Anion receptors: A new class of amide/quaternized amine macrocycles and the chelate effect

Inorganic Chemistry

Volumn 42, Issue 5, 2003, Pages 1397-1399

  Hossain, Alamgir ^a   Kang, Sung Ok ^a   Powell, Douglas ^a   Bowman James, Kristin ^a  

^a UNIVERSITY OF KANSAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; ANION; CHELATE; HALIDE; HYDROGEN; MACROCYCLIC COMPOUND; PHENYL GROUP; PYRIDINE DERIVATIVE; QUATERNARY AMMONIUM DERIVATIVE; RECEPTOR;

ARTICLE; BINDING AFFINITY; CHELATION; COMBINATORIAL CHEMISTRY; CRYSTAL STRUCTURE; HYDROGEN BOND;

EID: 0037430170     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic0263140     Document Type: Article

References (28)

1. Supramolecular Chemistry of Anions; Bianchi, A., Bowman-James, K., García-España, E., Eds; Wiley-VCH: New York, 1997.
2. Schneider, H.-J.; Yatsimirsky, A. Principles and Methods in Supramolecular Chemistry; John Wiley and Sons: New York. 2000.
3. Beer, P. D.; Smith, D. K. Prog. Inorg. Chem. 1997, 46, 1-96.
4. Danby, A.; Seib, L.; Alcock, N. W.; Bowman-James, K. Chem. Commun. 2000, 973-974.
5. Kavallieratos, K.; Danby, A.; Van Berkel, G. J.; Kelly, M. A.; Sachleben, R. A.; Moyer, B. A.; Bowman-James, K. Anal. Chem. 2000. 72, 5258-5264.
6. Qian, Q.; Wilson, G. S.; Bowman-James, K.; Girault, H. H. Anal. Chem. 2001, 73, 497-503.
7. Kavallieratos, K.; de Gala, S. R.; Austin, D. J.; Crabtree, R. H. J. Am. Chem. Soc. 1997, 119, 2325-2326.
8. Kavallieratos, K.; Bertao, C. M.; Crabtree, R. H. J. Org. Chem. 1999, 64, 1675-1683.
9. Valiyaveettil, S.; Engbersen, J. F. J.; Verboom, W.; Reinhoudt, D. N. Angew. Chem., Int. Ed. Engl. 1993, 32, 900-901.
10. Beer, P. D.; Drew, M. G. B.; Gradwell, K. J. Chem. Soc., Perkin Trans. 2, 2000, 511-519.
11. Kubik, S.; Goddard, R. Proc. Natl. Acad. Sci. U.S.A. 2002, 99, 5127-5132.
12. Choi, K.; Hamilton, A. D. J. Am. Chem. Soc. 2001, 123, 2456-2457.
13. Hossain, M. A.; Llinares, J. M.; Powell, D.; Bowman-James, K. Inorg. Chem. 2001, 40, 2936-2937.
14. Luecke, H.; Quiocho, F. A. Nature 1990, 347, 402-406.
15. He, J. J.; Quiocho, F. A. Science 1991, 251, 1479-1481.
16. Wisner, J. A.; Beer, P. D.; Drew, M. G. B. Angew. Chem., Int. Ed. 2001, 40, 3606-3609.
17. Kral, V.; Rusin, O.; Schmidtchen, F. P. Org. Lett. 2001, 3, 873-876.
18. 2), 8.12 (m, 6H, 7ArH), 9.38 (s, 4H, NH).
19. 2), 6.77 (t, 8H, ArH), 6.91 (t, 16H, ArH), 7.16 (s, 16H, ArH), 8.00 (d, 4H, ArH), 8.07 (t, 2H, ArH), 9.33 (s, 4H, NH).
20. - was isolated and was used directly for crystallization without further analysis.
21. 2 = 1.043.
22. 2 = 0.973.
23. Huang, B.; Parquette, J. R. Org. Lett. 2000, 2, 239-242.
24. Szumna, A.; Gryko, D. T.; Jurczak, J. Heterocycles 2002, 56, 361-368.
25. Baer, A. J.; Koivisto, B. D.; Côté, A. P.; Taylor, N. J.; Hanan, G. S.; Nierengarten, H.; Van Dorsselaer, A. Inorg. Chem. 2002, 41, 4987-4989.
26. -, which were 1 mM. TMS was used as an external reference in capillary tube.
27. Hynes, M. J. J. Chem. Soc., Dalton Trans. 1993, 311-312.
28. Schneider, H.-J.; Kramer, R.; Simova, S.; Schneider, U. J. Am. Chem. Soc. 1988, 110, 6442-6448.