Nanofibers of 1,3-diphenyl-2-pyrazoline induced by cetyltrimethylammonium bromide micelles

Angewandte Chemie - International Edition

Volumn 42, Issue 25, 2003, Pages 2883-2886

  Fu, Hongbing ^a   Xiao, Debao ^a   Yao, Jiannian ^a   Yang, Guoqiang ^a  

^a INSTITUTE OF CHEMISTRY   (China)

Author keywords

Aggregation; Micelles; Nanostructures; Photochemistry; Pi interactions

Indexed keywords

AGGLOMERATION; CRYSTALS; MICELLES; NANOSTRUCTURED MATERIALS; PHASE COMPOSITION;

NANOFIBERS;

AROMATIC COMPOUNDS;

1,3 DIPHENYL 2 PYRAZOLINE; CETRIMIDE; PYRAZOLINE DERIVATIVE; SURFACTANT; UNCLASSIFIED DRUG;

AQUEOUS SOLUTION; ARTICLE; COLLOID; CRYSTALLIZATION; MICELLE; NANOPARTICLE; PARTICLE SIZE; REACTION ANALYSIS; STRUCTURE ANALYSIS;

EID: 0038711355     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200350961     Document Type: Article

References (29)

1. H. Kasai, H. S. Nalwa, H. Oikawa, S. Okada, H. Matsuda, N. Minami, A. Kakuta, K. Ono, A. Mukoh, H. Nakanishi, Jpn. J. Appl. Phys. Part 2 1992, 31, L1132.
2. A. Ibanez, S. Maximov, A. Guiu, C. Chaillout, P. L. Baldeck, Adv. Mater. 1998, 10, 1540.
3. D. Horn, J. Rieger, Angew. Chem. 2001, 113, 4460;
4. Angew. Chem. Int. Ed. 2001, 40, 4331.
5. a) H. B. Fu, J. N. Yao, J. Am. Chem. Soc. 2001, 123, 1434;
6. b) H. B. Fu, B. H. Loo, D. B. Xiao, R. M. Xie, X. H. Ji, J. N. Yao, B. W. Zhang, L. Q. Zhang, Angew. Chem. 2002, 114, 1004; Angew. Chem. Int. Ed. 2002, 41, 962;
7. Angew. Chem. Int. Ed. 2002 41 962
8. c) R. M. Xie, D. B. Xiao, H. B. Fu, X. H. Ji, W. S. Yang, J. N. Yao, New J. Chem. 2001, 25, 1362.
9. J. K. Lee, W. K. Koh, W. S. Chae, Y. R. Kim, Chem. Commun. 2002, 138.
10. B. K. An, S. K. Kwon, S. D. Jung, S. Y. Park, J. Am. Chem. Soc. 2002, 124, 14410.
11. X. C. Gong, T. Milic, C. Xu, J. D. Batteas, C. M. Drain, J. Am. Chem. Soc. 2002, 124, 14290.
12. X. G. Peng, L. Manna, W. D. Yang, J. Wichham, E. Scher, A. Kadavanich, A. P. Alivisatos, Nature 2000, 404, 59.
13. a) Y. Y. Yu, S. S. Chang, C. L. Lee, C. R. C. Wang, J. Phys. Chem. B 1997, 101, 6661;
14. b) S. Link, M. B. Mohamed, M. A. El-Sayed, J. Phys. Chem. B 1999, 103, 3073.
15. a) N. R. Jana, C. J. Murphy, Chem. Commun. 2001, 617;
16. b) C. J. Murphy, N. R. Jana, Adv. Mater. 2002, 14, 80.
17. Silinsh, E. A. Organic Molecular Crystals: Their Electronic States; Springer-Verlag: Berlin, 1980;
18. b) M. Pope, C. E. Swenberg, Electronic Processes in Organic Crystals; Oxford Univ. Press: Oxford, 1982.
19. B. Duffin, Acta Crystallogr. Sect. B 1968, 24, 1256.
20. F. Wilkinson, G. P. Kelly, C. Michael, J. Photochem. Photobiol. A 1990, 52, 309.
21. T. Imae, R. Kamiya, S. Ikeda, J. Colloid Interface Sci. 1985, 108, 215.
22. Tuning the value of N by varying the injected quantity of DP/ ethanol stock solution could obtain the same results. Moreover, stepwise injection also produced nanofibers.
23. Solubilization in Surfactant Aggregates (Eds.: S. D. Christian, F. F. Scamehorn), Marcel Dekker, New York, 1995.
24. T. Shikata, H. Hirata, T. Kotaka, Langmuir 1988, 4, 354.
25. P. Lianos, J. Lang, C. Strazielle, R. Zana, J. Phys. Chem. 1982, 86, 1019.
26. a) S. Özçelik, D. L. Akins, J. Phys. Chem. B 1999, 103, 8926-8929;
27. b) E. S. Emerson, M. A. Conlin, A. E. Rosenoff, K. S. Norland, H. Rodriguez, D. Chin, G. R. Bird, J. Phys. Chem. 1967, 71, 2396;
28. c) M. Kasha, H. R. Rawls, M. A. El-Bayoumi, Pure Appl. Chem. 1965, 11, 371.
29. The angle between the pyrazoline plane and the crystallographic a axis is calculated to be 53.52°. Thus, α = 53.52°-(β-90°) ≈ 50.7°.