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dc.contributor.advisorLewis, David E.
dc.contributor.authorKppidlansky, Kyle M.
dc.date.accessioned2010-11-05T21:05:17Z
dc.date.available2010-11-05T21:05:17Z
dc.date.issued2010-04
dc.identifier.urihttp://digital.library.wisc.edu/1793/47122
dc.descriptionColor poster with text and diagrams.en
dc.description.abstractIt has long been believed that the heterocycle ring of a naphthalimide dye was resistant to nucleophilic attach. However, our research has shown that reacting N-aryl-4-sustituted-1,8-naphthalimides with nucleophic primary amimes has resulted in addition to the heterocyclic ring with loss of the aromatic amine to give an apparent net substitution at the nitrogen atom.en
dc.description.sponsorshipUniversity of Wisconsin--Eau Claire Office of Research and Sponsored Programs; Petroleum Research Funden
dc.language.isoen_USen
dc.relation.ispartofseriesUSGZE AS589en
dc.subjectNaphthalimidesen
dc.subjectAmine nucleophilesen
dc.subjectAminesen
dc.subjectPostersen
dc.titleReactivity of N-aryl-4-substituted-1,8-naphthalimides towards Amine Nucleophilesen
dc.typePresentationen


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