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Article: Supramolecular daisy chains

TitleSupramolecular daisy chains
Authors
Issue Date2001
Citation
Journal of Organic Chemistry, 2001, v. 66, n. 21, p. 6857-6872 How to Cite?
AbstractTwo series of self-complementary daisy chain monomers, in which a secondary ammonium ion-containing arm is grafted onto a macrocycle with either a [24]- or [25]crown-8 constitution, have been synthesized. In the solid- and 'gas'-phases, the parent [24]crown-8-based monomer forms dimeric superstructures, as revealed by X-ray crystallography and mass spectrometry, respectively. Elucidation of the complicated solution-phase behavior of this compound was facilitated by the synthesis and study of both deuterated, and fluorinated, analogues. These investigations revealed that the cyclic dimeric superstructure also dominates in solution, except when extremes of either concentration (low), temperature (high), or solvent polarity (highly polar, e.g., dimethyl sulfoxide) are employed. Whereas, upon aggregation, the [24]crown-8-based daisy chain monomers have the capacity to form stereoisomeric superstructures further complicating the study of this series of compounds. The assembly of [25]crown-8-based monomers gives only achiral superstructures. The weaker association exhibited between secondary dialkylammonium ions and crown ethers with a [25]crown-8 constitution, however, resulted in limited oligomerization-only dimeric and trimeric superstructures were formed at experimentally attainable concentrations-of [25]crown-8-based daisy chain monomers.
Persistent Identifierhttp://hdl.handle.net/10722/332499
ISSN
2023 Impact Factor: 3.3
2023 SCImago Journal Rankings: 0.724
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorCantrill, S. J.-
dc.contributor.authorYoun, G. J.-
dc.contributor.authorStoddart, J. F.-
dc.contributor.authorWilliams, D. J.-
dc.date.accessioned2023-10-06T05:11:59Z-
dc.date.available2023-10-06T05:11:59Z-
dc.date.issued2001-
dc.identifier.citationJournal of Organic Chemistry, 2001, v. 66, n. 21, p. 6857-6872-
dc.identifier.issn0022-3263-
dc.identifier.urihttp://hdl.handle.net/10722/332499-
dc.description.abstractTwo series of self-complementary daisy chain monomers, in which a secondary ammonium ion-containing arm is grafted onto a macrocycle with either a [24]- or [25]crown-8 constitution, have been synthesized. In the solid- and 'gas'-phases, the parent [24]crown-8-based monomer forms dimeric superstructures, as revealed by X-ray crystallography and mass spectrometry, respectively. Elucidation of the complicated solution-phase behavior of this compound was facilitated by the synthesis and study of both deuterated, and fluorinated, analogues. These investigations revealed that the cyclic dimeric superstructure also dominates in solution, except when extremes of either concentration (low), temperature (high), or solvent polarity (highly polar, e.g., dimethyl sulfoxide) are employed. Whereas, upon aggregation, the [24]crown-8-based daisy chain monomers have the capacity to form stereoisomeric superstructures further complicating the study of this series of compounds. The assembly of [25]crown-8-based monomers gives only achiral superstructures. The weaker association exhibited between secondary dialkylammonium ions and crown ethers with a [25]crown-8 constitution, however, resulted in limited oligomerization-only dimeric and trimeric superstructures were formed at experimentally attainable concentrations-of [25]crown-8-based daisy chain monomers.-
dc.languageeng-
dc.relation.ispartofJournal of Organic Chemistry-
dc.titleSupramolecular daisy chains-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/jo010405h-
dc.identifier.pmid11597203-
dc.identifier.scopuseid_2-s2.0-0035914106-
dc.identifier.volume66-
dc.identifier.issue21-
dc.identifier.spage6857-
dc.identifier.epage6872-
dc.identifier.isiWOS:000171613900003-

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