Temperature dependence of the inclusion-dissociation behavior of the inclusion complexes between cationic substituted 3H-indoles and β-cyclodextrin. Design of a novel type of semi-rotaxane

Journal of Photochemistry and Photobiology A: Chemistry

Volumn 173, Issue 1, 2005, Pages 42-50

  Chen, Yilong ^a   Xu, Tongkuan ^a   Shen, Xinghai ^a   Gao, Hongcheng ^a  

^a PEKING UNIVERSITY   (China)

Author keywords

Cyclodextrin; Inclusion dissociation interaction; Solvation effect; Substituted 3H indole; Temperature effect

Indexed keywords

EID: 20444366545     PISSN: 10106030     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jphotochem.2005.01.001     Document Type: Article

References (51)

1. S. Li W.C. Purdy Chem. Rev. 92 1992 1457
2. J. Szejtli Cyclodextrin Technology 1988 Kluwer Academic Publishers Dordrecht, The Netherlands
3. M.L. Bender M. Komiyama Cyclodextrin Chemistry 1978 Springer-Verlag Berlin
4. A.F. Danil de Namor R. Traboulssi D.F.V. Lewis J. Am. Chem. Soc. 112 1990 8442
5. M.V. Rekharsky Y. Inoue Chem. Rev. 98 1998 1875
6. Y. Inoue T. Hakushi Y. Liu L. Tong B. Shen D. Jin J. Am. Chem. Soc. 115 1993 475
7. Y. Inoue Y. Liu L. Tong B. Shen D. Jin J. Am. Chem. Soc. 115 1993 10637
8. M.V. Rekharsky M.P. Mayhew R.N. Goldberg P.D. Ross Y. Yamashoji Y. Inoue J. Phys. Chem. B 101 1997 87
9. M.V. Rekharsky R.N. Goldberg F.P. Schwarz Y.B. Tewari P.D. Ross Y. Yamashoji Y. Inoue J. Am. Chem. Soc. 117 1995 8830
10. J.E. Leffler J. Org. Chem. 20 1955 1202
11. I. Tabushi Y. Kiyosuke T. Sugimoto K. Yamamura J. Am. Chem. Soc. 100 1978 916
12. P.K. Zarzycki H. Lamparczyk J. Chem. Educ. 73 1996 459
13. (a) M. Saito T. Shimomura Y. Okumura K. Ito J. Chem. Phys. 114 2001 1
14. (b) Y. Okumura K. Ito R. Hayakawa Phys. Rev. Lett. 80 1998 5003
15. (a) C. Zhang, Ph.D. Thesis, Peking University, Beijing, 2002.
16. (b) C. Zhang X. Shen H. Gao Spectrosc. Spect. Anal. 23 2003 217
17. (c) C. Zhang X. Shen H. Gao Chem. Phys. Lett. 363 2002 515
18. P.V. Demarco A.L. Thakkar Chem. Commun. 1970 2
19. F. Cramer W. Saenger H. Spatz J. Am. Chem. Soc. 89 1967 14
20. R.P. Rohrbach L.J. Rodriguez E.M. Eyring J.F. Wojcik J. Phys. Chem. 81 1977 944
21. (a) X. Shen M. Belletête G. Durocher J. Phys. Chem. B 102 1998 1877
22. (b) X. Shen M. Belletête G. Durocher Chem. Phys. Lett. 301 1999 193
23. (a) H. Asanuma M. Kakazu M. Shibata T. Hishiya M. Komiyama Chem. Commun. 1997 1971
24. (b) P. Claudy J.M. Letoffe P. Germain J.P. Bastide A. Bayol S. Blasquez R.C. Rao B. Gonzalez J. Thermal Anal. 37 1991 2497
25. T. Xu X. Shen H. Gao Chinese Chem. Lett. 15 2004 26
26. P. Skrabal J. Steiger H. Zellinger Helv. Chim. Acta 58 1975 800
27. A. Popowycz, M.Sc. Thesis, University of Montreal, Montreal, 1991.
28. J. Martin D. Johannes Acta Chem. Scand. Serb. B 36 1982 241
29. 2O: C, 63.89; H, 9.76; N, 3.73. Found: C, 63.60; H, 9.63; N, 3.65.
30. (a) S. Nigam G. Durocher J. Phys. Chem. 100 1996 7135
31. (b) S. Nigam G. Durocher J. Photochem. Photobiol. A: Chem. 103 1997 143
32. (a) X. Shen M. Belletête G. Durocher J. Phys. Chem. B 101 1997 8212
33. (b) X. Shen M. Belletête G. Durocher Langmuir 13 1997 5830
34. (c) X. Shen M. Belletête G. Durocher Chem. Phys. Lett. 298 1998 201
35. M. Belletête R.S. Sarpal G. Durocher Can. J. Chem. 72 1994 2239
36. The absorbance values are with some errors due to the scattering in absorption spectra resulting from the large size of the 1:3 inclusion complexes (see Ref. 18a and see also: J.F. Rabeh, Experimental Methods in Polymer Chemistry, J. Wiley & Sons, New York, 1980, pp. 191).
37. G.G. Guilbault Practical Fluorescence 1973 Marcel Dekker New York
38. C.A. Parker Photoluminescence of Solution 1968 Elsevier Amsterdam
39. (a) R. Yang K. Li K. Wang F. Liu N. Li F. Zhao Spectrochim. Acta A 59 2003 153
40. (b) S. Hamai J. Phys. Chem. B 103 1999 293
41. (c) S. Hamai J. Phys. Chem. B 101 1997 1707
42. (d) D.R. Alston T.H. Lilley J.F. Stoddart J. Chem. Soc., Chem. Commun. 1985 1600
43. (e)(e) J. Li Y. Wei L. Ding C. Dong Spectrochim. Acta A 59 2003 2759
44. (a) H. Gharibi S. Jalili T. Rajabi Colloids Surf. A 175 2000 361
45. (b) J. Peeters P. Neeskens J. Adriaensen M. Brewster J. Incl. Phenom. Macro. 44 2002 75
46. H.A. Benesi J.H. Hildebrand J. Am. Chem. Soc. 71 1949 2703
47. H.F.M. Nelissen F. Venema R.M. Uittenbogaard M.C. Feiters R.J.M. Nolte J. Chem. Soc. Perkin Trans. 2 1997 2045
48. A. Benrebouh Y.H. Zhang X.X. Zhu Maromol. Rapid Commun. 21 2000 685
49. T.W.N. Bieze A.C. Barnes C.J.M. Huige J.E. Enderby J.C. Leyte J. Phys. Chem. 98 1994 6568
50. K.J. Liu J.L. Parsons Macromolecules 2 1969 529
51. D. Rudan-Tasic C. Klofutar J. Mol. Liquid 103/104 2003 187