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dc.contributor.authorDaphnomili, D.en
dc.contributor.authorGrammatikopoulou, M.en
dc.contributor.authorRaptopoulou, C.en
dc.contributor.authorCharalambidis, G.en
dc.contributor.authorLazarides, T.en
dc.contributor.authorCoutsolelos, A. G.en
dc.date.accessioned2015-11-24T16:39:52Z-
dc.date.available2015-11-24T16:39:52Z-
dc.identifier.issn1565-3633-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8200-
dc.rightsDefault Licence-
dc.subjectdipyrromethanesen
dc.subjectporphyrinsen
dc.titleA Synthetic Approach of New Trans-Substituted Hydroxylporphyrinsen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1155/2010/307696-
heal.identifier.secondary<Go to ISI>://000279731400001-
heal.identifier.secondaryhttp://downloads.hindawi.com/journals/bca/2010/307696.pdf-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2010-
heal.abstractThe synthesis of new trans A(2)B(2)-substituted porphyrins bearing oxygenic substituent (methoxy, acetoxy, hydroxy) at the periphery of the ring are described. All of the synthesized products were characterized by (1)H-N.M.R., (13)C-N.M.R., and H.R.M.S. Electrochemical studies revealed two one-electron oxidations and two reductions. In addition, the X-ray structure of one methoxy-derivative was determined.en
heal.publisherHindawi Publishing Corporationen
heal.journalNameBioinorg Chem Applen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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