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Article: Helical chirality in donor-acceptor catenanes

TitleHelical chirality in donor-acceptor catenanes
Authors
Issue Date2004
Citation
Organic Letters, 2004, v. 6, n. 7, p. 1095-1098 How to Cite?
AbstractA [2]catenane in which the macrocyclic polyether, bisparaphenylene[34] crown-10, is interlocked with the tetracationic cyclophane, cyclobis-(paraquat- p-phenylene), is shown by dynamic 1H NMR spectroscopy, using (i) neutral and (ii) anionic chiral shift reagents (CSRs), to exist at low temperatures (197 K) in acetone-d6 solutions as 1:1 and 2:1 mixtures of diastereoisomeric complexes and salts, respectively, as a consequence of the helical chirality associated with the [2]catenane interacting with the CSRs.
Persistent Identifierhttp://hdl.handle.net/10722/332617
ISSN
2023 Impact Factor: 4.9
2023 SCImago Journal Rankings: 1.245
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorVignon, Scott A.-
dc.contributor.authorWong, Jason-
dc.contributor.authorTseng, Hsian Rong-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:12:55Z-
dc.date.available2023-10-06T05:12:55Z-
dc.date.issued2004-
dc.identifier.citationOrganic Letters, 2004, v. 6, n. 7, p. 1095-1098-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/10722/332617-
dc.description.abstractA [2]catenane in which the macrocyclic polyether, bisparaphenylene[34] crown-10, is interlocked with the tetracationic cyclophane, cyclobis-(paraquat- p-phenylene), is shown by dynamic 1H NMR spectroscopy, using (i) neutral and (ii) anionic chiral shift reagents (CSRs), to exist at low temperatures (197 K) in acetone-d6 solutions as 1:1 and 2:1 mixtures of diastereoisomeric complexes and salts, respectively, as a consequence of the helical chirality associated with the [2]catenane interacting with the CSRs.-
dc.languageeng-
dc.relation.ispartofOrganic Letters-
dc.titleHelical chirality in donor-acceptor catenanes-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ol0364881-
dc.identifier.scopuseid_2-s2.0-2342486531-
dc.identifier.volume6-
dc.identifier.issue7-
dc.identifier.spage1095-
dc.identifier.epage1098-
dc.identifier.isiWOS:000220508600007-

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