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dc.contributor.authorElemes, Y.en
dc.contributor.authorSilverman, S. K.en
dc.contributor.authorSheu, C. M.en
dc.contributor.authorKao, M.en
dc.contributor.authorFoote, C. S.en
dc.contributor.authorAlvarez, M. M.en
dc.contributor.authorWhetten, R. L.en
dc.date.accessioned2015-11-24T16:46:03Z-
dc.date.available2015-11-24T16:46:03Z-
dc.identifier.issn0570-0833-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9023-
dc.rightsDefault Licence-
dc.subjectall-carbon moleculesen
dc.subjectenol ethersen
dc.subjectc-60en
dc.subjectestersen
dc.titleReaction of C-60 with Dimethyldioxirane - Formation of an Epoxide and a 1,3-Dioxolane Derivativeen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI 10.1002/anie.199203511-
heal.identifier.secondary<Go to ISI>://A1992HX98600035-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/anie.199203511/asset/199203511_ftp.pdf?v=1&t=hmstwv7f&s=552b8ca42c739a579e3915cb393db12e1a134eea-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate1992-
heal.abstractNot an oxygen-bridged annulene (structural type 1) but rather an epoxide (structural type 2) is the product of the reaction of dimethyldioxirane with C60. In a competing reaction, a 1,3-dioxolane (structural type 3) is formed-probably by a diradical mechanism. Cleavage of acetone from 3 leading to 2 was not observed at temperatures up to 110-degrees-C. Compound 3 could provide access to ring-opened fullerenes.en
heal.journalNameAngewandte Chemie-International Edition in Englishen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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