Stabilisation of charge-separated states via gain of aromaticity and planarity of the donor moiety in C60-based dyads

Chemical Communications

Volumn , Issue 2, 2000, Pages 113-114

  Martín, Nazario ^a   Sánchez, Luis ^a   Guldi, Dirk M ^b  

^a UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

^b UNIVERSITY OF NOTRE DAME   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; MOLECULAR STABILITY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OXIDATION; SYNTHESIS;

EID: 0034695693     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a908770b     Document Type: Article

References (18)

1. L. Echegoyen and L. Echegoyen, Acc. Chem. Res., 1998, 31, 593.
2. H. Kurreck and M. Hüber, Angew. Chem., Int. Ed. Engl., 1995, 34, 849.
3. N. Martín, L. Sánchez, B. Illescas and I. Pérez, Chem. Rev., 1998, 98, 2527.
4. H. Imahori and Y. Sakata, Adv. Mater., 1997, 9, 537; H. Imahori and Y. Sakata, Eur. J. Org. Chem., 1999, 2445.
5. H. Imahori and Y. Sakata, Adv. Mater., 1997, 9, 537; H. Imahori and Y. Sakata, Eur. J. Org. Chem., 1999, 2445.
6. K. A. Jolliffe, S. J. Langford, M. G. Ranasinghe, M. J. Shephard and M. N. Paddon-Row, J. Org. Chem., 1999, 64, 1238.
7. N. Martín, L. Sánchez, M. A. Herranz and D. M. Guldi, submitted for publication.
8. N. Martín, L. Sánchez, C. Seoane, E. Ortí, P. M. Viruela and R. Viruela, J. Org. Chem., 1998, 63, 1268; M. R. Bryce, A. J. Moore, M. Hasan, G. J. Ashwell, A. T. Fraser, W. Clegg, M. B. Hursthouse and A. I. Karaulov, Angew. Chem., Int. Ed. Engl., 1990, 29, 1450.
9. N. Martín, L. Sánchez, C. Seoane, E. Ortí, P. M. Viruela and R. Viruela, J. Org. Chem., 1998, 63, 1268; M. R. Bryce, A. J. Moore, M. Hasan, G. J. Ashwell, A. T. Fraser, W. Clegg, M. B. Hursthouse and A. I. Karaulov, Angew. Chem., Int. Ed. Engl., 1990, 29, 1450.
10. T. Suzuki, Q. Li, K. C. Khemani, F. Wudl and Ö. Almarsson, Science, 1991, 254, 1186.
11. N. Martín, I. Pérez, L. Sánchez and C. Seoane, J. Org. Chem., 1997, 62, 5690.
12. For the first preparation of fulleroids from p-tosylhydrazones, see: J. C. Hummelen, B.W. Knight, F. LePeq and F. Wudl, J. Org. Chem., 1995, 60, 532.
13. M. Prato, V. Luccini, M. Maggini, E. Stimpfl, G. Scorrano, G. Eirmann, T. Suzuki and F. Wudl, J. Am. Chem. Soc., 1993, 115, 8479.
14. M. Maggini, A. Karlsson, G. Scorrano, G. Sandona, G. Farnia and M. Prato, J. Chem. Soc., Chem. Commun., 1994, 589.
15. M. Eiermann, F. Wudl, M. Prato and M. Maggini, J. Am. Chem. Soc., 1994, 116, 8364.
16. D. M. Guldi, N. Martín and L. Sánchez, unpublished results.
17. D. M. Guldi, H. Hungerbühler and K.-D. Asmus, J. Phys. Chem., 1995, 99, 9380.
18. max at 1070 nm is identical to the photolytically generated spectrum and, thus, serves as additional confirmation for the spectral assignment.