Anion complexation by calix[4]arene-TTF conjugates

Dyes and Pigments

Volumn 92, Issue 1, 2012, Pages 668-673

  Flídrová, Karolína ^a   Tkadlecová, Marcela ^a   Lang, Kamil ^b   Lhoták, Pavel ^a  

^a INSTITUTE OF CHEMICAL TECHNOLOGY   (Czech Republic)

^b INSTITUTE OF INORGANIC CHEMISTRY   (Czech Republic)

Author keywords

Anion recognition; Calix 4 arene; NMR titration; Receptor; Tetrathiafulvalene; UV vis spectroscopy

Indexed keywords

ANION RECOGNITION; CALIX[4]ARENES; NMR TITRATION; RECEPTOR; TETRATHIAFULVALENES; UV/ VIS SPECTROSCOPY;

NEGATIVE IONS;

EID: 80051994127     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2011.06.001     Document Type: Article

References (38)

1. For books on calixarenes see: C.D. Gutsche Calixarenes: an introduction 2nd ed. 2008 The Royal Society of Chemistry, Thomas Graham House Cambridge
2. J. Vicens, J. Harrowfield, and L. Backlouti Calixarenes in the nanoworld 2007 Springer Dordrecht
3. Z. Asfari, V. Böhmer, J. Harrowfield, and J. Vicens Calixarenes 2001 2001 Kluwer Academic Publishers Dordrecht
4. L. Mandolini, and R. Ungaro Calixarenes in action 2000 Imperial College Press London
5. C.D. Gutsche J.F. Stoddart, Calixarenes revisited: monographs in supramolecular chemistry vol. 6 1998 The Royal Society of Chemistry Cambridge
6. For recent books and reviews on anion recognition see: J.L. Sessler, P.A. Gale, and W.S. Cho Anion receptor chemistry 2006 The Royal Society of Chemistry Cambridge
7. F.P. Schmidtchen Chem Soc Rev 39 2010 3916 3935
8. P.A. Gale Coord Chem Rev 250 2006 3219 3244
9. P.A. Gale, S.E. Garcia-Garrido, and J. Garric Chem Soc Rev 37 2008 151 190
10. B.L. Schottel, H.T. Chifotides, and K.R. Dunbar Chem Soc Rev 37 2008 68 83
11. R. Vilar Recognition of anions Structure and bonding vol. 129 2008 Springer Berlin
12. For review on calixarene-based anion receptors see: Matthews SE, Beer PD. In: Calixarenes; 2001. p. 421-39 (see Ref. [1c]).
13. P. Lhoták Top Curr Chem 255 2005 65 96
14. S.E. Matthews, and P.D. Beer Supramol Chem 17 2005 411 435
15. For some recent examples of urea-substituted calixarene-bases receptors see: B. Schazmann, N. Alhashimy, and D. Diamond J Am Chem Soc 128 2006 8607 8614
16. J.N. Babu, V. Bhalla, M. Kumar, R.K. Mahajan, and R.K. Puri Tetrahedron Lett 49 2008 2772 2775
17. E. Quinlan, S.E. Matthews, and T. Gunnlaugsson J Org Chem 72 2007 7497 7503
18. B. Schazmann, and D. Diamond New J Chem 31 2007 587 592
19. K. Lang, P. Curinová, M. Dudic, P. Prosková, I. Stibor, and V. Stastny Tetrahedron Lett 46 2005 4469 4472
20. P. Lhoták, J. Svoboda, and I. Stibor Tetrahedron 62 2006 1253 1257
21. I. Stibor, J. Budka, V. Michlová, M. Tkadlecová, M. Pojarová, and P. Curinová New J Chem 32 2008 1597 1607
22. J. Kroupa, I. Stibor, M. Pojarová, M. Tkadlecová, and P. Lhoták Tetrahedron 64 2005 10075 10079
23. P. Curinová, I. Stibor, J. Budka, J. Sykora, K. Lang, and P. Lhoták New J Chem 33 2009 612 619
24. For examples of calixarene-TTF conjugates see: M.H. Lee, Q.Y. Cao, S.K. Kim, J.L. Sessler, and J.S. Kim J Org Chem 76 2011 870 874
25. B.T. Zhao, M.J. Blesa, N. Mercier, F. LeDerf, and M. Salle New J Chem 29 2005 1164 1167
26. M.J. Blesa, B.T. Zhao, M. Allain, F. LeDerf, and M. Salle Chem Eur J 12 2006 1906 1914
27. J. Lyskawa, D. Canevet, M. Allain, and M. Salle Tetrahedron Lett 51 2010 5868 5872
28. B.T. Zhao, Z. Zhou, Z.N. Yan, E. Belhadj, F. LeDerf, and M. Salle Tetrahedron Lett 51 2010 5815 5818
29. A. Casnati, M. Fochi, P. Minari, A. Pochini, M. Reggiani, and R. Ungaro Gazz Chim Ital 126 1996 99 106
30. E. Kelderman, L. Derhaeg, G.J.T. Heesink, W. Veroom, J.F.J. Engbersen, and N.F. Van Hulst Angew Chem Int Ed Engl 31 1992 1075 1077
31. -1). Similar dimerization can be also found in: J. Scheerder, R.H. Vreekamp, J.F.J. Engbersen, W. Verboom, J.P.M. van Duynhoven, and D.N. Reinhoudt J Org Chem 61 1996 3476 3481
32. J. Garin, J. Orduna, S. Uriel, A.J. Moore, M.R. Bryce, and S. Wegener Synthesis 5 1994 489 493
33. D. Canevet, M. Salle, G. Zhang, D. Zhang, and D. Zhu Chem Commun 2009 2245 2269
34. J.S. Park, E. Karnas, K. Ohkudo, P. Chen, K.M. Kadish, and S. Fukuzumi Science 329 2010 1324 1327
35. J.S. Park, F. LeDerf, C.M. Bejger, V.M. Lynch, J.L. Sessler, and K.A. Nielsen Chem Eur J 16 2010 848 854
36. J. Lyskawa, M. Salle, J.Y. Balandier, F. LeDerf, E. Levillain, and M. Allain Chem Commun 2006 2233 2235
37. M. Yoshizawa, K. Kumazawa, and M. Fujita J Am Chem Soc 127 2005 13456 13457
38. A.Y. Ziganshina, Y.H. Ko, W.S. Jeon, and K. Kim Chem Commun 2004 806 807