The anion recognition based on calixarene derivatives

Progress in Chemistry

Volumn 18, Issue 12, 2006, Pages 1668-1676

  Han, Jun ^a   Yan, Chaoguo ^a  

^a YANGZHOU UNIVERSITY   (China)

Author keywords

Anion recognition; Calixarene; Molecular recognition; Supramolecular chemistry

Indexed keywords

EID: 33846477188     PISSN: 1005281X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (52)

1. Huang Z T, Yang L M. Progress in Chemistry, 1994, 6: 173-177
2. Gusche C D. Acc. Chem. Res., 1983, 16: 161-170
3. Liu Y, Zhang H Y, Li L, Wang H. Nanometer Supramolecular Chemistry. Beijing: Chemical Industry Press, 2004. 117-119
4. Beer P D, Gale P A. Angew. Chem. Int. Ed. Engl., 2001, 40: 486-516
5. Bohmer V. Angew. Chem. Int. Ed. Engl., 1995, 34: 713-745
6. Beer P D, Drew M G B, Hesek D, Shade M, Szemes F. Chem. Commun., 1996, 2161-2162
7. Beer P D, Drew M G B, Hesek D, Nam K C. Chem. Commun., 1997, 107-108
8. Gale P A, Chen Z, Drew M G B, Heath J A, Beer P D. Polyhedron, 1998, 17: 405-412
9. Dumazet I, Beer P D. Tetrahedron Lett., 1999, 40: 785-788
10. Beer P D, Gale P A, Hesek D. Tetrahedron Lett., 1995, 36: 767-770
11. Beer P D, Shade M. Chem. Commun., 1997, 2377-2378
12. Stastny V, Lhotak P, Michlova V, Stibora I, Sykora J. Tetrahedron, 2002, 58: 7207-7211
13. Miao R, Zheng Q Y, Chen C F, Huang Z T. Tetrahedron Lett., 2005, 46: 2155-2158
14. Tomapatanaget B. Tetrahedron Lett., 2001, 42: 8105-8109
15. Liu S Y, He Y B, Qing G Y, Xu K X, Qin H J. Tetrahedron: Asymmetry, 2005, 16: 1527-1534
16. Sdira S B, Felix C P, Giudicelli M B A, et al. J. Org. Chem., 2003, 68: 6632-6638
17. Schmidtchen F P, Berger M. Chem. Rev., 1997, 97: 1609-1646
18. Antonisse M M G, Reinhoudt D N. Chem. Commun., 1998, 443-448
19. Pan T R, Chantarasiri N, Tuntulani T. Tetrahedron Lett., 2003, 44: 29-32
20. Lang K, Curinova P, Dudic M, Proskova P, Stibor I, Sastny V, Lhotak P. Tetrahedron Lett., 2005, 46: 4469-4472
21. Gutsche C D, Calixarenes, in Monographs in Supramolecular Chemistry (ed. Stoarddt J F). Londan: Royal Society of Chemistry, 1989
22. Vicens J, Bohmer V (eds.). Calixarenes, a Versatile Class of Macrocyclic Compounds. Dordrecht: Kluwer, 1991
23. Bohmer V. Angew. Chem. Int. Ed. Engl., 1995, 34: 713-745
24. Izatt R M, Lanb J D, Hawkins R T, Brown P R, Izatt S R, Christensen J J. J. Am. Chem. Soc., 1983, 105: 1782-1785
25. Browne C M, Ferguson G, McKervey M A, Mulholland D L, O'Connor T, Parvez M. J. Am. Chem. Soc., 1985, 107: 2703-2712
26. Jeong H, Choi E M, Kang S O, Nam K C, Jeon S. J. Electroanal. Chem., 2000, 485: 154-160
27. Budka J, Lhotak P, Michlova V, Stibor I. Tetrahedron Lett., 2001, 42: 1583-1586
28. Lee J Y, Kim S K, Jung J H, Kim J S. J. Org. Chem., 2005, 70: 1463-1466
29. Xiao Y J, Wu X J, Zeng Z Y, He Y B, Meng L Z, Wu C T. Acta Chimica Sinica, 2003, 61(12): 1986-1990
30. Liu S Y, Wang F J, Kui L H, Xiao W, Meng L Z, He Y B. B Science in China, Series B, 2003, 33(6): 504-510
31. Casnati A, Massera C, Pelizzi N, Stibor I, Pinkassik E. Tetrahedron Lett., 2002, 43: 7311-7314
32. Beer P D, Timoshenko V, Maestri M, Balzani P P V. Chem. Commun., 1999, 1755-1756
33. Kotch F W, Sidorov V, Lam Y F, Kayser K J, Li H, Kaucher M S, Davis J T. J. Am. Chem. Soc., 2003, 125: 15140-15150
34. Tumcharern G, Tuntulani T, Coles S J, Hursthouse M B, Kilburn J D. Org. Lett., 2003, 5(26): 4971-4974
35. Ge Y, Liu L, Wang Y Y, Yan C G, Acta Chimica Sinica, 2005, 63(6): 533-537
36. Nabeshima T, Saiki T, Iwabuchi J, Akine S. J. Am. Chem. Soc., 2005, 127: 5507-5511
37. Dudic M, Lhota'k P, Stibor I, Lang K, Proskova P. Org. Lett., 2003, 5(2): 149-152
38. Arduini A, Brindani E, Giorgi G, Pochini A, Secchi A. J. Org. Chem., 2002, 67: 6188-6194
39. Liu S Y, He Y B, Wu J L, Wei L H, Qin H J, Meng L Z, Hu L. Org. Biomol. Chem., 2004, 2: 1582-1586
40. Rojsajjakul T, Veravong S, Tumcharen G, et al. Tetrahedron, 1997, 53: 4669-4680
41. Liu F, Lu G Y, He W J, Mei Y H, Zhu L G. Synthesis, 2001, 607-611
42. Liu F, Lu G Y, He W J, Wang Z S, Zhu L G. Chin. J. Chem., 2001, 19: 317-320
43. Liu F, Lu G Y, He W J, Liu M H, Zhu L G, Wu H M. New J. Chem., 2002, 26: 601-606
44. Camiolo S, Gale P A, Ogden M I, Skelton B W, White A H. J. Chem. Soc. Perkin Trans 2, 2001, 1294-1298
45. Wolf N J, Georgiev E M, Yordanov A T, Whittlesey B R, Fred H K, Roundhill D M. Polyhedron, 1999, 18: 885-896
46. Georgiev E M, Wolf N, Roundhill D M. Polyhedron, 1997, 16: 1581-1584
47. Yilmaz A, Memon S, Yilmaz M. Tetrahedron, 2002, 58: 7735-7740
48. Ediz O, Tabakci M, Memon S, Yilmaz M, Roundhill D M. Supramol. Chem., 2004, 16(3): 199-204
49. de Namora A F D, Piro O E, Castellano E E, et al. J. Inorganica Chimica Acta, 1999, 285: 142-144
50. Tuntulani T, Poompradub S, Thavornyutikarn P, Jaiboon N, Ruangpornvisuti V, Chaichit N, Asfaric Z, Vicensc J. Tetrahedron, 2002, 58: 10277-10285
51. Beer P D, Drew M G B, Gradwell K. J. Chem. Soc. Perkin Trans 2, 2000, 511-519
52. Tabakci M, Memon S, Yilmaz M, Roundhill D M. Journal of Inclusion Phenomena and Macrocyclic Chem., 2003, 45: 265-270