Novel two-dimensional molecular space material with regular double bonds

Chemistry of Materials

Volumn 19, Issue 3, 2007, Pages 335-337

  Yu, F T ^a   Yao, K ^a   Shi, L Y ^a   Wang, H Z ^b   Fu, Y ^a   You, X Q ^a  

^a SHANGHAI UNIVERSITY   (China)

^b DONGHUA UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; INFRARED SPECTROSCOPY; IONIZATION OF LIQUIDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ORGANIC ACIDS; REACTION KINETICS; X RAY DIFFRACTION;

ACRYLIC ACID; AMIDES; AMINO GROUPS; DOUBLE BONDS;

UNSATURATED COMPOUNDS;

EID: 33847242643     PISSN: 08974756     EISSN: None     Source Type: Journal    
DOI: 10.1021/cm0620842     Document Type: Article

References (34)

1. Vakarin, E. V.; Badiali, J. P. J. Phys. Chem. B 2002, 106, 7721.
2. Vaysse, C.; Guerlou-Demourgues, L.; Delmas, C.; Duguet, E. Macromolecules 2004, 37, 45.
3. Leroux, F.; Besse, J. P. Chem. Mater. 2001, 13, 3507.
4. Vieille, L.; Taviot-Guého, C.; Besse, J. P.; Leroux, F. Chem. Mater. 2003, 15, 4369.
5. Iyi, N.; Kurashima, K.; Fujita, T. Chem. Mater. 2002, 14, 583.
6. Roland-Swanson, C.; Besse, J. P.; Leroux, F. Chem. Mater. 2004, 16, 5512.
7. Iyi, N.; Matsumoto, T.; Kaneko, Y.; Kitamura, K. Chem. Mater. 2004, 16, 2926.
8. Müller, R.; Hrobarikova, J.; Calberg, C.; Jérôme, R.; Grandjean, J. Langmuir 2004, 20, 2982.
9. Kooli, F.; Khimyak, Y. Z.; Alshahateet, S. F.; Chen, F. X. Langmuir 2005, 21, 8717.
10. Beaudot, P.; De Roy, M. E.; Besse, J. P. Chem. Mater. 2004, 16, 935.
11. Darder, M.; López-Blanco, M.; Aranda, P.; Leroux, F.; Ruiz-Hitzky, E. Chem. Mater. 2005, 17, 1969.
12. Frey, G. L.; Reynolds, K. J.; Friend, R. H.; Cohen, H.; Feldman, Y. J. Am. Chem. Soc. 2003, 125, 5998.
13. Hu, G.; O'Hare, D. J. Am. Chem. Soc. 2005, 127, 17808.
14. Liu, Z. P.; Ma, R. Z.; Osada, M.; Iyi, N.; Ebina, Y.; Takada, K.; Sasaki, T. J. Am. Chem. Soc. 2006, 128, 4872.
15. Xu, Z. P.; Stevenson, G. S.; Lu, C. Q.; Lu, G. Q.; Bartlett, P. F.; Gray, P. P. J. Am. Chem. Soc. 2006, 128, 36.
16. Gardner, E.; Huntoon, K. M.; Pinnavaia, T. J. Adv. Mater. 2001, 13, 1263.
17. Triantafillidis, C. S.; LeBaron, P. C.; Pinnavaia, T. J. Chem. Mater. 2002, 14, 4088.
18. Yao, K.; Taniguchi, M.; Nakata, M.; Takahashi, M.; Yamagishi, A. Langmuir 1998, 14, 2410.
19. Yao, K.; Taniguchi, M.; Nakata, M.; Takahashi, M.; Yamagishi, A. Langmuir 1998, 14, 2890.
20. Yao, K.; Nishimura, S.; Imai, Y.; Wang, H. Z.; Ma, T. L.; Abe, E.; Tateyama, H.; Yamagishi, A. Langmuir 2003, 19, 321.
21. Zhong, Z. H.; Ding, W. P.; Hou, W. H.; Chen, Y. Chem. Mater. 2001, 13, 538.
22. Allada, R. K.; Pless, J. D.; Nenoff, T. M. Navrotsky, A. Chem. Mater. 2005, 17, 2455.
23. Moujahid, E. M.; Dubois, M.; Besse, J.; Leroux, F. Chem. Mater. 2002, 14, 3799.
24. Fujita, S.; Sato, H.; Kakegawa, N.; Yamagishi, A. J. Phys. Chem. B 2006, 110, 2533.
25. So, H.; Jung, H.; Choy, J.; Belford, R. L. J. Phys. Chem. B 2005, 109, 3324.
26. Sasai, R.; Iyi, N.; Fujita, T.; Arbeloa, F. L.; Martínez, V. M.; Takagi, K.; Itoh, H. Langmuir 2004, 20, 4715.
27. Matsumoto, Y.; Unal, U.; Kimura, Y.; Ohashi, S.; Izawa, K. J. Phys. Chem. B 2005, 109, 12748.
28. Tong, Z. W.; Shichi, T.; Takagi, K. J. Phys. Chem. B 2002, 106, 13306.
29. Hagerman, M. E.; Salamone, S. J.; Herbst, R. W.; Payeur, A. L. Chem. Mater. 2003, 15, 443.
30. Choudary, B. M.; Madhi, S.; Chowdari, N. S.; Kantam, M. L.; Sreedhar, B. J. Am. Chem. Soc. 2002, 124, 14127.
31. Greenwell, H. C.; Stackhouse, S.; Coveney, P. V.; Jones, W. J. Phys. Chem. B 2003, 107, 3476.
32. Yao, K.; Imai, Y.; Shi, L. Y.; Abe, E.; Adachi, Y.; Nishikubo, K.; Tateyama, H. Chem. Lett. 2004, 33, 1112.
33. Yao, K.; Imai, Y.; Shi, L. Y.; Dong, A. M.; Abe, E.; Adachi, Y.; Nishikubo, K.; Tateyama, H. J. Colloid Interface Sci. 2005, 285, 259.
34. The layered aminophenylsilica was synthesized by the slow titration of HCl into a mixture of p-aminophenyltrimethoxysilane (APhTMS, 2.78 mmol) and sodium dodecyl sulfate (2.92 mmol) in aqueous solution with stirring at room temperature (pH 2-3). The APhTMS-dodecyl sulfate complex (APhTMS-DS) was obtained as a light pink precipitate. The layered APhTMS-Cl was obtained from the APhTMS-DS by washing with a mixture of hydrochloric acid and ethanol. All the reagents were purchased from the Aldrich Chemical Co.