Highly Efficient and Selective Recognition of Dicyanoaurate(I) by a Bambusuril Macrocycle in Water
Status PubMed-not-MEDLINE Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
GA20-13922S
Grantová Agentura České Republiky
LM2018121
Ministerstvo Školství, Mládeže a Tělovýchovy
CZ.02.1.01/0.0/0.0/17_043/0009632
Ministerstvo Školství, Mládeže a Tělovýchovy
LM2018127
Ministerstvo Školství, Mládeže a Tělovýchovy
857560
H2020 Research Infrastructures
PubMed
36056559
DOI
10.1002/anie.202210184
Knihovny.cz E-zdroje
- Klíčová slova
- Anion Binding, Bambusurils, Dicyanoaurate, Gold Extraction, Host-Guest Complexes,
- Publikační typ
- časopisecké články MeSH
Dicyanoaurate(I) anion, [Au(CN)2 ]- , plays a central role in the current industrial production of gold, as its extraction from crude ore samples represents the most money-consuming step. Herein, we present the strongest host-guest recognition of dicyanoaurate anion using the bambusuril receptor in water, a highly competitive solvent. The micromolar stability of such a complex facilitated the up to date most efficient supramolecular stripping of dicyanoaurate from activated carbon at ambient temperature. Thermodynamic characteristics of bambusuril binding with [Au(CN)2 ]- differing from binding of other inorganic chaotropic anions are rationalized, as well as the bambusuril selectivity for [Au(CN)2 ]- over [Ag(CN)2 ]- .
Department of Chemistry Faculty of Science Masaryk University Kamenice 5 62500 Brno Czech Republic
RECETOX Faculty of Science Masaryk University Kamenice 5 62500 Brno Czech Republic
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Modern Supramolecular Gold Chemistry: Gold-Metal Interactions and Applications (Ed.: A. Laguna), Wiley, Hoboken, 2008.
Gold Ore Processing: Project Development and Operations (Ed.: M. D. Adams), Elsevier, Singapore, 2016.
F. Scherbaum, A. Grohmann, B. Huber, C. Krüger, H. Schmidbaur, Angew. Chem. Int. Ed. Engl. 1988, 27, 1544-1546;
Angew. Chem. 1988, 100, 1602-1604.
M. A. Rawashdeh-Omary, M. A. Omary, H. H. Patterson, J. Am. Chem. Soc. 2000, 122, 10371-10380.
M. A. Rawashdeh-Omary, M. A. Omary, H. H. Patterson, J. P. Fackler, J. Am. Chem. Soc. 2001, 123, 11237-11247.
W. Meng, A. B. League, T. K. Ronson, J. K. Clegg, W. C. Isley, D. Semrouni, L. Gagliardi, C. J. Cramer, J. R. Nitschke, J. Am. Chem. Soc. 2014, 136, 3972-3980.
W. Meng, J. K. Clegg, J. R. Nitschke, Angew. Chem. Int. Ed. 2012, 51, 1881-1884;
Angew. Chem. 2012, 124, 1917-1920.
N. N. Andersen, K. Eriksen, M. Lisbjerg, M. E. Ottesen, B. O. Milhøj, S. P. A. Sauer, M. Pittelkow, J. Org. Chem. 2019, 84, 2577-2584.
W. Liu, L. O. Jones, H. Wu, C. L. Stern, R. A. Sponenburg, G. C. Schatz, J. F. Stoddart, J. Am. Chem. Soc. 2021, 143, 1984-1992.
J. Svec, M. Necas, V. Sindelar, Angew. Chem. Int. Ed. 2010, 49, 2378-2381;
Angew. Chem. 2010, 122, 2428-2431.
T. Lizal, V. Sindelar, Isr. J. Chem. 2018, 58, 326-333.
H. Valkenier, O. Akrawi, P. Jurček, K. Sleziaková, T. Lízal, K. Bartik, V. Šindelář, Chem 2019, 5, 429-444.
V. Havel, V. Sindelar, ChemPlusChem 2015, 80, 1601-1606.
M. A. Yawer, V. Havel, V. Sindelar, Angew. Chem. Int. Ed. 2015, 54, 276-279;
Angew. Chem. 2015, 127, 278-281.
M. Rekharsky, Y. Inoue, J. Am. Chem. Soc. 2000, 122, 4418-4435.
Deposition Numbers 2133370 and 2133371 contain the supplementary crystallographic data for this paper. These data are provided free of charge by the joint Cambridge Crystallographic Data Centre and Fachinformationszentrum Karlsruhe Access Structures service.
L. Ezzedinloo, K. A. Zenere, Z. Xie, M. Ahmed, S. Scottwell, M. Bhadbhade, H. E. A. Brand, J. K. Clegg, C. Hua, N. F. Sciortino, L. C. Parker, B. J. Powell, C. J. Kepert, S. M. Neville, Chem. Eur. J. 2021, 27, 5136-5141.
A. Djemel, O. Stefanczyk, M. Marchivie, E. Trzop, E. Collet, C. Desplanches, R. Delimi, G. Chastanet, Chem. Eur. J. 2018, 24, 14760-14767.
W.-F. Yeung, W.-T. Wong, J.-L. Zuo, T.-C. Lau, J. Chem. Soc. Dalton Trans. 2000, 629-631.
J. J. Zakrzewski, B. Sieklucka, S. Chorazy, Inorg. Chem. 2020, 59, 1393-1404.
V. A. Milway, L. N. Dawe, L. K. Thompson, Can. J. Chem. 2014, 92, 966-974.
M. Monim-ul-Mehboob, M. Ramzan, W. Zierkiewicz, M. Michalczyk, R. Mahmood, M. Altaf, S. Nadeem, M. Akhtar, S. Ahmad, Russ. J. Coord. Chem. 2018, 44, 198-206.
V. Havel, V. Sindelar, M. Necas, A. E. Kaifer, Chem. Commun. 2014, 50, 1372-1374.
T. Fiala, L. Ludvíková, D. Heger, J. Švec, T. Slanina, L. Vetráková, M. Babiak, M. Nečas, P. Kulhánek, P. Klán, V. Sindelar, J. Am. Chem. Soc. 2017, 139, 2597-2603.
T. Fiala, V. Sindelar, Supramol. Chem. 2016, 28, 810-816.
T. Fiala, K. Sleziakova, K. Marsalek, K. Salvadori, V. Sindelar, J. Org. Chem. 2018, 83, 1903-1912.
A. C. Sedgwick, J. T. Brewster, T. Wu, X. Feng, S. D. Bull, X. Qian, J. L. Sessler, T. D. James, E. V. Anslyn, X. Sun, Chem. Soc. Rev. 2021, 50, 9-38.
F. Biedermann, H.-J. Schneider, Chem. Rev. 2016, 116, 5216-5300.
F. Biedermann, V. D. Uzunova, O. A. Scherman, W. M. Nau, A. De Simone, J. Am. Chem. Soc. 2012, 134, 15318-15323.
S. Kubik, ChemistryOpen 2022, 11, e202200028.
P. S. Cremer, A. H. Flood, B. C. Gibb, D. L. Mobley, Nat. Chem. 2018, 10, 8-16.
K. I. Assaf, W. M. Nau, Angew. Chem. Int. Ed. 2018, 57, 13968-13981;
Angew. Chem. 2018, 130, 14164-14177.
E. A. Mezhov, G. A. Reymarov, N. L. Khananishvili, V. S. Schmidt, Radiokhimiya 1992, 34, 9-50.
Y. Marcus, J. Chem. Soc. Faraday Trans. 1991, 87, 2995-2999.
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