Luminescent europium tetraazamacrocyclic complexes with wide range pH sensitivity

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Thorfinnur Gunnlaugsson


Abstract

The complexes [EuL1]3+ and [EuL2] function as luminescent pH sensors over an extended pH range; two distinguishable pH switching ranges are observed: the delayed europium emission is switched on in acidic solution, whereas the fluorescence emission spectra show a pronounced pH dependence only in alkaline media.


References

  1. Fluorescent Chemosensors for Ions and Molecular Recognition, ed. A. W. Czarnik, ACS Symp. Ser., Washington DC, 1993 Search PubMed; R. A. Bissell, A. P. de Silva, H. Q. N. Gunaratne, P. L. M. Lynch, G. E. M. Maguire and K. R. A. S. Sandanayake, Chem. Soc. Rev., 1992, 21, 187 Search PubMed; R. A. Bissell, A. P. de Silva, H. Q. N. Gunaratne, P. L. M. Lynch, G. E. M. Maguire, C. P. McCoy and K. R. A. S. Sandanayake, Top. Curr. Chem., 1993, 168, 223 RSC; A. W. Czarnik, Acc. Chem. Res., 1994, 27, 302.
  2. A. Mayer and S. Neuenhofer, Angew. Chem., Int. Ed. Engl., 1994, 33, 1044 CrossRef; E. F. G. Dickson, A. Pollak and E. P. Diamandis, J. Photochem. Photobiol. B, 1995, 27, 3 CrossRef CAS.
  3. R. A. Bissell and A. P. de Silva, J. Chem. Soc., Chem. Commun., 1991, 1148 RSC; R. Grigg, J. M. Holmes, S. K. Jones and W. D. J. A. Norbert, J. Chem. Soc., Chem. Commun., 1994, 185 RSC.
  4. J.-C. G. Bunzli, in Lanthanide Probes in Life, Chemical and Earth Sciences, Theory and Practice, ed. J.-C. G. Bunzli and G. R. Choppin, Elsevier, New York, 1989, p. 219 Search PubMed; D. Parker and J. A. G. Williams, J. Chem. Soc., Dalton Trans., 1996, 3613 Search PubMed; J. Chem. Soc., Perkin Trans. 2, 1995, 1305 RSC; A. Beeby and S. Faulkner, Chem. Phys. Lett., 1997, 266, 116 RSC; A. Beeby, R. S. Dickins, S. Faulkner, D. Parker and J. A. G. Williams, Chem. Commun., 1997, 1401 Search PubMed.
  5. A. P. de Silva, H. Q. N. Gunaratne and T. E. Rice, Angew. Chem., Int. Ed. Engl., 1996, 35, 2116 CrossRef CAS.
  6. D. Parker, in Comprehensive Supramolecular Chemistry, ed. J.-M. Lehn, D. D. Macnicol, J. L. Atwood, J. E. Davis, D. N. Reinhoudt and F. Vogtle, Pergamon, Oxford, 1996, vol. 10, ch. 17, pp. 487–536 Search PubMed; D. Parker, Chem. Br., 1994, 818 Search PubMed.
  7. A. Beeby, D. Parker and J. A. G. Williams, J. Chem. Soc., Perkin Trans. 2, 1996, 1565 RSC; A. Beeby, M. Murru, D. Parker and J. A. G. Williams, J. Chem. Soc., Chem. Commun., 1993, 1116 RSC; S. Aime, M. Botta, D. Parker and J. A. G. Williams, J. Chem. Soc., Dalton Trans., 1996, 17 RSC.
  8. D. Parker, K. Senanayake and J. A. G. Williams, Chem. Commun., 1997, 1777 RSC; D. Parker and J. A. G. Williams, Chem. Commun., 1998, 245 RSC.
  9. D. Parker and J. A. G. Williams, J. Chem. Soc., Perkin Trans. 2, 1996, 1581 RSC.
  10. E. U. Akkaya, M. E. Huston and A. W. Czarnik, J. Am. Chem. Soc., 1990, 112, 3590 CrossRef CAS.
  11. R. S. Dickins, D. Parker, A. S. de Sousa and J. A. G. Williams, Chem. Commun., 1996, 697 RSC.
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