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Non-Traditional Aromatic Topologies and Biomimetic Assembly Motifs as Components of Functional Pi-Conjugated Oligomers
Authors:John D Tovar  Stephen R Diegelmann  Patricia A Peart
Institution:1.Department of Chemistry, Johns Hopkins University, 3400 N. Charles St., Baltimore, MD, 21218 USA; E-Mails: (S.R.D.); (P.A.P.);2.Department of Materials Science and Engineering, Johns Hopkins University, 3400 N. Charles St., Baltimore, MD, 21218 USA;3.Institute for NanoBioTechnology, Johns Hopkins University, 3400 N. Charles St., Baltimore, MD, 21218 USA
Abstract:This article will highlight our recent work using conjugated oligomers as precursors to electroactive polymer films and self-assembling nanomaterials. One area of investigation has focused on nonbenzenoid aromaticity in the context of charge delocalization in conjugated polymers. In these studies, polymerizable pi-conjugated units were coupled onto unusual aromatic cores such as methano10]annulene. This article will also show how biologically-inspired assembly of molecularly well-defined oligopeptides that flank pi-conjugated oligomers has resulted in the aqueous construction of 1-dimensional nanomaterials that encourage electronic delocalization among the pi-electron systems.
Keywords:conjugated polymers  self-assembly  aromaticity
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