N-(2-Alkoxyphenyl)-substituted double rhodanine indoline dyes for zinc oxide dye-sensitized solar cell

Tetrahedron

Volumn 68, Issue 22, 2012, Pages 4286-4291

  Matsui, Masaki ^a   Shiota, Takahiro ^a   Kubota, Yasuhiro ^a   Funabiki, Kazumasa ^a   Jin, Jiye ^b   Yoshida, Tsukasa ^a   Higashijima, Shinji ^c   Miura, Hidetoshi ^c  

^a GIFU UNIVERSITY   (Japan)

^b SHINSHU UNIVERSITY   (Japan)

^c Chemicrea Co Ltd   (Japan)

Author keywords

Aggregation; Dye sensitized solar cell; Indoline dyes; Sensitizers; Zinc oxide

Indexed keywords

1 BROMO 2 BUTOXYBENZENE; 1 BROMO 2 DODECYLOXYBENZENE; 1 BROMO 2 OCTADECYLOXYBENZENE; 1 BROMO 2 OCTYLOXYBENZENE; 4 (2 BUTOXYPHENYL) 1,2,3,3A,4,8B HEXAHYDROCYCLOPENTA[B]INDOLE; 4 (2 BUTOXYPHENYL) 1,2,3,3A,4,8B HEXAHYDROCYCLOPENTA[B]INDOLE 7 CARBALDEHYDE; 4 (2 DODECYLOXYPHENYL) 1,2,3,3A,4,8B HEXAHYDROCYCLOPENTA[B]INDOLE; 4 (2 DODECYLOXYPHENYL) 1,2,3,3A,4,8B HEXAHYDROCYCLOPENTA[B]INDOLE 7 CARBALDEHYDE; 4 (2 METHOXYPHENYL) 1,2,3,3A,4,8B HEXAHYDROCYCLOPENTA[B]INDOLE; 4 (2 METHOXYPHENYL) 1,2,3,3A,4,8B HEXAHYDROCYCLOPENTA[B]INDOLE 7 CARBALDEHYDE; 4 (2 OCTADECAOXYPHENYL) 1,2,3,3A,4,8B HEXAHYDROCYCLOPENTA[B]INDOLE; 4 (2 OCTADECYLOXYPHENYL) 1,2,3,3A,4,8B HEXAHYDROCYCLOPENTA[B]INDOLE 7 CARBALDEHYDE; 4 (2 OCTYLOXYPHENYL) 1,2,3,3A,4,8B HEXAHYDROCYCLOPENTA[B]INDOLE; 4 (2 OCTYLOXYPHENYL) 1,2,3,3A,4,8B HEXAHYDROCYCLOPENTA[B]INDOLE 7 CARBALDEHYDE; BENZENE DERIVATIVE; ELECTROLYTE; RHODANINE; UNCLASSIFIED DRUG; ZINC OXIDE;

ABSORPTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL BOND; CHROMATOPHORE; FLUORESCENCE SPECTROSCOPY; LIGHT ABSORPTION; OXIDATION REDUCTION POTENTIAL; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SOLAR ENERGY;

EID: 84860489351     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.03.060     Document Type: Article

References (11)

1. D. Kuang, S. Uchida, R. Humphry-Baker, S.M. Zakeeruddin, and M. Grätzel Angew. Chem., Int. Ed. 47 2008 1923 1927
2. L. Schmidt-Mende, U. Bach, R. Humphry-Baker, T. Horiuchi, H. Miura, S. Ito, S. Uchida, and M. Grätzel Adv. Mater. 17 2005 813 815
3. T. Horiuchi, H. Miura, and S. Uchida J. Photochem. Photobiol., A: Chem. 164 2004 29 32
4. T. Horiuchi, H. Miura, K. Sumioka, and S. Uchida J. Am. Chem. Soc. 126 2004 12218 12219
5. T. Horiuchi, H. Miura, and S. Uchida Chem. Commun. 2003 3036 3037
6. S. Ito, S.M. Zakeeruddin, R. Humphry-Baker, P. Liska, R. Charvet, P. Comte, M.K. Nazeeruddin, P. Péchy, M. Takata, H. Miura, S. Uchida, and M. Grätzel Adv. Mater. 18 2006 1202 1205
7. M. Matsui, T. Fujita, Y. Kubota, K. Funabiki, J. Jin, T. Yoshida, and H. Miura Dyes Pigm. 86 2010 143 148
8. M. Matsui, T. Fujita, Y. Kubota, K. Funabiki, H. Miura, and M. Shiro Bull. Chem. Soc. Jpn. 83 2010 709 711
9. S. Ito, H. Miura, S. Uchida, M. Takata, K. Sumioka, P. Liska, P. Comte, P. Péchy, and M. Grätzel Chem. Commun. 2008 5194 5196
10. M. Matsui, M. Kotani, Y. Kubota, K. Funabiki, J. Jin, T. Yoshida, S. Higashijima, and H. Miura Dyes Pigments 91 2011 145 152
11. S. Higashijima, H. Miura, T. Fujita, Y. Kubota, K. Funabiki, T. Yoshida, and M. Matsui Tetrahedron 67 2011 6289 6293