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Electron Spin Dynamics of Photoexcited Corannulene-Lithium Complexes in Tetrahydrofuran. Fourier Transform Electron Paramagnetic Resonance

  • Gil Zilber
  • , Mordecai Rabinovitz*
  • , Gil Zilber
  • , Vladimir Rozenshtein
  • , Haim Levanon
  • , Pei Chao Cheng
  • , Lawrence T. Scott
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Tetrahydrofuran (THF) solutions of corannulene (Cor) reduced by lithium metal exhibit electron paramagnetic resonance (EPR) features that depend on the reduction stage of Cor, the temperature, and the nuclear spin (isotope effect). Photoexcitation of these solutions results in EPR emissive spectra, attributed to the trianion, Cor3•-, and to the photoelectron, e-Photo- These electron spin polarized (ESP) effects are discussed within the framework of intramolecular electron transfer reactions of ion complexes of highly charged constituents, in conjunction with ESP mechanisms that take into account radical—triplet interactions.

Original languageEnglish
Pages (from-to)10720-10725
Number of pages6
JournalJournal of the American Chemical Society
Volume117
Issue number43
DOIs
StatePublished - 1995

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