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Purpurinimide-fullerene dyads: Introduction of fullerene moiety at various peripheral positions of the purpurinimide system

  • Roswell Park Cancer Institute
  • Rutgers - The State University of New Jersey, New Brunswick

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

(Equation Presented) Fullerene was regioselectively introduced at various peripheral positions of N-hexyl-purpurinimide for photoinduced electron transfer studies. Remarkably different effects of the position of the fullerene moiety in the formation of atropisomers were observed.

Original languageEnglish
Pages (from-to)2393-2396
Number of pages4
JournalOrganic Letters
Volume6
Issue number14
DOIs
StatePublished - Jul 8 2004

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