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Syntheses and photochemical properties of octasubstituted phthalocyaninato zinc complexes
Journal of Porphyrins and Phthalocyanines ( IF 0.9 ) Pub Date : 2002-08-25 , DOI: 10.1002/jpp.388 SUZANNE E. MAREE 1 , TEBELLO NYOKONG 1
Journal of Porphyrins and Phthalocyanines ( IF 0.9 ) Pub Date : 2002-08-25 , DOI: 10.1002/jpp.388 SUZANNE E. MAREE 1 , TEBELLO NYOKONG 1
Affiliation
In this work a selection of octasubstituted phthalocyaninato zinc complexes were synthesized and their photochemistry studied. The substituents included cholesterol (3a), estrone (3b), naphthol (3c) and phenoxy groups substituted with CH3 (3d), C ( CH 3 )3 (at two positions, 3e), C ( CH 3 )3 (3f), NO2 (3g), NH 2 (3h), COH (3i), COOH (3j), and H (3k). In general, complexes containing electron-donating groups attached to the phenoxy ring (e.g. 3e and 3f) were found to be photochemically unstable with photobleaching quantum yields of the order of 10-3 . In the presence of electron-withdrawing groups (3g, 3i, and 3j) the photobleaching quantum yields were of the order of 10-6 to 10-5 . Singlet oxygen quantum yields (ΦΔ ) ranged from 0.01 to 0.73. The lowest ΦΔ was observed for the highly aggregated complex 3c. All the complexes showed aggregation at high concentrations. Electrochemical reduction using a thin-layer spectroelectrochemistry cell showed that the complexes become more monomeric following reduction.
中文翻译:
八取代酞菁锌配合物的合成及光化学性质
在这项工作中,合成了一种选择的八取代酞菁锌配合物并研究了它们的光化学。取代基包括胆固醇 (3a)、雌酮 (3b)、萘酚 (3c) 和被 CH 取代的苯氧基3 (3d), C (CH3 )3 (在两个位置,3e),C(CH3 )3 (3f),否2 (3g),NH2 (3h)、COH (3i)、COOH (3j) 和 H (3k)。通常,发现含有连接到苯氧基环(例如 3e 和 3f)的给电子基团的配合物在光化学上不稳定,光漂白量子产率约为 10-3 . 在存在吸电子基团(3g、3i 和 3j)的情况下,光漂白量子产率约为 10-6 到 10-5 . 单线态氧量子产率 (ΦΔ ) 范围从 0.01 到 0.73。最低ΦΔ 观察到高度聚集的复合物 3c。所有配合物在高浓度下均显示聚集。使用薄层光谱电化学电池进行电化学还原表明,还原后配合物变得更加单体。
更新日期:2002-08-25
中文翻译:
八取代酞菁锌配合物的合成及光化学性质
在这项工作中,合成了一种选择的八取代酞菁锌配合物并研究了它们的光化学。取代基包括胆固醇 (3a)、雌酮 (3b)、萘酚 (3c) 和被 CH 取代的苯氧基