Study of inclusion complex of β-cyclodextrin and Ortho-Anisidine; Photophysical and electrochemical behaviors

Journal of Molecular Structure

Volumn 987, Issue 1-3, 2011, Pages 214-224

  Srinivasan, K ^a   Vaheethabanu, J ^a   Manisankar, P ^a   Stalin, T ^a  

^a ALAGAPPA UNIVERSITY   (India)

Author keywords

Cyclodextrin; Cyclicvoltammetry; Inclusion complex; Ortho Anisidine; pH Effects; RasMol tool

Indexed keywords

ANODIC PEAK POTENTIAL; ANODIC PEAKS; BUFFER SOLUTIONS; ELECTROCHEMICAL BEHAVIORS; ELECTROCHEMICAL STUDIES; HOST-GUESTS; INCLUSION COMPLEX; INCLUSION COMPLEXATION; INCLUSION INTERACTION; ORTHO-ANISIDINE; PHOTOPHYSICAL; RASMOL TOOL; SEM; SOLID INCLUSION COMPLEXES; SPONTANEOUS PROCESS; THERMODYNAMIC PARAMETER; UV-VISIBLE;

COMPLEXATION; ELECTROCHEMISTRY; SCANNING ELECTRON MICROSCOPY; X RAY DIFFRACTION;

PH EFFECTS;

EID: 79551565554     PISSN: 00222860     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molstruc.2010.12.026     Document Type: Article

References (32)

1. H. Suzuki Electronic Absorption Spectra and Geometry of Organic Molecules 1967 Academic Press New York p. 568
2. S.L. Wang, J.M. Lin, S.E. Shu, and C.Y. Chern J. Photochem. Photobiol. A: Chem. 210 2010 54 60
3. L. Jinxia, M. Zhanga, J. Chaoa, and S. Shuang Spectrochim. Acta Part A 73 2009 752 756
4. G. Astray, C.G. Barreiro, J.C. Mejuto, R.R. Otero, and J.S. Gandara Food Hydrocoll. 23 2009 1631 1640
5. T. Stalin, and N. Rajendiran Spectrochim. Acta 61A 2005 3087 3096
6. T. Stalin, R. Anitha Devi, and N. Rajendiran Spectrochim. Acta 61A 2005 2495 2504
7. T. Stalin, and N. Rajendiran J. Mol. Struct. 794 2006 35 45
8. T. Stalin, and N. Rajendiran J. Photochem. Photobiol. A; Chem. 177 2006 144 155
9. T. Stalin, K. Sivakumar, and N. Rajendiran Spectrochim. Acta 62 2005 991 999
10. T. Stalin, and N. Rajendiran Chem. Phys. 322 2006 311 322
11. T. Stalin, and N. Rajendiran J. Incl. Phenom. 55 2006 21 29
12. T. Stalin, and N. Rajendiran J. Photochem. Photobiol. A; Chem. 182 2006 137 150
13. T. Stalin, and N. Rajendiran Ind. J. Chem. 45 2006 1113 1120
14. S.S. Maity, S. Samanta, P.S. Sardar, A. Pal, S. Dasgupta, and S. Ghosh Chem. Phys. 354 2008 162 173
15. K. Sivakumar, and S. Balaji J. Chem. Sci. 119 2007 571 579
16. S. Patil Poly. Inter. 46 1998 99 105
17. G. Wang, Z. Yang, X. Li, and C. Li Carbon 43 2005 2564 2570
18. Xinhua Dai, Yiwei Tan, and Jian Xu Langmuir 18 2002 9010 9016
19. M.J. Jorgenson, and D.R. Harter J. Am. Chem. Soc. 85 1963 878 883
20. G. Yagil J. Phys. Chem. 71 1967 1034 1044
21. T. Stalin, M. Shanmugam, D. Ramesh, V. Nagalakshmi, R. Kavitha, and R. Rajamohan Spectrochim. Acta Part A 71 2008 125 132
22. N. Rajendiran Afinidad LVI 481 1999 170 174
23. N. Rajendiran, and M. Swaminathan J. Photochem. Photobiol. Sect. A 90 1995 109 116
24. N. Rajendiran, and M. Swaminathan Bull. Chem. Soc. Jpn. 68 1995 2797 2808
25. N. Rajendiran, and M. Swaminathan Bull. Chem. Soc. Jpn. 69 1996 2447 2452
26. H.A. Bensi, and J.H. Hildebrand J. Am. Chem. Soc. 71 1949 2703 2707
27. G. Gaitano, P.R.S. Rozas, J.R. Isasi, A.G. Martínez, and G. Tardajos J. Phys. Chem. B 108 2004 14154 14162
28. M. Chen, G. Diao, and E. Zhang Chemosphere 63 2006 522 529
29. L. Szente, vol. 3, Pergamon Press, Oxford, 1996, pp. 253-278.
30. H.Y. Wang, J.H. Xia Guang Feng, and Y.L. Pang Spectrochim. Acta Part A 65 2006 100 105
31. S. Scalia, A. Molinari, A. Casolari, and A. Maldotti Eur. J. Pharm. Sci. 22 2004 241 249
32. T. Pralhad, and K. Rajendrakumar J. Pharm. Biomed. Anal. 34 2004 333 339