Simple and efficient generation of white light emission from organophosphorus building blocks

Advanced Functional Materials

Volumn 19, Issue 22, 2009, Pages 3625-3631

  Romero Nieto, Carlos ^a   Durben, Stefan ^a   Kormos, Lla M ^a   Baumgartner, Thomas ^a  

^a UNIVERSITY OF CALGARY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO FUNCTIONAL GROUP; BUILDING BLOCKES; FLUORESCENCE RESONANCE ENERGY TRANSFER; INCANDESCENT LIGHT BULBS; ORGANIC ELECTRONIC MATERIALS; PHOSPHOLES; PHOTOPHYSICAL PROPERTIES; STRUCTURE PROPERTY; THREE COMPONENT; WHITE FLUORESCENCE; WHITE LIGHT EMISSION;

AMINES; ENERGY TRANSFER; FLUORINE CONTAINING POLYMERS; FUNCTIONAL GROUPS; INCANDESCENT LAMPS; LIGHT EMISSION; POLYSTYRENES;

FLUORESCENCE;

EID: 72849134298     PISSN: 1616301X     EISSN: 16163028     Source Type: Journal    
DOI: 10.1002/adfm.200901540     Document Type: Article

References (57)

1. a) Organic Light Emitting Devices (Eds: K. Müllen, U. Scherf), Wiley-VCH, Weinheim, Germany 2005.
2. b)Handbook of Conducting Polymers, 3rd ed. (Eds: T. A. Skotheim, J. R. Reynolds), CRC Press, Boca Raton, FL 2006.
3. a) C. D. Dimitrakopoulos, P. R. L. Malenfant, Adv. Mater. 2002, 14, 99.
4. b) J. E. Anthony, Angew. Chem. 2008, 120,460;
5. Angew. Chem. Int. Ed. 2008, 47, 452.
6. c) A. R. Murphy, J. M. J. Fréchet, Chem. Rev. 2007, 107, 1066.
7. d) S. Allard, M. Forster, B. Souharce, H. Thiem, U. Scherf, Angew. Chem. 2008, 120, 4138;
8. Angew. Chem. Int. Ed. 2008, 47, 4070.
9. a) B. C. Thompson, J. M. J. Fréchet, Angew. Chem. 2008, 120, 62;
10. Angew. Chem. Int. Ed. 2008, 47, 58.
11. b) S. Günes, H. Neugebauer, N. S. Sariciftci, Chem. Rev. 2007, 107, 1324.
12. a) M. J. D. Bosdet, W. E. Piers, Can. J. Chem. 2009, 87, 8.
13. b) M. Elbing, G. C. Bazan, Angew. Chem. 2008, 120, 846;
14. Angew. Chem. Int. Ed. 2008, 47, 834.
15. c) C. D. Entwistle, T. B. Marder, Chem. Mater. 2004, 16, 4574.
16. d) F. Jäkle, Coord. Chem. Rev. 2006, 250, 1107.
17. e) S. Yamaguchi, A. Wakamiya, Pure Appl. Chem. 2006, 78, 1413.
18. a) M.Shimizu, H. Tatsumi, K. Mochida, K. Oda, T. Hiyama, Chem.-Asian J. 2008, 3, 1238.
19. b) M. Hissler, P. W. Dyer, R. Réau, Coord. Chem. Rev. 2003, 244, 1.
20. c) A. C. Grimsdale, K. L. Chan, R. E. Martin, P. G. Jokisz, A. B. Holmes, Chem. Rev. 2009, 109, 897.
21. d) S. Yamaguchi, C. H. Xu, T. Okamoto, Pure Appl. Chem. 2006, 721.
22. e) S. Yamaguchi, K. Tamao, Chem. Lett. 2005, 34, 2.
23. a) Y. Matano, H. Imahori, Org. Biomol. Chem. 2009, 7,1258.
24. b) J. Crassous, R. Réau, Dalton Trans. 2008, 6865.
25. c) M. G. Hobbs, T. Baumgartner, Eur. J. Inorg. Chem. 2007,3611.
26. d) T. Baumgartner, R. Réau, Chem. Rev. 2006,106, 4681
27. (Correction: Chem. Rev. 2007, 107, 303 ).
28. e) F. Mathey, Angew. Chem. 2003, 115, 1616;
29. Angew. Chem. Int. Ed. 2003, 42, 1578.
30. f) D. P. Gates, Top. Curr. Chem. 2005, 250, 107.
31. a) C. Adachi, M. A. Baldo, M. E. Thompson, S. R. Forrest, J. Appl. Phys. 2001, 90, 5048.
32. b) H. Yersln, Top. Curr. Chem. 2004, 247, 1.
33. c) B. W. D'Andrade, S. R. Forrest, Adv. Mater. 2004, 16, 1585.
34. d) Y. Sun, N. C. Giebink, H. Kanno, B. Ma, M. E. Thompson, S. R. Forrest, Nature 2006, 440, 908.
35. e) B. W. D'Andrade, Nat. Photonics 2006, 1, 33.
36. f) C. J. Humphreys, MRS Bulletin 2008, 33, 456.
37. a) G. Tu, C. Mei, Q. Zhou, Y. Cheng, Y. Geng, L. Wang, D. Ma, X. Jing, F. Wang, Adv. Funct. Mater. 2006, 16, 101.
38. b) J. Liu, X. Guo, L. Bu, Z. Xie, Y. Cheng, Y. Geng, L. Wang, X. Jing, F. Wang, Adv. Funct. Mater. 2007, 17, 1917.
39. O Fadhel, M. Gras, N. Lemaitre, V. Deborde, M. Hissler, B. Geffroy, R. Réau, Adv. Mater. 2009, 21, 1261.
40. a) T. Baumgartner, T. Neumann, B. Wirges, Angew. Chem. 2004, 116, 6323;
41. Angew. Chem. Int. Ed. 2004, 43, 6197.
42. b) T. Baumgartner, W. Bergmans, T. Kárpáti, T. Neumann, M. Nieger, L. Nyulászi, Chem. - Eur. J. 2005, 11, 4687.
43. a) T. Neumann, Y. Dienes, T. Baumgartner, Org. Lett. 2006, 8, 495.
44. b) Y. Dienes, M. Eggenstein, T. Kárpáti, T. C. Sutherland, L. Nyulászi, T. Baumgartner, Chem. - Eur. J. 2008, 14, 9878.
45. c) Y. Ren, Y. Dienes, S. Hettel, M. Parvez, B. Hoge, T. Baumgartner, Organometallics 2009, 28, 734.
46. d) C. Romero-Nieto, S. Merino, J. Rodríguez-López, T. Baumgartner, Chem. -Eur.J. 2009, 15, 4135.
47. Y. Dienes, S. Durben, T. Kárpáti, T. Neumann, U. Englert, L. Nyulászi, T. Baumgartner, Chem. - Eur.J. 2007, 13, 7487.
48. a) Y. Xie, B. M. Wu, F. Xue, S. C. Ng, T. C. W. Mak, T. S. A. Hor, Organometallics 1998, 17, 3988.
49. b) H.-J. Son, W.-S. Han, J.-Y. Chun, S.-N. Kwon, J. Ko, S. O. Kang, Organometallics 2008, 27, 2464.
50. J. R. Lakowicz, Principles of Fluorescence Spectroscopy, 3rd ed. Springer, New York, NY 2006.
51. In a somewhat related study, Bazan and co-workers have recently reported the bandgap control in π-conjugated oligomers using Lewis acids: G. C. Welch, R. Coffin, J. Peet, G. C. Bazan, J. Am. Chem. Soc. 2009, 131, 10802.
52. F. D'Anna, P. Vitale, R. Noto, J. Org. Chem, 2009, 74, 6224.
53. This ratio was established to be ideal from the two-color mixing studies. A larger amount of the blue component is necessary to avoid complete FRET, which would ultimately eliminate the contribution of this species.
54. J. Whitaker, Electronic Displays: Technology, Design, and Applications, McGraw-Hill, New York, NY 1994, p. 92.
55. M. Cocchi, J. Kalinowski, D. Virgili, V. Fattori, S. Develay, J. A. G. Williams, Appl. Phys. Lett. 2007, 90, 163508.
56. H. Meng, W. Huang, J. Org. Chem. 2000, 65, 3894.
57. K. Diemert, B. Kottwitz, W. Kuchen, Phosphorus, Sulfur Silicon Relat. Elem. 1986, 26, 307.