Metal–organic polyhedra containing 36 and 24 folds of amide groups for selective luminescent recognition of natural disaccharides

Chemical Communications

Volumn 48, Issue 48, 2012, Pages 6022-6024

  Jiao, Yang ^a   Zhang, Jing ^a   Zhang, Lejie ^a   Lin, Zhihua ^a   He, Cheng ^a   Duan, Chunying ^a  

^a DALIAN UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; DISACCHARIDE; LACTOSE; METAL ORGANIC FRAMEWORK; SUCROSE; METAL; MONOSACCHARIDE;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; FLUORESCENCE ANALYSIS; CHEMISTRY; LUMINESCENCE;

AMIDES; DISACCHARIDES; LUMINESCENCE; METALS; MONOSACCHARIDES;

EID: 84861608763     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c2cc30497j     Document Type: Article

References (34)

1. B. Ernst, G. W. Hart and P. Sinay, Carbohydrates in Chemistry and Biology, Wiley-VCH, Weinheim, 2000
2. A. P. Davis and T. D. James, in Functional Synthetic Receptors, ed. T. Schrader and A. D. Hamilton, Wiley-VCH, Weinheim, Germany, 2005, pp. 45-109
3. T. K. Dam, C. F. Brewer, Chem. Rev., 2002, 102, 387-429
4. M. Mazik, Chem. Soc. Rev., 2009, 38, 935-956
5. T. K. Lindhorst, Essentials of Carbohydrate Chemistry and Biochemistry, Wiley-VCH, Weinheim, 2000
6. A. Varki, R. Cummings, J. Esko, H. Freeze, G. Hart and J. Marth, in Essentials of Glycobiology, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1999
7. O. Francesconi, A. Ienco, G. Moneti, C. Nativi, S. Roelens, Angew. Chem. Int. Ed., 2006, 45, 6693-6696
8. D. Rodríguez-Lucena, J. M. Benito, C. O. Mellet, J. M. G. Fernández, Chem. Commun., 2007 831-833
9. M. Mazik, M. Kuschel, Eur. J. Org. Chem., 2008 1517-1526
10. T. Ishi-i, M. A. Mateos-Timoneda, P. Timmerman, M. Crego-Calama, D. N. Reinhoudt, S. Shinkai, Angew. Chem. Int. Ed., 2003, 42, 2300-2305
11. R. D. Hubbard, S. R. Horner, B. L. Miller, J. Am. Chem. Soc., 2001, 123, 5810
12. O. Rusin, K. Lang, V. Král, Chem.-Eur. J., 2002, 8, 655
13. M. Mazik, A. König, J. Org. Chem., 2006, 71, 7854
14. J. L. Hou, X. B. Shao, G. J. Chen, Y. X. Zhou, X. K. Jiang, Z. T. Li, J. Am. Chem. Soc., 2004, 126, 12386-12387
15. D. B. Walker, G. Joshi, A. P. Davis, Cell. Mol. Life Sci., 2009, 66, 3177-3191
16. Jack K. Clegg, Feng Li, Katrina A. Jolliffe, George V. Meehan, Leonard F. Lindy, Chem. Commun., 2011, 47, 6042-6044
17. Y. Ferrand, M. P. Crump, A. P. Davis, Science, 2007, 318, 619-622
18. T. J. Ryan, G. Lecollinet, T. Velasco, A. P. Davis, Proc. Natl. Acad. Sci. U. S. A., 2002, 99, 4863-4866
19. M. D. Ward, Chem. Commun., 2009 4487-4499
20. B. H. Northrop, Y.-R. Zheng, K.-W. Chi, P. J. Stang, Acc. Chem. Res., 2009, 42, 1554-1563
21. L. Cronin, Angew. Chem. Int. Ed., 2006, 45, 3576-3578
22. C. Schmuck, Angew. Chem. Int. Ed., 2007, 46, 5830-5832
23. E. Barea, J. A. R. Navarro, J. M. Salas, M. Quiro, M. Willermann, B. Lippert, Chem.-Eur. J., 2003, 9, 4414-4474
24. S. Tashiro, M. Kobayashi, M. Fujita, J. Am. Chem. Soc., 2006, 128, 9280-9281
25. C. J. Hastings, D. Fiedler, R. G. Bergman, K. N. Raymond, J. Am. Chem. Soc., 2008, 130, 10977-10983
26. Abe, Y. Chida, H. Kurokawa, M. Inouye, J. Org. Chem., 2011, 76, 3366-3371
27. N. P. Barwell, A. P. Davis, J. Org. Chem., 2011, 76, 6548-6557
28. Y. Q. Chen, X. Z. Wang, X.-B. Shao, J. L. Hou, X. Z. Chen, X. K. Jiang, Z. T. Li, Tetrahedron, 2004, 60, 10253-10256
29. F. A. Quiocho, Pure Appl. Chem., 1989, 61, 1293-1306
30. N. K. Vyas, M. N. Vyas, F. A. Quiocho, Science, 1988, 242, 1290-1295
31. C. He, Z. Lin, Z. He, C. Duan, C. Xu, Z. Wang, C. Yan, Angew. Chem. Int. Ed., 2008, 47, 877-881
32. Y. Liu, X. Wu, C. He, Y. Jiao, C. Duan, Chem. Commun., 2009 7554-7556
33. L. Zhao, S. Y. Qu, C. He, R. Zhang, C. Y. Duan, Chem. Commun., 2011, 47, 9387-9389
34. K. A. Connors, Binding Constants, John Wiley, New York, 1987