene, 2.3 × 10-17; 2-methylnaphthalene, 3.6 × 10-17 and 2,3-dimethylnaphthalene, 5.3 × 10-17. These data for naphthylene and the alkylnaphthalenes are in good agreement with our previous absolute and relative N2O5 reaction rate constants, and show that the NO3 radical reactions with aromatic compounds proceed by overall H-atom abstraction from substituent-XH bonds (where X = C or O), or by NO3 radical addition to unsaturated substituent groups while the N2O5 reactions only occur for aromatic compounds containing two or more fused six-membered aromatic rings.
    Zusätzliches Material: 12 Ill.
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  • 241
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 549-563 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Changes in the magnitude of 〈ΔEdown〉, the average downward collisional energy transferred between a highly vibrationally excited reactant molecule and an inert bath gas, upon perdeuteration of the substrate are reported for tert-butyl bromide dilute in Ar, Kr, N2, and CO2. The technique of pressure-dependent very low-pressure pyrolysis (VLPP) was used to obtain the absolute values of 〈ΔEdown〉, which are for C4H9Br, 230 (Ar), 285 (Kr), 270 (N2), and 365 (CO2) while for C4D9Br, 200 (Ar), 250 (Kr), 220 (N2), and 335 (CO2), all in cm-1 at ca. 720 K. The estimated uncertainties in these values are ca. ± 10%. These observed 〈ΔEdown〉, values and trends found with results from this series of isotope studies, are compared with current theoretical models. Extrapolated high-pressure temperature-dependent rate coefficients (s-1) for the thermal decomposition of reactant are 1013.8±0.3 exp(-175 ± 8 kJ mol-1/RT) for C4H9Br and 1014.3±0.3 exp(-183 ± 8 kJ mol-1/RT) for C4D9Br. These results are in accord with other studies and the expected isotope effect.
    Zusätzliches Material: 6 Ill.
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  • 242
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 577-592 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Gas phase slow combustion of (chloro)benzene in O2/N2 mixtures, and induced by addends such as tert butylhydroperoxide, cyclohexane, or methanol, leads to (chloro)-phenol as the only important aromatic product. Using C6H6/C6D6 mixtures, formation of phenol/perdeuterophenol was studied between 520-1080 K. The temperature dependence of this product ratio was found to obey the Arrhenius expression for the intermolecular isotope effect log kH/kD = -0.14 ± 0.03 + (1240 ± 80)/2.303RT (R in cal/mol K). Essentially the same result was obtained for the intramolecular isotope effect, measuring the change in isomer distribution for the chlorophenols formed from p-deuterio-chlorobenzene versus those for chlorobenzene.These results are in accordance with H(D)-abstraction by ·OH, via a linear transition state, as the first and (relative) rate determining step. Whereas above 1000 K, at reduced pressure, the intramolecular isotope effect continues to prevail, C6H6/C6D6 do not show differences in rate of formation of C6H5OH/C6D5OH. Under these conditions, the only effective reaction of arene to phenol appears to be set in by addition of O(3P).
    Zusätzliches Material: 1 Ill.
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  • 243
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 661-665 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 244
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 687-697 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The kinetics of the reaction between nitric acid and formaldehyde have been studied by spectrophotometry. The reaction is autocatalytic. A two-step mechanism is proposed, which accounts for this behavior and describes the effect of reactant concentrations on the characteristics of the kinetic curves: the length of the induction period, ti, the maximum rate, rmax of nitrous acid production and the final product concentration, cf.
    Zusätzliches Material: 7 Ill.
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  • 245
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 719-729 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Ethylene at concentrations of 2.7 × 10-3 to 1.0 × 10-2 mol L-1 has been pyrolyzed at 900 K in a flow system. The products ethane and hydrogen have been analyzed by gas chromatography. The results are consistent with a mechanism in which these products are initially formed as follows: Reaction [1] occurs only 1 to 2% as often as the addition reaction, The latter reaction is close to equilibrium. Taking the rate constant, k4, and the equilibrium constant, K2, from the literature and making small adjustments for minor processes, k1 is found to be (9 ± 3) × 107 L mol-1 s-1. Here the uncertainty is intended to encompass errors in the present work and in the literature parameters.A secondary source of hydrogen was also observed. Its dependence on ethylene concentration was consistent with formation from an intermediate with six carbon atoms, such as cyclohexene.
    Zusätzliches Material: 3 Ill.
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  • 246
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 731-747 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The thermal decomposition of 1,2 butadiene has been studied behind reflected shock waves over the temperature and total pressure ranges of 1300-2000 K and 0.20-0.55 atm using mixtures of 3% and 4.3% 1,2 butadiene in Ne. The major products of the pyrolysis are C2H2, C4H2, C2H4, CH4 and C6H6. Toluene was observed as a minor product in a narrow temperature range of 1500-1700 K. In order to model successfully the product profiles which were obtained by time-of-flight mass spectrometry, it was necessary to include the isomerization reaction of 1,2 to 1,3 butadiene. A reaction mechanism consisting of 74 reaction steps and 28 species was formulated to model the time and temperature dependence of major products obtained during the course of decomposition. The importance of C3H3 in the formation of benzene is demonstrated.
    Zusätzliches Material: 9 Ill.
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  • 247
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 775-786 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In order to bring more information on the thermodynamic and kinetic behavior of nitryl chloride in aprotic media, we have surveyed exhaustively the first NO2Cl-reduction step in sulfolane (at the platinum electrode), taking into account our preliminary results about the electrochemical properties of NO2Cl in aprotic solvents. We have excluded the intervention of the weak ionic dissociation of NO2Cl (NO2Cl ⇆ NO2+ + Cl- [I]) and its slow molecular decomposition as: 2NO2Cl ⇄ Cl2 + 2NO2• (⇄ N2O4) [II] in this process. We have admitted the occurrence of a rapid chemical reaction which controls kinetically the electrochemical system studied: \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm NO} + {\rm NO}_{\rm 2} {\rm Cl}\buildrel {k^*} \over \longrightarrow {\rm NOCl} + {\rm NO}_{\rm 2}^ \cdot {\rm}[{\rm III]} $\end{document}. By analyzing the kinetic currents resulting from the 1 st cathodic wave of NO2Cl at the temperature range 303-323 K, the rate constant, k*, and the activation energy, E*, of reaction [III] have been determined. These results and those previously found in the gas phase are discussed.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 248
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The third order rate coefficients for the addition reaction of Cl with NO2, Cl + NO2 + M → ClNO2 (ClONO) + M; k1, were measured to be k1(He) = (7.5 ± 1.1) × 10-31 cm6 molecule-2 s-1 and k1(N2) = (16.6 ± 3.0) × 10-31 cm6 molecule-2 s-1 at 298 K using the flash photolysis-resonance fluorescence method. The pressure range of the study was 15 to 500 torr He and 19 to 200 torr N2. The temperature dependence of the third order rate coefficients were also measured between 240 and 350 K. The 298 K results are compared with those from previous low pressure studies.
    Zusätzliches Material: 1 Tab.
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  • 249
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 250
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 195-215 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A general numerical method and program for simulation of the kinetics of multistep reactions is described, with details for collation of data, construction of a mechanistic model, and simulation of reciprocal relaxation times and calculation of individual rate constants. The working scheme of the program includes an initial approximate simulation by adjustment of the rate constants followed by their optimization with a Powell minimization subroutine. The procedure is applied to aromatic nucleophilic addition.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 251
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 241-265 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The kinetics and products of the homogeneous gas-phase reactions of the OH radical with the chloroethenes were investigated at 298 ± 2 K and atmospheric pressure. Using a relative rate technique and ethane as a scavenger for the chlorine atoms produced in these OH radical reactions, rate constants (in units of 10-12 cm3 molecule-1s-1) of 8.11 ± 0.24, 2.38 ± 0.14, and 1.80 ± 0.03 were obtained for 1,1-dichloroethene, cis-1, 2-dichloroethene and trans-1,2-dichloroethene, respectively. Under these conditions, the major products observed by long pathlength FT-IR absorption spectroscopy were HCHO and HC(O)Cl from vinyl chloride; HC(O)Cl from cis- and trans-1,2-dichloroethene; HCHO and COCl2 from 1,1-dichloroethene; HC(O)Cl and COCl2 from trichloroethene; and COCl2 from tetrachloroethene. In the absence of a Cl atom scavenger, significant yields of the chloroacetyl chlorides, CHxCl3-xC(O)Cl, were observed from 1,1-dichloro-, trichloro- and tetrachloroethene, indicating that these products resulted from reactions involving chlorine atoms. The yields of all of these products are reported and the mechanisms of these gas-phase reactions discussed. In addition, OH radical reaction rate constants were redetermined, in the presence of a Cl atom scavenger, for cis- and trans-1,3-dichloropropene and 3-chloro-2-chloromethyl-1-propene, being (in units of 10-12 cm3 molecule-1 s-1) 8.45 ± 0.41, 14.4 ± 0.8, and 33.5 ± 3.0, respectively.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 252
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 339-342 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 253
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 365-378 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The hexacyanoferrate(III)-thallium(I) reaction in aqueous acetic acid containing large concentrations of hydrochloric acid is considerably accelerated both by hydrogen and chloride ions as well as increasing acetic acid in the medium. The experimental results obey the rate law (1) where β1 to β6 \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{rcl} {{\rm (1)}} & {- \frac{{{\rm d[Fe(CN)}_{\rm 6} ^{{\rm 3 -}}]}}{{dt}} = \frac{{\{\beta _4 k_a [{\rm H}^ +] + \beta _5 k_b [{\rm H}^ +]^2 \} \beta _2 [{\rm Cl}^ -]^2 [{\rm Fe(CN)}_{\rm 6} ^{{\rm 3 -}}]_T [Tl^ +]_T}}{{\{1 + \beta _4 [{\rm H}^ +] + \beta _5 [{\rm H}^ +]^2 + \beta _6 [{\rm H}^ +]^3 \} \{1 + \beta _1 [{\rm Cl}^ -] + \beta _2 [{\rm Cl}^ -]^2 + \beta _2 [{\rm Cl}^ -]^3 \}}}}\end{array}$$\end{document} are the cumulative stability constants of the species TlCl, TlCl2-, TlCl32-, HFe(CN)62-, H2Fe(CN)6- and H3Fe(CN)6 respectively and ka and kb are the rate constants associated with the mono- and di-protonated oxidant species. The main active species are H2Fe(CN)6- and TlCl2-.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 254
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 541-547 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Absolute rate constants were determined at 298 K for the gas phase reactions of hydroxyl radicals with several C5 through C7 aliphatic alcohols and ethers using the flash photolysis resonance fluorescence technique. The values obtained (in units of 10-12 cm3 molecule-1 s-1) were: 3-methyl-2-butanol, (12.4 ± 0.7); 2-pentanol, (11.8 ± 0.8); 3-pentanol, (12.2 ± 0.7); cyclopentanol, (10.7 ± 0.7); 1-hexanol, (12.4 ± 0.7); 2-hexanol, (12.1 ± 0.7); 1-heptanol, (13.6 ± 1.3); methyl-n-butylether, (16.4 ± 0.6); ethyl-n-butylether, (22.8 ± 0.9); ethyl-t-butylether, (8.12 ± 0.32); and methyl-t-amylether, (7.91 ± 0.42). These results are discussed in terms of group reactivities in such molecules and are compared with values estimated from an additive structure-reactivity index.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 255
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 256
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 621-632 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: H2S accelerates the thermal isomerization of cis-2-pentene (P2c) to 1-pentene (P1) and trans-2-pentene (P2t) to around 800 K. This effect is interpreted on the basis of a free radical mechanism in which 2-pentenyl and thiyl radicals are the main chain carriers. P1 formation is essentially explained by the competing processes: P2t formation is due to addition-elimination processes: the importance of which has been evaluated against process (-4μ): The following ratios of rate constants have been measured and are discussed: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{rcl} k_{10} /k_2 &\approx& 10^{- 3.19\, \pm \,2.3}\,{\rm \,exp(31,200}\, \pm \,{\rm 800/}RT)\,{\rm \,mol}^{{\rm - 1}}\,{\rm \,cm}^{\rm 3}\\ k_{11} /k_{- 4\mu} &\approx& 10^{.89\, \pm \,.49}\,{\rm \,exp(2100}\, \pm \,17{\rm 00/}RT) \end{array} $$\end{document}(RT in cal mol-1).
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 257
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 645-659 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Since thymine dimerization is the main photochemical lesion occuring in uv irradiated DNA, an understanding of the mechanism of dimerization is biologically significant. Both photosensitized and direct dimerization are important in DNA, but because photosensitized thymine dimerization has been less thoroughly investigated, this has been the major topic of study in this laboratory. By comparing experimental results with those obtained by computer simulation, attempts have been made to deduce mechanisms for photosensitization by acetone, acetophenone, and benzophenone.Photolysis of photosensitized solutions was performed using a xenon lamp and quantitative detection of dimer was achieved using h.p.l.c. techniques. A program designed to solve differential rate equations was used for the computer simulation of reaction mechanisms.Based on the results obtained it has been confirmed that acetone photosensitization over the entire range of thymine concentration considered (10-4 mol dm-3 to 10-2 mol dm-3) proceeds via diffusion controlled triplet transfer from the photosensitizer to thymine, followed by bimolecular collision of ground and excited state thymine monomers. For acetophenone and benzophenone photosensitization this method applied at low thymine concentrations, but at higher concentrations (〈10-3 mol dm-3) predicted far lower yields than those observed experimentally. The effect of thymine base stacking was then considered, but it was found that this did not significantly increase the dimer yield. A mechanism involving association of thymine and photosensitizer molecules was therefore proposed. This mechanism was found to give reasonably good agreement between experimental and computed data. On the basis of present data the authors regard this as the most likely mechanism for thymine dimerization and work is in progress to confirm this proposal.
    Zusätzliches Material: 8 Ill.
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  • 258
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 713-718 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A kinetic analysis of the thermal decomposition of methylamino and aminomethyl radicals into methyleneimine, reactions (1) and (2): leads to ΔHf0(CH2=NH) = 25.0 ± 3 kcal/mol in excellent agreement with ion cyclotron resonance spectroscopy measurements and to a pi bond energy of Eπ = 55.0 kcal/mol in CH2=NH which is comparable but smaller than to the corresponding value in CH2=CH2 (63.7 kcal/mol). Assuming that Eπ(CH2=NH) = 0.5 [Eπ(CH2=CH2) + Eπ(NH=NH)] then requires that Eπ(NH=NH) = 46.8 kcal/mol in diimine and BDE(N2H3-H) = 87.5 kcal/mol i.e. about 11.5 kcal/mol larger than current data for hydrazine but otherwise consistent with additional evidence.The entropy and heat capacity of methyleneimine, calculated from recent infrared and microwave spectroscopic data using the rigid rotor harmonic oscillator approximation, are also reported.
    Zusätzliches Material: 1 Tab.
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  • 259
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 759-773 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The kinetics of the reaction between CH3 and HCl was studied in a tubular reactor coupled to a photoionization mass spectrometer. Rate constants were measured as a function of temperature (296-495 K) and were fitted to an Arrhenius expression: k1 = 5.0(±0.7) × 10-13 exp{-1.4(±0.3) kcal mol-1/RT} cm3 molecule-1 s-1. This information was combined with known kinetic parameters of the reverse reaction to obtain Second Law determinations of the methyl radical heat of formation {34.7(±0.6) kcal mol-1} and entropy {46(±2) cal mol-1 K-1} at 298 K. Using the known entropy of CH3, a more accurate Third Law determination of the CH3 heat of formation at this temperature was also obtained {34.8(±0.3) kcal mol-1}. The values of k1 obtained in this study are between those reported in prior investigations. The results were also used to test the accuracy of the thermochemical information which can be obtained from kinetic studies of R + HX (X = Cl, Br, I) reactions of the type described here.
    Zusätzliches Material: 3 Ill.
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  • 260
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 787-809 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Rate constants for the unimolecular dissociation of 1,3-butadiene have been measured with the pulsed laser flash absorption technique, following butadiene disappearance at 222 nm. The results are in excellent agreement with previous laser-schlieren measurements interpreted with a ΔH°298 = 100 kcal/mol heat of dissociation. A new RRKM calculation agreeing with both sets of rate constants gives log k∞(s-1) = 17.03 ± 0.3 - 94(kcal/mol)/RT. These data and product measurements using ARAS, single-pulse product analysis, and time-of-flight mass spectrometry, in shock tubes, all provide independent evidence against any major participation by molecular reactions in the dissociation. The only dissociation channel, or combination of channels, consistent with all the measurements is C-C scission to two vinyl radicals. However, the extremely slow rate of H-atom formation seen in ARAS experiments then requires an unacceptably low rate of vinyl dissociation.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
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  • 261
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 979-990 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A recently developed solution of the master equation for unimolecular and recombination reactions is extended to give new means for incorporating angular momentum (J) conservation in the fall-off regime for multichannel reactions. The calculated pressure dependence of a typical multichannel unimolecular dissociation reaction (thermal dissociation of 1-iodopropane) shows that if one of the channels has a transition state with a moment of inertia (I†) significantly different from that of the parent molecule (I) (e.g., a “simple-fission” type), neglect of angular momentum conservation causes the predicted branching ratio to be grossly in error at lower pressures. Specifically, if I† 〉 I the rate coefficient is underestimated whereas if I† 〈 I the rate coefficient is overestimated.
    Zusätzliches Material: 2 Ill.
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  • 262
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 263
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The first-order rate constants, k1, for 1,2-ethanediolysis (within the content of 1,2-ethanediol of 5% to 90%, v/v) and 2-ethoxyethanolysis (within the 2-ethoxyethanol content of 5% to 60%, v/v) of phenyl salicylate, PSH, in alkaline aqueous mixed solvents, fit to a relationship: k1 = k[ROH]T/(1 + K[ROH]T) where k and K represent the secondorder rate constant for the reaction of alkanol, ROH, with ionized phenyl salicylate, PS-, and association constant for the dimerization of ROH, respectively, and [ROH]T is the total concentration of ROH. Similar relationship between k1 and [ROH]T has been found for 1,2-ethanediolysis of PS- studied in mixed solvents containing 1,2-ethanediol and MeCN. In the alkaline aqueous mixed solvents containing 2-ethoxyethanol, the k1-[ROH]T profile reveals the change in the solvent structure of the reaction medium at 〉60% (v/v) of ROH content. It is proposed that alkanols exist in polymeric form, (ROH)n, and the alkanolysis of PS- involves the pre-equilibrium formation of monomeric ROH from (ROH)n, followed by an intramolecular general base-catalyzed nucleophilic attack at carbonyl carbon of ester. A slight negative KCl salt- and slight positive n-Bu4NI salt-effect are obtained for 1,2-ethanediolysis while a significant positive n-Bu4NI salt-effect is obtained for 2-ethoxyethanolysis of PS-.
    Zusätzliches Material: 3 Ill.
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  • 264
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 265
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 603-608 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Pyrazole elimination and vinyl bromide were found as products in the Flash Vacuum Pyrolysis of (β-Bromo ethyl)-pyrazole. To obtain kinetic parameters (Ea) we carried out competitive reactions using (β-chloro ethyl)-pyrazole as an internal standard. A thermochemical study to calculate Δ(ΔHƒ∘) for this reaction was carried out.
    Zusätzliches Material: 3 Tab.
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  • 266
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 633-643 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Highly excited 2-butyl radicals have been generated by addition of hot hydrogen atoms to but-2-ene. Atoms of initial energy 130 kJ mol-1 and 161 kJ mol-1 were produced by photolysis of H2S. Rates of decomposition of the highly excited 2-butyl radicals were monitored by analysis of stabilization and decomposition products, and the extent of energy-loss of the hydrogen atoms in nonreactive collisions assessed by measuring the effect of added xenon on product yields. A model involving the cross-section for the addition reaction, energy transfer in nonreactive collisions between hydrogen atoms and but-2-ene, RRKM rate constants for decomposition of excited 2-butyl radicals, and collisional energy transfer from the radicals, has been used to calculate product yields for comparison with experimental values. It is concluded that the cross-section for addition of hydrogen atoms of energy about 130 kJ mol-1 to but-2-ene is 0.055 ± 0.028 nm2. This value is compatible with the A factor for the thermal addition reaction.
    Zusätzliches Material: 4 Ill.
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  • 267
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 26-26 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 268
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 51-62 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Acuchem is a program for solving the system of differential equations describing the temporal behavior of spatially homogeneous, isothermal, multicomponent chemical reaction systems. It is designed to provide modelers, data evaluators, and laboratory scientists with an easy to use program for modeling complex chemical reactions, and for presenting the results in tabular or graphical form. The program is described and some examples of its application given. Acuchem is designed to operate on the IBM Personal Computer family and other compatible microcomputers, and is available in a compiled version on a floppy disk.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 269
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 75-92 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: N2(A3Σu+), the lowest electronically excited state of N2, has a long and distinguished history due to its role in nitrogen discharges and the nitrogen afterglow. Recently, the production of N2(A) via photolysis and chemiluminescent reactions has been newly explored, and new facets of its reactivity have been uncovered. N2(A) is unusual, in that its deactivation probability in collision with small molecules spans many orders of magnitude, and is frequently strongly dependent on the vibrational content of N2(A). This behavior and the observed product channels can be understood in terms of a simple model for the energy transfer process. Brief comparison with reactions of related species is made.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 270
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 117-129 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Absolute rate constants are measured for the reactions: OH + CH2O, over the temperature range 296-576 K and for OH + 1,3,5-trioxane over the range 292-597 K. The technique employed is laser photolysis of H2O2 or HNO3 to produce OH, and laser-induced fluorescence to directly monitor the relative OH concentration. The results fit the following Arrhenius equations: k (CH2O) = (1.66 ± 0.20) × 10-11 exp[-(170 ± 80)/RT] cm3 s-1 and k(1,3,5-trioxane) = (1.36 ± 0.20) × 10-11 exp[-(460 ± 100)/RT] cm3 s-1. The transition-state theory is employed to model the OH + CH2O reaction and extrapolate into the combustion regime. The calculated result covering 300 to 2500 K can be represented by the equation: k(CH2O) = 1.2 × 10-18 T2.46 exp(970/RT) cm3 s-1. An estimate of 91 ± 2 kcal/mol is obtained for the first C—H bond in 1,3,5-trioxane by using a correlation of C—H bond strength with measured activation energies.
    Zusätzliches Material: 4 Ill.
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  • 271
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 272
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 1-8 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The pyrolysis of methyl 4-bromocrotonate in the temperature range 300-340°C and pressure range 74-170 torr has been shown to be homogeneous, unimolecular, and to follow a first-order rate law. The reaction was carried out in a static system, seasoned with allyl bromide, and in the presence of the radical chain exhibitor toluene. The rate coefficients are represented by the Arrhenius expression: log k1(s-1) = (13.30 ± 0.66) - (185.2 ± 7.5) kJ mol-1 (2.303RT)-1. The carbomethoxy group appears to provide anchimeric assistance in the process of dehydrobromination and lactone products formation. The partial rates for the parallel reaction have been estimated, reported, and discussed. The pyrolysis elimination is explained in terms of an intimate ion pair-type of mechanism.
    Zusätzliches Material: 10 Tab.
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  • 273
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 467-491 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 274
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 493-493 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 275
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 849-855 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The Taylor dispersion technique has been used to measure the diffusion coefficients of nine compounds in dilute solution in isopropanol at 300 K. These compounds correspond, by the difference of a single hydrogen atom, to nine free radicals, for which the rate constants for bimolecular (termination) reactions have been previously measured under the same conditions by e.s.r. Comparison of the two sets of results show the termination reactions to be essentially diffusion-controlled, and, assuming no activation-energy effect, interaction parameters for the termination reactions are calculated and discussed.
    Zusätzliches Material: 1 Ill.
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  • 276
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 815-826 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The ultraviolet absorption spectra of chloromethylperoxy and fluoromethylperoxy radicals, CH2ClO2 and CH2FO2, and the kinetics of their respective self reactions have been studied in the gas phase using a flash photolysis technique. The absorption spectra for both radicals were quantified over the wavelength range 210 and 290 nm. The measured absorption cross-sections \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} \sigma _{{\rm CH}_{\rm 2} {\rm ClO}_{\rm 2}} (250{\rm nm)} = (3.14 \pm 0.45) \times 10^{- 18} {\rm cm}^{\rm 2} {\rm molecule}^{- 1} \\ \sigma _{{\rm CH}_{\rm 2} {\rm FO}_{\rm 2}} (240{\rm nm)} = (3.72 \pm 0.45) \times 10^{- 18} {\rm cm}^{\rm 2} {\rm molecule}^{- 1} \\ \end{array} $$\end{document} were used to derive the observed self-reaction rate constants (for reactions 1 and 2) over the temperature range 228-380 K, defined as -d[CH2XO2]/dt = 2k[CH2XO2]2, where X represents Cl or F. The rate constants at 298 K were found to be independent of pressure over the range 25-400 torr N2 with values of k1(298 K) = (3.78 ± 0.45) × 10-12 and k2(298 K) = (3.07 ± 0.65) × 10-12 in units of cm3 molecule-1 s-1. The kinetic data over the complete temperature range are represented by the Arrhenius expressions: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} k_1 = (3.1 \pm 1.1) \times 10^{- 13} \exp [(735 \pm 95)/{\rm T] cm}^{\rm 3} {\rm molecule}^{- 1} {\rm s}^{- 1} \\ k_2 = (3.3 \pm 1.2) \times 10^{- 13} \exp [(700 \pm 100)/{\rm T] cm}^{\rm 3} {\rm molecule}^{- 1} {\rm s}^{- 1} \\\end{array} $$\end{document} where the error limits represent 2σ from linear least squares analysis. These results are discussed with respect to previous measurements of the absorption spectra and reactions of alkylperoxy radicals.
    Zusätzliches Material: 4 Ill.
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  • 277
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The Modified Simplex Method (MSM) coupled with contour diagrams is used to determine the rate constants of a kinetic scheme involving three sequential second order processes.Reaction between glutathione and the dithiocarbamate fungicide tetramethylthiuram disulfide produces the oxidized form of glutathione which is then reduced in the presence of NADPH. The concentration of the reducing agent is monitored as a function of time. In the absence of simplifying assumption a closed form solution of the rate equations does not exist. Computed curves of NADPH concentration versus time were generated using the software SIMULCIN.The rate constant values are optimized by the MSM procedure to obtain the best agreement between calculated and experimental data. The significance, validity limits of the estimated rate constants and the relevance of these in vitro data to previous in vivo studies are discussed.
    Zusätzliches Material: 9 Ill.
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  • 278
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 857-866 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The rate of reaction between NO and HNO3 and the rate of thermal decomposition of HNO3 have been measured by FTIR spectroscopy. The measurements were made in a teflon lined batch reactor having a surface to volume ratio of 14 m-1. During the experiments, with initial HNO3 concentrations between 2 and 12 ppm and NO concentrations between 2 and 30 ppm, a reactant stoichiometry of unity and a first order NO and HNO3 dependence were confirmed. The observed rate constant for the reaction \documentclass{article}\pagestyle{empty}\begin{document}$${\rm HNO}_{\rm 3} + {\rm NO} \longrightarrow {\rm HNO}_{\rm 2} + {\rm NO}_2$$\end{document} at 22°C and atmospheric pressure was determined to 1.1 (±0.3) 10-5 ppm-1 min-1. At atmospheric pressure, HNO3 decomposes into NO2 and other products with a first order HNO3 dependence and with a rate constant of 2.0 (±0.2) 10-3 min-1. The apparent activation energy for the decomposition is 13 (±4) kJ mol-1.
    Zusätzliches Material: 2 Ill.
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  • 279
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 885-895 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The 147 nm photolysis of 3,3 dimethylbut-1-ene leads mainly to the formation of very hot (≅375 kJ/mol) α,α-dimethallyl radicals. On the other hand, that of 3-methyl-cis-and trans-pentene-2, as well as that of 2,3-dimethylbut-1-ene is a source of very hot α,β-dimethallyl radicals. These allylic radicals are coolled down using pressure and are allowed to combine with available methyl radicals. From the formation of various C6H12 products, it is concluded that the very hot α,α- radical isomerizes towards the α,β-structure at low pressures and vice versa. The equilibrium constant of the following process has been evaluated to be 1.72 ± 0.30. \documentclass{article}\pagestyle{empty}\begin{document}$${\rm CH}_3{\rm C}({\rm CH}_3){\rm CHCH}_2 ^ * \Leftrightarrow {\rm CH}_2 {\rm C}({\rm CH}_{\rm 3}){\rm CHCH}_3 ^ *$$\end{document}
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 280
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Dibenzoylmesitylene undergoes protiodeacylation in 89.8% (w/w) sulfuric acid at ca. 90°C, with subsequent sulfonation, to give mesitylenedisulfonic acid. The reaction involves a single-path sequence of four first-order reactions. The corresponding reaction of acetylbenzoylmesitylene can proceed by two possible routes: it is shown that about 94% of the overall reaction at 75° involves initial protiodeacetylation and about 6% initial protiodebenzoylation. The kinetic analyses provide estimates of concentration ratios as functions of time, and of the buildup and decay of intermediates in the reactions.
    Zusätzliches Material: 3 Tab.
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  • 281
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 153-164 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Highly dilute mixtures of 1,3-butadiene and 1,3-butadiene-1,1,4,4-d4 were pyrolyzed behind reflected and incident shock waves, respectively. Concentrations of H and D atoms were measured by resonance absorption spectroscopy. In the early stages of the reaction, nearly equal amounts of H and D were formed from CD2CHCHCD2, indicating that loss of H from C2 followed by loss of D from C1 is a more important reaction than breaking of the central C—C bond. Overall, rate constants for atom-forming reactions are much slower than rate constants for disappearance of butadiene in earlier experiments, suggesting that most of the butadiene disappears by processes that do not involve H or D atoms or by radicals that produce them rapidly.
    Zusätzliches Material: 2 Ill.
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  • 282
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 187-190 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The present study was undertaken to quantitatively measure the concentration of ions produced by a microwave discharge source commonly used in the production of atomic species. Using a double floating probe to monitor the ion content, the results indicate that the flow of ions was less than 1.8 × 10-6 times the total flow of particles from the discharge cavity. Due to the low ion mole fraction, it is concluded that ion-molecule reactions are not competitive with previousry reported atom-molecule reactions.
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  • 283
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 284
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 283-295 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The rate constant for the HO2 self reaction has been determined as a function of methanol vapor concentration at 278 K and 299 K. A molecular modulation technique was used in which HO2 radicals were photochemically produced in flowing gas mixtures comprised of Cl2, CH3OH, N2 and O2 with HO2 monitored in the UV at 220 nm. A positive linear dependence of the second order rate constant on methanol concentration was found and this effect increased with decreasing temperature. The rate constant for the HO2 self reaction can be described by \documentclass{article}\pagestyle{empty}\begin{document}$$k = 9.2 \cdot 10^{- 15} {\rm \,exp(1700/}T)\,+ \,2.1 \cdot 10^{- 34} {\rm \,exp(3000/}T)[{\rm CH}_{\rm 3} {\rm OH]cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}} {\rm \,s}^{{\rm - 1}}$$\end{document} in nitrogen at atmospheric pressure and in the methanol concentration range 1 · 1016 to 3 · 1017 molecules cm-3.
    Zusätzliches Material: 3 Ill.
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  • 285
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 286
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 349-363 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The photolysis of 2-methylcyclohexanone has been studied in the gas phase at 313 nm, mainly at 100°C, over a range of pressures. The Hg(63P1) photosensitized decomposition has also been investigated at 100°C. Under conditions of high excitation and/or little collisional quenching the major products are carbon monoxide and the hydrocarbons: 1-hexene, trans-and cis-2-hexene and methylcyclopentane, with minor aldehyde formation. The various product ratios are presented in tabular form. At lower excitation energies, and with increased collisional deactivation, trans- and cis-5-heptenal become important products, and the trans/cis aldehyde ratio is seen to be slightly pressure dependent when all the systems are compared. Similarly, there is a small pressure dependence for the Σ hexenes/methylcyclopentane ratio. From experiments at 250°C the temperature dependence of this ratio was established, and for thermalized hexane-1,5-diyl an activation energy difference (Ed - Ec) = -1.3 kcal mol-1 has been determined for the disproportionation and combination of the biradical. The mechanism for the photolysis is discussed in terms of triplet state photochemistry and biradical intermediates as developed, in particular, by Frey and coworkers, this Journal, 16, 1337 (1984).
    Zusätzliches Material: 3 Tab.
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  • 287
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 433-441 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: At 298 K the rate constant for the decomposition of N-chloroleucine has the constant value 3.20 × 10-4 s-1 over the range pH 5-12, increases with increasing acidity at pH 〈 5, and increases with pH at pH 〉 12. A mechanism is put forward which explains these results.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 288
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 165-175 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Pyrolysis of a dilute mixture of neopentane (2,2-dimethylpropane) has been studied behind incident shock waves at an average pressure of 0.35 atm; the reaction was followed by absorption spectroscopy for H atoms. In the temperature range 1230-1455 K, the rate constant for dissociation of neopentane to t-butyl and methyl radicals is 1.1 E 13 exp(-62 kcal/RT) s-1. These data and some of the literature results, between 1000 and 1450 K, can be fitted by an RRKM model of the hindered Gorin type, with five active internal rotors in the complex. To match our data with other literature data down to 800 K, a vibrational model was more satisfactory, but this did not fit very low pressure pyrolysis data in the 1000-1100 K range. Apparently, the VLPP data are too high because of heterogeneous processes or chain reactions.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 289
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Elementary bimolecular processes that involve formation of a chemically activated intermediate species are common. We address the general problem of modeling these processes and describe the necessary and sufficient information that must be specified to assure that a kinetics model will extrapolate the rate constants for those reactions over wide ranges of temperature and pressure. The approach is illustrated for the system centered around the HOCO intermediate. Here, specification of the temperature and pressure dependence of three rate constants, k(T,P) and the temperature dependence of two equilibrium constants, K(T), is necessary and sufficient, viz: Rate constants are cast in the form of an analytical expression, suggested by Troe, and appropriate parameters are tabulated.
    Zusätzliches Material: 4 Ill.
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  • 290
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988) 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 291
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 103-110 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The temperature dependence of the rate of the reaction of OH with 2-(dimethylamino)-ethanol, (CH3)2NCH2CH2OH (DMAE) was investigated over the temperature range, 234 to 364 K. The reaction was studied using the flash photolysis-resonance fluorescence technique. The room temperature rate constant determined for this reaction was (10.3 ± 2.0) × 10-11 cm3 molecule-1 s-1, with essentially no temperature dependence evident within the uncertainty in the experiments. A value of (9.0 ± 2.0) × 10-11 cm3 molecule-1 s-1 is believed to best describe the reaction over the entire temperature range. The room temperature rate constant is about twice the value reported previously for this reaction. The overall reaction of OH with DMAE was apportioned to the reactivity of OH for abstracting individual H- atoms from different types of C—H bonds and the O—H bond within the molecule. This technique predicts the overall rate constant for the OH-DMAE reaction to within about 15% of the experimental value and makes it possible to estimate the yields of the initial radical products of the OH attack on DMAE. A mechanism is proposed for the subsequent atmospheric reactions that would occur in the photooxidation of DMAE.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 292
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 145-151 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The rates of elimination of seven cycloalkyl acetates containing between 5 and 15 ring carbons have been determined in a static system over a temperature range 280-370°C and a pressure range 35-234 torr. The unimolecular reactions, carried out in the presence of the inhibitor cyclohexene, are homogeneous in seasoned vessels and follow a first-order rate law. The rate coefficients are exemplified by that found for cyclopentyl acetate: \documentclass{article}\pagestyle{empty}\begin{document}$$\log {\rm}k_1 ({\rm s}^{{\rm - 1}}) = (12.68 \pm 0.14) - (179.8 \pm 1.5){\rm \,kJ\,mol}^{{\rm - 1}} {\rm (2}{\rm .303}RT)^{- 1}$$\end{document} The sequence of relative rates is analogous to that found in most solution reactions of these compounds. The contribution of ring strain to energy barriers of these compounds is described.
    Zusätzliches Material: 1 Ill.
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  • 293
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 217-222 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Flash vacuum pyrolysis of (β-chloro ethyl)-pyrazole was studied. Pyrazole elimination and vinyl chloride formation were found. Competitive reactions with (β-chloro ethyl)-pyrazole were carried out using N-ethyl-3,5-dimethyl pyrazole as internal standard to obtain the kinetic parameters (Ea). Δ(ΔHƒ∘) for this reaction was calculated.
    Zusätzliches Material: 4 Tab.
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  • 294
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 387-395 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Rate constants for the reactions of oxirane with alkanethiols in the presence of basic catalyst were studied at the temperature range of 20-50°C. A mechanism of these reactions has been proposed and appropriate kinetic equation has been presented.
    Zusätzliches Material: 3 Ill.
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  • 295
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 415-431 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The rate constant of the reaction of OH with DMS has been measured relative to OH + ethene in a 420 l reaction chamber at 760 torr total pressure and 298 ± 3 K in N2 + O2 buffer gas using the 254 nm photolysis of H2O2 as the OH source. In agreement with a recent absolute rate determination of the reaction the measured effective rate constant was found to increase with increasing partial pressure of O2 in the system, for 760 torr air a rate constant of (8.0 ± 0.5) × 10-12 cm3 s-1 was obtained.Product studies have been performed on the reaction in air using FTIR absorption spectrometry for detection of reactants and products. On a molar basis, SO2 was formed with a yield of 70% and dimethyl sulfone (CH3SO2CH3) with a yield of approximately 20%. These results are considerably different to those obtained in other product studies which were carried out in the presence of NOx. These differences are compared and their relevance for the atmospheric oxidation mechanisms of DMS is discussed.
    Zusätzliches Material: 5 Ill.
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  • 296
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 501-511 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Kinetics of oxidation of ethylene glycol and glycerol by acidic solution of N-bromoacetamide (NBA) in the presence of ruthenium (III) chloride as a homogeneous catalyst and mercuric acetate as scavenger in the temperature range of 30-50°C have been reported. The reactions follow identical kinetics, being zero-order in substrate and first-order in Ru(III). First order dependence of the reaction on NBA at its low concentrations tends to zero order in the higher concentration range. Positive effect of [H-] and [Cl-] has been observed. A negative effect of acetamide and ionic strength of the medium is observed while D2O and mercuric acetate show zero effect on the reaction velocity. Various activation parameters have been computed. The main product of the oxidation is corresponding acid. (H2OBr)+ has been postulated as the oxidizing species. A suitable mechanism in conformity with the kinetic data has been proposed.
    Zusätzliches Material: 3 Ill.
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  • 297
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    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 565-575 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The gas phase kinetics of the bromine catalyzed elimination of HCl from 1,1,1-trichloroethane has been studied over a five fold variation of (CH3CCl3)/(Br2) and from 565 to 634 K. The most important reactions in the mechanism are found to be: The preferred analysis of the kinetic data results in log(k1/M-1 s-1) = 11.3 ± 0.3 - (19.9 ± 1.0) × 103/4.575 T. From these results one calculates the C - H bond dissociation energy in CH3CCl3 to be 103.8 ± 2 kcal mol-1, and the heat of formation of 2,2,2-trichloroethyl to be 17.7 ± 2 kcal mol-1.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 298
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 877-884 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reactions of poly(4-vinylbiphenyl) (denoted as PVB) polymers and biphenyl molecules with solvated electrons in the 2-methyltetrahydrofuran (MTHF) solvent have been studied at 100-120 K by electron-pulse radiolysis. The formation of PVB polymer anions as well as biphenyl anions was observed by the electron-pulse irradiation of the MTHF-PVB(or biphenyl) solution. The anions are formed by two processes; a rapid formation during the pulse irradiation (〈20 ns) and a slow formation after the pulse irradiation. The slow formation is due to a diffusion-controlled reaction between solutes, such as PVB and biphenyl, and solvated electrons. It was found that the reaction efficiency, expressed in monomer unit, of PVB polymers is 1/27 of that of biphenyl molecules. The reaction radius for the electron capture reaction of PVB polymers is estimated as 200-370 A, which is much larger than the gyration radius (107 A) of polymer coils in MTHF solution.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 299
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 9-25 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Vinylacetylene and 2-butyne mixtures were pyrolyzed at 350-450°C in the absence and presence of O2 and NO. The major product of the reaction is a polymer, but o-xylene is also produced and was studied as the species of interest. The C8H10 formation rate is first-order in C4H4 and C4H6. The rate coefficient is best fitted by \documentclass{article}\pagestyle{empty}\begin{document}$$\log {\rm [}k{\rm (C}_{\rm 8} {\rm H}_{{\rm 10}}),{\rm M}^{{\rm -1}}\, {\rm s}^{{\rm - 1}}] = (4.33 \pm 0.58) - (80.1 \pm 7.4)/2.3RT$$\end{document} though it is not inconsistent with \documentclass{article}\pagestyle{empty}\begin{document}$$\log {\rm [}k{\rm (C}_{\rm 8} {\rm H}_{{\rm 10}}),{\rm M}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}] = (7.93) - (125.9)/2.3RT$$\end{document} where R is the ideal gas constant in kJ/mol-K. O-xylene formation occurs by two processes: a concerted molecular mechanism (⋍67%) and a singlet diradical mechanism (⋍33%).
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 300
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 41-49 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Absolute rate constants were determined for the gas phase reactions of OH radicals with a series of linear aliphatic ethers using the flash photolysis resonance fluorescence technique. Experiments were performed over the temperature range 240-440 K at total pressures (using Ar diluent gas) between 25-50 Torr. The kinetic data for dimethylether (k1), diethylether (k2), and dipropylether (k3) were used to derive the Arrhenius expressions \documentclass{article}\pagestyle{empty}\begin{document}$$k_1 = (6.7 \pm 1.5) \times 10^{- 12} {\rm \,exp[- (300} \pm {\rm 70)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$k_2 = (5.6 \pm 1.7) \times 10^{- 12} {\rm \,exp[(270} \pm 10{\rm 0)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}$$\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$$k_3 = (11 \pm 3) \times 10^{- 1 2} {\rm \,exp[(150} \pm 8{\rm 0)/}T]{\rm \,cm}^{\rm 3}\, {\rm \,molecule}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}}$$\end{document} At 296 K, the measured rate constants (in units of 10-13 cm3 molecule-1 s-1) were: k1 = (24.9 ± 2.2), k2 = (136 ± 9), and k3 = (180 ± 22). Room temperature rate constants for the OH reactions with several other aliphatic ethers were also measured. These were (in the above units): di-n-butylether, (278 ± 36); di-n-pentylether, (347 ± 20); ethyleneoxide, (0.95 ± 0.05); propyleneoxide, (4.95 ± 0.52); and tetrahydrofuran, (178 ± 16). The results are discussed in terms of the mechanisms for these reactions and are compared to previous literature data.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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