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Journal Article

1,4‐Dihydro‐1,2,4‐benzotriazin‐Radikalkationen

MPS-Authors
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Neugebauer,  Franz A.
Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons238355

Umminger,  Irmgard
Max Planck Institute for Medical Research, Max Planck Society;

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https://onlinelibrary.wiley.com/doi/epdf/10.1002/cber.19811140709
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https://doi.org/10.1002/cber.19811140709
(Any fulltext)

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Citation

Neugebauer, F. A., & Umminger, I. (1981). 1,4‐Dihydro‐1,2,4‐benzotriazin‐Radikalkationen. Chemische Berichte, 114(7), 2423-2430. doi:10.1002/cber.19811140709.


Cite as: https://hdl.handle.net/21.11116/0000-0004-E3A8-E
Abstract
1,4‐Dihydro‐1,2,4‐benzotriazinyl‐Radikale (4) werden in Gegenwart starker Säuren protoniert. Die Konstitution der Radikalkationen wurde durch ESR‐spektroskopische Untersuchung deuterierter Derivate gesichert.