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1
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0002637831
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Fluorescent Chemosensors for Ion and Molecule Recognition
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American Chemical Society: Washington, DC
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Czarnik, A. W. Fluorescent Chemosensors for Ion and Molecule Recognition; ACS Symposium Series 538; American Chemical Society: Washington, DC, 1993.
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Czarnik, A.W.1
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0003652229
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Chemosensors for Ion and Molecule Recognition
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Kluwer Academic Publishers: London
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Desvergne, J. P.; Czarnik, A. W. Chemosensors for Ion and Molecule Recognition; NATO Asi Series, Series C; Kluwer Academic Publishers: London, 1997.
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For, selected reviews, see
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McCoy, C.P.5
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de Silva, A. P.; Fox, D. B.; Huxley, A. J. M.; Moody, T. S. Coord. Chem. Rev. 2000, 205, 41-57.
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(b) Lee, D. H.; Im, J. H.; Lee, J. H.; Hong, J. I. Tetrahedron Lett. 2002, 43, 9637-9640.
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Tetrahedron Lett
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Lee, D.H.1
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0036009980
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(c) Costero, A. M.; Andreu, R.; Monrabal, E.; Martínez- Mañez, R.; Sancenón, F.; Soto, J. J. Chem. Soc., Dalton Trans. 2002, 1769-1775.
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Costero, A.M.1
Andreu, R.2
Monrabal, E.3
Martínez- Mañez, R.4
Sancenón, F.5
Soto, J.6
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(e) Costero, A. M.; Gil, S.; Sanchis, J.; Peransi, S.; Sanz, V.; Williams, J. A. G. Tetrahedron 2004, 60, 6327-6334.
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Tetrahedron
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Costero, A.M.1
Gil, S.2
Sanchis, J.3
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(f) Costero, A. M.; Sanchis, J.; Gil, S.; Sanz, V.; Williams, J. A. G. J. Mater. Chem. 2005, 15, 2848-2853.
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Sanchis, J.2
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(g) Costero, A. M.; Bañuls, M. J.; Aurell, M. J.; Ochando, L. E.; Domenech, A. Tetrahedron 2005, 61, 10309-10320.
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Tetrahedron
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Costero, A.M.1
Bañuls, M.J.2
Aurell, M.J.3
Ochando, L.E.4
Domenech, A.5
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16
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0000129332
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For recent examples of other cyclopeptide-based chemosensors, see
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For recent examples of other cyclopeptide-based chemosensors, see: Leipert, D.; Nopper, D.; Bauser, M.; Gauglitz, G.; Jung, G. Angew. Chem. 1998, 110, 3503-3505;
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Angew. Chem
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Leipert, D.1
Nopper, D.2
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Jung, G.5
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17
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0032542306
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Angew. Chem., Int. Ed. 1998, 37, 3311-3314.
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Chem., Int. Ed
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Angew1
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33645079885
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Ngu-Schwemlein, M.; Butko, P.; Cook, B.; Whigham, T. J. Pept. Res. Suppl. 1 2005, 66, 72-81.
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J. Pept. Res. Suppl
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Ngu-Schwemlein, M.1
Butko, P.2
Cook, B.3
Whigham, T.4
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19
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McDonough, M. J.; Reynolds, A. J.; Lee, W. Y. G.; Jolliffe, K. A. Chem. Commun. 2006, 2971-2973.
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Chem. Commun
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McDonough, M.J.1
Reynolds, A.J.2
Lee, W.Y.G.3
Jolliffe, K.A.4
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20
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34447647634
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Zhang, Y. H.; Yin, Z. M.; He, J. Q.; Cheng, J. P. Tetrahedron Lett. 2007, 48, 6039-6043.
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Tetrahedron Lett
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Zhang, Y.H.1
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He, J.Q.3
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21
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0037202170
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(a) Kubik, S.; Kirchner, R.; Nolting, D.; Seidel, J. J. Am. Chem. Soc. 2002, 124, 12752-12760.
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J. Am. Chem. Soc
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(d) Rodriguez-Docampo, Z.; Pascu, S. I.; Kubik, S.; Otto, S. J. Am. Chem. Soc. 2006, 128, 11206-11210.
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J. Am. Chem. Soc
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Rodriguez-Docampo, Z.1
Pascu, S.I.2
Kubik, S.3
Otto, S.4
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Eller, L. R.; Stepien, M.; Fowler, C. J.; Lee, J. T.; Sessler, J. L.; Moyer, B. A. J. Am. Chem. Soc. 2007, 129, 11020-11021.
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Eller, L.R.1
Stepien, M.2
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Lee, J.T.4
Sessler, J.L.5
Moyer, B.A.6
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26
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37249008883
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Additional peaks are visible in the spectrum around the peak of the 1:1 sulfate complex evenly spaced by exactly 14 mass units. These peaks could correspond to sulfate complexes containing derivatives of 1 with different numbers of methyl groups in the biphenyl substituents. As HPLC and NMR spectroscopic characterization gave no indication of major impurities in the sample used for the measurement we believe that partial decomposition of 1 occurs during ionization.
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Additional peaks are visible in the spectrum around the peak of the 1:1 sulfate complex evenly spaced by exactly 14 mass units. These peaks could correspond to sulfate complexes containing derivatives of 1 with different numbers of methyl groups in the biphenyl substituents. As HPLC and NMR spectroscopic characterization gave no indication of major impurities in the sample used for the measurement we believe that partial decomposition of 1 occurs during ionization.
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27
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37249050063
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The binding isotherms obtained by the ITC titrations were all fitted by using the model of substrate binding to receptors with a single set of identical binding sites although formation of higher complexes in the case of iodide complexation cannot be ruled out
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The binding isotherms obtained by the ITC titrations were all fitted by using the model of substrate binding to receptors with a single set of identical binding sites although formation of higher complexes in the case of iodide complexation cannot be ruled out.
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28
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37249090450
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Calculations were performed by using MacSpartan '04 (Wavefunction Inc.) on the P enantiomers of A, B, and C (positive dihedral angle) with anti-oriented formyl groups. The biphenyl linker in the sulfate complex of 1 adopts the M conformation (negative dihedral angle).
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Calculations were performed by using MacSpartan '04 (Wavefunction Inc.) on the P enantiomers of A, B, and C (positive dihedral angle) with anti-oriented formyl groups. The biphenyl linker in the sulfate complex of 1 adopts the M conformation (negative dihedral angle).
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29544435887
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Benmenni, L.; Alilou, E. H.; Giorgi, M.; Pierrot, M.; Reglier, M. J. Chem. Cryst. 1994, 24, 345-352.
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Benmenni, L.1
Alilou, E.H.2
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Reglier, M.5
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0032500097
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Costero, A. M.; Andreu, C.; Martínez-Mañez, R.; Soto, J.; Ochando, L. E.; Amígo, J. M. Tetrahedron 1998, 54, 8159-8170.
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(1998)
Tetrahedron
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Costero, A.M.1
Andreu, C.2
Martínez-Mañez, R.3
Soto, J.4
Ochando, L.E.5
Amígo, J.M.6
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34
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34248205248
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For a recent related study, see
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For a recent related study, see: Allen, B. D.; Benniston, A. C.; Harriman, A.; Llarena, I.; Sams, C. A. J. Phys. Chem. A 2007, 111, 2641-2649.
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J. Phys. Chem. A
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Allen, B.D.1
Benniston, A.C.2
Harriman, A.3
Llarena, I.4
Sams, C.A.5
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