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Volumn 112, Issue 11, 2008, Pages 4396-4405

Quinoxaline-fused porphyrins for dye-sensitized solar cells

Author keywords

[No Author keywords available]

Indexed keywords

ABSORPTION; DIRECT ENERGY CONVERSION; ELECTROCHEMICAL PROPERTIES; ELECTROMAGNETIC WAVE ABSORPTION; ENERGY ABSORPTION; LIGHT ABSORPTION; MOLECULAR MODELING; MOLECULAR ORBITALS; ROCKETS; SOLAR CELLS; SOLAR ENERGY;

EID: 42449151360     PISSN: 19327447     EISSN: 19327455     Source Type: Journal    
DOI: 10.1021/jp710400p     Document Type: Article
Times cited : (182)

References (115)
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    • Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A., Jr.; Vreven, T.; Kudin, K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez, C.; Pople, J. A. Gaussian 03, revision C.02; Gaussian, Inc.: Wallingford, CT, 2004.
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    • Giraudeau, A.1    Callot, H.J.2    Jorgan, J.3    Ezhar, I.4    Gross, M.5
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    • Catalano, M. M.; Crossley, M. J.; Harding, M. M.; King, L. G. Chem. Commun. 1984, 1535. While the Ni (II) counterpart of copper porphyrin 2, 5,10,15,20-tetrakis(2,4,6-trimethylphenyl)porphyrinatonickel (II), displayed the similar reactivity for the nitration, demetallation of the nickel porphyrin showed too low yield in these experiments.
    • Catalano, M. M.; Crossley, M. J.; Harding, M. M.; King, L. G. Chem. Commun. 1984, 1535. While the Ni (II) counterpart of copper porphyrin 2, 5,10,15,20-tetrakis(2,4,6-trimethylphenyl)porphyrinatonickel (II), displayed the similar reactivity for the nitration, demetallation of the nickel porphyrin showed too low yield in these experiments.
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    • Both 2,3-Dioxo-5,10,15,20-tetrakis(2,4,6-trimethylphenyl)chlori- natocopper (II) and 2,3-dioxo-5,10,15,20-tetrakis(2,4,6-trimethylphenyl)- chlorinatonickel (II) showed higher stability than the free base one, and could be used for the Schiff base forming reaction with the diamine compounds, but demetallations of the resulting carboxyquinoxalino[2,3-β]-porphyrins were practically impossible, at least in our experiments.
    • Both 2,3-Dioxo-5,10,15,20-tetrakis(2,4,6-trimethylphenyl)chlori- natocopper (II) and 2,3-dioxo-5,10,15,20-tetrakis(2,4,6-trimethylphenyl)- chlorinatonickel (II) showed higher stability than the free base one, and could be used for the Schiff base forming reaction with the diamine compounds, but demetallations of the resulting carboxyquinoxalino[2,3-β]-porphyrins were practically impossible, at least in our experiments.
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    • Initially, it was attempted in dichloromethane or ethanol solutions; however, neither of the trials were successful
    • Initially, it was attempted in dichloromethane or ethanol solutions; however, neither of the trials were successful.
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    • We cannot rule out the probability of the carbonyl oxygen coordination to the TiO2 surface. Readers who are interested in the possible adsorption modes of carboxylic acid group onto the TiO2 surface should be referred to the reference. Vittadini, A, Selloni, A, Rotzinger, F. P, Grätzel, M. J. Phys. Chem. B 2000, 104, 1300
    • 2 surface should be referred to the reference. Vittadini, A.; Selloni, A.; Rotzinger, F. P.; Grätzel, M. J. Phys. Chem. B 2000, 104, 1300.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.