Supramolecular assemblies with calix[6]arenes and copper ions: From dinuclear to trinuclear linear arrangements of hydroxo - Cu(II) complexes

Inorganic Chemistry

Volumn 45, Issue 3, 2006, Pages 1069-1077

  Izzet, Guillaume ^a   Akdas, Huriye ^a   Hucher, Nicolas ^c   Giorgi, Michel ^d   Prangé, Thierry ^b   Reinaud, Olivia ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b UNIVERSITÉ PARIS DESCARTES   (France)

^c UNIVERSITÉ DU HAVRE   (France)

^d AIX MARSEILLE UNIVERSITY   (France)

Author keywords

[No Author keywords available]

Indexed keywords

1 BENZYLIMIDAZOLE; 1-BENZYLIMIDAZOLE; CALIXARENE; COPPER; IMIDAZOLE DERIVATIVE; ORGANOMETALLIC COMPOUND;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; METHODOLOGY; SENSITIVITY AND SPECIFICITY; SYNTHESIS; ULTRAVIOLET SPECTROPHOTOMETRY; X RAY CRYSTALLOGRAPHY;

CALIXARENES; COPPER; CRYSTALLOGRAPHY, X-RAY; IMIDAZOLES; MODELS, MOLECULAR; MOLECULAR CONFORMATION; ORGANOMETALLIC COMPOUNDS; SENSITIVITY AND SPECIFICITY; SPECTROPHOTOMETRY, ULTRAVIOLET;

EID: 32544459143     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic051221e     Document Type: Article

References (48)

1. Review of bioinorganic enzymology: Chem. Rev. 1996, 96, 2237-3042.
2. (a) Kaim, W.; Rail, J. Angew. Chem., Int. Ed. 1996, 35, 43-60.
3. (b) Solomon, E. I.; Chen, P.; Metz, M.; Lee, S.-K.; Palmer, A. E. Angew. Chem., Int. Ed. 2001, 40, 4570-4590.
4. For recent reviews on Cu-enzyme modeling, see (a) Hatcher, L. Q.; Karlin, K. D. J. Biol. Inorg. Chem. 2004, 9, 669-683.
5. (b) Lewis, E. A.; Tolman, W. B. Chem. Rev. 2004, 104, 1047-1076.
6. (c) Mirica, L. M.; Ottenwaelder, X.; Stack, T. D. P. Chem. Rev. 2004, 104, 1013-1045.
7. Blanchard, S.; Le Clainche, L.; Rager, M.-N.; Chansou, B.; Tuchagues, J.-P.; Duprat, A. F; Le Mest, Y.; Reinaud, O. Angew. Chem., Int. Ed. 1998, 37, 2732-2735.
8. Rondelez, Y.; Sénèque, O.; Rager, M.-N.; Duprat, A. F.; Reinaud, O. Chem. Eur. J. 2000, 6, 4218-4226.
9. (a) Le Clainche, L.; Giorgi, M.; Reinaud, O. Inorg. Chem. 2000, 39, 3436-3437.
10. (b) Le Clainche, L.; Rondelez, Y.; Sénèque, O.; Blanchard, S.; Campion, M.; Giorgi, M.; Duprat, A. F.; Le Mest, Y.; Reinaud, O. C. R. Acad. Sci, Sér. IIc 2000, 3, 811-819.
11. Izzet, G.; Frapart, Y.-M., Prangé, T.; Provost, K.; Michalowicz, A.; Reinaud, O. Inorg. Chem. 2005, 44, 9743-9751.
12. Birker, P. J. M. W. L.; Godefroi, E. F.; Helder, J.; Reedijk, J. J. Am. Chem. Soc. 1982, 104, 7556-7560.
13. Otsuka, H.; Araki, K.; Shinkai, S. J. Org. Chem. 1994, 59, 1542-1547.
14. Le Clainche, L. Ph.D. Thesis, Paris VI University, 2000.
15. Otwinowsky, Z.; Minor, W. Methods Enzymol. 1997, 276, 307-326.
16. Miller, R.; Gallo, S. M.; Khalak, H. G.; Weeks, C. M. J. Appl. Crystallogr. 1994, 27, 613-621.
17. Sheldrick, G. M. SHELXL97. Program for the refinement of crystal structures, University of Göttingen: Göttingen, Germany, 1997.
18. Bruker-Nonius. Kappa CCD Reference Manual; Nonius B. V., P.O. Box 811, 2600 Av., Delft, The Netherlands, 1998.
19. (a) Kitajima, N.; Koda, T.; Hashimoto, S.; Kitagawa, T.; Moro-oka, Y. J. Am. Chem. Soc. 1991, 113, 5664-5671.
20. (b) Kitajima, N.; Fujisawa, K.; Fujimoto, C.; Moro-oka, Y.; Hashimoto, S.; Kitagawa, T.; Toriumi, K.; Tatsumi, K.; Nakamura, A. J. Am. Chem. Soc. 1992, 114, 1277-1291.
21. (c) Spencer, D. J. E.; Reynolds, A. M.; Holland, P. L.; Jazdzewski, B. A.; Duboc-Toia, C.; Le Pape, L.; Yokota, S.; Tachi, Y.; Itoh, S.; Tolman, W. B. Inorg. Chem. 2002, 41, 6307-6321.
22. (d) Lam, B. M. T.; Halfen, J. A.; Young, V. G., Jr.; Hagadorn, J. R.; Holland, P. L.; Lledós, A.; Cucurull-Sánchez, L.; Novoa, J. J.; Alvarez, S.; Tolman, W. B. Inorg. Chem. 2000, 39, 4059-4072.
23. (e) Mukherjee, J.; Mukherjee, R. Inorg. Chim. Acta 2002, 337, 429-438.
24. (f) Zhang, C. X.; Liang, H.-C.; Kim, E.-I.; Shearer, J.; Helton, M. E.; Kim, E.; Kaderli, S.; Incarvito, C. D.; Zuberbühler, A. D.; Rheingold, A. L.; Karlin, K. D. J. Am. Chem. Soc. 2003, 125, 634-635.
25. Hathaway, B. J.; Billing, D. E. Coord. Chem. Rev. 1970, 5, 143-207.
26. (a) Epstein, J. M.; Figgis, B. N.; White, A. H.; Willis, A. C. J. Chem. Soc., Dalton Trans. 1974, 18, 1954-1961.
27. (b) Baker, W. A., Jr.; Helm, F. T. J. Am. Chem. Soc. 1975, 97, 2295-2296.
28. (c) Matsumoto, N.; Nishida, Y.; Kida, S.; Ueda, I. Bull. Chem. Soc. Jpn. 1976, 49, 117-121.
29. (d) Chiari, B.; Piovesana, O.; Tarantelli, T.; Zanazzi, P. F. Inorg. Chem. 1985, 24, 4615-4619.
30. (e) Ferguson, G.; Langrick, C. R.; Parker, D.; Matthes, K. J. Chem. Soc., Chem. Commun. 1985, 1609-1610.
31. (f) Veit, R.; Girerd, J.-J.; Kahn, O.; Robert, F.; Jeannin, Y. Inorg. Chem. 1986, 25, 4175-4180.
32. (g) Curtis, N. F.; Gainsford, G. J.; Morgan, K. R. Aust. J. Chem. 1988, 41, 1545-1555.
33. (h) Smolander, K.; Leisto, K. Inorg. Chim. Acta 1990, 169, 151-155.
34. (i) Sillanpää, R.; Rissanen, K. Acta Chem. Scand. 1990, 44, 1013-1017.
35. (j) Myllyviita, S.; Sillanpää, R.; Kolnaar, J. J. A.; Reedijk, J. J. Chem. Soc., Dalton Trans. 1995, 13, 2209-2213.
36. (k) Kannan, S.; Pillai, M. R. A.; Droege, P. A.; Jurisson, S.; Barnes, C. L. Inorg. Chim. Acta 1997, 254, 397-400.
37. (l) Higgs, T. C.; Spartalian, K.; O'Connor, C. J.; Matzanke, B. F.; Carrano, C. J. Inorg. Chem. 1998, 37, 2263-2272.
38. (m) Cronin, L.; Mount, A. R.; Parsons, S.; Robertson, N. J. Chem. Soc., Dalton Trans. 1999, 12, 1925-1928.
39. (n) Bu, X.-H.; Du, M.; Shang, Z.-L.; Zhang, R.-H.; Liao, D.-Z.; Shionoya, M.; Clifford, T. Inorg. Chem. 2000, 39, 4190-4199.
40. (o) Song, Y.; Gamez, P.; Roubeau, O.; Lutz, M.; Spek, A. L.; Reedijk, J. Eur. J. Inorg. Chem. 2003, 2924-2928.
41. (a) Cronin, L.; Walton, P. H. Inorg. Chim. Acta 1998, 269, 241-245.
42. (b) Gutierrez, L.; Alzuet, G.; Real, J. A.; Cano, J.; Borras, J.; Castineiras, A. Inorg. Chem. 2000, 39, 3608-3614.
43. (c) Gutierrez, L.; Alzuet, G.; Real, J. A.; Cano, J.; Borras, J.; Castineiras, A. Eur. J. Inorg. Chem. 2002, 2094-2102.
44. Journaux, Y.; Lloret, F.; Kahn, O. Inorg. Chem. 1990, 29, 3048-3051.
45. (a) Darbost, U.; Zeng, X.; Rager, M-N.; Giorgi, M.; Jabin, L; Reinaud, O. Eur. J. Inorg. Chem. 2004, 4371-4374.
46. (b) Sénèque, O.; Rager, M.-N.; Giorgi, M.; Prangé, T.; Tomas, A.; Reinaud, O. J. Am. Chem. Soc. 2005, 127, 14833-14840.
47. When the anisol units of a calixarene are π-metalated, the cavity becomes more acidic and can host anions. See Staffilani, M.; Hancock, K. S. B.; Steed, J. W.; Holman, K. T.; Atwood, J. L.; Juneja, R. K.; Burkhalter, R. S. J. Am., Chem. Soc. 1997, 119, 6324-6335.
48. Strong conformational couplings between the metal center and the calix[6]arene structure have been highlighted in other instances. See ref 19b and Rondelez, Y.; Sénèque, O.; Rager, M.-N.; Duprat, A.; Reinaud, O. Chem. Eur. J. 2000, 6, 4218-4226.