Cation chelating [2]catenanes and cyclophanes based on 2,2'-bipyridine

Tetrahedron Letters

Volumn 38, Issue 20, 1997, Pages 3577-3580

  Benniston, Andrew C ^a   Mackie, Philip R ^a   Harriman, Anthony ^b  

^a UNIVERSITY OF GLASGOW   (United Kingdom)

^b UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

2,2' BIPYRIDINE DERIVATIVE; METAL COMPLEX; OSMIUM; RUTHENIUM;

ARTICLE; COMPLEX FORMATION; DRUG SYNTHESIS; IN VITRO STUDY; MASS SPECTROMETRY; METAL BINDING;

EID: 0030922521     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00667-9     Document Type: Article

References (20)

1. Bissell, R. A.; Cordova, E.; Kaifer, A. E.; Stoddart, J. F. Nature, 1994, 369, 133-137.
2. Benniston, A.C.; Harriman, A. Angew. Chem. Int. Ed. Engl. 1993, 32, 1495-1461.
3. Willner, I.; Rubin, S. Angew. Chem. Int. Ed. Engl. 1996, 35, 367-385.
4. Benniston, A. C. Chem. Soc. Rev. 1996, 25, 427-436.
5. Chambron, J-C.; Harriman, A.; Heitz, V.; Sauvage, J-P. J. Am. Chem. Soc. 1993, 115, 7419-7425.
6. Gunter, M. J.; Johnston, M. R. J. Chem. Soc., Chem. Commun. 1994, 829-830.
7. Benniston, A. C.; Harriman, A.; Lynch, V. M. Tetrahedron Lett. 1994, 35, 1473-1477.
8. Vögtle, F.; Müller, V. M.; Müller, U.; Bauer, M.; Rissanen, K. Angew. Chem. Int. Ed. Engl. 1993, 32, 1295-1297.
9. Amibilino, D. B.; Dietrich-Buchecker, C. O.; Livoreil, A.; Pérez-García, L.; Sauvage, J-P.; Stoddart, J-F. J. Am. Chem. Soc. 1996, 118, 3905-3913.
10. 2(9:1). see: Gould, S.; Strouse, G. F.; Meyer, T. J.; Sullivan, P. B.; Inorg. Chem. 1991, 30, 2942-2949.
11. +.
12. Stoddart, J. F.; Philp, D. Synlett, 1991, 7, 445-458 and references therein.
13. +.
14. 2+, prepared according to: Kendrick, M. S.; Dawson, J. H. Inorg. Chimica. Acta. 1985, 97, L41.
15. 5+.
16. The acronym 34C10 corresponds to 1,4,7,10,13,20,23,26,29,32-decaoxa[13.13]paracyclophane.
17. + consistent with the "free" cyclophane ligand. Other peaks in the mass spectral records are also compatible with products in which one and two α,α'-dibromo-p-xylenes had reacted and formed oligomers.
18. max (nm): 255; 290; 370; 425; 495.
19. max (nm): 255; 295; 370; 430; 490.
20. Using the asymmetric crown 46C14 this general method of ring closure has been used to generate metallated catenanes, the results of which are to be published later.