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Porphyrin-naphthodiimide Interactions as a Structural Motif in Foldamers and Supramolecular Assemblies

Zulkifli Merican, Ken Johnstone, Maxwell John Gunter

Research output: Contribution to journalArticlepeer-review

14 Citations (Scopus)

Abstract

π-π Stacking interactions between electron deficient naphthalenediimides (NDI) and electron-rich porphyrins (POR) leading to charge transfer are shown to be prevalent in linked NDI-POR and POR-NDI-POR structures. For flexibility-linked systems, intramolecular interactions lead to S-shaped foldamers in solution, whereas intermolecular association is predominant in more rigid systems. The foldamer structures can be interrupted by competing aromatic solvents, by six-coordination of metallated porphyrin derivatives, by protonation of the free base porphyrin in non-metallated structures, and in facially sterically hindered porphyrins.
Original languageEnglish
Pages (from-to)2534-2543
JournalOrganic & Biomolecular Chemistry
Volume6
Issue number14
DOIs
Publication statusPublished - 2008

Keywords

  • Nanochemistry and Supramolecular Chemistry

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