Experimental and theoretical studies on the inclusion complexation of syringic acid with α-, β-, γ- and heptakis(2,6-di-O-methyl)- β-cyclodextrin

Chemical and Pharmaceutical Bulletin

Volumn 56, Issue 4, 2008, Pages 468-474

  Song, Le Xin ^a   Wang, Hai Ming ^a   Xu, Peng ^a   Yang, Yan ^b   Zhang, Zi Qiang ^a  

^a UNIVERSITY OF SCIENCE AND TECHNOLOGY OF CHINA   (China)

^b ANHUI UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Cyclodextrin; Formation constant; Inclusion complex; Parameterized model 3; Syringic acid

Indexed keywords

ALPHA CYCLODEXTRIN; BETA CYCLODEXTRIN; BETA CYCLODEXTRIN DERIVATIVE; EUGENOL; GAMMA CYCLODEXTRIN; GUAIACOL; HEPTAKIS(2,6 O DIMETHYL) BETA CYCLODEXTRIN; PHENOL DERIVATIVE; SYRINGIC ACID;

AQUEOUS SOLUTION; ARTICLE; COMPLEX FORMATION; FLUORESCENCE SPECTROSCOPY; MOLECULAR INTERACTION; NONLINEAR SYSTEM; PROTON NUCLEAR MAGNETIC RESONANCE;

ALGORITHMS; CHEMISTRY, PHYSICAL; CYCLODEXTRINS; DRUG CARRIERS; GALLIC ACID; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; SOLUTIONS; SPECTROMETRY, FLUORESCENCE;

EID: 42049105332     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.56.468     Document Type: Article

References (31)

1. Szejtli J., Chem. Rev., 98, 1743-1753 (1998).
2. Song L. X., Teng C. F., Yang Y., J. Inclusion Phenom. Macrocyclic Chem., 54, 221-232 (2006).
3. Wenz G., Han B. H., Muller A., Chem. Rev., 106, 782-817 (2006).
4. Rekharsky M. V., Inoue Y., Chem. Rev., 98, 1875-1917 (1998).
5. Liu Y., Han B. H., Zhang H. Y., Curr. Org. Chem., 8, 35-46 (2004).
6. Connors K. A., J. Pharm. Sci., 84, 843-848 (1995).
7. Kitano H., Endo H., Gemmei-ide M., Kyogoku M., J. Inclusion Phenom. Macrocyclic Chem., 47, 83-90 (2003).
8. Huang M. J., Watts J. D., Bodor N., Int. J. Quantum Chem., 65, 1135-1152 (1997).
9. Yang Y., Song L. X., J. Inclusion Phenom. Macrocyclic Chem., 53, 27-33 (2005).
10. Liu L., Guo Q. X., J. Phys. Chem. B, 103, 3461-3467 (1999).
11. Huang M. J., Yi M. Y., Int. J. Quantum Chem., 100, 771-778 (2004).
12. Bertrand G. L., Faulkner J. R., Jr., Han S. M., Armstrong D. W., J. Phys. Chem., 93, 6863-6867 (1989).
13. Leyva E., Moctezuma E., Strouse J., Garcia-Garibay M. A., J. Inclusion Phenom. Macrocyclic Chem., 39, 41-46 (2001).
14. Tran C. D., Lacerda S. H. D., Anal. Chem., 74, 5337-5341 (2002).
15. Stewart J. J. P., J. Comput. Chem., 10, 221-264 (1989).
16. Stewart J. J. P., J. Comput.-Aided Mol. Des., 4, 1-45 (1990).
17. Chacko K. K., Saenger W., J. Am. Chem. Soc., 103, 1708-1715 (1981).
18. Lindner K., Saenger W., Carbohydr. Res., 99, 103-115 (1982).
19. Harata K., Bull. Chem. Soc. Jpn., 60, 2763-2767 (1987).
20. Aree T., Hoier H., Schulz B., Reck G., Saenger W. R., Angew. Chem. Int. Ed. Engl., 39, 897-899 (2000).
21. Wang H. M., Song L. X., Chem. Lett., 36, 596-597 (2007).
22. Klamt A., Schuurmann G., J. Chem. Soc. Perkin Trans. 2, 1993, 799-805 (1993).
23. Liu Y., Song Y., Chen Y., Yang Z. X., Ding F., J. Phys. Chem. B, 109, 10717-10726 (2005).
24. Song L. X., Wang H. M., Yang Y., Acta Chim. Sinica, 65, 1593-1599 (2007).
25. Tilloy S., Crowyn G., Monflier E., van Leeuwen P. W. N. M., Reek J. N. H., New J. Chem., 30, 377-383 (2006).
26. Coly A., Aaron J. J., Anal. Chim. Acta, 360, 129-141 (1998).
27. Stalin T., Sivakumar G., Shanthi B., Sekar A., Rajendiran N., J. Photochem. Photobiol. A, 177, 144-155 (2006).
28. Tucker E. E., Chirstian S. D., J. Am. Chem. Soc., 106, 1942-1945 (1984).
29. Schneider H. J., Hacket F., Rudiger V., Ikeda H., Chem. Rev., 98, 1755-1785 (1998).
30. Song L. X., Wang H. M., Xu P., Zhang Z. Q., Liu Q. Q., Bull. Chem. Soc. Jpn., 80, 2313-2322 (2007).
31. Yang Y., M.S. Thesis, University of Science and Technology of China, Hefei, China, 2005, pp. 33-37.