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  • Chemistry  (8)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 46 (1960), S. 355-364 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Water vapor sorption isotherms of a commercial dextrin prepared by dry acid treatment, amylose recrystallized from n-butanol, and amylopectin precipitated from methanol were determined at various temperatures in the range of 10-40°C. The differential thermodynamic functions for water vapor sorption on the various materials were calculated, and B.E.T. constants were determined. A striking characteristic of the thermodynamic functions is the strong similarity for amylopectin and amylose. A model for the sorption is proposed. X-ray patterns for the starch samples equilibrated with water vapor at various relative pressures of water vapor were determined. The major changes are explicable on the basis of intramicellar swelling. As the relative pressures increase, the crystalline patterns gradually fade and disappear. However, some new spacings appear with increased sorption in amylose and amylopectin. These spacings are explained on the basis of the formation of transitory lattices during the swelling of the starch crystallites.
    Additional Material: 7 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 3 (1971), S. 25-37 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study of the structural isomerization rate of chemically activated 1,1-dimethylcyclopropane from singlet methylene addition to the double bond of isobutene is reported. Singlet methylenes were produced from the 4358- and 3660-Å photolysis of diazomethane in the presence of added oxygen. Theoretical rates calculated via RRKM theory are in excellent agreement with experiment for calculations utilizing activated complex structures and critical energies consistent with known thermal Arrhenius parameters, and excitation energies consistent with previous determinations of ΔHf00(CH2) + E*(CH2) = 116.1 and 112.6 kcal/mole for diazomethane photolyses at 3660 and 4358 Å, respectively.
    Additional Material: 5 Ill.
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  • 3
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The total decomposition rates of the chemically activated alkanes n-butane, n-pentane, isopentane, and neohexane were measured using an internal comparison technique. Chemical activation was by the C—H insertion reaction of excited singlet-state methylene radicals. A total of ten rate constants ranging from 4.6 × 105 to 2.3 × 107 sec-1 were measured for these alkanes at different excitation energies. These rates correlate via RRKM theory calculations with thermal A-factors in the range of 1016.1 to 1017.1 sec-1 for free rotoractivated complex models and in the range of 1016.4 to 1017.8 sec-1 for vibrator-activated complex models. It was found that high critical energies for decomposition, “tight” radical models, and activated complex models with free internal rotations were required to correlate the decomposition rates of these alkanes with estimated alkyl radical recombination rates. The correlation is just barely possible even for these favorable extremes, indicating that there may be a basic discrepancy between the recombination rate and decomposition rate data for alkanes.
    Additional Material: 7 Ill.
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  • 4
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An experimental study of the decomposition kinetics of chemically activated 2-methyl-l-butene and 3-methyl-l-butene produced from photolysis of diazomethane-isobutene-neopentane-oxygen mixtures is reported. The experimental rate constants for 3-methyl-l-butene decomposition were 1.74 ± 0.44 × 108 sec-1 and 1.01 ± 0.25 × 108 sec-1 at 3660 and 4358 Å, respectively. 2-Methyl-l-butene experimental decomposition rate constants were found to be 5.94 ± 0.59 × 107 sec-1 at 3660 Å and 3.42 ± 0.34 × 107 sec-1 at 4358 Å. Activated complex structures giving Arrhenius A-factors calculated from absolute rate theory of 1016.6 ± 0.5 sec-1 for 3-methyl-l-butene and 1016.2 ± 0.4 sec-1 for 2-methyl-l-butene, both calculated at 1000°K, were required to fit RRKM theory calculated rate constants to the experimental rate constants at reasonable E0 and E* values. Corrected calculations (adjusted E0 values) on previous results for 2-pentene decomposition gave an Arrhenius A-factor of 1016.45 ± 0.35 sec-1 at 1000°K. The predicted A-factors for these three alkene decompositions giving resonance-stabilized methylully radicals are in good internal agreement. The fact that these A-factors are only slightly less than those for related alkane decompositions indicates that methylallylic resonance in the decomposition products leads to only a small amount of tightening in the corresponding activated complexes. This tightening is a significantly smaller factor than the large reduction in the critical energy due to resonance stabilization.
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 7 (1975), S. 547-555 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The decomposition rate of chemically activated ethyltrimethylgermane from the reaction 1CH2 + (CH3)4Ge, where 1CH2 was produced from diazomethane photolysis at 3660 Å, is 8.6 × 105 sec-1. This result combined with RRKM theory and critical energy estimates yields an Arrhenius A factor of log[A (sec-1)/methyl] = 14.7 ± 0.8 for methyl rupture from germanium.Log A values for methyl rupture from carbon, silicon, and germanium linearly correlate with the vibrational-rotational entropies of the corresponding tetramethyls. Extrapolation predicts log[A (sec-1)/methyl] = 14.4 and 14.3 for methyl rupture from tin and lead, respectively.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 7 (1975), S. 879-894 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The specific decomposition rates of chemically activated methylcyclobutane produced from CH2(1A1) reaction with cyclobutane have been determined. CH2(1A1)was produced from ketene photolyses at 3340 and 3130 Å and from diazomethane photolyses at 4358 and 3660 Å. Comparisons of the excitation energies of the methylcyclobutane, determined by RRKM theory calculations, and the experimental results for the ketene systems, with thermochemically predicted maximum excitation energies, favor an Arrhenius A factor in the range of 5 × 1015 to 1 × 1016 sec-1 for methylcyclobutane. This result is consistent with (1) the comparison of RRKM theory calculations and the experimental unimolecular falloff for methylcyclobutane, (2) the comparison of experimental A factors for cyclobutane and other alkylcyclobutane decompositions, and (3) two out of three reported experimental A factors for methylcyclobutane. An analysis of these and previous results leads to a value of the CH2(1A1) ↔ CH2(3B1) energy splitting of 9±3 kcal/mole.
    Additional Material: 3 Ill.
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  • 7
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The decomposition kinetics of chemically activated methyl-d1-methylsilane-d2 (DMS-d3*) and ethylsilane-d3 (ES-d3*) from the Si-D and C-H insertion reactions of CH2 (1A1) with methylsilane-d3 have been studied. The total rate constants for decomposition of chemically activated DMS-d3 and ES-d3 have been measured. The individual rate constants for molecular elimination of CH3D, CH2D2, and D2 from DMS-d3* and for molecular elimination of CH3CH2D and D2 from ES-d3* have been measured. All of the above rate constants exhibit the expected kinetic isotope effect when compared to those found previously in the undeuterated system. RRKM theory calculations of the rate constants for the expected C-Si and Si-D bond rupture processes, based on energetics and activated comple× models deduced previously for the undeuterated system, were carried out. In the case of DMS-d3* the RRKM theory calculations of rate constants for the bond rupture processes combined with experimental rate constants for the molecular elimination processes gave a total rate constant for decomposition in agreement with the measured value. The results of a high-pressure study of the CH3D/CH2D2 ratio from chemically activated DMS-d3 decomposition were consistent with complete randomization of internal energy up to a pressure of 4 atmospheres (lifetime of ∼1.7 × 10×11 sec). This is not an unexpected result in light of earlier work.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 5 (1973), S. 77-92 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemically activated ethane, with an excitation energy of 114.9 ± 2 kcal/mole, was formed by reaction with methane of excited singlet methylene radicals produced by the 4358 Å photolysis of diazomethane. A decomposition rate constant of (4.6 ± 1.2) × 109 sec-1 was measured for the chemically activated ethane. This result agrees, via RRKM theory, with most other chemically activated ethane data, and the result predicts, via RRKM and absolute rate theory for E0 = 85.8 kcal/mole, E* = 114.9 kcal/mole, and kE = 4.6 × 101 sec-1, a thermal A-factor at 600°K of 1016.6±0.2 sec-1, in approximate agreement with the more recent experimental values. Combining 2 kcal/mole uncertainties in E0 and E* with the uncertainty in our rate constant yields an A-factor range of 1016.6±0.7 sec-1. It is emphasized that this large uncertainty in the A-factor results from an improbable combination of uncertainty limits for the various parameters. These decomposition results predict, via absolute rate theory (with E0(recombination) = 0) and statistical thermodynamic equilibrium constants, methyl radical recombination rates at 25°C of between 4.4 × 108 to 3.1 × 109 l.-mole-1-sec-1, which are 60 to 8 times lower, respectively, than the apparently quite reliable experimental value. A value of E0(recombination) greater than zero offers no improvement, and a value less than zero would be quite unusual. Activated complexes consistent with the experimental recombination rate and E0(recombination) = 0 greatly overestimate the experimental chemical activation and high pressure thermal decomposition rate data. Absolute rate theory as it is applied here in a straightforward way has failed in this case, or a significant amount of internally consistent data are in serious error. Some corrections to our previous calculations for higher alkanes are discussed in Appendix II.
    Additional Material: 3 Ill.
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