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dc.contributor.authorWard, Jas S.
dc.contributor.authorGomila, Rosa M.
dc.contributor.authorFrontera, Antonio
dc.contributor.authorRissanen, Kari
dc.date.accessioned2022-03-24T11:49:24Z
dc.date.available2022-03-24T11:49:24Z
dc.date.issued2022
dc.identifier.citationWard, J. S., Gomila, R. M., Frontera, A., & Rissanen, K. (2022). Iodine(i) complexes incorporating sterically bulky 2-substituted pyridines. <i>RSC Advances</i>, <i>12</i>(14), 8674-8682. <a href="https://doi.org/10.1039/d2ra01390h" target="_blank">https://doi.org/10.1039/d2ra01390h</a>
dc.identifier.otherCONVID_117399984
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/80363
dc.description.abstractThe silver(I) and iodine(I) complexes of the 2-substituted pyridines 2-(diphenylmethyl)pyridine (1) and 2-(1,1-diphenylethyl)pyridine (2), along with their potential protonated side products, were synthesised to investigate the steric limitations of iodine(I) complex formation. The complexes were characterised by 1H and 1H–15N HMBC NMR, X-ray crystallography, and DFT calculations. The solid-state structures for the silver(I) and iodine(I) complexes were extensively compared to the literature and analysed by DFT to examine the influence of the sterically bulky pyridines and their anions.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherRoyal Society of Chemistry (RSC)
dc.relation.ispartofseriesRSC Advances
dc.rightsCC BY-NC 3.0
dc.titleIodine(i) complexes incorporating sterically bulky 2-substituted pyridines
dc.typeresearch article
dc.identifier.urnURN:NBN:fi:jyu-202203242050
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.pagerange8674-8682
dc.relation.issn2046-2069
dc.relation.numberinseries14
dc.relation.volume12
dc.type.versionpublishedVersion
dc.rights.copyright© 2022 The Author(s). Published by the Royal Society of Chemistry
dc.rights.accesslevelopenAccessfi
dc.type.publicationarticle
dc.relation.grantnumber317259
dc.subject.ysohopea
dc.subject.ysoröntgenkristallografia
dc.subject.ysokemia
dc.subject.ysosupramolekulaarinen kemia
dc.subject.ysokemialliset yhdisteet
dc.subject.ysojodi
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p7409
jyx.subject.urihttp://www.yso.fi/onto/yso/p29058
jyx.subject.urihttp://www.yso.fi/onto/yso/p1801
jyx.subject.urihttp://www.yso.fi/onto/yso/p37759
jyx.subject.urihttp://www.yso.fi/onto/yso/p324
jyx.subject.urihttp://www.yso.fi/onto/yso/p18902
dc.rights.urlhttps://creativecommons.org/licenses/by-nc/3.0/
dc.relation.doi10.1039/d2ra01390h
dc.relation.funderResearch Council of Finlanden
dc.relation.funderSuomen Akatemiafi
jyx.fundingprogramAcademy Project, AoFen
jyx.fundingprogramAkatemiahanke, SAfi
jyx.fundinginformationThe authors gratefully acknowledge the Magnus Ehrnrooth Foundation (J. S. W.), the MICIU/AEI of Spain (A. F. project PID2020-115637GB-I00, FEDER), the Academy of Finland (K. R. grant no. 317259), and the University of Jyvaskyla, Finland for financial support.
dc.type.okmA1


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