Please use this identifier to cite or link to this item: https://dspace.univ-ouargla.dz/jspui/handle/123456789/5547
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAli DOUADI-
dc.contributor.authorGérard AUDRAN-
dc.contributor.authorPaul BREMOND-
dc.contributor.authorKineticsen_US
dc.date.accessioned2013-
dc.date.available2013-
dc.date.issued2013-
dc.identifier.issn2170-0672-
dc.identifier.urihttp://dspace.univ-ouargla.dz/jspui/handle/123456789/5547-
dc.descriptionAST Annales des Sciences et Technologieen_US
dc.description.abstractThe alkoxyamines (or trialkylhydroxylamines) R1R2NOR3 are very labile molecules able to undergo a homolytic rupture at physiological temperature to give a stable nitroxide radical for diagnostic applications and a highly reactive alkyl radical for therapeutic applications. In this work, we present the results of an alkoxyamine homolysis and the influence of solvent on this radical decomposition.en_US
dc.language.isofren_US
dc.relation.ispartofseriesvolume 5 numéro 2 AST 2013;-
dc.subjectAlkoxyamineen_US
dc.subjectHomolysisen_US
dc.subjectSolvent effecten_US
dc.subjectActivation energyen_US
dc.titleEtude cinétique de la décomposition radicalaire de la liaison C-ON d’une alcoxyamine : effet de solvanten_US
dc.typeArticleen_US
Appears in Collections:volume 5 numéro 2 AST 2013

Files in This Item:
File Description SizeFormat 
A050209.pdf557,45 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.