Convenient synthesis of functionalized 4,4′-disubstituted-2,2′- bipyridine with extended π-system for dye-sensitized solar cell applications

Tetrahedron Letters

Volumn 51, Issue 47, 2010, Pages 6161-6165

  Klein, Cédric ^a   Baranoff, Etienne ^a   Nazeeruddin, Md Khaja ^a   Grätzel, Michael ^a  

^a EPFL   (Switzerland)

Author keywords

Bipyridine; Dye sensitized solar cells; Extended systems; Horner Emmons Wadsworth reaction

Indexed keywords

2,2' BIPYRIDINE; RUTHENIUM;

ARTICLE; BIOSYNTHESIS; CELL ACTIVITY; CHEMICAL STRUCTURE; CHEMOSENSITIZATION; ELECTRON; HETERONUCLEAR NUCLEAR MAGNETIC RESONANCE; HORNER WADSWORTH EMMONS REACTION; ISOMER; NONHUMAN;

EID: 77958501442     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.09.077     Document Type: Article

References (20)

1. C.-Y. Chen, S.-J. Wu, C.-G. Wu, J.-G. Chen, and K.-C. Ho Angew. Chem., Int. Ed. 45 2006 5822
2. C.-Y. Chen, S.-J. Wu, C.-G. Wu, J.-G. Chen, and K.-C. Ho Adv. Mater. 19 2007 3888
3. F. Gao, Y. Wang, J. Zhang, D. Shi, M. Wang, R. Humphry-Baker, P. Wang, S.-M. Zakeeruddin, and M. Grätzel Chem. Commun. 2008 2635
4. H. Choi, C. Baik, S. Kim, M.-S. Kang, X. Xu, H.S. Kang, S.-O. Kang, J.J. Ko, M.K. Nazeeruddin, and M. Grätzel New J. Chem. 32 2008 2233
5. T.L. Bouder, P. Massiot, and H. Le Bozec Tetrahedron Lett. 39 1998 6869
6. T.L. Bouder, L. Viau, J.-P. Guegan, O. Maury, and H. Le Bozec Eur. J. Org. Chem. 2002 3024
7. O. Maury, J.-P. Guégan, T. Renouard, A. Hilton, P. Dupau, N. Sandon, L. Toupet, and H. Le Bozec New J. Chem. 25 2001 1553
8. L. Viau, O. Maury, and H. Le Bozec Tetrahedron Lett. 45 2004 125
9. V. Aubert, V. Guerchais, E. Ishow, K. Hoang-Thi, I. Ledoux, K. Nakatani, and H. Le Bozec Angew. Chem., Int. Ed. 47 2008 577
10. T. Chatterjee, M. Sarma, and S.K. Das Tetrahedron Lett. 51 2010 1985
11. I. Gillaizeau-Gauthier, F. Odobel, M. Alebbi, R. Argazzi, E. Costa, C.A. Bignozzi, P. Qu, and G.J. Meyer Inorg. Chem. 40 2001 6073
12. C.L. Fraser, N.R. Anastasi, and J.S. Lamba J. Org. Chem. 62 1997 9314
13. S.A. Savage, A.P. Smith, and C.L. Fraser J. Org. Chem. 63 1998 10048
14. 11
15. C.-Y. Chen, S.-J. Wu, C.-G. Wu, J.-G. Chen, and K.-C. Ho Adv. Funct. Mater. 17 2007 29
16. H. Qin, S. Wenger, M. Xu, F. Gao, X. Jing, P. Wang, S.-M. Zakeeruddin, and M. Grätzel J. Am. Chem. Soc. 130 2008 9202
17. Y. Cao, Y. Bai, Q. Yu, Y. Cheng, S. Liu, D. Shi, F. Gao, and P. Wang J. Phys. Chem. C 113 2009 6290
18. T. Renouard, and M. Grätzel Tetrahedron 57 2001 8145
19. 3, 298 K, 50 MHz, δ ppm) 14.3, 61.3, 118.0, 121.2, 125.6, 127.8, 128.2, 133.3, 133.8, 144.6, 147.7, 149.7, 156.4, 161.9.
20. 3, 298 K, 50 MHz, δ ppm) 14.4, 22.6, 25.9, 29.2, 31.6, 68.3, 104.6, 118.4, 120.9, 122.7, 123.3, 124.8, 125.2, 125.7, 126.1, 126.9, 127.0, 130.4, 132.3, 146.3, 149.5, 155.7, 156.6.