Journal of the Chemical Society B Physical Organic, pages 378-380
Radicals produced during γ-irradiation of 1-substituted 5-amino-tetrazoles
Publication type: Journal Article
Publication date: 1970-01-01
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ISSN: 00456470
Organic Chemistry
Physical and Theoretical Chemistry
Abstract
The 1-methyl site of alkyl substituted 5-aminotetrazoles was found to be the most susceptible to γ-irradiation. The main paramagnetic radicals formed were identified as CH3· and R–CH2·(R = substittuted 5-aminotetrazole). With a 5-nitraminotetrazole claeavage of the nitramino N–N bond, yielding an NO2· radical, was the major interaction.
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Butler R. N., Catton R. C., Symons M. C. R. Radicals produced during γ-irradiation of 1-substituted 5-amino-tetrazoles // Journal of the Chemical Society B Physical Organic. 1970. pp. 378-380.
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Butler R. N., Catton R. C., Symons M. C. R. Radicals produced during γ-irradiation of 1-substituted 5-amino-tetrazoles // Journal of the Chemical Society B Physical Organic. 1970. pp. 378-380.
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TY - JOUR
DO - 10.1039/j29700000378
UR - https://doi.org/10.1039/j29700000378
TI - Radicals produced during γ-irradiation of 1-substituted 5-amino-tetrazoles
T2 - Journal of the Chemical Society B Physical Organic
AU - Butler, R N
AU - Catton, R. C.
AU - Symons, M. C. R.
PY - 1970
DA - 1970/01/01
PB - Royal Society of Chemistry (RSC)
SP - 378-380
SN - 0045-6470
ER -
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@article{1970_Butler,
author = {R N Butler and R. C. Catton and M. C. R. Symons},
title = {Radicals produced during γ-irradiation of 1-substituted 5-amino-tetrazoles},
journal = {Journal of the Chemical Society B Physical Organic},
year = {1970},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/j29700000378},
pages = {378--380},
doi = {10.1039/j29700000378}
}