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dc.contributor.authorKhariushin, Ivan V.
dc.contributor.authorOvsyannikov, Alexander S.
dc.contributor.authorBaudron, Stéphane A.
dc.contributor.authorWard, Jas S.
dc.contributor.authorKiesilä, Anniina
dc.contributor.authorRissanen, Kari
dc.contributor.authorKalenius, Elina
dc.contributor.authorChessé, Matthieu
dc.contributor.authorNowicka, Beata
dc.contributor.authorSolovieva, Svetlana E.
dc.contributor.authorAntipin, Igor S.
dc.contributor.authorBulach, Véronique
dc.contributor.authorFerlay, Sylvie
dc.date.accessioned2024-12-19T06:13:41Z
dc.date.available2024-12-19T06:13:41Z
dc.date.issued2025
dc.identifier.citationKhariushin, I. V., Ovsyannikov, A. S., Baudron, S. A., Ward, J. S., Kiesilä, A., Rissanen, K., Kalenius, E., Chessé, M., Nowicka, B., Solovieva, S. E., Antipin, I. S., Bulach, V., & Ferlay, S. (2025). Face-controlled chirality induction in octahedral thiacalixarene-based porous coordination cages. <i>Nanoscale</i>, <i>Early online</i>. <a href="https://doi.org/10.1039/d4nr03622k" target="_blank">https://doi.org/10.1039/d4nr03622k</a>
dc.identifier.otherCONVID_244490036
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/99064
dc.description.abstractNanosized chiral octahedral M32 coordination cages were prepared via self-assembly of sulfonylcalix[4]arene tetranuclear M(II) clusters (M = Co or Ni) with enantiomerically enriched linkers based on tris(dipyrrinato)cobalt(III) complexes, appended with peripheral carboxylic groups. Two pairs of enantiomers of cages were obtained and unambiguously characterized from a structural point of view, using single crystal X-ray diffraction. Chiral-HPLC was used to evidence the enantiomers. In the solid state, the compounds present intrinsic and extrinsic porosity: the intrinsic porosity is linked with the size of the cages, which present an inner diameter of ca. 19 Å. The obtained solid-state supramolecular architectures demonstrated good performances as adsorbents for water and 2-butanol guest molecules.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherRoyal Society of Chemistry
dc.relation.ispartofseriesNanoscale
dc.rightsIn Copyright
dc.titleFace-controlled chirality induction in octahedral thiacalixarene-based porous coordination cages
dc.typeresearch article
dc.identifier.urnURN:NBN:fi:jyu-202412197875
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn2040-3364
dc.relation.volumeEarly online
dc.type.versionacceptedVersion
dc.rights.copyright© The Royal Society of Chemistry 2025
dc.rights.accesslevelembargoedAccessfi
dc.type.publicationarticle
dc.subject.ysosupramolekulaarinen kemia
dc.subject.ysonanorakenteet
dc.subject.ysokompleksiyhdisteet
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p37759
jyx.subject.urihttp://www.yso.fi/onto/yso/p25315
jyx.subject.urihttp://www.yso.fi/onto/yso/p30190
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1039/d4nr03622k
jyx.fundinginformationThis work was supported by the University of Strasbourg, Fondation Jean-Marie Lehn, Doctoral Verdnaskii scholarship from the French Embassy (I. V. K.), the CNRS and the Russian Science Foundation (Project No. 19-73-20035 to A. S. O., S. E. S. and I. S. A.). The University of Jyväskylä is acknowledged for the use of SCXRD and MS instrumentation.
dc.type.okmA1


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