Homolytic substitution in aromatic heterocycles

Alam, Shahidul


Alam, Shahidul (1983) Homolytic substitution in aromatic heterocycles.

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A radical is a species with an unpaired electron. The classical research papers of Gomberg1 on the triphenylmethyl radical (I) (reaction 1 and 2), and the study by Lund and [diagram] Bodenstein 2 (1906) of the H2 an Br2 hain reaction, mark thebeginning of organic free-radical chemistry. Radical kinetics openedup with the radical-mirror removal experiments of Paneth et. al. 3 (1929) (reaction 3) and others. 4. [diagram] (3) The pyrolysis of tetramethyl lead (900--1200°K; 1 s, residence in quartz furnace) produced species (methyl radicals) which were capable of removing mirrors of lead, antimony and zinc. The rates and products observed made possible the first measurements of radical concentration and of radical reactivity.The Rice-HerzfieId mechanisms 5 (1934) gave a detailed scheme of elementary radical reactions to account for the rates and products of complex pyrolysis reactions.

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This version's date is: 1983
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Item TypeThesis (Doctoral)
TitleHomolytic substitution in aromatic heterocycles
AuthorsAlam, Shahidul
Uncontrolled KeywordsOrganic Chemistry; Pure Sciences; Aromatic; Aromatic Heterocycles; Aromatic Heterocycles; Heterocycles; Homolytic; Substitution



Deposited by () on 01-Feb-2017 in Royal Holloway Research Online.Last modified on 01-Feb-2017


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