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Article: Polyvalent Scaffolds. Counting the Number of Seats Available for Eosin Guest Molecules in Viologen-Based Host Dendrimers

TitlePolyvalent Scaffolds. Counting the Number of Seats Available for Eosin Guest Molecules in Viologen-Based Host Dendrimers
Authors
Issue Date2004
Citation
Journal of the American Chemical Society, 2004, v. 126, n. 2, p. 568-573 How to Cite?
AbstractWe have prepared and investigated two dendrimers based on a 1,3,5-trisubstituted benzenoid-type core, containing 9 and 21 viologen units in their branches, respectively, and terminated with tetraarylmethane derivatives. We have shown that, in dichloromethane solution, such highly charged cationic species give rise to strong host-guest complexes with the dianionic form of the red dye eosin. Upon complexation, the absorption spectrum of eosin becomes broader and is slightly displaced toward lower energies, whereas the strong fluorescence of eosin is completely quenched. Titration experiments based on fluorescence measurements have shown that each viologen unit in the dendrimers becomes associated with an eosin molecule, so that the number of positions ("seats") available for the guest molecules in the hosting dendrimer is clearly established, e.g., 21 for the larger of the two dendrimers. The host-guest interaction can be destroyed by addition of chloride ions, a procedure which permits eosin to escape from the dendrimer's interior in a controlled way and to regain its intense fluorescence. When chloride anions are precipitated out by addition of silver cations, eosin molecules re-enter the dendrimer's interior and their fluorescence again disappears.
Persistent Identifierhttp://hdl.handle.net/10722/332558
ISSN
2023 Impact Factor: 14.4
2023 SCImago Journal Rankings: 5.489
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMarchioni, Filippo-
dc.contributor.authorVenturi, Margherita-
dc.contributor.authorCredi, Alberto-
dc.contributor.authorBalzani, Vincenzo-
dc.contributor.authorBelohradsky, Martin-
dc.contributor.authorElizarov, Arkadij M.-
dc.contributor.authorTseng, Hsian Rong-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:12:27Z-
dc.date.available2023-10-06T05:12:27Z-
dc.date.issued2004-
dc.identifier.citationJournal of the American Chemical Society, 2004, v. 126, n. 2, p. 568-573-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10722/332558-
dc.description.abstractWe have prepared and investigated two dendrimers based on a 1,3,5-trisubstituted benzenoid-type core, containing 9 and 21 viologen units in their branches, respectively, and terminated with tetraarylmethane derivatives. We have shown that, in dichloromethane solution, such highly charged cationic species give rise to strong host-guest complexes with the dianionic form of the red dye eosin. Upon complexation, the absorption spectrum of eosin becomes broader and is slightly displaced toward lower energies, whereas the strong fluorescence of eosin is completely quenched. Titration experiments based on fluorescence measurements have shown that each viologen unit in the dendrimers becomes associated with an eosin molecule, so that the number of positions ("seats") available for the guest molecules in the hosting dendrimer is clearly established, e.g., 21 for the larger of the two dendrimers. The host-guest interaction can be destroyed by addition of chloride ions, a procedure which permits eosin to escape from the dendrimer's interior in a controlled way and to regain its intense fluorescence. When chloride anions are precipitated out by addition of silver cations, eosin molecules re-enter the dendrimer's interior and their fluorescence again disappears.-
dc.languageeng-
dc.relation.ispartofJournal of the American Chemical Society-
dc.titlePolyvalent Scaffolds. Counting the Number of Seats Available for Eosin Guest Molecules in Viologen-Based Host Dendrimers-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ja037318m-
dc.identifier.scopuseid_2-s2.0-0346008049-
dc.identifier.volume126-
dc.identifier.issue2-
dc.identifier.spage568-
dc.identifier.epage573-
dc.identifier.isiWOS:000188197800050-

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