Multi-maleimides bearing electron-donating chromophores: Reversible fluorescence and aggregation behavior

Journal of the American Chemical Society

Volumn 126, Issue 39, 2004, Pages 12200-12201

  Zhang, Xin ^a   Li, Zi Chen ^a   Li, Kai Bo ^a   Du, Fu Sheng ^a   Li, Fu Mian ^a  

^a PEKING UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

MALEIMIDE DERIVATIVE;

ARTICLE; CHROMATOPHORE; DIELS ALDER REACTION; ELECTRON; ELECTRON TRANSPORT; FLUORESCENCE; MICHAEL ADDITION; POLYMERIZATION; X RAY ANALYSIS;

AMIDES; MALEIMIDES; MICROSCOPY, ATOMIC FORCE; SPECTROMETRY, FLUORESCENCE; SUCCINATES;

EID: 4644317800     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0487527     Document Type: Article

References (16)

1. (a) Chen, X.; Dam, M. A.; Ono, K.; Mal, A. K.; Shen, H.; Nutt, S. R.; Sheran, K.; Wudl, F. Science 2002, 85, 1496.
2. (b) Tanaka, F.; Thayumanavan, R.; Barbas, C. F., III. J. Am. Chem. Soc. 2003, 125, 8523.
3. (c) Zhang, X.; Jin, Y. H.; Du, F. S.; Li, Z. C.; Li, F. M. Macromolecules 2003, 36, 3115.
4. Gousse, C.; Gandini, A.; Hodge, P. Macromolecules 1998, 31, 314.
5. (a) Gousse, C.; Gandini. A. Polym. Int. 1999, 48, 723.
6. (b) Kamahori, K.; Tada, S.; Ito, K.; Itsuno. S. Macromolecules 1999, 32, 541.
7. (a) Imai, Y.; Itoh, H.; Naka, K.; Chujo, Y. Macromolecules 2000, 33, 4343.
8. (b) Chen, X.; Wudl, F.; Mal, A. K.; Shen, H.; Nutt. S. R. Macromolecules 2003, 36, 1802.
9. Gheneim, R.; Perez-Berumem, C.; Gandini. A. Macromolecules 2002, 35, 7246.
10. (a) McElhanon, J. R.; Wheeler. D. R. Org. Lett. 2001, 3, 2681.
11. (b) Mcelhanon, J. R.; Russick, E. M.; Wheeler, D. R.; Loy, D. A.; Aubert, J. H. J. Appl. Polym. Sci. 2002, 85, 1496.
12. 3), respectively.
13. -/A) of the acceptor using the relationship of Chen (Chen, E. C. M.; Wentworth, W. E. J. Chem. Phys. 1975, 63, 3183).
14. 00(D*) is the excitation energy, and C is the electrostatic interaction term.
15. Mison, P.; Sillion. B. Adv. Polym. Sci. 1999, 140, 137.
16. TMPA-F and TMPA-FA obtained initially are a mixed exo,exo,exo-lendo,endo, endo-isomers, The pure exo, exo, exo-isomer can be obtained by heating the mixed isomers in chloroform with an addition of furan or furfural alcohol at 40 °C for 2 days, where the endo,endo, endo-isomer was converted completely into the (exo,exo,exo)-isomer. The exo,exo,exo-isomer is relative stable, which does not reconvert into endo,endo,endo-isomer before retro-Diels-Alder occurring.