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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 9 (1996), S. 729-738 
    ISSN: 0894-3230
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A qualitative analysis is presented of the interrelationships between phase transformations and organic chemical reactivity in the solid state, taking into consideration general thermochemical relationships and the thermodynamics of heterophase equilibrium. Two cases, where isomerization reactions depend on the solid-state solubility of the reactant and product, are considered and show that the formation of a new phase can influence both the reaction yield and rate. For example, it is shown that crystallization of a new phase from a crystalline or amorphous solid solution can supply the thermodynamic driving force for chemical transformation. Formation of a new phase may influence solid-state kinetics depending on the solubility of a reactant in the new phase and the relative rates of chemical transformation and formation of the new phase. It is further shown that even for simple monomolecular reactions, kinetic curves for the overall process can consist of up to five parts, depending on the type of phase diagram involved. These principles have been applied to some examples of solid-state isomerization in a way that allows the choice of a proper kinetic scheme and an explanation of the direction and maximum yield observed for a particular reaction.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 29 (1997), S. 339-348 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: To better understand the general interrelationships between chemical transformations and physical transformations in solid-state reactions, we have studied the kinetics of methyl transfer in polycrystalline samples of tetraglycine methyl ester [TGME] over the temperature range of 83°C-115°C. Changes in the concentrations of the reactant and various intermediates (sarcosyltriglycine methyl ester METGME, and tetraglycine TG) and products (sarcosyltriglycine METG and N N-dimethyl glycyl triglycine Me2TG) were measured over the entire time course of the reaction using HPLC. Corresponding measurements of physical transformations occurring during the course of the reactions were made using X-ray powder diffractometry and differential scanning calorimetry. Kinetic curves for the loss of TGME in the range of 83°C-115°C have a sigmoldal shape and collapse into one curve when plotted in terms of reduced time. t/t0.5, as do plots of intermediate and product concentration plotted in the same manner. The first 25% of the reaction proceeds homogeneously through what is believed to be the formation of a crystalline solid solution of the intermediates and products in the reactant. The acceleratory character of the kinetic curves in the single-phase portion of the reaction has been described by a kinetic scheme that contains a concentration-dependent rate constant. The apperance of a new crystalline phase beyond 35% of the reaction changes the reaction mechanism from a bulk reaction to an interface-controlled process that causes further acceleration of the methyl transfer. The apparent activation energies for both single-phase and heterophase stages of the reaction are about 100-130 kJ/mole © 1997 John Wiley & Sons, Inc. Int J Chem Kinet 29: 339-348, 1997
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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