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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 213 (1973), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 12 (1979), S. 57-62 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Изучена кинетика каталитического эпоксидирования пропилена гидроперекисью этилбензола. Сама реакция эпоксидирования — это молекулярное взаимодействие между пропиленом и комплексом катализатора с гидроперекисью. Ряд побочных продуктов образуется в радикальных реакциях. Данный механизм описывает кинетику как эпоксидирования так и каталитического разложения гидроперекиси.
    Notes: Abstract The mechanism of the catalytic epoxidation of propylene with α-phenylethyl hydroperoxide has been investigated. The epoxidation step is a molecular interaction between propylene and a complex formed from hydroperoxide and catalyst, while part of side products is formed in free radical reactions. This mechanism is valid for the kinetics of both epoxidation and catalytic decomposition of hydroperoxide.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract Бьло найдено, что в отсутствии кислорода и света насыщенные углеводороды самопроизвольно реагируют с нитрозобензолами. Для интерпретации этого общего явления было предположено новое направление реакции. В свете полученных данных следует обращатя особое внимание при интерпретации экспериментальных результатов в случае применения нитрозобензолов в качестве спиновых ловушек, ингибиторов, а также для синтетических целей при проведении опытов в насыщенных углеводродах как растворителях, которые, по предположению являются инертными.
    Notes: Abstract We have found that nitrosobenzenes spontaneously react with saturated hydrocarbons in the absence of oxygen and light. For interpretation of this general phenomenon a new reaction pathway has been assumed. In light of these results special care should be taken when applying nitrosobenzenes for inhibition and spin trapping as well as organic synthesis in saturated organic solvents, which are supposed to be inert.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 1191-1202 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A general mechanism was proposed for the title reactions which describes the kinetics of hydroperoxide decomposition as well as product accumulation throughout the whole reaction period in an analytical form. The following catalytic steps were included: where the deactivation takes place as a result of radical-catalyst interaction inside the cage. The resulting equations give satisfactory description of the literature data in the case of various catalysts and hydroperoxides.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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