Miller, Joseph and Paul, D.B. and Wong, L.Y. and Kelso, A.G. (1970) Phenylation of azobenzene. Journal of the Chemical Society B: Physical Organic. pp. 62-65. ISSN 0045-6470, DOI https://doi.org/10.1039/J29700000062.
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Official URL: https://doi.org/10.1039/J29700000062
Abstract
The substituent effect of the phenylazo-group in homolytic phenylation has been measured with azobenzene as substrate and nitrobenzene as reference compound. Even after allowance for the large number of sites of substitution the phenylazo-group was shown to equal the nitro-group in its activating power. Isomer ratios and partial rate factors have been determined and are discussed. © Royal Society of Chemistry.
Item Type: | Article |
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Funders: | UNSPECIFIED |
Uncontrolled Keywords: | Phenylation; azobenzene |
Subjects: | Q Science > Q Science (General) Q Science > QD Chemistry |
Divisions: | Faculty of Science > Department of Chemistry |
Depositing User: | Mr Jasny Razali |
Date Deposited: | 22 Mar 2021 04:42 |
Last Modified: | 22 Mar 2021 04:42 |
URI: | http://eprints.um.edu.my/id/eprint/24536 |
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