Face-controlled chirality induction in octahedral thiacalixarene-based porous coordination cages
Khariushin, 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. Nanoscale, Early online. https://doi.org/10.1039/d4nr03622k
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2025Access restrictions
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© The Royal Society of Chemistry 2025
Nanosized 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.
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Royal Society of ChemistryISSN Search the Publication Forum
2040-3364Publication in research information system
https://converis.jyu.fi/converis/portal/detail/Publication/244490036
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This 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.License
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