Reversing selectivity of bambusuril macrocycles toward inorganic anions by installing spacious substituents on their portals

. 2025 Jan 15 ; 16 (3) : 1288-1292. [epub] 20241206

Status PubMed-not-MEDLINE Jazyk angličtina Země Velká Británie, Anglie Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid39677942

Two chiral bambusurils, which are diastereomers to each other, show remarkable differences in their binding affinity and selectivity toward inorganic anions as determined by isothermal titration calorimetry. These differences are explained by quantum-chemical calculations.

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Busschaert N. Caltagirone C. Van Rossom W. Gale P. A. Chem. Rev. 2015;115:8038–8155. doi: 10.1021/acs.chemrev.5b00099. PubMed DOI

McNaughton D. A. Ryder W. G. Gilchrist A. M. Wang P. Fares M. Wu X. Gale P. A. Chem. 2023;9:3045–3112.

Chen L. Berry S. N. Wu X. Howe E. N. W. Gale P. A. Chem. 2020;6:61–141.

Anion-binding catalysis, ed. O. García Mancheño, Wiley-VCH, Weinheim, 2022

Macreadie L. K. Gilchrist A. M. McNaughton D. A. Ryder W. G. Fares M. Gale P. A. Chem. 2022;8:46–118.

Qin L. Vervuurt S. J. N. Elmes R. B. P. Berry S. N. Proschogo N. Jolliffe K. A. Chem. Sci. 2020;11:201–207. doi: 10.1039/C9SC04786G. DOI

Zhou W. Li A. Gale P. A. He Q. Cell Rep. Phys. Sci. 2022;3:100875. doi: 10.1016/j.xcrp.2022.100875. DOI

Evans N. H. Beer P. D. Angew. Chem., Int. Ed. 2014;53:11716–11754. doi: 10.1002/anie.201309937. PubMed DOI

Gale P. A. Chem. Commun. 2011;47:82–86. doi: 10.1039/C0CC00656D. PubMed DOI

Steed J. W. and Atwood J. L., Supramolecular Chemistry, Wiley, Chichester, 2edn, 2009, repr. with corr

d'Ischia M., Napolitano A. and Pezzella A., in Comprehensive Heterocyclic Chemistry III, ed. A. R. Katritzky, C. A. Ramsden, E. F. V. Scriven and R. J. K. Taylor, Elsevier, Oxford, 2008, pp. 353–388

Kaabel S. Adamson J. Topić F. Kiesilä A. Kalenius E. Öeren M. Reimund M. Prigorchenko E. Lõokene A. Reich H. J. Rissanen K. Aav R. Chem. Sci. 2017;8:2184–2190. doi: 10.1039/C6SC05058A. PubMed DOI PMC

Lizal T. Sindelar V. Isr. J. Chem. 2018;58:326–333. doi: 10.1002/ijch.201700111. DOI

Reany O. Mohite A. Keinan E. Isr. J. Chem. 2018;58:449–460. doi: 10.1002/ijch.201700138. DOI

Svec J. Necas M. Sindelar V. Angew. Chem., Int. Ed. 2010;49:2378–2381. doi: 10.1002/anie.201000420. PubMed DOI

Havel V. Svec J. Wimmerova M. Dusek M. Pojarova M. Sindelar V. Org. Lett. 2011;13:4000–4003. doi: 10.1021/ol201515c. PubMed DOI

Chvojka M. Madea D. Valkenier H. Šindelář V. Angew. Chem., Int. Ed. 2024;63:e202318261. doi: 10.1002/anie.202318261. PubMed DOI

Havel V. Babiak M. Sindelar V. Chem.–Eur. J. 2017;23:8963–8968. doi: 10.1002/chem.201701316. PubMed DOI

Havel V. Sindelar V. ChemPlusChem. 2015;80:1601–1606. doi: 10.1002/cplu.201500345. PubMed DOI

Sokolov J. Šindelář V. Chem.–Eur. J. 2018;24:15482–15485. doi: 10.1002/chem.201802748. PubMed DOI

Valkenier H. Akrawi O. Jurček P. Sleziaková K. Lízal T. Bartik K. Šindelář V. Chem. 2019;5:429–444.

Liu Y. Sengupta A. Raghavachari K. Flood A. H. Chem. 2017;3:411–427.

Neese F. Rev. Comput. Mol. Sci. 2012;2:73–78. doi: 10.1002/wcms.81. DOI

Brandenburg J. G. Bannwarth C. Hansen A. Grimme S. J. Chem. Phys. 2018;148:064104. doi: 10.1063/1.5012601. PubMed DOI

Adamo C. Barone V. J. Chem. Phys. 1999;110:6158–6170. doi: 10.1063/1.478522. DOI

Perdew J. P. Burke K. Ernzerhof M. Phys. Rev. Lett. 1996;77:3865–3868. doi: 10.1103/PhysRevLett.77.3865. PubMed DOI

Neese F. Wennmohs F. Hansen A. Becker U. Mov. Front. Quantum Chem. 2009;356:98–109.

Grimme S. Ehrlich S. Goerigk L. J. Comput. Chem. 2011;32:1456–1465. doi: 10.1002/jcc.21759. PubMed DOI

Weigend F. Ahlrichs R. Phys. Chem. Chem. Phys. 2005;7:3297–3305. doi: 10.1039/B508541A. PubMed DOI

Boys S. F. Bernardi F. Mol. Phys. 1970;19:553–566. doi: 10.1080/00268977000101561. DOI

Marenich A. V. Cramer C. J. Truhlar D. G. J. Phys. Chem. B. 2009;113:6378–6396. doi: 10.1021/jp810292n. PubMed DOI

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