A supramolecular oligophenylenevinylene-C60 conjugate

Tetrahedron Letters

Volumn 44, Issue 15, 2003, Pages 3043-3046

  Gutiérrez Nava, Manuel ^a   Nierengarten, Hélène ^b   Masson, Patrick ^a   Van Dorsselaer, Alain ^b   Nierengarten, Jean François ^a  

^a INSTITUT DE PHYSIQUE ET CHIMIE DES MATÉRIAUX DE STRASBOURG   (France)

^b UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIA; CARBON; CARBON 60; CHEMICAL COMPOUND; CROWN ETHER; FULLERENE DERIVATIVE; OLIGOPHENYLENEVINYLENE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL PARAMETERS; LUMINESCENCE; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE;

EID: 0037424731     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)00561-6     Document Type: Article

References (26)

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4. Supramolecular complexes obtained from fullerene derivatives bearing a pyridyl moiety and metalloporphyrins have been described, for examples, see: (a) Armaroli, N.; Diederich, F.; Echegoyen, L.; Habicher, T.; Flamigni, L.; Marconi, G.; Nierengarten, J.-F. New J. Chem. 1999, 23, 77-83; (b) D'Souza, F.; Deviprasad, G. R.; Rahman, M. S.; Choi, J.-P. Inorg. Chem. 1999, 38, 2157-2160; (c) Da Ros T.; Prato, M.; Gildi, D. M.; Alessio, E.; Ruzzi, M.; Pasimeni, L. Chem. Commun. 1999, 635-636; (d) Guldi, D. M.; Da Ros, T.; Braiuca, P.; Prato, M.; Alessio, E. J. Mater. Chem. 2002, 12, 2001-2008.
5. Supramolecular complexes obtained from fullerene derivatives bearing a pyridyl moiety and metalloporphyrins have been described, for examples, see: (a) Armaroli, N.; Diederich, F.; Echegoyen, L.; Habicher, T.; Flamigni, L.; Marconi, G.; Nierengarten, J.-F. New J. Chem. 1999, 23, 77-83; (b) D'Souza, F.; Deviprasad, G. R.; Rahman, M. S.; Choi, J.-P. Inorg. Chem. 1999, 38, 2157-2160; (c) Da Ros T.; Prato, M.; Gildi, D. M.; Alessio, E.; Ruzzi, M.; Pasimeni, L. Chem. Commun. 1999, 635-636; (d) Guldi, D. M.; Da Ros, T.; Braiuca, P.; Prato, M.; Alessio, E. J. Mater. Chem. 2002, 12, 2001-2008.
6. Supramolecular complexes obtained from fullerene derivatives bearing a pyridyl moiety and metalloporphyrins have been described, for examples, see: (a) Armaroli, N.; Diederich, F.; Echegoyen, L.; Habicher, T.; Flamigni, L.; Marconi, G.; Nierengarten, J.-F. New J. Chem. 1999, 23, 77-83; (b) D'Souza, F.; Deviprasad, G. R.; Rahman, M. S.; Choi, J.-P. Inorg. Chem. 1999, 38, 2157-2160; (c) Da Ros T.; Prato, M.; Gildi, D. M.; Alessio, E.; Ruzzi, M.; Pasimeni, L. Chem. Commun. 1999, 635-636; (d) Guldi, D. M.; Da Ros, T.; Braiuca, P.; Prato, M.; Alessio, E. J. Mater. Chem. 2002, 12, 2001-2008.
7. Supramolecular complexes obtained from fullerene derivatives bearing a pyridyl moiety and metalloporphyrins have been described, for examples, see: (a) Armaroli, N.; Diederich, F.; Echegoyen, L.; Habicher, T.; Flamigni, L.; Marconi, G.; Nierengarten, J.-F. New J. Chem. 1999, 23, 77-83; (b) D'Souza, F.; Deviprasad, G. R.; Rahman, M. S.; Choi, J.-P. Inorg. Chem. 1999, 38, 2157-2160; (c) Da Ros T.; Prato, M.; Gildi, D. M.; Alessio, E.; Ruzzi, M.; Pasimeni, L. Chem. Commun. 1999, 635-636; (d) Guldi, D. M.; Da Ros, T.; Braiuca, P.; Prato, M.; Alessio, E. J. Mater. Chem. 2002, 12, 2001-2008.
8. 60 with a donor moiety by using hydrogen bonds have been described, for examples, see: (a) Diederich, F.; Echegoyen, L.; Gomez-Lopez, M.; Kessinger, R.; Stoddart, J. F. J. Chem. Soc., Perkin Trans. 2 1999, 1577-1586; (b) Martinez-Diaz, M. V.; Fender, N. S.; Rodriguez-Morgade, M. S.; Gomez-Lopez, M.; Diederich, F.; Echegoyen, L.; Stoddart, J. F.; Torres, T. J. Mater. Chem. 2002, 12, 2095-2099; (c) Beckers, E. H. A.; van Hal, P. A.; Schenning, A. P. H. J.; El-ghayoury, A.; Peeters, E.; Rispens, M. T.; Hummelen, J. C.; Meijer, E. W.; Janssen, R. A. J. J. Mater. Chem. 2002, 12, 2054-2060; (d) Beckers, E. H. A.; Schenning, A. P. H. J.; van Hal, P. A.; El-ghayoury, A.; Sanchez, L.; Hummelen, J. C.; Meijer, E. W.; Janssen, R. A. Chem. Commun. 2002, 2888-2889; (e) Guldi, D. M.; Ramey, J.; Martinez-Diaz, M. V.; de la Escosura, A.; Torres, T.; Da Ros, T.; Prato, M. Chem. Commun. 2002, 2774-2775.
9. 60 with a donor moiety by using hydrogen bonds have been described, for examples, see: (a) Diederich, F.; Echegoyen, L.; Gomez-Lopez, M.; Kessinger, R.; Stoddart, J. F. J. Chem. Soc., Perkin Trans. 2 1999, 1577-1586; (b) Martinez-Diaz, M. V.; Fender, N. S.; Rodriguez-Morgade, M. S.; Gomez-Lopez, M.; Diederich, F.; Echegoyen, L.; Stoddart, J. F.; Torres, T. J. Mater. Chem. 2002, 12, 2095-2099; (c) Beckers, E. H. A.; van Hal, P. A.; Schenning, A. P. H. J.; El-ghayoury, A.; Peeters, E.; Rispens, M. T.; Hummelen, J. C.; Meijer, E. W.; Janssen, R. A. J. J. Mater. Chem. 2002, 12, 2054-2060; (d) Beckers, E. H. A.; Schenning, A. P. H. J.; van Hal, P. A.; El-ghayoury, A.; Sanchez, L.; Hummelen, J. C.; Meijer, E. W.; Janssen, R. A. Chem. Commun. 2002, 2888-2889; (e) Guldi, D. M.; Ramey, J.; Martinez-Diaz, M. V.; de la Escosura, A.; Torres, T.; Da Ros, T.; Prato, M. Chem. Commun. 2002, 2774-2775.
10. 60 with a donor moiety by using hydrogen bonds have been described, for examples, see: (a) Diederich, F.; Echegoyen, L.; Gomez-Lopez, M.; Kessinger, R.; Stoddart, J. F. J. Chem. Soc., Perkin Trans. 2 1999, 1577-1586; (b) Martinez-Diaz, M. V.; Fender, N. S.; Rodriguez-Morgade, M. S.; Gomez-Lopez, M.; Diederich, F.; Echegoyen, L.; Stoddart, J. F.; Torres, T. J. Mater. Chem. 2002, 12, 2095-2099; (c) Beckers, E. H. A.; van Hal, P. A.; Schenning, A. P. H. J.; El-ghayoury, A.; Peeters, E.; Rispens, M. T.; Hummelen, J. C.; Meijer, E. W.; Janssen, R. A. J. J. Mater. Chem. 2002, 12, 2054-2060; (d) Beckers, E. H. A.; Schenning, A. P. H. J.; van Hal, P. A.; El-ghayoury, A.; Sanchez, L.; Hummelen, J. C.; Meijer, E. W.; Janssen, R. A. Chem. Commun. 2002, 2888-2889; (e) Guldi, D. M.; Ramey, J.; Martinez-Diaz, M. V.; de la Escosura, A.; Torres, T.; Da Ros, T.; Prato, M. Chem. Commun. 2002, 2774-2775.
11. 60 with a donor moiety by using hydrogen bonds have been described, for examples, see: (a) Diederich, F.; Echegoyen, L.; Gomez-Lopez, M.; Kessinger, R.; Stoddart, J. F. J. Chem. Soc., Perkin Trans. 2 1999, 1577-1586; (b) Martinez-Diaz, M. V.; Fender, N. S.; Rodriguez-Morgade, M. S.; Gomez-Lopez, M.; Diederich, F.; Echegoyen, L.; Stoddart, J. F.; Torres, T. J. Mater. Chem. 2002, 12, 2095-2099; (c) Beckers, E. H. A.; van Hal, P. A.; Schenning, A. P. H. J.; El-ghayoury, A.; Peeters, E.; Rispens, M. T.; Hummelen, J. C.; Meijer, E. W.; Janssen, R. A. J. J. Mater. Chem. 2002, 12, 2054-2060; (d) Beckers, E. H. A.; Schenning, A. P. H. J.; van Hal, P. A.; El-ghayoury, A.; Sanchez, L.; Hummelen, J. C.; Meijer, E. W.; Janssen, R. A. Chem. Commun. 2002, 2888-2889; (e) Guldi, D. M.; Ramey, J.; Martinez-Diaz, M. V.; de la Escosura, A.; Torres, T.; Da Ros, T.; Prato, M. Chem. Commun. 2002, 2774-2775.
12. 60 with a donor moiety by using hydrogen bonds have been described, for examples, see: (a) Diederich, F.; Echegoyen, L.; Gomez-Lopez, M.; Kessinger, R.; Stoddart, J. F. J. Chem. Soc., Perkin Trans. 2 1999, 1577-1586; (b) Martinez-Diaz, M. V.; Fender, N. S.; Rodriguez-Morgade, M. S.; Gomez-Lopez, M.; Diederich, F.; Echegoyen, L.; Stoddart, J. F.; Torres, T. J. Mater. Chem. 2002, 12, 2095-2099; (c) Beckers, E. H. A.; van Hal, P. A.; Schenning, A. P. H. J.; El-ghayoury, A.; Peeters, E.; Rispens, M. T.; Hummelen, J. C.; Meijer, E. W.; Janssen, R. A. J. J. Mater. Chem. 2002, 12, 2054-2060; (d) Beckers, E. H. A.; Schenning, A. P. H. J.; van Hal, P. A.; El-ghayoury, A.; Sanchez, L.; Hummelen, J. C.; Meijer, E. W.; Janssen, R. A. Chem. Commun. 2002, 2888-2889; (e) Guldi, D. M.; Ramey, J.; Martinez-Diaz, M. V.; de la Escosura, A.; Torres, T.; Da Ros, T.; Prato, M. Chem. Commun. 2002, 2774-2775.
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26. 2 was similar to the value deduced from the NMR binding studies. This titration was performed according to the procedure described by Armaroli and co-workers in Ref. 2a.