A luminescent tricarbonylchlororhenium(I) complex featuring a flexible “crown ether” ligand. Manipulation of photoexcited state properties via binding of small cations[hair space]

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Suzanne Bélanger, Michelle Gilbertson, Dong I. Yoon, Charlotte L. Stern, Xiaojun Dang and Joseph T. Hupp


Abstract

A luminescent complex, [Re(CO)3(Cl)(LL)] where LL is 1,11-bis(4-pyridylcarboxy)-3,6,9-trioxaundecane, was prepared, and the crystal structures of two solvates were determined. The flexible polyether chain of the chelating ligand adopts an all gauche conformation about the aliphatic C–C bonds, and does not appear to introduce any appreciable constraints on the geometry at the octahedral metal center. The cavity formed by the “crown ether” has a diameter of ca. 7 Å. Binding of cations causes a decrease of the luminescence lifetime of the ReIILL excited state, consistent with an “energy gap” effect and with a rapid excited-state equilibrium between bound and unbound moieties. Binding constants were determined for several alkali metal ions, and for the ammonium cation. The chemical affinity of the crown-functionalized ligand is not specific for any of the cations studied, but, instead, is similar for a range of cations. Comparative studies with a complex containing ester-functionalized pyridine ligands, but lacking the polyether linkage necessary to form the crown, also showed excited state binding of small cations, indicating that the anionic ester pyridyl fragment, rather than the polyether fragment, is responsible for the binding.


References

  1. D. I. Yoon, C. A. Berg-Brennan, H. Lu and J. T. Hupp, Inorg. Chem., 1992, 31, 3192 CrossRef CAS.
  2. C. A. Berg-Brennan, D. I. Yoon and J. T. Hupp, J. Am. Chem. Soc., 1993, 115, 2048 CrossRef CAS; C. A. Berg-Brennan, D. I. Yoon, R. V. Slone, A. P. Kazala and J. T. Hupp, Inorg. Chem., 1996, 35, 2032 CrossRef.
  3. M. Absi, C. L. Stern, D. I. Yoon and J. T. Hupp, Acta Crystallogr., Sect. C, 1997, 53, 1054 CrossRef.
  4. A. K. Williams, D. I. Yoon and J. T. Hupp, unpublished work.
  5. Y. Shen and B. P. Sullivan, J. Chem. Educ., 1997, 74, 685 CrossRef CAS.
  6. D. B. MacQueen and K. S. Schanze, J. Am. Chem. Soc., 1991, 113, 6108 CrossRef.
  7. R. V. Slone, D. I. Yoon, R. M. Calhoun and J. T. Hupp, J. Am. Chem. Soc., 1995, 117, 11813 CrossRef CAS.
  8. C. K. Johnson, ORTEP II, Report ORNL-5138, Oak Ridge National Laboratory, Oak Ridge, TN, 1976; R. N. Dominey, B. Hauser, J. Hubbard and J. Dunham, Inorg. Chem., 1991, 30, 4754 Search PubMed; E. R. Civitello, P. S. Dragovich, T. B. Karpishin, S. G. Novick, G. Bierach, J. F. O'Connell and T. D. Westmoreland, Inorg. Chem., 1993, 32, 237 CrossRef CAS; V. J. Catalano, W. E. Larson, M. M. Olmstead and H. B. Gray, Inorg. Chem., 1994, 33, 4502 CrossRef CAS; V. W.-W. Yam, V. C.-Y. Lau and K.-K. Cheung, Organometallics, 1995, 14, 2749 CrossRef CAS.
  9. N. M. Iha and G. Ferraudi, J. Chem. Soc., Dalton. Trans., 1994, 2565 RSC.
  10. Y.-L. Yang, J.-D. Chen, Y.-C. Lin, M.-C. Cheng and Y. Yang, J. Organomet. Chem., 1994, 467, C6 CrossRef CAS.
  11. S. Bélanger, J. T. Hupp and C. L. Stern, Acta Crystallogr., Sect. C, 1998, 54, 1596 CrossRef.
  12. B. L. Allwood, H. M. Colquhoun, S. M. Doughty, F. H. Kohnke, A. M. Z. Slawin, J. F. Stoddart, D. J. Williams and R. J. Zarzycki, J. Chem. Soc., Chem. Commun., 1987, 1054 RSC; B. L. Allwood, H. Shahriari-Zavareh, J. F. Stoddart and D. J. Williams, J. Chem. Soc., Chem. Commun., 1987, 1058 RSC; B. L. Allwood, N. Spencer, H. Shahriari-Zavareh, J. F. Stoddart and D. J. Williams, J. Chem. Soc., Chem. Commun., 1987, 1061, 1064 RSC; A. M. Z. Slawin, N. Spencer, J. F. Stoddart and D. J. Williams, J. Chem. Soc., Chem. Commun., 1987, 1070 RSC; H. M. Colquhoun, J. F. Stoddart, D. J. Williams, J. B. Wolstenholme and R. Zarzycki, Angew. Chem., Int. Ed. Engl., 1981, 20, 1051 CrossRef; H. M. Colquhoun, E. P. Goodings, J. M. Maud, J. F. Stoddart, J. B. Wolstenholme and D. J. Williams, J. Chem. Soc., Perkin Trans. 2, 1985, 607 RSC; M. A. Bush and M. R. Truter, J. Chem. Soc., Perkin Trans. 2, 1972, 345 RSC; F. H. Kohnke, J. F. Stoddart, B. L. Allwood and D. J. Williams, Tetrahedron Lett., 1985, 26, 1681 CrossRef CAS; B. L. Allwood, F. H. Kohnze, J. F. Stoddart and D. J. Williams, Angew. Chem., Int. Ed. Engl., 1985, 24, 581 CrossRef; B. L. Allwood, F. H. Kohnze, A. M. Z. Slawin, J. F. Stoddart and D. J. Williams, J. Chem. Soc., Chem. Commun., 1985, 311 RSC.
  13. See, for example, L. Fabbrizzi and A. Poggi, Chem. Soc. Rev., 1995, 24, 197 Search PubMed.
  14. J. V. Caspar, Ph.D. Thesis, The University of North Carolina at Chapel Hill, 1982; J. V. Caspar and T. J. Meyer, J. Phys. Chem., 1983, 87, 952 Search PubMed.
  15. J. de Meulenaer and H. Tompa, Acta Crystallogr., 1965, 19, 1014 CrossRef CAS.
  16. P. T. Beurskens, G. Admiraal, G. Beurskens, W. P. Bosman, S. Garcia-Granda, R. O. Gould, J. M. M. Smits and C. Smykalla, The DIRDIF program system, Technical Report of the Crystallography Laboratory, University of Nijmegen, 1992.
  17. TEXSAN, Single Crystal Structure Analysis Software, Version 1.7, Molecular Structure Corporation, The Woodlands, TX, 1995.
  18. International Tables for Crystallography, Kluwer, Dordrecht, 1992, Vol. C, Tables 4.2.6.8 and 6.1.1.1 Search PubMed.
  19. P. J. Giordano and M. S. Wrighton, J. Am. Chem. Soc., 1979, 101, 2888 CrossRef CAS.
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