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dc.creatorEngel, PS
dc.creatorDuan, SM
dc.creatorHe, SL
dc.creatorTsvaygboym, K
dc.creatorWang, CR
dc.creatorWu, AY
dc.creatorYing, YM
dc.creatorSmith, WB
dc.date.accessioned2022-01-31T17:27:28Z
dc.date.available2022-01-31T17:27:28Z
dc.date.issued2003
dc.identifier.urihttps://doi.org/10.3998/ark.5550190.0004.c11
dc.identifier.urihttps://repository.tcu.edu/handle/116099117/49963
dc.description.abstractThe azoxy functional group, though relatively uncommon, is found in several natural products and in liquid crystalline compounds. Azoxyalkanes are generally very stable to heat and light and are not subject to attack by radicals. Intramolecular radical reactions, however, can lead to cyclic aminyl nitroxides and hydrazyls, which rearrange further or undergo fragmentation. The azoxy group greatly stabilizes an attached carbon-centered radical but the chemistry of the resulting alpha-azoxy radicals is not completely understood.
dc.language.isoenen_US
dc.publisherArkat Usa Inc
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceArkivoc
dc.subjectazoxy
dc.subjectradical
dc.subjectaminyl nitroxide
dc.subjecthydrazonyloxide
dc.titleThe free radical chemistry of the azoxy group
dc.typeArticle
dc.rights.holderArkat Usa Inc
dc.rights.licenseCC BY 4.0
local.collegeCollege of Science and Engineering
local.departmentChemistry and Biochemistry
local.personsSmith (CHEM)


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