Allosteric anion recognition by metal complexation of tris(bipyridine-imidazolium) ligand

Tetrahedron Letters

Volumn 48, Issue 8, 2007, Pages 1493-1496

  Sato, Kiyoshi ^a   Sadamitsu, Yuichi ^a   Arai, Sadao ^b   Yamagishi, Takamichi ^a  

^a TOKYO METROPOLITAN UNIVERSITY   (Japan)

^b TOKYO MEDICAL UNIVERSITY   (Japan)

Author keywords

C H X hydrogen bonding; Allosteric effect; Anion recognition; Imidazolium; Pseudocryptand

Indexed keywords

ANION; BIPYRIDINE DERIVATIVE; BROMINE; CHLORINE; IMIDAZOLE DERIVATIVE; IODINE; IRON; RUTHENIUM;

ALLOSTERISM; ANION TRANSPORT; ARTICLE; LIGAND BINDING; MOLECULAR DYNAMICS; MOLECULAR MODEL; MOLECULAR RECOGNITION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY;

EID: 33846345306     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.12.118     Document Type: Article

References (37)

1. Saalfrank R.W., and Demleitner B. In: Sauvage J.P. (Ed). Transition Metals in Supramolecular Chemistry (1999), John Wiley and Sons, New York 1-52
2. Reviews of metal-templated receptors:. Linton B., and Hamilton A.D. Chem. Rev. 97 (1997) 1669-1680
3. Nabeshima T. Coord. Chem. Rev. 148 (1996) 151-169
4. Recent examples of metal controlled molecular recognition:. Lee A.B., and Hong J.-I. Tetrahedron Lett. 39 (1998) 4317-4320
5. Schwabacher A.W., Stefanescu A.D., and Rehman A. J. Org. Chem. 64 (1999) 1784-1788
6. Al-Sayah M.H., and Branda N.R. Angew. Chem., Int. Ed. 39 (2000) 945-947
7. Haino T., Yamanaka Y., Araki H., and Fukazawa Y. Chem. Commun. (2002) 402-403
8. Katoh A., Kudo H., and Saito R. J. Supramolecular Chem. 2 (2002) 79-84
9. Telfer S.G., Bernardinelli G., and Williams A.F. Dalton Trans. (2003) 435-440
10. Nabeshima T., Yoshihira Y., Saiki T., Akine S., and Horn E. J. Am. Chem. Soc. 125 (2003) 28-29
11. Katoh A., Kudo H., and Saito R. Heterocycles 66 (2005) 285-297
12. Baylies C.J., Riis-Johannessen T., Harding L.P., Jeffery J.C., Moon R., Rice C.R., and Whitehead M. Angew. Chem., Int. Ed. 44 (2005) 6909-6912
13. Nabeshima T., Tanaka Y., Saiki T., Akine S., Ikeda C., and Sato S. Tetrahedron Lett. 47 (2006) 3541-3544
14. Amendola V., Boiocchi M., Colasson B., and Fabbrizzi L. Inorg. Chem. 45 (2006) 6138-6147 and references cited therein
15. For recent reviews of anion recognition:. Sessler J.L., Gale P.A., and Cho W.S. Anion Receptor Chemistry (2006), Royal Society of Chemistry, Cambridge, UK
16. Steed J.W. Chem. Commun. (2006) 2637-2649
17. Yoon J., Kim S.K., Singh N.J., and Kim K.S. Chem. Soc. Rev. 35 (2006) 355-360
18. Kubik S., Reyheller C., and Stüwe S. J. Inclusion Phenom. Macrocyclic Chem. 52 (2005) 137-187
19. Special Issue on Anion Sensing, Top. Curr. Chem., 2005, 255, 1-229.
20. Special Issue on Synthetic Anion Receptor Chemistry, Coord. Chem. Rev., 2003, 240, 1-226.
21. Beer P.D., and Gale P.A. Angew. Chem., Int. Ed. 40 (2001) 486-516
22. Sato K., Arai S., and Yamagishi T. Tetrahedron Lett. 40 (1999) 5219-5222
23. See also:. Ihm H., Yun S., Kim H.G., Kim J.K., and Kim K.S. Org. Lett. 4 (2002) 2897
24. Polin J., Schmohel E., and Balzani V. Synthesis (1998) 321-324
25. Liu H.-K., Sun W.-Y., Ma D.-J., Yu K.B., and Tang W.-X. Chem. Commun. (2000) 591-592
26. Ziessel R., and Lehn J.-P. Helv. Chim. Acta 73 (1990) 1149-1162
27. Beeston R.F., Aldridge W.S., Treadway J.A., Fitzgerald M.C., DeGraff B.A., and Stitzel S.E. Inorg. Chem. 37 (1998) 4368-4379
28. Hamann C., von Zelewsky A., Neels A., and Stoeckli-Evans H. Dalton Trans. (2004) 402-406
29. 2+) will be published in full paper.
30. aapp. Schneider H.-J., and Yatsimirsky A. Principles and Methods in Supramolecular Chemistry (2000), John Wiley and Sons, New York 144-145
31. Fielding L. Tetrahedron 56 (2000) 6151-6170
32. Wong W.W.H., Phipps D.E., and Beer P.D. Polyhedron 23 (2004) 2821-2829
33. Vichers M.S., Martindale K.S., and Beer P.D. J. Mater. Chem. 15 (2005) 2784-2790
34. max = 640 nm).
35. Sato K., Onitake T., Arai S., and Yamagishi T. Heterocycles 60 (2003) 779-784
36. Sato K., Sadamitsu Y., Arai S., Shimada T., Inoue H., and Yamagishi T. Heterocycles 66 (2005) 119-127
37. During course of this manuscript preparation, a similar Fe(II) complex with ethyl groups at 2,4,6-position of benzene has been reported very recently:. Amendola V., Boiocchi M., Colasson B., Fabbrizzi L., Douton M.-J.R., and Ugozzoli F. Angew. Chem., Int. Ed. 45 (2006) 6920-6924