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dc.contributor.authorTwum, Kwaku
dc.contributor.authorNadimi, Sanaz
dc.contributor.authorOsei, Frank Boateng
dc.contributor.authorPuttreddy, Rakesh
dc.contributor.authorOjong, Yvonne Bessem
dc.contributor.authorHayward, John J.
dc.contributor.authorRissanen, Kari
dc.contributor.authorTrant, John F.
dc.contributor.authorBeyeh, Ngong Kodiah
dc.date.accessioned2023-02-02T09:51:56Z
dc.date.available2023-02-02T09:51:56Z
dc.date.issued2023
dc.identifier.citationTwum, K., Nadimi, S., Osei, F. B., Puttreddy, R., Ojong, Y. B., Hayward, J. J., Rissanen, K., Trant, J. F., & Beyeh, N. K. (2023). The “nitrogen effect” : Complexation with macrocycles potentiates fused heterocycles to form halogen bonds in competitive solvents. <i>Chemistry : An Asian Journal</i>, <i>18</i>(6), Article e202201308. <a href="https://doi.org/10.1002/asia.202201308" target="_blank">https://doi.org/10.1002/asia.202201308</a>
dc.identifier.otherCONVID_176548163
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/85300
dc.description.abstractWeak intermolecular forces are typically very difficult to observe in highly competitive polar protic solvents as they are overwhelmed by the quantity of competing solvent. This is even more challenging for three-component ternary assemblies of pure organic compounds. In this work, we overcome these complications by leveraging the binding of fused aromatic N-heterocycles in an open resorcinarene cavity to template the formation of a three-component halogen-bonded ternary assembly in a protic polar solvent system.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherWiley-VCH Verlag
dc.relation.ispartofseriesChemistry : An Asian Journal
dc.rightsIn Copyright
dc.subject.otherhalogen bond
dc.subject.otherresorcinarenes
dc.subject.otherternary assemblies
dc.subject.otherdimeric capsules
dc.subject.otherN-Heterocycles
dc.titleThe “nitrogen effect” : Complexation with macrocycles potentiates fused heterocycles to form halogen bonds in competitive solvents
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202302021582
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.relation.issn1861-4728
dc.relation.numberinseries6
dc.relation.volume18
dc.type.versionacceptedVersion
dc.rights.copyright© 2023 Wiley-VCH GmbH
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber317259
dc.subject.ysoorgaaniset yhdisteet
dc.subject.ysohalogeenit
dc.subject.ysoliuottimet
dc.subject.ysotyppi
dc.subject.ysokemia
dc.subject.ysomolekyylit
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p3841
jyx.subject.urihttp://www.yso.fi/onto/yso/p4164
jyx.subject.urihttp://www.yso.fi/onto/yso/p20402
jyx.subject.urihttp://www.yso.fi/onto/yso/p10988
jyx.subject.urihttp://www.yso.fi/onto/yso/p1801
jyx.subject.urihttp://www.yso.fi/onto/yso/p2984
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1002/asia.202201308
dc.relation.funderResearch Council of Finlanden
dc.relation.funderSuomen Akatemiafi
jyx.fundingprogramAcademy Project, AoFen
jyx.fundingprogramAkatemiahanke, SAfi
jyx.fundinginformationWe gratefully acknowledge financial support from the American Chemical Society (NKB: ACS-PRF grant no. 39427), Oakland University, MI, the Academy of Finland (KR: grant no. 317259), and the University of Jyväskylä. We also acknowledge the financial support from the Natural Sciences and Engineering Research Council of Canada (JFT: grant no. 2018-06338) and the Ontario Early Researcher Award (JFT: grant no. ER18-14-114)
dc.type.okmA1


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