By Anthony W. Czarnik
content material: Supramolecular chemistry, fluorescence, and sensing / Anthony W. Czarnik --
Synthesis and research of crown ethers with alkali-metal-enhanced fluorescence : quest for flashy crowns / L.R. Sousa, B. Son, T.E. Trehearne, R.W. Stevenson, S.J. Ganion, B.E. Beeson, S. Barnell, T.E. Mabry, M. Yao, C. Chakrabarty, P.L. Bock, C.C. Yoder, and S. Pope --
Ion popularity detected by means of alterations in photoinduced cost or strength move / Bernard Valeur, Jean Bourson, and Jacques Pouget --
Fluorescent photoinduced electron-transfer sensors : the easy common sense and its extensions / Richard A. Bissell, A. Prasanna de Silva, H.Q. Nimal Gunaratne, P.L. Mark Lynch, Colin P. McCoy, Glenn E.M. Maguire, and K.R.A. Samankumara Sandanayake --
Tunable fluorescence of a few macrocyclic anthracenophanes / H. Bouas-Laurent, J-P. Desvergne, F. Fages, and P. Marsau --
Fluorescent cyclodextrins for detecting natural compounds with molecular popularity / Akihiko Ueno --
Intrinsic chromophores and fluorophores in artificial molecular receptors / Thomas W. Bell, Daniel L. Beckles, Peter J. Cragg, Jia Liu, James Maioriello, Andrew T. Papoulis, and Vincent J. Santora --
Fluorescent sign transduction in molecular sensors and dosimeters / Anthony W. Czarnik --
Fluorescent and photochemical probes of dynamic biochemical indications within residing cells / Roger Y. Tsien --
1,2-Bis(2-aminophenoxy)ethane-N, N, N', N', -tetraacetic acid conjugates used to degree intracellular Ca² focus / Michael A. Kuhn --
Fluorescent chemosensors for tracking potassium in blood and throughout organic membranes / Divakar Masilamani and Mariann E. Lucas --
Fluorescent probes in reviews of proteases / provide A. Krafft and Gary T. Wang --
Lifetime-based sensing utilizing phase-modulation fluorometry / H. Szmacinski and J.R. Lakowicz.
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Extra resources for Fluorescent Chemosensors for Ion and Molecule Recognition
In contrast to acetonitrile, the sigmoidal shape of the titration curve observed in propylene carbonate (Figure 10) is remarkable and characteristic of cooperative binding. 5x1ο M . The structure of the complex is likely to be helical, as often observed with oligoethylene glycol ethers (27). ; ACS Symposium Series; American Chemical Society: Washington, DC, 1993. ch003 40 FLUORESCENT CHEMOSENSORS FOR ION AND MOLECULE RECOGNITION Figure 8. Emission and excitation spectra of D X A under the same conditions as those indicated in Figure 7.
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Chem. 1985, 260, 3440. (6) Konopelski, J. ; Bouas-Laurent, H . J. Chem. , Chem. Commun. 1985, 433. (7) Bouas-Laurent, H . ; Daney, M . -H. J. Am. Chem. Soc. 1986, 108, 315. (8) Tundo. ; Fendler, J. H . J. Am. Chem. Soc. 1980, 102, 1760. (9) Haugland, R. P. : Eugene, OR, 1992, pp 142-152. (10) Moore, E. D. ; Tsien, R. ; Fay. F. S. Fed. Am. Soc. Exp. Biol. J. 1988, 2(4), Abs. 2660. (11) de Silva, A. ; de Silva, S. A. J. Chem. , Chem. Commun. 1986, 1709. (12) de Silva, A. ; Sandanayake, K. R. A. S.
Fluorescent Chemosensors for Ion and Molecule Recognition by Anthony W. Czarnik