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Nyokong, T.5
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16
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8144221391
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The hexadecacarboxy analogues were prepared similarly. See
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The hexadecacarboxy analogues were prepared similarly. See: Choi, C.-F.; Tsang, P.-T.; Huang, J.-D.; Chan, E. Y. M.; Ko, W.-H.; Fong, W.-P.; Ng, D. K. P. Chem. Commun. 2004, 2236.
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Ko, W.-H.5
Fong, W.-P.6
Ng, D.K.P.7
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17
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0027468478
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Compounds 2-4 were prepared previously directly from the corresponding carboxy-substituted phthalonitriles, but very few characterization data were given. See: (a) Wöhrle, D.; Eskes, M.; Shigehara, K.; Yamada, A. Synthesis 1993, 194.
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Compounds 2-4 were prepared previously directly from the corresponding carboxy-substituted phthalonitriles, but very few characterization data were given. See: (a) Wöhrle, D.; Eskes, M.; Shigehara, K.; Yamada, A. Synthesis 1993, 194.
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18
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0000937283
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(b) Nazeeruddin, M. K.; Humphry-Baker, R.; Grätzel, M.; Wöhrle, D.; Schnurpfeil, G.; Schneider, G.; Hirth, A.; Trombach, N. J. Porphyrins Phthalocyanines 1999, 3, 230.
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Nazeeruddin, M.K.1
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Grätzel, M.3
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Schnurpfeil, G.5
Schneider, G.6
Hirth, A.7
Trombach, N.8
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22
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27844482920
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Under this alkaline condition, the isoindole nitrogens of 3 may undergo complete deprotonation giving a single rather than split Q band as most of the metal-free phthalocyanines do. See: Leclaire, J.; Dagiral, R.; Fery-Forgues, S.; Coppel, Y.; Donnadieu, B.; Caminade, A.-M.; Majorai, J.-P. J. Am. Chem. Soc. 2005, 127, 15762.
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Under this alkaline condition, the isoindole nitrogens of 3 may undergo complete deprotonation giving a single rather than split Q band as most of the metal-free phthalocyanines do. See: Leclaire, J.; Dagiral, R.; Fery-Forgues, S.; Coppel, Y.; Donnadieu, B.; Caminade, A.-M.; Majorai, J.-P. J. Am. Chem. Soc. 2005, 127, 15762.
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