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Electrochemical Characterization and Metallization of Two Novel Asymmetric Meso-Subtstituted Porphyrins

机译:两种新型不对称内消旋取代卟啉的电化学表征和金属化

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Electrochemical characterization and metallization of two novel meso-susbstituted porphyrins werecarried out by sweep and step potential techniques. Redox potentials of 5,10,15-tris(p-chlorophenyl)- 20-(2-hydroxy-3-methoxyphenyl)porphyrin and 5,10,15-tris(p-methoxyphenyl)-20-(p-chlorophenyl)porphyrin were identified, and their respective diffusion coefficients at 25 1 C in CH2Cl2 usingtetrabutylammonium hexafluorophosphate as supporting electrolyte were determined. The dianionradical formation potentials were found to be influenced by the electrodonor effects of the porphyrinsubstituents. The metallization process of the porphyrins were carried out by controlled potentialelectrolysis using an aluminum sacrificial anode to form the metallic ions in situ. The aluminummetalloporphyrin formation of each porphyrin was confirmed by UV-Vis, IR and atomic absorptionspectroscopy.
机译:通过扫描电势和步进电势技术进行了两种新型的内消旋卟啉的电化学表征和金属化。 5,10,15-三(对氯苯基)-20-(2-羟基-3-甲氧基苯基)卟啉和5,10,15-三(对甲氧基苯基)-20-(对氯苯基)卟啉的氧化还原电位进行了鉴定,并以六氟磷酸四丁铵为支持电解质,测定了它们在25 1 C下在CH2Cl2中的扩散系数。发现二价阴离子形成势受卟啉取代基的电给体作用影响。卟啉的金属化过程是使用铝牺牲阳极通过受控电势电解进行的,以原位形成金属离子。通过UV-Vis,IR和原子吸收光谱法证实了每个卟啉的铝金属卟啉形成。

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