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dc.contributor.authorRodewald, Marko
dc.contributor.authorRautiainen, J. Mikko
dc.contributor.authorNiksch, Tobias
dc.contributor.authorGörls, Helmar
dc.contributor.authorOilunkaniemi, Raija
dc.contributor.authorWeigand, Wolfgang
dc.contributor.authorLaitinen, Risto Sakari
dc.date.accessioned2020-07-06T06:14:41Z
dc.date.available2020-07-06T06:14:41Z
dc.date.issued2020
dc.identifier.citationRodewald, M., Rautiainen, J. M., Niksch, T., Görls, H., Oilunkaniemi, R., Weigand, W., & Laitinen, R. S. (2020). Chalcogen‐Bonding Interactions in Telluroether Heterocycles [Te(CH2)m]n (n=1-4; m=3-7). <i>Chemistry : A European Journal</i>, <i>26</i>(61), 13806-13818. <a href="https://doi.org/10.1002/chem.202002510" target="_blank">https://doi.org/10.1002/chem.202002510</a>
dc.identifier.otherCONVID_36261854
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/71067
dc.description.abstractThe Te…Te secondary bonding interactions (SBI) in solid heterocyclic telluroethers were explored by preparing and structurally characterizing a series of [Te(CH2)m]n (n = 1‐4; m = 3‐7) species. The SBIs in 1,7‐Te2(CH2)10, 1,8‐Te2(CH2)12, 1,5,9‐Te3(CH2)9, 1,8,15‐Te3(CH2)18, 1,7,13,19‐Te4(CH2)20, 1,8,15,22‐Te4(CH2)24, and 1,9,17,25‐Te4(CH2)28 led to the tubular packing of the molecules, as has been observed previously for related thio‐ and selenoether rings. The nature of the intermolecular interactions was explored by solid‐state PBE0‐D3/pob‐TZVP calculations involving periodic boundary conditions. The packing of molecules in 1,7,13,19‐Te4(CH2)20, 1,8,15,22‐Te4(CH2)24, and 1,9,17,25‐Te4(CH2)28 form infinite shafts. The electron densities at bond critical points indicate a narrow range of Te…Te bond orders of 0.12‐0.14. The formation of the shafts can be rationalized by frontier orbital overlap and charge‐transfer.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesChemistry : A European Journal
dc.rightsCC BY 4.0
dc.subject.otherdensity functional calculations
dc.subject.otherheterocycles
dc.subject.othernoncovalent interactions
dc.subject.othersolid-state structures
dc.subject.othertellurium
dc.titleChalcogen‐Bonding Interactions in Telluroether Heterocycles [Te(CH2)m]n (n=1-4; m=3-7)
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202007065240
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineEpäorgaaninen ja analyyttinen kemiafi
dc.contributor.oppiaineInorganic and Analytical Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange13806-13818
dc.relation.issn0947-6539
dc.relation.numberinseries61
dc.relation.volume26
dc.type.versionpublishedVersion
dc.rights.copyright© 2020 The Authors. Published by Wiley-VCH GmbH.
dc.rights.accesslevelopenAccessfi
dc.subject.ysotelluuri
dc.subject.ysoeetterit
dc.subject.ysotiheysfunktionaaliteoria
dc.subject.ysokemialliset sidokset
dc.subject.ysoorganometalliyhdisteet
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p22857
jyx.subject.urihttp://www.yso.fi/onto/yso/p3840
jyx.subject.urihttp://www.yso.fi/onto/yso/p28852
jyx.subject.urihttp://www.yso.fi/onto/yso/p10130
jyx.subject.urihttp://www.yso.fi/onto/yso/p28123
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1002/chem.202002510
jyx.fundinginformationWe are grateful to Finnish CSC-IT Center for Science Ltd, The Finnish Grid and Cloud Infrastructure (urn:nbn:fi:researchinfras-2016072533), and Prof. H. M. Tuononen (University of Jyväskylä) for provision of computational resources. We are thankful to Dr. P. Bellstedt, Dipl-Phys. F. Pielenz, B. Rambach (NMR Platform of the FSU Jena), Dr. N. Ueberschaar, M. Heineck, S. Schönau (MS Platform FSU Jena) as well as Dipl.-Ing. B. Fähndrich (surface area measurements).
dc.type.okmA1


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