Synthesis and characterization of perylene tetracarboxylic bisester monoimide derivatives

Dyes and Pigments

Volumn 76, Issue 3, 2008, Pages 810-816

  Zhang, Xiaobing ^a   Wu, Yangfang ^a   Li, Jianzhong ^a   Li, Fan ^a   Li, Min ^a  

^a BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

Author keywords

Energy level; Perylene derivatives; Photoluminescence

Indexed keywords

BAND STRUCTURE; DIMERS; ELECTROCHEMICAL PROPERTIES; ELECTRON ENERGY LEVELS; ELECTRON TRANSPORT PROPERTIES; ELECTRONIC STRUCTURE; FLUORESCENCE; INORGANIC COMPOUNDS; MOLECULAR STRUCTURE; PHOTOLUMINESCENCE; SYNTHESIS (CHEMICAL);

ALKYL CHAIN; PERYLENE DERIVATIVES;

DERIVATIVES;

CHEMICAL PROPERTY; COLOR; ELECTROCHEMISTRY; FLUORESCENCE; LUMINESCENCE; MOLECULAR STRUCTURE; OPTICAL PROPERTY; SOLUBILITY; SOLVENT; SYNTHESIS;

EID: 34548661060     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2007.02.006     Document Type: Article

References (30)

1. Liu D., De Feyter S., Cotlet M., Stefan A., Wiesler U.M., Herrmann A., et al. Macromolecules 36 (2003) 5918-5925
2. Würthner F. Chem Commun (2004) 1564-1579
3. Seguy I., Jolinat P., Destruel P., Farenc J., Mamy R., Bock H., et al. J Appl Phys 89 10 (2001) 5442-5448
4. Rainer D., Marina L., Pablo B., Matthias G., and Frank W. Macromolecules 38 (2005) 1315-1325
5. O'Neil M.P., Niemczyk M.P., Svec W.A., Gosztola D., Gaines III G.L., and Wasielewski M.R. Science 257 III (1992) 63
6. Schneider M., Hagen J., Haarer D., and Mu{combining double acute accent}llen K. Adv Mater 12 5 (2000) 351-354
7. Ranke P., Rleyl I., Simmerer J., Haarer D., Bacher A., and Schmidt H.W. Appl Phys Lett 71 (1997) 1332-1334
8. Osman MA, Zeller HR, Markert J. EP 47027; 1982.
9. Benning S.A., Hassneider T., Keuker-Baumann S., Bock H., Della Sala F., Frauenheim T., et al. Liq Cryst 28 7 (2001) 1105-1113
10. Moryson H., Kozlowski K., and Bauman D. Mol Cryst Liq Cryst 331 (1999) 2299-2307
11. Bauman D., Mykowska E., and Wolarz E. Mol Cryst Liq Cryst 321 (1998) 777-791
12. Haßheider T., Benning S.A., Lauhof M.W., Kitzerow H.S., Bock H., Watson M.D., et al. Mol Cryst Liq Cryst 413 (2004) 2597-2608
13. Tang C.W. Appl Phys Lett 48 (1986) 183-185
14. Oukachmih M., Destruel P., Seguy I., Ablart G., Jolinat P., Archambeau S., et al. Sol Energy Mater Sol Cells 85 4 (2005) 535-543
15. Yakimov A., and Forrest S.R. Appl Phys Lett 80 (2002) 1667-1669
16. Breeze A.J., Salomn A., Ginley D.S., Gregg B.A., Tillmann H., and Hörhold H.H. Appl Phys Lett 81 (2002) 3085-3087
17. Schmidt-Mende L., Fechtenkötter A., Mu{combining double acute accent}llen K., Moons E., Friend R.H., and MacKenzie J.D. Science 293 (2001) 1119
18. Qu J.Q., Zhang J.Y., Grimsdale A.C., and Müllen K. Macromolecules 37 (2004) 8297-8306
19. Schlichting P., Rohr U., and Mu{combining double acute accent}llen K. Eur J Org Chem 2 (1997) 395-407
20. Pan J.F., Zhu W.H., Li S.F., Xu J., and Tian H. Eur J Org Chem (2006) 986-1001
21. Pan J.F., Zhu W.H., Li S.F., Zeng W.J., Cao Y., and Tian H. Polymer 46 (2005) 7658-7669
22. Benning S., Kitzerow H.S., Bock H., and Achard M.F. Liq Cryst 27 7 (2000) 901-906
23. Seguy I., Jolinat P., Destrael P., Mamy R., Allouchi H., and Courelle C. ChemPhysChem 2 7 (2001) 448-452
24. Pasaogullari N., Icil H., and Demuth M. Dyes Pigments 69 (2006) 118-127
25. Tröster H. Dyes Pigments 4 (1983) 171-177
26. Nagao Y. Prog Org Coat 31 (1997) 43-49
27. Langhals H., and Jona W. Eur J Org Chem (1998) 847-851
28. Huang W., Yan D.Y., Lu Q.H., and Huang Y. Eur Polym J 39 6 (2003) 1099-1104
29. Yan P., Chowdhury A., Holman M.W., and Adams D.M. J Phys Chem B 109 (2005) 724-730
30. Mercadante R., Trsic M., Duff J., and Aroca R. J Mol Struct 394 (1997) 215-226