Study of inclusion complex between 2,6-dinitrobenzoic acid and β-cyclodextrin by 1H NMR, 2D 1H NMR (ROESY), FT-IR, XRD, SEM and photophysical methods

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 130, Issue , 2014, Pages 105-115

  Srinivasan, Krishnan ^a   Stalin, Thambusamy ^a  

^a ALAGAPPA UNIVERSITY   (India)

Author keywords

2,6 Dinitrobenzoic acid; Inclusion complex; Cyclodextrin

Indexed keywords

CYCLIC VOLTAMMETRY; ULTRAVIOLET VISIBLE SPECTROSCOPY;

ELECTROCHEMICAL ANALYSIS; HOST-GUEST INCLUSION COMPLEXES; INCLUSION COMPLEX; SCHEMATIC REPRESENTATIONS; SOLID INCLUSION COMPLEXES; THERMODYNAMIC PARAMETER; UV VISIBLE SPECTROSCOPY;

CYCLODEXTRINS;

BENZOIC ACID; BETA CYCLODEXTRIN; BETA CYCLODEXTRIN DERIVATIVE; ELECTROLYTE; NITROBENZOIC ACID DERIVATIVE; OLIGOSACCHARIDE;

CHEMISTRY; CONFORMATION; ELECTROCHEMISTRY; INFRARED SPECTROSCOPY; MOLECULAR DOCKING; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OXIDATION REDUCTION REACTION; PH; PHOTOCHEMISTRY; PROTON NUCLEAR MAGNETIC RESONANCE; SCANNING ELECTRON MICROSCOPY; SPECTROPHOTOMETRY; THERMODYNAMICS; X RAY DIFFRACTION;

BENZOIC ACID; BETA-CYCLODEXTRINS; ELECTROCHEMISTRY; ELECTROLYTES; HYDROGEN-ION CONCENTRATION; MAGNETIC RESONANCE SPECTROSCOPY; MICROSCOPY, ELECTRON, SCANNING; MOLECULAR CONFORMATION; MOLECULAR DOCKING SIMULATION; NITROBENZOATES; OLIGOSACCHARIDES; OXIDATION-REDUCTION; PHOTOCHEMISTRY; PROTON MAGNETIC RESONANCE SPECTROSCOPY; SPECTROPHOTOMETRY; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; THERMODYNAMICS; X-RAY DIFFRACTION;

EID: 84899582865     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2014.03.106     Document Type: Article

References (23)

1. V. Stefano, and B. Bruno J. Chem. Thermodyn. 41 7 2009 880 887
2. H. Long, Y.X. Zhu, and P.T. Kissinger Chin. J. Anal. Chem. 31 2003 631 634
3. X. Guo, Z. Wang, and S. Zhou Talanta 64 2004 135 139
4. G. Crini Prog. Polym. Sci. 30 2005 38 70
5. M. Kitaoka, and K. Hayashi J. Inclusion Phenom. Macrocycl. Chem. 44 2002 429 431
6. G. Crini Dyes Pigm. 77 2008 415 426
7. E.Y. Ozmen, and M. Yilmaz J. Hazard. Mater. 148 2007 303 310
8. L. Ducoroy, M. Bacquet, B. Martel, and M. Morcellet React. Funct. Polym. 68 2008 594 600
9. S. Berto, M.C. Bruzzoniti, R. Cavalli, D. Perrachon, E. Prenesti, C. Sarzanini, F. Trotta, and W. Tumiatti J. Inclusion Phenom. Macrocycl. Chem. 57 2007 637 643
10. E.M. Martin Dell Valle Process Biochem. 39 2004 1033 1046
11. D.S. Duhovny, Y. Inbar, R. Nussinov, and H.J. Wolfson Nucl. Acids Res. 33 2005 363 367
12. M.L. Connolly J. Appl. Crystallogr. 16 1983 548 558
13. C. Zhang, G. Vasmatzis, J.L. Cornette, and C. DeLisi J. Mol. Biol. 267 1997 707 726
14. G. Yagil J. Phys. Chem. 71 1967 1034 1044
15. M.J. Jorgenson, and D.R. Hartter J. Am. Chem. Soc. 85 1963 878 883
16. K. Srinivasan, T. Stalin, J. Vaheethabanu, and P. Manisankar J. Mol. Struct. 987 2011 214 224
17. K. Srinivasan, T. Stalin, K. Kayalvizhi, and K. Sivakumar Spectrochim. Acta A 79 2011 169 178
18. T. Stalin, M. Shanmugam, D. Ramesh, V. Nagalakshmi, R. Kavitha, and R. Rajamohan Spectrochim. Acta A Mol. Biomol. Spectrosc. 71 2008 125 132
19. H.A. Bensi, and J.H. Hildebrand J. Am. Chem. Soc. 71 1949 2703 2707
20. G. Gaitano, P.R.S. Rozas, J.R. Isasi, A.G. Martínez, and G. Tardajos J. Phys. Chem. B 108 2004 14154 14162
21. T. Sohajda, S. Beni, E. Varga, R. Ivanyi, A. Racz, L. Szente, and B. Noszal J. Pharm. Biomed. 50 2009 737 745
22. H.Y. Wang, J.H. Feng, and Y.L. Pang Spectrochem. Acta A 65 2006 100 105
23. R.O. Williams, V. Mahaguna, and M. Sriwongjanya Eur. J. Pharm. Biopharm. 46 1998 355 360