New ruthenium complexes with 4-(1H-pyrrol-1-yl)-substituted polypyridine ligands - Electrochemical and spectroscopic properties

European Journal of Inorganic Chemistry

Volumn , Issue 20, 2004, Pages 3984-3986

  Martineau, David ^b   Gros, Philippe ^a   Beley, Marc ^b   Fort, Yves ^a  

^a NANCY UNIVERSITÉ   (France)

^b LIMBP   (France)

Author keywords

N donor ligands; Nitrogen heterocycles; Ruthenium

Indexed keywords

AROMATIC COMPOUNDS; NITROGEN; RUTHENIUM COMPOUNDS;

BIPYRIDINES; ELECTROCHEMICALS; N-DONOR LIGANDS; NITROGEN HETEROCYCLES; PHOTOPHYSICAL; POLYPYRIDINE LIGANDS; PYRROLE RING; RUTHENIUM COMPLEXES; SPECTROSCOPIC PROPERTY; TERPYRIDINES;

LIGANDS;

NITROGEN; PYRIDINE DERIVATIVE; PYRROLE DERIVATIVE; RUTHENIUM COMPLEX;

ARTICLE; COMPLEX FORMATION; ELECTROCHEMICAL ANALYSIS; REACTION ANALYSIS; REDUCTION; SPECTROSCOPY; SYNTHESIS;

EID: 8144229481     PISSN: 14341948     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejic.200400385     Document Type: Article

References (20)

1. [1a] A. Juris, V. Balzani, F. Barigelletti, S. Campagna, P. Belser, A. von Zelewsky, Coord. Chem. Rev. 1988. 84, 85.
2. [1b] B. O'Regan, M. Grätzel, Nature 1991, 353, 737.
3. [1c] A. Hagfeldt, M. Grätzel, Chem. Rev. 1995, 95, 49.
4. [1d] R. Argazzi, A. Bignozzi, G. M. Hasselmann, G. J. Meyer, Inorg. Chem. 1998, 27, 4533.
5. [1e] X. Schulze, J. Serin, A. Adronov, J. M. J. Fréchet, Chem. Commun. 2001, 1160.
6. [1f] M. I. J. Poison, N. J. Taylor, G. S. Hanan, Chem. Commun. 2002, 1356.
7. [1g] E. Figgemeier, V. Aranyos, E. C. Constable, R. W. Handel, C. E. Housecroft, C. Risinger, A. Hagfeldt, E. Mukhtar, Inorg. Chem. Commmun. 2004, 7, 117.
8. M. J. Cook, A. P. Lewis, G. S. McAulife, V. Skarda, A. J. Thomson, J. Chem. Soc., Perkin Trans. 2 1984, 1293.
9. [3a] J. Hjelm, E. C. Constable, E. Figgemeier, A. Hagfeldt, R. Handel, C. E. Housecroft, E. Mukhtar, E. Chofield, Chem. Commun. 2002, 284.
10. [3b] E. R. Schofield, Ph. D. Dissertation, University of Basel, Switzerland, 1999.
11. [4a] Ph. Gros, Y. Fort, Eur. J. Org. Chem. 2002, 3375.
12. [4b] D. Cuperly, Ph. Gros, Y. Fort, J. Org. Chem. 2002, 67, 238.
13. Detailed studies on selective lithiation of 1 and coupling reactions will be published in due course.
14. B. P. Sullivan, J. A. Baumann, T. J. Meyer, D. J. Salmon, H. Lehmann, A. Ludi, J. Am. Chem. Soc. 1977, 99, 7368.
15. E. C. Constable, C. E. Housecroft, E. R. Schofield, S. Encinas, N. Armaroli, F. Barigelletti, L. Flamigni, E. Figgenmeier, J. G. Vos. Chem. Commun. 1999, 869.
16. K. Nakamaru, Bull. Chem. Soc. Jpn. 1982, 55, 1639.
17. M. Maestri, N. Armaroli, V. Balzani, E. W. Constable, A. M. W. Cargill Thomson, Inorg. Chem. 1995, 34, 2759.
18. F. Barigelletti, A. Juris, V. Balzani, P. Belser, A. von Zelewsky, Inorg. Chem. 1987, 26, 4115
19. 1H NMR spectrum of 5a did not allow to distinguish between the fac- and mer isomer.
20. M. L. Stone, G. A. Crosby, Chem. Phys. Lett. 1981, 79, 169.