Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/1350
Title: Porphyrin-naphthodiimide Interactions as a Structural Motif in Foldamers and Supramolecular Assemblies
Contributor(s): Merican, Zulkifli (author); Johnstone, Ken (author); Gunter, Maxwell John (author)
Publication Date: 2008
DOI: 10.1039/b804267e
Handle Link: https://hdl.handle.net/1959.11/1350
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.
Publication Type: Journal Article
Source of Publication: Organic & Biomolecular Chemistry, 6(14), p. 2534-2543
Publisher: Royal Society of Chemistry
Place of Publication: UK
ISSN: 1477-0520
Field of Research (FOR): 030302 Nanochemistry and Supramolecular Chemistry
Peer Reviewed: Yes
HERDC Category Description: C1 Refereed Article in a Scholarly Journal
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