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dc.contributor.authorHu, Johnny
dc.contributor.authorWard, Jas S.
dc.contributor.authorChaumont, Alain
dc.contributor.authorRissanen, Kari
dc.contributor.authorVincent, Jean-Marc
dc.contributor.authorHeitz, Valérie
dc.contributor.authorJacquot de Rouville, Henri-Pierre
dc.date.accessioned2020-09-07T05:46:50Z
dc.date.available2020-09-07T05:46:50Z
dc.date.issued2020
dc.identifier.citationHu, J., Ward, J. S., Chaumont, A., Rissanen, K., Vincent, J.-M., Heitz, V., & Jacquot de Rouville, H.-P. (2020). A Bis‐Acridinium Macrocycle as Multi‐Responsive Receptor and Selective Phase‐Transfer Agent of Perylene. <i>Angewandte Chemie</i>, <i>59</i>(51), 23206-23212. <a href="https://doi.org/10.1002/anie.202009212" target="_blank">https://doi.org/10.1002/anie.202009212</a>
dc.identifier.otherCONVID_41916568
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/71652
dc.description.abstractA bis‐acridinium cyclophane incorporating switchable acridinium moieties linked by a 3,5‐dipyridylanisole spacer was studied as a multi‐responsive host for polycyclic aromatic hydrocarbon guests. Complexation of perylene was proven to be the most effective and was characterized in particular by a charge transfer band as signal output. Effective catch and release of the guest was triggered by both chemical (proton/hydroxide) and redox stimuli. Moreover, the dicationic host was also easily switched between organic and perfluorocarbon phases for application related to the enrichment of perylene from a mixture of polycyclic aromatic hydrocarbons.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherWiley-VCH Verlag
dc.relation.ispartofseriesAngewandte Chemie
dc.rightsIn Copyright
dc.subject.otherisäntä-vieras kemia
dc.subject.othermulti-responsive receptor
dc.subject.otherphase transfer
dc.subject.otheracridinium
dc.subject.otherperfluorocarbons
dc.subject.otherhost-guest chemistry
dc.titleA Bis‐Acridinium Macrocycle as Multi‐Responsive Receptor and Selective Phase‐Transfer Agent of Perylene
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202009075761
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.pagerange23206-23212
dc.relation.issn1433-7851
dc.relation.numberinseries51
dc.relation.volume59
dc.type.versionacceptedVersion
dc.rights.copyright© 2020 Wiley‐VCH GmbH
dc.rights.accesslevelopenAccessfi
dc.subject.ysoPFC-yhdisteet
dc.subject.ysosupramolekulaarinen kemia
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p16398
jyx.subject.urihttp://www.yso.fi/onto/yso/p37759
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1002/anie.202009212
jyx.fundinginformationThis work was supported by the CNRS, the University of Strasbourg, the University of Bordeaux and the University of Jyväskylä. We gratefully acknowledge the International Center for Frontier Research in Chemistry ic-FRC (www.icfrc.fr) for financial support. We are grateful to the Fédération de Chimie Le Bel FR 2010 of the University of Strasbourg. JH thanks the French Ministry of National Education for a PhD Fellowship.
dc.type.okmA1


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