Comment on conversion of nitric oxide into a nitroxide radical using 2,3-dimethylbutadiene and 2,5-dimethylhexadiene

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Abstract

ESR spectroscopic evidence is given to suggest that NO2 initiates radical formation instead of the previously assumed ring-closure mechanism in the reaction of nitric oxide with 2,3-dimethyl-1,3-butadiene and 2,5-dimethyl-2,4-hexadiene.

Original languageEnglish
Pages (from-to)145
Number of pages1
JournalJournal of the Chemical Society, Chemical Communications
Issue number2
DOIs
Publication statusPublished - 1994

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Nitric oxide
Butadiene
Paramagnetic resonance
Nitric Oxide
nitroxyl
2,3-dimethyl-1,3-butadiene

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

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title = "Comment on conversion of nitric oxide into a nitroxide radical using 2,3-dimethylbutadiene and 2,5-dimethylhexadiene",
abstract = "ESR spectroscopic evidence is given to suggest that NO2 initiates radical formation instead of the previously assumed ring-closure mechanism in the reaction of nitric oxide with 2,3-dimethyl-1,3-butadiene and 2,5-dimethyl-2,4-hexadiene.",
author = "A. Rockenbauer and L. Korecz",
year = "1994",
doi = "10.1039/C39940000145",
language = "English",
pages = "145",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "2",

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T1 - Comment on conversion of nitric oxide into a nitroxide radical using 2,3-dimethylbutadiene and 2,5-dimethylhexadiene

AU - Rockenbauer, A.

AU - Korecz, L.

PY - 1994

Y1 - 1994

N2 - ESR spectroscopic evidence is given to suggest that NO2 initiates radical formation instead of the previously assumed ring-closure mechanism in the reaction of nitric oxide with 2,3-dimethyl-1,3-butadiene and 2,5-dimethyl-2,4-hexadiene.

AB - ESR spectroscopic evidence is given to suggest that NO2 initiates radical formation instead of the previously assumed ring-closure mechanism in the reaction of nitric oxide with 2,3-dimethyl-1,3-butadiene and 2,5-dimethyl-2,4-hexadiene.

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U2 - 10.1039/C39940000145

DO - 10.1039/C39940000145

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