References
- O'Regan, B.; Gratzel, M. Nature 1991, 353, 737. https://doi.org/10.1038/353737a0
- Gratzel, M. Nature 2001, 414, 338. https://doi.org/10.1038/35104607
- Chiba, Y.; Islam, A.; Watanabe, Y.; Komiya, R.; Koide, N.; Han, L. Jpn. J. Appl. Phys. 2006, 45, L638. https://doi.org/10.1143/JJAP.45.L638
- Nazeeruddin, M. K.; Angelis, F. D.; Fantacci, S.; Selloni, A.; Viscardi, G.; Liska, P.; Ito, S.; Takeru, B.; Grätzel, M. J. Am. Chem. Soc. 2005, 127, 16835. https://doi.org/10.1021/ja052467l
- Wang, Z.-S.; Yamaguchi, T; Sugihara, H.; Arakawa, H. Langmuir 2005, 21, 4272. https://doi.org/10.1021/la050134w
- Wang, P.; Zakeeruddin, S. M.; Moser, J. E.; Nazeeruddin, M. K.; Sekiguchi, T.; Gratzel, M. Nat. Mater. 2003, 2, 402. https://doi.org/10.1038/nmat904
- Mishra, A.; Fischer, M. K.; Bauerle, P. Angew. Chem., Int. Ed. 2009, 48, 2474. https://doi.org/10.1002/anie.200804709
- Labana, S. S.; Lababa, L. L. Chem. Rew. 1967, 67, 1. https://doi.org/10.1021/cr60245a001
- Herbst, W.; Hunger, K. Industrial Pigments; VCH: Weinheim, 1993; 447.
- Lincke, G. Dyes and Pigments 2002, 52, 169. https://doi.org/10.1016/S0143-7208(01)00085-7
- Manabe, K.; Kusabayashi, S.; Yokoyama, M. Chem. Lett. 1987, 609.
- Marco, P. D.; Fattori, V.; Giro, G.; Kalinowski, J. Mol. Cryst. Liq. Cryst. 1992, 217, 223. https://doi.org/10.1080/10587259208046905
- Tsutsui, T.; Aminaka, E.; Fujita, Y.; Hamada, Y.; Saito, S. Synth. Met. 1993, 57, 4157. https://doi.org/10.1016/0379-6779(93)90574-G
- Shi, J.; Tang, C. W. Appl. Phys. Lett. 1997, 70, 1665. https://doi.org/10.1063/1.118664
- Jabbour, G. E.; Kawabe, Y.; Shaheen, S. E.; Wang, J. F.; Morrell, M. M.; Kippelen, B.; Peyghambarian, N. Appl. Phys. Lett. 1997, 71, 1762. https://doi.org/10.1063/1.119392
- Feyter, S. D.; Gesquiere, A.; Schryver, F. C. D.; Keller, U.; Mullen, K. Chem. Mater. 2002, 14, 989. https://doi.org/10.1021/cm011053y
- Mu, Z.; Wang, Z.; Zhang, X.; Ye, K.; Wang, Y. J. Phys. Chem. B 2004, 108, 19955. https://doi.org/10.1021/jp046942y
- Yang, X.; Mu, Z.; Wang, Z.; Zhang, X.; Wang, J.; Wang, Y. Langmuir 2005, 20, 7225.
- Ortiz, A.; Flora, W. H.; D'Ambruoso, G. D.; Armstrong, N. R.; McGrath, D. V. Chem. Commun. 2005, 444.
- Liu, J.; Gao, B.; Cheng, Y.; Xie, Z.; Geng, Y.; Wang, L.; Jing, X.; Wang, F. Macromolecules 2008, 41, 1162. https://doi.org/10.1021/ma071235z
- Sakong, C.; Kim, Y. D.; Choi, J.-H.; Yoon, C.; Kim, J. P. Dyes and Pigments 2011, 88, 166. https://doi.org/10.1016/j.dyepig.2010.06.003
- Liu, P. H.; Tian, H.; Chang, C. P. J. Photochem. Photobiol. A 2000, 137, 99. https://doi.org/10.1016/S1010-6030(00)00361-0
- Smith, J. A.; West, R. M.; Allen, M. J. Fluoresc. 2004, 14, 151. https://doi.org/10.1023/B:JOFL.0000016287.56322.eb
- Marson, C. M. Tetrahedron 1992, 48, 3659. https://doi.org/10.1016/S0040-4020(01)92263-X
- Smith, J. A. inventor; GE Healthcare UK Limited, assignee. United States Patent US 7335771. 2008 Feb 26.
- Pomel, V.; Klicic, J.; Covini, D.; Church, D. D.; Shaw, J. P.; Roulin, K.; Burgat-Charvilon, F.; Valognes, D.; Camps, M.; Chabert, C.; Gillieron, C.; Francon, B.; Perrin, D.; Leroy, D.; Gretener, D.; Nichols, A.; Vitte, P. A.; Carboni, S.; Rommel, C.; Schwarz, M. K.; Rückle, T. J. Med. Chem. 2006, 49, 3857. https://doi.org/10.1021/jm0601598
- Roquet, S.; Cravino, A.; Leriche, P.; Aleveque, O.; Frere, P.; Roncali, J. J. Am. Chem. Soc. 2006, 128, 3459. https://doi.org/10.1021/ja058178e
- Thomas, K. R. J.; Hsu, Y. C.; Lin, J. T.; Lee, K. M.; Ho, K. C.; Lai, C. H.; Cheng, Y. M.; Chou, P. T. Chem. Mater. 2008, 20, 1830. https://doi.org/10.1021/cm702631r
- Morley, J. O.; Push, D. J. Chem. Soc. Faraday Trans. 1991, 87, 3021. https://doi.org/10.1039/ft9918703021
- Wu, I. Y.; Lin, J. T.; Li, C. S.; Tsai, C.; Wen, Y. S.; Hsu, C. C.; Yeh, F. F.; Liou, S. Organometallics 1998, 17, 2188. https://doi.org/10.1021/om970947i
- March, J. Advanced Organic Chemistry, 4th ed.; Wiley: New York, U.S.A., 1992; p 45.
- Ramakishna, G.; Ghosh, H. N. J. Phys. Chem. A 2002, 106, 2545. https://doi.org/10.1021/jp013803x
- Wu, W.; Yang, J.; Hua, J.; Tang, J.; Zhang, L.; Long, Y.; Tian, H. J. Mater. Chem. 2010, 20, 1772. https://doi.org/10.1039/b918282a
- Hwang, S.; Lee, J. H.; Park, C.; Lee, H.; Kim, C.; Park, C.; Lee, M. H.; Lee, W.; Park, J.; Kim, K.; Park, N. G.; Kim, C. Chem. Commun. 2007, 4887.
- Hara, K.; Tachibana, Y.; Ohga, Y.; Shinpo, A.; Sugab, S.; Sayamaa, K.; Sugihara, H.; Arakawa, H. Sol. Energy Mater. Sol. Cells 2003, 77, 89. https://doi.org/10.1016/S0927-0248(02)00460-9
- Hara, K.; Sato, T.; Katoh, R.; Furube, A.; Ohga, Y.; Shinpo, A.; Suga, S.; Sayama, K.; Sugihara, H.; Arakawa, H. J. Phys. Chem. B 2003, 107, 597. https://doi.org/10.1021/jp026963x
- Kuang, D.; Walter, P.; Nuesch, F.; Kim, S.; Ko, J.; Comte, P.; Zakeeruddin, S. M.; Nazeeruddin, M. K.; Gratzel, M. Langmuir 2007, 23, 10906. https://doi.org/10.1021/la702411n
- Hagberg, D. P.; Marinado, T.; Karlsson, K. M.; Nonomura, K.; Qin, P.; Boschloo, G.; Brinck, T.; Hagfeldt, A.; Sun, L. J. Org. Chem. 2007, 72, 9550. https://doi.org/10.1021/jo701592x
- Tae, E. L.; Lee, S. H.; Lee, J. K.; Yoo, S. S.; Kang, E. J.; Yoon, K. B. J. Phys. Chem. B 2005, 109, 22513. https://doi.org/10.1021/jp0537411
- Li, C.; Yang, X.; Chen, R.; Pan, J.; Tian, H.; Zhu, H.; Wang, X.; Hagfeldt, A.; Sun, L. Sol. Energy Mater. Sol. Cells 2007, 91, 1863. https://doi.org/10.1016/j.solmat.2007.07.002
- Ferrere, S.; Zaban, A.; Gregg, B. A. J. Phys. Chem. B 1997, 101, 4490. https://doi.org/10.1021/jp970683d
- Ferrere, S.; Gregg, B. A. J. Phys. Chem. B 2001, 105, 7602. https://doi.org/10.1021/jp011612o
- Ferrere, S.; Gregg, B. A. New J. Chem. 2002, 26, 1155. https://doi.org/10.1039/b203260k
- Shibano, Y.; Umecyama, T.; Matano, Y.; Imahori, H. Org. Lett. 2007, 9, 1971. https://doi.org/10.1021/ol070556s
- Fortage, J.; Séverac, M.; Houarner- Rassin, C.; Pellegrin, Y.; Blart, E.; Odobel, F. J. Photochem. Photobiol. A 2008, 197, 156. https://doi.org/10.1016/j.jphotochem.2007.12.034
- Jin, Y.; Hua, J.; Wu, W.; Ma, X.; Meng, F. Synth. Met. 2008, 158, 64. https://doi.org/10.1016/j.synthmet.2007.12.005
Cited by
- Efficient and stable organic DSSC sensitizers bearing quinacridone and furan moieties as a planar π-spacer vol.22, pp.46, 2012, https://doi.org/10.1039/c2jm31929b
- Effects of Exciton Polarity in Charge-Transfer Polymer/PCBM Bulk Heterojunction Films vol.5, pp.11, 2014, https://doi.org/10.1021/jz5005957
- Sensitizers with rigidified-aromatics as the conjugated spacers for dye-sensitized solar cells vol.3, pp.38, 2015, https://doi.org/10.1039/C5TC02356D
- Quinacridone-based π-conjugated electronic materials vol.4, pp.42, 2016, https://doi.org/10.1039/C6TC03621J
- Structural effect of carbazole-based coadsorbents on the photovoltaic performance of organic dye-sensitized solar cells vol.1, pp.32, 2011, https://doi.org/10.1039/c3ta11508a
- A comprehensive spectral, photophysical and electrochemical study of synthetic water-soluble acridones. A new class of pH and polarity sensitive fluorescent probes vol.166, pp.None, 2011, https://doi.org/10.1016/j.dyepig.2019.03.028
- Enhanced photoelectric and photocatalysis performances of quinacridone derivatives by forming D-π-A-A structure vol.201, pp.None, 2011, https://doi.org/10.1016/j.solener.2020.03.053
- An electron rich indaceno [2,1-b:6,5-b′] dithiophene derivative as a high intramolecular charge transfer material in dye sensitized solar cells vol.45, pp.5, 2011, https://doi.org/10.1039/d0nj06067d