Liquid-crystalline fullerene-ferrocene dyads

Journal of Materials Chemistry

Volumn 14, Issue 8, 2004, Pages 1266-1272

  Campidelli, Stéphane ^a   Vázquez, Ester ^b   Milic, Dragana ^b   Prato, Maurizio ^b   Barberá, Joaquín ^c   Guldi, Dirk M ^d   Marcaccio, Massimo ^e   Paolucci, Demis ^e   Paolucci, Francesco ^e   Deschenaux, Robert ^a  

^a UNIVERSITÉ DE NEUCHÂTEL   (Switzerland)

^b UNIVERSITY OF TRIESTE   (Italy)

^c CSIC   (Spain)

^d UNIVERSITY OF NOTRE DAME   (United States)

^e UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DENDRIMERS; ELECTROCHEMISTRY; FULLERENES; MATHEMATICAL MODELS; REACTION KINETICS; REDOX REACTIONS; X RAY DIFFRACTION;

CYCLOADDITION REACTIONS; D-LAYER SPACING; ENANTIOTROPIC SMECTIC A PHASE; LIQUID-CRYSTALLINE FULLERENE-FERROCENE DYADS;

SMECTIC LIQUID CRYSTALS;

CRYSTALLIN; FERROCENE; FULLERENE;

ARTICLE; CHEMICAL REACTION; CRYSTAL STRUCTURE; CYCLOADDITION; ELECTROCHEMISTRY; ELECTRON TRANSPORT; ENANTIOSELECTIVITY; LIGHT; MOLECULAR MODEL; OXIDATION; PHOTOCHEMISTRY; PHYSICAL CHEMISTRY; REDUCTION; SUPRAMOLECULAR CHEMISTRY; TEMPERATURE; X RAY DIFFRACTION;

EID: 11144353605     PISSN: 09599428     EISSN: None     Source Type: Journal    
DOI: 10.1039/b316085h     Document Type: Article

References (31)

1. D. M. Guldi and M. Prato, Acc. Chem. Res., 2000, 33, 695.
2. N. Martín, L. Sánchez, B. Illescas and I. Pérez, Chem. Rev., 1998, 98, 2527.
3. H. Imahori and Y. Sakata, Eur. J. Org. Chem., 1999, 2445.
4. D. M. Guldi, Chem. Commun., 2000, 321.
5. D. M. Guldi, Chem. Soc. Rev., 2002, 31, 22.
6. D. Carbonera, M. Di Valentin, C. Corvaja, G. Agostini, G. Giacometti, P. A. Liddell, D. Kuciauskas, A. L. Moore, T. A. Moore and D. Gust, J. Am. Chem. Soc., 1998, 120, 4398.
7. J.-F. Nierengarten, J.-F. Eckert, J.-F. Nicoud, L. Ouali, V. Krasnikov and G. Hadziioannou, Chem. Commun., 1999, 617.
8. J.-F. Eckert, J.-F. Nicoud, J.-F. Nierengarten, S.-G. Liu, L. Echegoyen, F. Barigelletti, N. Armaroli, L. Ouali, V. Krasnikov and G. Hadziioannou, J. Am. Chem. Soc., 2000, 122, 7467.
9. E. Peeters, P. A. van Hal, J. Knol, C. J. Brabec, N. S. Sariciftci, J. C. Hummelen and R. A. J. Janssen, J. Phys. Chem. B, 2000, 104, 10174.
10. A. Marcos Ramos, M. T. Rispens, J. K. J. van Duren, J. C. Hummelen and R. A. J. Janssen, J. Am. Chem. Soc., 2001, 123, 6714.
11. C. J. Brabec, N. S. Sariciftci and J. C. Hummelen, Adv. Funct. Mater., 2001, 11, 15.
12. A. Cravino, G. Zerza, M. Maggini, S. Bucella, M. Svensson, M. R. Andersson, H. Neugebauer and N. S. Sariciftci, Chem. Commun., 2000, 2487.
13. A. Cravino, G. Zerza, H. Neugebauer, M. Maggini, S. Bucella, E. Menna, M. Svensson, M. R. Andersson, C. J. Brabec and N. S. Sariciftci, J. Phys. Chem. B, 2002, 106, 70.
14. D. Gust, T. A. Moore and A. L. Moore, Acc. Chem. Res., 2001, 34, 40.
15. D. M. Guldi, M. Maggini, G. Scorrano and M. Prato, J. Am. Chem. Soc., 1997, 119, 974.
16. R. Deschenaux, M. Even and D. Guillon, Chem. Commun., 1998, 537.
17. M. Even, B. Heinrich, D. Guillon, D. M. Guldi, M. Prato and R. Deschenaux, Chem. Eur. J., 2001, 7, 2595.
18. C. Bingel, Chem. Ber., 1993, 126, 1957.
19. J.-P. Bourgeois, F. Diederich, L. Echegoyen and J.-F. Nierengarten, Helv. Chem. Acta, 1998, 81, 1835.
20. S. Campidelli and R. Deschenaux, Helv. Chim. Acta, 2001, 84, 589.
21. K. Kordatos, T. Da Ros, S. Bosi, E. Vásquez, M. Bergamin, C. Cusan, F. Pellarini, V. Tomberli, B. Baiti, D. Pantarotto, V. Georgakilas, G. Spalluto and M. Prato, J. Org. Chem., 2001, 66, 4915.
22. T. Chuard and R. Deschenaux, J. Mater. Chem., 2002, 12, 1944.
23. B. Dardel, D. Guillon, B. Heinrich and R. Deschenaux, J. Mater. Chem., 2001, 11, 2814.
24. F. Paolucci, M. Carano, P. Ceroni, L. Mottier and S. Roffia, J. Electrochem. Soc., 1999, 146, 3357.
25. S. Cattarin, P. Ceroni, D. M. Guldi, M. Maggini, E. Menna, F. Paolucci, S. Roffia and G. Scorrano, J. Mater. Chem., 1999, 9, 2743.
26. T. Da Ros, M. Prato, M. Carano, P. Ceroni, F. Paolucci and S. Roffia, J. Am. Chem. Soc., 1998, 120, 11645.
27. For peaks I-IV in the CV curve of Fig. 3c, a four (unequal) step sigmoidal curve is obtained after convolution, where each step is proportional to n of the corresponding CV peak: A. J. Bard and L. R. Faulkner, Electrochemical Methods. Fundamentals and Applications, Wiley, New York, 2000.
28. A similar trend was seen in a fullerene-ferrocene reference dyad, which lacks the mesogenic unit, confirming that the latter has no meaningful impact on the fullerene singlet excited state deactivation.
29. D. M. Guldi, M. Maggini, G. Scorrano and M. Prato, Res. Chem. Intermed., 1997, 23, 561.
30. D. M. Guldi, C. Luo, N. A. Kotov, T. Da Ros, S. Bosi and M. Prato, J. Phys. Chem. B, 2003, 107, 7293.
31. M. D. Thomas and G. L. Hug, Comput. Chem., 1998, 22, 491.