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(2008)
Calixarenes: An Introduction
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Gutsche, C.D.1
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2
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84892021501
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J. Vicens, J. Harrowfield, L. Backlouti, Springer Dordrecht
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J. Vicens, J. Harrowfield, L. Backlouti, Calixarenes in the Nanoworld 2007 Springer Dordrecht
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Calixarenes in the Nanoworld
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3
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0004287470
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Z. Asfari, V. Böhmer, J. Harrowfield, J. Vicens, Kluwer Academic Dordrecht
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Z. Asfari, V. Böhmer, J. Harrowfield, J. Vicens, Calixarenes 2001 2001 Kluwer Academic Dordrecht
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Calixarenes 2001
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6
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77956395392
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For recent reviews/books on anion-recognition see:
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For recent reviews/books on anion-recognition see:
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8
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66649133258
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R. Vilar, Springer GmbH Berlin
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R. Vilar, Recognition of Anions 2008 Springer GmbH Berlin
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Recognition of Anions
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14
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0004091542
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A. Bianchi, K. Bowman-James, E. Garcia-Espana, Wiley-VCH New York, NY
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A. Bianchi, K. Bowman-James, E. Garcia-Espana, Supramolecular Chemistry of Anions 1997 Wiley-VCH New York, NY
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(1997)
Supramolecular Chemistry of Anions
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15
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77956393607
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For review on calixarene-based anion receptors see:
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For review on calixarene-based anion receptors see:
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20
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77956392207
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For some recent examples of urea-substituted calixarene-bases receptors from our group see:
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For some recent examples of urea-substituted calixarene-bases receptors from our group see:
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21
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0038680403
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M. Dudic, P. Lhoták, I. Stibor, K. Lang, and P. Prosková Org. Lett. 5 2003 149 152
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K. Lang, P. Curinová, M. Dudic, P. Prosková, I. Stibor, V. Stastny, and P. Lhoták Tetrahedron Lett. 46 2005 4469 4472
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Lang, K.1
Curinová, P.2
Dudic, M.3
Prosková, P.4
Stibor, I.5
Stastny, V.6
Lhoták, P.7
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J. Kroupa, I. Stibor, M. Pojarova, M. Tkadlecova, and P. Lhotak Tetrahedron 64 2008 10075 10079
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Lhotak, P.5
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I. Stibor, J. Budka, V. Michlová, M. Tkadlecová, M. Pojarová, P. Cuínová, and P. Lhoták New J. Chem. 32 2008 1597 1607
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Budka, J.2
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Lhoták, P.7
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P. Cuínová, I. Stibor, J. Budka, J. Sykora, K. Lang, and P. Lhoták New J. Chem. 33 2009 612 619
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Lang, K.5
Lhoták, P.6
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D. Coquiere, S. Le Gac, U. Darbost, O. Seneque, I. Jabin, and O. Reinaud Org. Biomol. Chem. 7 2009 2485 2500
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Reinaud, O.6
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Kerckhoffs, J.M.C.A.2
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Reinhoudt, D.N.4
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77956392570
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note
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The biding constants were calculated using the computer program OPIUM (Kyvala M.) freely available at: http://www.natur.cuni.cz/∼kyvala/opium. html. All our attempts to measure the stoichiometry of complexes using Job plot analysis have failed as the small complexation constants did not lead to well resolved maximum in the corresponding plots. Anyhow, the complexation curves gave the best fit using 1:1 stoichiometry.
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36
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77956393027
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For complexation of neutral molecules (gases) by the cavity of 1,3-alternates see Ref. 5c.
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For complexation of neutral molecules (gases) by the cavity of 1,3-alternates see Ref. 5c.
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38
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0242560405
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A. Altomare, M.C. Burla, M. Camalli, G.L. Cascarano, C. Giacovazzo, A. Guagliardi, A.G.G. Moliterni, G. Polidori, and R. Spagna J. Appl. Crystallogr. 32 1999 115 119
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Altomare, A.1
Burla, M.C.2
Camalli, M.3
Cascarano, G.L.4
Giacovazzo, C.5
Guagliardi, A.6
Moliterni, A.G.G.7
Polidori, G.8
Spagna, R.9
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Betteridge, P.W.1
Carruthers, J.R.2
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Watkin, D.J.5
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