Interactions of 1-hexyl-3-methylimidazolium bromide with acetone

Chinese Journal of Chemical Physics

Volumn 19, Issue 5, 2006, Pages 447-450

  Zhai, Cui Ping ^a,c   Wang, Jian Ji ^b   Xuan, Xiao Peng ^b   Wang, Han Qing ^a   Chen, Miao ^a  

^a LANZHOU INSTITUTE OF CHEMICAL PHYSICS   (China)

^b HENAN NORMAL UNIVERSITY   (China)

^c HENAN UNIVERSITY   (China)

Author keywords

1 hexyl 3 methylimidazolium bromide ionic liquid; 1h and 13C NMR; Acetone; Chemical shift; Interaction

Indexed keywords

CHEMICAL SHIFT; HYDROGEN BONDS; IONIC LIQUIDS;

13C NMR; COMPUTATIONAL RESULTS; HYDROGEN NUCLEI; INTERACTION; MOLE FRACTION; ROOM TEMPERATURE IONIC LIQUIDS;

ACETONE;

EID: 33846010175     PISSN: 16740068     EISSN: None     Source Type: Journal    
DOI: 10.1360/cjcp2006.19(5).447.4     Document Type: Article

References (27)

1. P. Bonhôte, A. P. Dias, N. Papageorgiou, K. Kalyanasundaram and M. Grätzel, Inorg. Chem. 35, 1168 (1996).
2. A. Noda, K. Hayamizu and M. Watanabe, J. Phys. Chem. B. 105, 4603 (2001).
3. P. J. Dyson, D. J. Ellis, D. G. Parker and T. Welton, Chem. Commun. 25 (1999).
4. B. M. Quinn, Z. F. Ding, R. Moulton and A. J. Bard, Langmuir 18, 1734 (2002).
5. B. Cabovska, G. P. Kreishman, D. F. Wassell and A. M. Stalcup, J. Chromatogra. A 1007, 179 (2003).
6. C. Cadena, J. L. Anthony, J. K. Shah, T. I. Morrow, J. F. Brennecke and E. J. Maginn, J. Am. Chem. Soc. 126, 5300 (2004).
7. H. M. Luo, S. Dai and P. V. Bonnesen, Anal. Chem. 78, 2773 (2004).
8. P. Wasserscheid and T. Welton, Ionic Liquids in Synthesis, GmbH & Co, KgaA, Weinheim: Wiley-VCH Verlag, 174 (2002).
9. T. Welton, Chem. Rev. 99, 2071 (1999).
10. P. Wasserscheid and W. Keim, Angew. Chem. Int. Ed. 39, 3772 (2000).
11. J. Dupont, R. F. Souza and P. A. Z. Suarez, Chem. Rev. 102, 3667 (2002).
12. A. Heintz, J. K. Lehmann and C. Wertz, J. Chem. Eng. Data. 48, 472 (2003).
13. J. M. Crosthwaite, S. N. V. K. Aki, E. J. Maginn and J. F. Brennecke, J. Phys. Chem. B. 108, 5113 (2004).
14. C. G. Hanke, N. A. Atamas and R. M. Lynden-Bell, Green Chem. 4, 107 (2002).
15. L. Crowhurst, P. R. Mawdsley, J. M. Perez-Arlandis, P. A. Salter and T. Welton, Phys. Chem. Chem. Phys. 5, 2790 (2003).
16. B. M. Su, S. G. Zhang and Z. C. Zhang, J. Phys. Chem. B 108, 19510 (2004).
17. C. P. Zhai, J. J. Wang, Y. Zhao, X. P. Xuan, J. M. Tang and H. Q. Wang, Z. Phys. Chem. 220, 775 (2006).
18. C. P. Zhai, J. J. Wang, Y. Zhao, X. P. Xuan and H. Q. Wang, Acta Phys. Chim. Sin. 22, 456 (2006).
19. M. W. Hanna and A. L. Ashbaugh, J. Phys. Chem. 68, 811 (1964).
20. A. A. Fannin, L. A. King, J. A. Levisky and J. S. Wilkes, J. Phys. Chem. 88, 2609 (1984).
21. J. D. Holbrey and K. R. Seddon, J. Chem. Soc. Dalton Tran. 2133 (1999).
22. J. G. Huddleston, A. E. Visser, W. M. Reichert, H. D. Willauer, G. A. Broker and R. D. Rogers, Green Chem. 3, 156 (2001).
23. L. Turi, Chem. Phys. Lett. 275, 35 (1997).
24. W. R. Fawcett, P. Brooksby, D. Verbovy, I. Bakó and G. Pálinkás, J. Mol. Liq. 118, 171 (2005).
25. A. G. Avent, P. A. Chaloner, M. P. Day, K. R Seddon and T. Welton, J. Chem. Soc., Dalton Trans. 3405 (1994).
26. A. Elaiwi, P. B. H. Chcock, K. R. Seddon, N. Srinivasan, Y. M. Tan, T. Welton and J. Azora, J. Chem. Soc., Dalton Trans. 3467 (1995).
27. R. Taylor and O. Kennard, J. Am. Chem. Soc. 104, 5063 (1982).