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Article: Designing Synthetic Cationic Molecular Receptors for Alcohols

TitleDesigning Synthetic Cationic Molecular Receptors for Alcohols
Authors
Issue Date1992
Citation
Angewandte Chemie International Edition in English, 1992, v. 31, n. 4, p. 478-480 How to Cite?
AbstractThe monoprotonation of diaza‐12‐crown‐6 derivatives converts these macrocycles to hosts for short‐chain alcohols; the association constant Ka is as high as 47 M−1. For the neutral diaza crown ether, on the other hand, Ka is only 1.1 M−1. X‐ray structure investigations show that the alcohol (R = Me) is held in place by two hydrogen bonds (see right). R = Me, Et, nPr, nBu; R′ = PhCH2, PhCH2CH2 (Figure Presented.) Copyright © 1992 by VCH Verlagsgesellschaft mbH, Germany
Persistent Identifierhttp://hdl.handle.net/10722/332696
ISSN
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMéndez, Luis-
dc.contributor.authorSingleton, Raymond-
dc.contributor.authorSlawin, Alexandra M.Z.-
dc.contributor.authorStoddart, J. Fraser-
dc.contributor.authorWilliams, David J.-
dc.contributor.authorWilliams, M. Kevin-
dc.date.accessioned2023-10-06T05:13:34Z-
dc.date.available2023-10-06T05:13:34Z-
dc.date.issued1992-
dc.identifier.citationAngewandte Chemie International Edition in English, 1992, v. 31, n. 4, p. 478-480-
dc.identifier.issn0570-0833-
dc.identifier.urihttp://hdl.handle.net/10722/332696-
dc.description.abstractThe monoprotonation of diaza‐12‐crown‐6 derivatives converts these macrocycles to hosts for short‐chain alcohols; the association constant Ka is as high as 47 M−1. For the neutral diaza crown ether, on the other hand, Ka is only 1.1 M−1. X‐ray structure investigations show that the alcohol (R = Me) is held in place by two hydrogen bonds (see right). R = Me, Et, nPr, nBu; R′ = PhCH2, PhCH2CH2 (Figure Presented.) Copyright © 1992 by VCH Verlagsgesellschaft mbH, Germany-
dc.languageeng-
dc.relation.ispartofAngewandte Chemie International Edition in English-
dc.titleDesigning Synthetic Cationic Molecular Receptors for Alcohols-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/anie.199204781-
dc.identifier.scopuseid_2-s2.0-33748233294-
dc.identifier.volume31-
dc.identifier.issue4-
dc.identifier.spage478-
dc.identifier.epage480-
dc.identifier.eissn1521-3773-
dc.identifier.isiWOS:A1992JD99400031-

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