Electrochemical probing of ground state electronic interactions in polynuclear complexes of a new heteroditopic ligand

Dalton Transactions

Volumn , Issue 13, 2004, Pages 1918-1927

  Constable, Edwin C ^a   Figgemeier, Egbert ^b   Housecraft, Catherine E ^a   Olsson, Jerry ^a   Zimmermann, Yves C ^a  

^a UNIVERSITY OF BASEL   (Switzerland)

^b UPPSALA UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEXATION; CYCLIC VOLTAMMETRY; ELECTROCHEMISTRY; ELECTRON TRANSITIONS; ENERGY ABSORPTION; ENERGY TRANSFER; GROUND STATE; SYNTHESIS (CHEMICAL);

DIFFERENTIAL PULSE VOLTAMMETRY; ELECTRONIC INTERACTIONS; INTERA-MOLECULAR ENERGY TRANSFER; LIGANDS;

NITROGEN COMPOUNDS;

EID: 3142780985     PISSN: 14779226     EISSN: None     Source Type: Journal    
DOI: 10.1039/b404602a     Document Type: Article

References (75)

1. F. Barigelletti and L. Flamigni, Chem. Soc. Rev., 2000, 29, 1.
2. M. D. Ward, Chem. Soc. Rev., 1995, 24, 121.
3. C. A. Bignozzi, R. Argazzi and C. J. Kleverlaan, Chem. Soc. Rev., 2000, 29, 87.
4. L. C. Sun, L. Hammarstrom, B. Akermark and S. Styring, Chem. Soc. Rev., 2001, 30, 36.
5. V. Balzani, P. Ceroni, A. Juris, M. Venturi, S. Campagna, F. Puntoriero and S. Serroni, Coord. Chem. Rev., 2001, 219, 545.
6. A. C. Benniston, V. Grosshenny, A. Harriman and R. Ziessel, Angew. Chem., Int. Ed. Engl., 1994, 33, 1884.
7. C. A. Bignozzi, R. Argazzi, J. R. Schoonover, K. C. Gordon, R. B. Dyer and F. Scandola, Inorg. Chem., 1992, 31, 5260.
8. C. A. Bignozzi, R. Argazzi, C. Chiorboli, F. Scandola, R. B. Dyer, J. R. Schoonover and T. J. Meyer, Inorg. Chem., 1994, 33, 1652.
9. C. A. Bignozzi, J. R. Schoonover and F. Scandola, A supramolecular approach to light harvesting and sensitisation of wide-bandgap semiconductors: Antenna effects and charge separation,in Molecular Level Artificial Photosynthetic Materials, John Wiley & Sons Inc., New York, 1997, vol. 44, pp. 1-95.
10. A. K. Bilakhiya, B. Tyagi and P. Paul, Polyhedron, 2000, 19, 1233.
11. S. Campagna, S. Serroni, F. Puntoriero, F. Loiseau, L. De Cola, C. L. Kleverlaan, J. Becher, A. P. Sorensen, P. Hascoat and N. Thorup, Chem.-Eur. J., 2002, 8, 4461.
12. C. Chiorboli, M. A. J. Rodgers and F. Scandola, J. Am. Chem. Soc., 2003, 125, 483.
13. R. L. Cleary, K. J. Byrom, D. A. Bardwell, J. C. Jeffery, M. D. Ward, G. Calogero, N. Armaroli, L. Flamigni and F. Barigelletti, Inorg. Chem., 1997, 36, 2601.
14. N. H. Damrauer and J. K. McCusker, J. Phys. Chem. A, 1999, 103, 8440.
15. L. De Cola and P. Belser, Coord. Chem. Rev., 1998, 177, 301.
16. L. De Cola, V. Balzani, F. Barigelletti, L. Flamigni, P. Belser, A. von Zelewsky, M. Frank and F. Vogtle, Mol. Cryst. Liq. Cryst. Sci. Technol. Sect. A: Mol. Cryst. Liq. Cryst., 1994, 252, 97.
17. H. Durr and S. Bossmann, Acc. Chem. Res., 2001, 34, 905.
18. M. Furue, K. Maruyama, Y. Kanematsu, T. Kushida and M. Kamachi, Coord. Chem. Rev., 1994, 132, 201.
19. M. Furue, M. M. Ishibashi, A. Satoh, T. Oguni, K. Maruyama, K. Sumi and M. Kamachi, Coord. Chem. Rev., 2000, 208, 103.
20. V. Grosshenny, A. Harriman, M. Hissler and R. Ziessel, J. Chem. Soc., Faraday Trans., 1996, 92, 2223.
21. M. T. Indelli, F. Scandola, J. P. Collin, J. P. Sauvage and A. Sour, Inorg. Chem., 1996, 35, 303.
22. O. Johansson, M. Borgstrom, R. Lomoth, M. Palmblad, J. Bergquist, L. Hammarstrom, L. C. Sun and B. Akermark, Inorg. Chem., 2003, 42, 2908.
23. A. Juris, L. Prodi, A. Harriman, R. Ziessel, M. Hissler, A. Elghayoury, F. Y. Wu, E. C. Riesgo and R. P. Thummel, Inorg. Chem., 2000, 39, 3590.
24. A. F. Morales, G. Accorsi, N. Armaroli, F. Barigelletti, S. J. Pope and M. D. Ward, Inorg. Chem., 2002, 41, 6711.
25. T. Ohno, K. Nozaki, N. Ikeda and M. Haga, Adv. Chem. Ser., 1991, 215.
26. T. Ohno, K. Nozaki and M. Haga, Inorg. Chem., 1992, 31, 548.
27. E. A. Plummer, J. W. Hofstraat and L. De Cola, Dalton Trans., 2003, 2080.
28. F. Scandola, R. Argazzi, C. A. Bignozzi, C. Chiorboli, M. Indelli and M. A. Rampi, Coord. Chem. Rev., 1993, 125, 283.
29. F. Scandola, R. Argazzi, C. A. Bignozzi and M. T. Indelli, J. Photochem. Photobiol. A: Chem., 1994, 82, 191.
30. M. Staffilani, P. Belser, F. Hartl, C. J. Kleverlaan and L. De Cola, J. Phys. Chem. A, 2002, 106, 9242.
31. A. Vlcek, Coord. Chem. Rev., 1998, 177, 219.
32. M. D. Ward, C. M. White, F. Barigelletti, N. Armaroli, G. Calogero and L. Flamigni, Coord. Chem. Rev., 1998, 171, 481.
33. S. Fanni, C. Di Pietro, S. Serroni, S. Campagna and J G. Vos, Inorg. Chem. Commun., 2000, 3, 42.
34. D. M. Guldi, M. Maggini, E. Menna, G. Scorrano, P. Ceroni, M. Marcaccio, F. Paolucci and S. Roffia, Chem.-Eur. J., 2001, 7, 1597.
35. M. Marcaccio, F. Paolucci, C. Paradisi, M. Carano, S. Roffia, C. Fontanesi, L. J. Yellowlees, S. Serroni, S. Campagna and V. Balzani, J. Electroanal. Chem., 2002, 532, 99.
36. M. Marcaccio, F. Paolucci, C. Paradisi, S. Roffia, C. Fontanesi, L. J. Yellowlees, S. Serroni, S. Campagna, C. Denti and V. Balzani, J. Am. Chem. Soc., 1999, 121, 10081.
37. M. Krejcik and A. Vlcek, Inorg. Chem., 1992, 31, 2390.
38. M. Carano, P. Ceroni, C. Fontanesi, M. Marcaccio, F. Paolucci, C. Paradisi and S. Roffia, Electrochim. Acta, 2001, 46, 3199.
39. S. Welter, K. Brunner, J. W. Hofstraat and L. De Cola, Nature, 2003, 421, 54.
40. E. C. Constable and M. D. Ward, J. Chem. Soc., Dalton Trans., 1990, 1405.
41. J. P. Collin, P. Laine, J. P. Launay, J. P. Sauvage and A. Sour, J. Chem. Soc., Chem. Commun., 1993, 434.
42. L. Hammarstrom, F. Barigelletti, L. Flamigni, M. T. Indelli, N. Armaroli, G. Calogero, M. Guardigli, A. Sour, J. P. Collin and J. P. Sauvage, J. Phys. Chem. A, 1997, 101, 9061.
43. A. J. Downard, G. E. Honey, L. F. Phillips and P. Steel, Inorg. Chem., 1991, 30, 2259.
44. M. Beley, S. Chodorowskikimmes, J. P. Collin, P. Laine, J. P. Launay and J. P. Sauvage, Angew. Chem., Int. Ed. Engl., 1994, 33, 1775.
45. E. Figgemeier, E. C. Constable, C. E. Housecroft and Y. C. Zimmermann, 2004, submitted for publication.
46. B. P. Sullivan, D. J. Salmon and T. J. Meyer, Inorg. Chem., 1978, 17, 3334.
47. F. Kröhnke, Synthesis, 1976, 1.
48. E. C. Constable, A. Thompson, D. A. Tocher and M. A. M. Daniels, New J. Chem., 1992, 16, 855.
49. D. A. Buckingham, A. M. Sargeson and F. P. Dwyer, Aust. J. Chem., 1964, 17, 622.
50. K. D. Demadis, E. S. El-Samanody, T. J. Meyer and P. S. White, Polyhedron, 1999, 18, 1587.
51. T. L. J. Huang and D. J. Brewer, Can. J. Chem., 1981, 59, 1689.
52. K. T. Potts and P. A. Winslow, J. Org. Chem., 1985, 50, 5405.
53. S. A. Savage, A. P. Smith and C. L. Fraser, J. Org. Chem., 1998, 63, 10048.
54. B. M. Kellybasetti, I. Krodkiewska, W. H. F. Sasse, G. P. Savage and G. W. Simpson, Tetrahedron Lett., 1995, 36, 327.
55. B. Imperiali, T. J. Prins and S. L. Fisher, J. Org. Chem., 1993, 58, 1613.
56. H. Brederec, G. Simchen and R. Wahl, Chem. Ber./Recl., 1968, 101, 4048.
57. M. G. Vetelino and J. W. Coe, Tetrahedron Lett., 1994, 35, 219.
58. P. Dupau, T. Renouard and H. LeBozec, Tetrahedron Lett., 1996, 37, 7503.
59. G. Denti, S. Serroni, S. Campagna, A. Juris, M. Ciano and V. Balzani, in Perspectives in Coordination Chemistry, ed. A. F. Williams, C. Floriani and A. E. Merbach, VHCA and VCH, Basel and Weinheim, 1992, pp. 153-164.
60. E. C. Constable, C. E. Housecraft and Y. Tao, to be published.
61. All values listed for the trimeric and dimeric compounds were determined by differential pulse voltammetry (DPV). These values were compared with numbers determined by cyclic voltammetry (CV), but did not differ significantly (<20 mV).
62. + as internal reference. The results are in accordance with the values taken from: A. Juris, V. Balzani, F. Barigelletti, S. Campagna, P. Belser and A. von Zelewsky, Coord. Chem. Rev., 1988, 84, 85-277.
63. E. C. Constable and A. Thompson, J. Chem. Soc., Dalton Trans., 1994, 1409.
64. C. Creutz and H. Taube, J. Am. Chem. Soc., 1973, 95, 1086.
65. J. P. Sauvage, J. P. Collin, J. C. Chambron, S. Guillerez, C. Coudret, V. Balzani, F. Barigelletti, L. De Cola and L. Flamigni, Chem. Rev., 1994, 94, 993.
66. V. Balzani, A. Juris, M. Venturi, S. Campagna and S. Serroni, Chem. Rev., 1996, 96, 759.
67. 4+ was dominated by one signal. In order to extract the redox potentials, the peak was fitted by two gaussian curves assuming two one-electron processes lying beneath.
68. P. Ceroni, A. Credi, V. Balzani, S. Campagna, G. S. Hanan, C. R. Arana and J. M. Lehn, Eur. J. Inorg. Chem., 1999, 1409.
69. A. J. Bard and L. R. Forster, Electrochemical Methods, Fundamentals and Applications, John Wiley & Sons, New York, 2nd edn., 2001.
70. Two reductions for the terpy were observed, although in Fig. 3(A) -dashed line - only one peak is shown.
71. It should also be mentioned that latest studies indicate that this assumption is not entirely correct for related compounds such as Ru and Os phenolate complexes: T. E. Keyes, D. Leane, R. J. Forster, C. G. Coates, J. J. McGarvey, N. Nieuwenhuyzen, E. Figgemeier and J. G. Vos, Inorg. Chem., 2002, 41, 5721.
72. E. C. Constable, C. E. Housecraft, E. R. Schofield, S. Encinas, N. Armaroli, F. Barigelletti, L. Flamigni, E. Figgemeier and J. G. Vos, Chem. Commun., 1999, 869.
73. M. Duati, S. Fanni and J. G. Vos, Inorg. Chem. Commun., 2000, 3, 68.
74. J. R. Winkler, T. L. Netzel, C. Creutz and N. Sutin, J. Am. Chem. Soc., 1987, 109, 2381.
75. Y. Kim and C. M. Lieber, Inorg. Chem., 1989, 28, 3990.