Synthesis of a new phenanthroline derived ligand with acceptor properties

Tetrahedron Letters

Volumn 37, Issue 31, 1996, Pages 5437-5440

  López, Rosa B ^a   Loeb, Bárbara L ^a   Boussie, Thomas ^b   Meyer, Thomas J ^b  

^a PONTIFICIA UNIVERSIDAD CATÓLICA DE CHILE   (Chile)

^b University of North Carolina at Chapel Hill   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PHENANTHROLINE DERIVATIVE;

ARTICLE; CYCLIC POTENTIOMETRY; DRUG SYNTHESIS; LIGAND BINDING; REACTION ANALYSIS;

EID: 0030605860     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01141-0     Document Type: Article

References (15)

1. 1. Bard, A. J. Science 1980, 207, 139.
2. 2. Meyer, T. J. Acc.Chem.Res. 1989, 22, 163.
3. 3. Meyer, T. J. in Photochemical Processes in Organized Molecular Systems, Honda, K. Ed. in Chief; Elsevier Science Publishers B. V., 1991, p.133.
4. 4. Tapolsky, G.; Duesing, R.; Meyer, T. J. Inorg.Chem. 1990, 29, 2285.
5. 5. Sauvage, J. P.; Collin, J. P.; Chambron, J. C.; Guillerez, S.; Coundret, C.; Balzani, V.; Barigelleti, F.; Della, L.; Falmigni, L. Chem.Rev. 1994, 94, 993.
6. 6. Lynne, W.; Rillema, P. Inorg.Chem. 1993, 32, 3836.
7. 7. a). Claude, J. P. Photophysics of Polypyridyl Complexes of Ru(II), Os(II), and Re(I), University of North Carolina at Chapel Hill, 1995.
8. b). Opperman, K. A.; Mecklenburg, S. L.; Meyer, T. J. Inorg.Chem. 1994, 33, 5295.
9. 8. Worl, L.; Duesing, R.; Chen, P. G.; Della-Ciana, L.; Meyer, T. J. J.Chem.Soc.Dalton Trans. 1991, 849.
10. 9. Druey, J.; Schmidth, P. Helv.Chim.Acta 1951, 33, 1080.
11. 10. Moody, C. J.; Rees, C. W.; Thomas, R. Tetrahedron 1992, 48, 3589.
12. 11. a). Robinson, J. W., Practical Handbook of Spectroscopy, CRC Press, Boca Raton, Florida, USA, 1991, p.133.
13. b). Láng, L.(ed.), Absorption Spectra in the Utraviolet and Visible Region, Vol. VIII, Academic Press, N.Y., USA, 1967.
14. 3Cl: 10.10 ppm (dd, H(1)); 9.87 ppm (dd, H(6)); 9.53 ppm (dd, H(3),H(4)); 8.95 ppm (d, H(8)); 8.79 ppm (d, H(7)); 8.35 ppm (m, H(9),H(12)); 8.12 ppm (m, H(2)); 8.07 ppm (m, H(5));7.9 ppm (m, H(10),H(11)).
15. 13. Krishman, S.; Kuhn, D. G.; Hamilton, G. A. J.Am.Chem.Soc. 1977, 99, 8121.