Low-band gap polymeric cyanine dyes absorbing in the NIR region

Macromolecular Rapid Communications

Volumn 29, Issue 8, 2008, Pages 651-658

  Geiger, Thomas ^a   Benmansour, Hadjar ^a   Fan, Bin ^a   Hany, Roland ^a   Nüesch, Frank ^a  

^a SWISS FEDERAL LABORATORIES FOR MATERIALS SCIENCE AND TECHNOLOGY   (Switzerland)

Author keywords

Electrochemistry; Photophysics; Polymeric cyanine dyes; Solar cells; Synthesis; UV vis spectroscopy

Indexed keywords

ABSORPTION; CHROMATOGRAPHIC ANALYSIS; COLLOIDS; CYCLIC VOLTAMMETRY; GELATION; INFRARED DEVICES; NUCLEAR MAGNETIC RESONANCE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POLYMERS; SOLAR ENERGY; ULTRAVIOLET SPECTROSCOPY;

BAND GAPS; BATHOCHROMIC SHIFTS; CYANINE DYES; DYE MOIETIES; ELEMENTARY ANALYSES; HIGHLY EFFICIENT; IR SPECTROSCOPIES; MOLAR ABSORPTION COEFFICIENTS; NEAR INFRARED; NIR REGIONS; NMR SPECTROSCOPIES; OPTICAL APPLICATIONS; PHOTOPHYSICS; PHOTOVOLTAIC DEVICES; POLYMERIC CYANINE DYES; SPECTRAL DOMAINS; SYNTHESIS; UV-VIS SPECTROSCOPY;

ABS RESINS;

EID: 45749120437     PISSN: 10221336     EISSN: 15213927     Source Type: Journal    
DOI: 10.1002/marc.200700860     Document Type: Article

References (32)

1. [1a] A. Moliton, R. C. Hiorns, Polym. Int 2004, 53, 1397;
2. [1b] H. Mustroph, M. Stollenwerk, V. Bressau, Angew. Chem. Int. Ed. 2006, 45, 2016;
3. [1c] C. J. Brabec, N. S. Saridftci, J. C. Hummelen, Adv. Funct. Mater. 2001, 11, 15;
4. [1d] N. S. Sariciftci, Mater. Today 2004, 7, 36;
5. [1e] S. Günes, H. Neugebauer, N. S. Sariciftci, Chem. Rev. 2007, 107, 1324.
6. [2a] E. Bundgaard, F. C. Krebs, Sol. Energy Mater. Sol. Cells 2007, 91, 954;
7. [2b] C. Winder, N. S. Sariciftci, J. Mater. Chem. 2004, 14, 1077.
8. [3a] J. Roncali, Chem Rev. 1997, 97, 173;
9. [3b] J. Roncali, Macromol. Rapid Commun. 2007, 28, 1761.
10. L. R. Dalton, A. W. Harper, R. Ghosn, W. H. Steier, M. Ziari, H. Fetterman, Y. Shi, R. V. Mustcich, A. K.-Y. Jen, K. J. Shea, Chem. Mater. 1995, 7, 1060.
11. E. E. Havinga, W. Tenhoeve, H. Wynberg, Polym. Bull. 1992, 29, 119.
12. th edition, Macmillan, New York, NY 1977, p. 714.
13. F. A. Castro, A. Faes, T. Geiger, C. F. O. Graeff, M. Nagel, F. Nuesch, R. Hany, Synth. Met. 2006, 156, 973.
14. M. Pailer, E. Renner-Kuhn, Monatsh. Chem. 1954, 85, 601.
15. G. Kossmehl, P. Bocionek, Macromol. Chem. Phys. 1981, 182, 3427.
16. [10a] Z. H. Peng, L. Qun, X. F. Zhou, S. Carroll, H. J. Geise, B. X. Peng, R. Dommisse, R. Carleer, I Mater. Chem. 1996, 6, 559;
17. [10b] Q. Li, J. Tan, B. X. Peng, Molecules 1997, 2, 91;
18. [10c] J. S. Kim, R. Kodagahally, L. Strekowski, G. Patonay, Talanta 2005, 67, 947.
19. [11a] Z. Zhu, Dyes Pigm. 1995, 27, 77;
20. [11b] A. Mishra, R. K. Behera, P. K. Behera, B. K. Mishra, G. B. Behera, Chem. Rev. 2000, 100, 1973;
21. [11c] W. König, Ber. Dtsch. Chem. Ges. 1922, 55, 3293;
22. [11d] F. M. Rowe, H. J. Twitchett, J. Chem. Soc. 1936, 33, 1704.
23. A. M. Kolesnikov, F. A. Mikhailenko, Zh. Org. Khim. 1982, 18, 441.
24. W. Y. Lee, J. Korean Chem. Soc. 1974, 18, 50.
25. I. G. Gut, J. Wirz, Angew. Chem. Int. Ed. Engl. 1994, 33, 1153.
26. [15a] G. Brocks, A. Toi, J. Phys. Chem. 1996, 100, 1838;
27. [15b] H. Meier, Angew. Chem. Int Ed. 2005, 44, 2482.
28. M. Kasha, H. R. Rawls, M. A. El-Bayoumi, Pure Appl. Chem. 1965, 11, 371.
29. [17a] M. van Faassen, P. L. de Boeij, J. Chem. Phys. 2004, 121, 10707;
30. [17b] B. Saha, M. Ehara, H. Nakatsuji, J. Phys. Chem. A 2007, 122, 5473.
31. R. O. Loutry, J. H. Sharp, Photogr. Sci. Eng. 1976, 20, 165.
32. T. Suzuki, Y. Maruyama, T. Akasaka, W. Ando, K. Kobayashi, S. Nagase, J. Am. Chem. Soc. 1994, 116, 1359.