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Crystal structure of (E)-1,2-diferrocenyl-1,2-bis­(furan-2-yl)ethene

dc.contributor.authorMloston, Grzegorz
dc.contributor.authorHamera-Fałdyga, Róża
dc.contributor.authorLinden, Anthony
dc.contributor.authorHeimgartner, Heinz
dc.date.accessioned2022-01-31T08:10:53Z
dc.date.available2022-01-31T08:10:53Z
dc.date.issued2018
dc.identifier.issn2056-9890
dc.identifier.urihttp://hdl.handle.net/11089/40538
dc.descriptionThe title compound, [Fe₂(C₅H₅)₂(C₂₀H₁₄O₂)], is the product of a new synthetic route towards tetraaryl/hetaryl-substituted ethenes that reduces the occurrence of side-products. In the crystal, the molecule is centrosymmetric and the cyclopentadienyl (Cp) rings are nearly coplanar and aligned slightly closer to a staggered conformation than to an eclipsed one. The ethene plane is tilted by 32.40 (18)° with respect to that of the substituted Cp ring and by 63.19 (19)° with respect to that of the furan ring. C—H··· π interactions link the molecules into a three-dimensional supramolecular framework.pl_PL
dc.description.sponsorshipFunding for this research was provided by: Maestro-3 (grant No. Dec-2012/06/A/ST5/00219 to R. Hamera-Fałdyga, G. Mlostoń); Institutspartnerschaft, Alexander von Humboldt Foundation, Bonn (grant to R. Hamera-Fałdyga, G. Mlostoń).pl_PL
dc.language.isoenpl_PL
dc.publisherInternational Union of Crystallographypl_PL
dc.relation.ispartofseriesActa Crystallographica Section E: Crystallographic Communications;74
dc.rightsUznanie autorstwa 4.0 Międzynarodowe*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectcrystal structurepl_PL
dc.subjectethenespl_PL
dc.subjectferrocenepl_PL
dc.titleCrystal structure of (E)-1,2-diferrocenyl-1,2-bis­(furan-2-yl)ethenepl_PL
dc.typeArticlepl_PL
dc.page.number625-629pl_PL
dc.contributor.authorAffiliationDepartment of Organic and Applied Chemistry, University of Łódź, Tamka 12, PL-91-403 Łódź, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Organic and Applied Chemistry, University of Łódź, Tamka 12, PL-91-403 Łódź, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Chemistry, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerlandpl_PL
dc.contributor.authorAffiliationDepartment of Chemistry, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerlandpl_PL
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dc.contributor.authorEmailanthony.linden@chem.uzh.chpl_PL
dc.identifier.doi10.1107/S2056989018005078
dc.relation.volume5pl_PL
dc.disciplinenauki chemicznepl_PL


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