Materials 2010, 3(2), 1269-1280; doi:10.3390/ma3021269
Review

Non-Traditional Aromatic Topologies and Biomimetic Assembly Motifs as Components of Functional Pi-Conjugated Oligomers

1,2,3,* email, 1,3email and 1email
Received: 6 January 2010; in revised form: 2 February 2010 / Accepted: 11 February 2010 / Published: 23 February 2010
(This article belongs to the Special Issue Conjugated Oligomers)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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 methano[10]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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MDPI and ACS Style

Tovar, J.D.; Diegelmann, S.R.; Peart, P.A. Non-Traditional Aromatic Topologies and Biomimetic Assembly Motifs as Components of Functional Pi-Conjugated Oligomers. Materials 2010, 3, 1269-1280.

AMA Style

Tovar JD, Diegelmann SR, Peart PA. Non-Traditional Aromatic Topologies and Biomimetic Assembly Motifs as Components of Functional Pi-Conjugated Oligomers. Materials. 2010; 3(2):1269-1280.

Chicago/Turabian Style

Tovar, John D.; Diegelmann, Stephen R.; Peart, Patricia A. 2010. "Non-Traditional Aromatic Topologies and Biomimetic Assembly Motifs as Components of Functional Pi-Conjugated Oligomers." Materials 3, no. 2: 1269-1280.

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