Molecular design of calixarene-based host molecules for inclusion of C60 in solution

Tetrahedron Letters

Volumn 37, Issue 1, 1996, Pages 73-76

  Araki, Koji ^a   Akao, Kiyotaka ^a   Ikeda, Atsushi ^a   Suzuki, Tsuyoshi ^b   Shinkai, Seiji ^a,b  

^a KYUSHU UNIVERSITY   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARENE;

CALIXARENE;

ARTICLE; COMPLEX FORMATION; DRUG DESIGN; DRUG SYNTHESIS; SPECTROPHOTOMETRY;

EID: 0030059389     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(95)02105-1     Document Type: Article

References (12)

1. Suzuki, T.; Nakashima, K.; Shinkai, S. Chem. Lett., 1994, 699-702.
2. Atwood, J. L.; Koutsantonis, G. A.; Raston, C. L. Nature, 1994, 368, 229-231.
3. Suzuki, T.; Shinkai, S.; unpublished results: also see Suzuki, T.; Nakashima, K.; Shinkai, S. Tetrahedron Lett., 1995, 36, 249-252.
4. Suzuki, T.; Shinkai, S.; unpublished results: also see Suzuki, T.; Nakashima, K.; Shinkai, S. Tetrahedron Lett., 1995, 36, 249-252.
5. Anderson, T.; Nilsson, K.; Sundahl, M.; Westman, G.; Wennerström, O. J. Chem. Soc., Chem. Commun., 1992, 604-606; Yoshida, Z.; Takekuma, H.; Matsubara, Y. Angew. Chem. Int. Ed. Engl., 1994, 33, 1597-1599; R. M. Williams and J. W. Verhoeven, Recl. Trav. Chim. Pays-Bas, 1992, 111, 531-532.
6. Anderson, T.; Nilsson, K.; Sundahl, M.; Westman, G.; Wennerström, O. J. Chem. Soc., Chem. Commun., 1992, 604-606; Yoshida, Z.; Takekuma, H.; Matsubara, Y. Angew. Chem. Int. Ed. Engl., 1994, 33, 1597-1599; R. M. Williams and J. W. Verhoeven, Recl. Trav. Chim. Pays-Bas, 1992, 111, 531-532.
7. Anderson, T.; Nilsson, K.; Sundahl, M.; Westman, G.; Wennerström, O. J. Chem. Soc., Chem. Commun., 1992, 604-606; Yoshida, Z.; Takekuma, H.; Matsubara, Y. Angew. Chem. Int. Ed. Engl., 1994, 33, 1597-1599; R. M. Williams and J. W. Verhoeven, Recl. Trav. Chim. Pays-Bas, 1992, 111, 531-532.
8. Sun, Y.-P.; Bunker, C. E.; Ma, B. J. Am. Chem. Soc., 1994, 116, 9692 and references cited therein.
9. 2N, 12H), 6.30 (s, ArH, 3H), 6.58 (d, J = 8.2 Hz, ArH, 6H), 6.78 (s, ArH, 6H), 6.88 (s, ArH, 6H), 7.15 (t, J = 7.9 Hz, ArH, 3H).
10. 60, one can regard that only the 1:1 complex formation is monitored by the spectroscopic change.
11. 8 at -85 - 30 °C. However, we could not detect the significant shift (the largest up-field shift was 0.0046 ppm for the calix[6]arene ArH protons).
12. The K value was scarcely affected by the wavelength used (>550 nm).