Document Detail


Porphyrin-naphthodiimide interactions as a structural motif in foldamers and supramolecular assemblies.
MedLine Citation:
PMID:  18600275     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
pi-pi 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 flexibly-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.
Authors:
Zulkifli Merican; Ken D Johnstone; Maxwell J Gunter
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Publication Detail:
Type:  Journal Article     Date:  2008-05-16
Journal Detail:
Title:  Organic & biomolecular chemistry     Volume:  6     ISSN:  1477-0520     ISO Abbreviation:  Org. Biomol. Chem.     Publication Date:  2008 Jul 
Date Detail:
Created Date:  2008-07-07     Completed Date:  2008-09-08     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101154995     Medline TA:  Org Biomol Chem     Country:  England    
Other Details:
Languages:  eng     Pagination:  2534-43     Citation Subset:  -    
Affiliation:
Chemistry, School of Science and Technology, University of New England, Armidale, NSW 2351, Australia.
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