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Cyclotriveratrylene Dendrimers

Published online by Cambridge University Press:  14 December 2012

Karla E. Sanchez-Montes,
Tatiana Klimova,
Mark E. Martínez-Klimov and
Marcos. Martínez-García
Karla E. Sanchez-Montes
Affiliation:
Instituto de Química, Universidad Nacional Autónoma de México, Cd. Universitaria, Circuito Exterior, Coyoacán, C.P. 04510, México D.F. E-mail: margar@servidor.unam.mx
Tatiana Klimova
Affiliation:
Facultad de Química, Universidad Nacional Autónoma de México, Cd. Universitaria, Circuito Interior, Coyoacán, C.P. 04510, México D.F.
Mark E. Martínez-Klimov
Affiliation:
Facultad de Química, Universidad Nacional Autónoma de México, Cd. Universitaria, Circuito Interior, Coyoacán, C.P. 04510, México D.F.
Marcos. Martínez-García*
Affiliation:
Instituto de Química, Universidad Nacional Autónoma de México, Cd. Universitaria, Circuito Exterior, Coyoacán, C.P. 04510, México D.F. E-mail: margar@servidor.unam.mx
*
*E-mail: margar@servidor.unam.mx
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Abstract

Dendrons with dodecyl ended groups joined benzyloxy moieties were attached to a cyclotriveratrylene core. The dendrimers were used in Diederich cyclopropanation reaction with the fullerene C60. The structure of the synthesized dendrimers was confirmed by 1H- and 13C-NMR, MALDI-TOF mass spectrometry and elemental analysis.

Keywords

OrganicChemical synthesis

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References

REFERENCES

Collet, A., Tetrahedron, 43, 5725 (1987).CrossRefGoogle Scholar
Hardie, M. J., Raston, C. L., Wells, B., Chem. Eur. J., 6, 3293 (2000).3.0.CO;2-4>CrossRefGoogle Scholar
Brotin, T., Dutasta, J. P., Chem. Rev., 109, 85 (2009).CrossRefGoogle Scholar
Rump, E. T., Rijkers, D. T. S., Hilbers, H. W., De Groot, P. G., Liskamp, R. M. J., Chem. Eur. J., 8, 4613 (2002).3.0.CO;2-R>CrossRefGoogle Scholar
Bardelang, D., Camerel, F., Ziessel, R., Schmutz, M., Hannon, M. J., J. Mater. Chem., 18, 489 (2008).CrossRefGoogle Scholar
McKeown, N. B., Gahnem, B., Msayib, K.J., Budd, P.M., Tattershall, C. E., Mahmood, K., Tan, S., Book, D., Langmi, H. W., Walton, A. Angew. Chem., Int. Ed., 45, 1804 (2006).CrossRefGoogle Scholar
Hardie, M. J., Sumby, C. J., Inorg. Chem., 43, 6872 (2004).CrossRefGoogle Scholar
Zhang, S., Echegoyen, L., J. Am. Chem. Soc., 127, 2006 (2005).CrossRefGoogle Scholar
Eckert, J. F., Byrne, D., Nicoud, J. F., Oswald, L, Nierengarten, J. F., Numata, M., Ikeda, A., Shinkai, S., Armaroli, A., New J Chem., 24, 749 (2000).CrossRefGoogle Scholar
Lijanova, I. V., Maturano, J. F., Chavez, J. G. D., Montes, K. E. S., Ortega, S. H., Klimova, T., Martinez-Garcia, M., Supramol. Chem., 21, 21 (2009).CrossRefGoogle Scholar
Bingel, C., Chem. Ber., 126, 1957 (1993).CrossRefGoogle Scholar