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Article
ProDOT-Assisted Isomerically Pure Indophenines
Journal of Organic Chemistry (2019)
  • Ted M. Pappenfus, University of Minnesota
  • Andrew J Helmin
  • Wyatt D Wilcox
  • Sarah M Severson
  • Daron E Janzen, St. Catherine University
Abstract
Reactions between 3,4-propylenedioxythiophenes (ProDOTs) and N-alkyl isatins under ambient conditions result in isomerically pure indophenine materials as confirmed by TLC and 1H NMR analysis. The resulting low band gap materials exhibit favorable inter- and intramolecular interactions, high thermal stabilities, low electronic transitions and amphoteric redox behavior.
Disciplines
Publication Date
Summer August 12, 2019
DOI
10.1021/acs.joc.9b01525
Citation Information
Ted M. Pappenfus, Andrew J Helmin, Wyatt D Wilcox, Sarah M Severson, et al.. "ProDOT-Assisted Isomerically Pure Indophenines" Journal of Organic Chemistry (2019)
Available at: http://works.bepress.com/daron-janzen/95/