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Anion Recognition by Diureido-calix[4]arenes in the 1,3-Alternate Conformation
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SYSNO ASEP 0332779 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Anion Recognition by Diureido-calix[4]arenes in the 1,3-Alternate Conformation Title Aniontové rozpoznání diureido-calix[4]arenů v 1,3-střídavé konformaci Author(s) Cuřínová, Petra (UCHP-M) RID, SAI, ORCID
Stibor, I. (CZ)
Budka, J. (CZ)
Sýkora, Jan (UCHP-M) RID, ORCID, SAI
Lang, Kamil (UACH-T) SAI, RID, ORCID
Lhoták, P. (CZ)Source Title New Journal of Chemistry. - : Royal Society of Chemistry - ISSN 1144-0546
Roč. 33, č. 3 (2009), s. 612-619Number of pages 8 s. Language eng - English Country GB - United Kingdom Keywords complexation ability ; biological systems ; anions Subject RIV CF - Physical ; Theoretical Chemistry R&D Projects GA203/06/0738 GA ČR - Czech Science Foundation (CSF) GA203/07/1424 GA ČR - Czech Science Foundation (CSF) IAA400720706 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR) CEZ AV0Z40720504 - UCHP-M (2005-2011) AV0Z40320502 - UACH-T (2005-2011) UT WOS 000263922500022 DOI 10.1039/b816790g Annotation A series of diureido-calix[4]arenes immobilised in the 1,3-alternate conformation was synthesised and systematically studied for their complexation ability. As revealed by 1H NMR and UV/vis titrations, this structural motif leads to very efficient ligands for anion recognition with high binding constants in nonpolar solvents. The comparison with the corresponding ligands possessing the cone conformation indicates that diureido-calix[4]arene in a 1,3-alternate conformation are very promising anion receptors with pronounced binding ability towards carboxylates. Workplace Institute of Chemical Process Fundamentals Contact Eva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227 Year of Publishing 2010
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