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dc.contributor.authorMevissen, Christian
dc.contributor.authorKwamen, Carel
dc.contributor.authorHimmel, Leonard
dc.contributor.authorChen, Xiaofei
dc.contributor.authorBrückner, Matthias
dc.contributor.authorHuda, Saskia
dc.contributor.authorGöb, Christian
dc.contributor.authorJenniches, Judith
dc.contributor.authorOppel, Iris
dc.contributor.authorWard, James
dc.contributor.authorRissanen, Kari
dc.contributor.authorAlbrecht, Markus
dc.date.accessioned2020-09-21T14:09:03Z
dc.date.available2020-09-21T14:09:03Z
dc.date.issued2020
dc.identifier.citationMevissen, C., Kwamen, C., Himmel, L., Chen, X., Brückner, M., Huda, S., Göb, C., Jenniches, J., Oppel, I., Ward, J., Rissanen, K., & Albrecht, M. (2020). Helicates with Ether‐Substituted Catechol Esters as Ligands. <i>European Journal of Organic Chemistry</i>, <i>2020</i>(32), 5161-5172. <a href="https://doi.org/10.1002/ejoc.202000843" target="_blank">https://doi.org/10.1002/ejoc.202000843</a>
dc.identifier.otherCONVID_41576175
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/71826
dc.description.abstractMono‐ or biscatechol esters with ether‐type substituents or spacers form either triple lithium bridged dimeric helicates or triple stranded helicates with the ability to bind three lithium cations in their interior. Hierarchical helicates with ether or thioether substituents show in solution a monomer‐dimer equilibrium which is independent of the heteroatom in the ester substituent. However, dimerization constants are significantly lower than for corresponding alkyl derivatives. Dinuclear helicates with oligoether spacers are well obtained in the presence of lithium cations. Upon removal of the cations the helicates expand and successive addition of LiCl results in compression again.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesEuropean Journal of Organic Chemistry
dc.rightsCC BY 4.0
dc.subject.otherhelicate
dc.subject.othertemplating
dc.subject.othermolecular switch
dc.subject.otherthermodynamics
dc.subject.othercatecholate
dc.titleHelicates with Ether‐Substituted Catechol Esters as Ligands
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202009215909
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineOrganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange5161-5172
dc.relation.issn1434-193X
dc.relation.numberinseries32
dc.relation.volume2020
dc.type.versionpublishedVersion
dc.rights.copyright© 2020 the Authors
dc.rights.accesslevelopenAccessfi
dc.subject.ysotermodynamiikka
dc.subject.ysoesterit
dc.subject.ysosupramolekulaarinen kemia
dc.subject.ysokompleksiyhdisteet
dc.subject.ysolitium
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p14558
jyx.subject.urihttp://www.yso.fi/onto/yso/p11144
jyx.subject.urihttp://www.yso.fi/onto/yso/p37759
jyx.subject.urihttp://www.yso.fi/onto/yso/p30190
jyx.subject.urihttp://www.yso.fi/onto/yso/p29475
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1002/ejoc.202000843
jyx.fundinginformationX. C. acknowledges the support by the Chinese Scholarship Council (CSC).
dc.type.okmA1


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