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dc.contributor.authorCarlsson, Anna-Carin C.
dc.contributor.authorMehmeti, Krenare
dc.contributor.authorUhrbom, Martin
dc.contributor.authorKarim, Alavi
dc.contributor.authorBedin, Michele
dc.contributor.authorPuttreddy, Rakesh
dc.contributor.authorKleinmaier, Roland
dc.contributor.authorNeverov, Alexei A.
dc.contributor.authorNekoueishahraki, Bijan
dc.contributor.authorGräfenstein, Jürgen
dc.contributor.authorRissanen, Kari
dc.contributor.authorErdélyi, Máté
dc.date.accessioned2016-08-26T09:56:35Z
dc.date.available2016-08-26T09:56:35Z
dc.date.issued2016
dc.identifier.citationCarlsson, A.-C. C., Mehmeti, K., Uhrbom, M., Karim, A., Bedin, M., Puttreddy, R., Kleinmaier, R., Neverov, A. A., Nekoueishahraki, B., Gräfenstein, J., Rissanen, K., & Erdélyi, M. (2016). Substituent Effects on the [N−I−N]+ Halogen Bond. <i>Journal of the American Chemical Society</i>, <i>138</i>(31), 9853-9863. <a href="https://doi.org/10.1021/jacs.6b03842" target="_blank">https://doi.org/10.1021/jacs.6b03842</a>
dc.identifier.otherCONVID_26157147
dc.identifier.otherTUTKAID_70869
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/51083
dc.description.abstractWe have investigated the influence of electron density on the three-center [N–I–N]+ halogen bond. A series of [bis(pyridine)iodine]+ and [1,2-bis((pyridine-2-ylethynyl)benzene)iodine]+ BF4– complexes substituted with electron withdrawing and donating functionalities in the para-position of their pyridine nitrogen were synthesized and studied by spectroscopic and computational methods. The systematic change of electron density of the pyridine nitrogens upon alteration of the para-substituent (NO2, CF3, H, F, Me, OMe, NMe2) was confirmed by 15N NMR and by computation of the natural atomic population and the π electron population of the nitrogen atoms. Formation of the [N–I–N]+ halogen bond resulted in >100 ppm 15N NMR coordination shifts. Substituent effects on the 15N NMR chemical shift are governed by the π population rather than the total electron population at the nitrogens. Isotopic perturbation of equilibrium NMR studies along with computation on the DFT level indicate that all studied systems possess static, symmetric [N–I–N]+ halogen bonds, independent of their electron density. This was further confirmed by single crystal X-ray diffraction data of 4-substituted [bis(pyridine)iodine]+ complexes. An increased electron density of the halogen bond acceptor stabilizes the [N···I···N]+ bond, whereas electron deficiency reduces the stability of the complexes, as demonstrated by UV-kinetics and computation. In contrast, the N–I bond length is virtually unaffected by changes of the electron density. The understanding of electronic effects on the [N–X–N]+ halogen bond is expected to provide a useful handle for the modulation of the reactivity of [bis(pyridine)halogen]+-type synthetic reagents.en
dc.languageeng
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.ispartofseriesJournal of the American Chemical Society
dc.subject.otherhalogeenisidos
dc.subject.otherhalogen bonds
dc.titleSubstituent Effects on the [N−I−N]+ Halogen Bond
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201608113767
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.date.updated2016-08-11T06:15:03Z
dc.type.coarjournal article
dc.description.reviewstatuspeerReviewed
dc.format.pagerange9853-9863
dc.relation.issn0002-7863
dc.relation.numberinseries31
dc.relation.volume138
dc.type.versionpublishedVersion
dc.rights.copyright© the Authors, 2016. This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber263256
dc.subject.ysokemialliset sidokset
dc.subject.ysosupramolekulaarinen kemia
dc.subject.ysomolekyylit
jyx.subject.urihttp://www.yso.fi/onto/yso/p10130
jyx.subject.urihttp://www.yso.fi/onto/yso/p37759
jyx.subject.urihttp://www.yso.fi/onto/yso/p2984
dc.rights.urlhttp://pubs.acs.org/page/policy/authorchoice_termsofuse.html
dc.relation.doi10.1021/jacs.6b03842
dc.relation.funderSuomen Akatemiafi
dc.relation.funderAcademy of Finlanden
jyx.fundingprogramAkatemiaprofessorin tehtävä, SAfi
jyx.fundingprogramResearch post as Academy Professor, AoFen
jyx.fundinginformationThe research leading to these results has received funding from the European Research Council under the European Union’s Seventh Framework Programme (FP7/2007-2013)/ERC Grant Agreement No. 259638. We thank the Swedish Research Council (ME 2007:4407; 621-2008-3562) and the Academy of Finland (KR: 263256 and 265328) for financial support, and Professor Stan Brown (Department of Chemistry, Queen’s University) for giving us access to equipment for the UV–vis kinetic experiments.


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Except where otherwise noted, this item's license is described as © the Authors, 2016. This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.