以取代水杨酸盐为轴向配体的铝(III)-对甲基-中四苯基卟啉配合物的电化学和光谱表征

IF 2.3 Q3 ELECTROCHEMISTRY
G. D. Bajju, Deepmala, S. K. Anand, Sujata Kundan, Narinder Singh
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引用次数: 1

摘要

合成了一系列含有轴向配位水杨酸阴离子[p-CH3TPP-Al (III)]的铝(III)-对甲基-中四苯基卟啉(p-CH3TPP-Al -X),其中X =水杨酸盐(SA)、4-氯水杨酸盐(4-CSA)、5-氯水杨酸盐(5-CSA)、5-氟水杨酸盐(5-FSA)、4-氨基水杨酸盐(4-ASA)、5-氨基水杨酸盐(5-ASA)、5-硝基水杨酸盐(5-NSA)和5-磺基水杨酸盐(5-SSA),并通过紫外可见(UV-vis)、红外(IR)光谱,质子核磁共振(1H NMR)光谱,13C NMR和元素分析。对所有合成的化合物进行了详细的电化学研究,比较了它们的氧化和还原机制,并解释了轴向配位对它们氧化还原性能的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemical and Spectroscopic Characterization of Aluminium(III)-para-methyl-meso-tetraphenylporphyrin Complexes Containing Substituted Salicylates as Axial Ligands
A series of aluminium(III)-p-methyl-meso-tetraphenylporphyrin (p-CH3TPP-Al(III)) containing axially coordinated salicylate anion [p-CH3TPP-Al-X)], where X = salicylate (SA), 4-chlorosalicylate (4-CSA), 5-chlorosalicylate (5-CSA), 5-flourosalicylate (5-FSA), 4-aminosalicylate (4-ASA), 5-aminosalicylate (5-ASA), 5-nitrosalicylate (5-NSA), and 5-sulfosalicylate (5-SSA), have been synthesized and characterized by various spectroscopic techniques including ultraviolet-visible (UV-vis), infrared (IR) spectroscopy, proton nuclear magnetic resonance (1H NMR) spectroscopy, 13C NMR, and elemental analysis. A detailed study of electrochemistry of all the synthesized compounds has been done to compare their oxidation and reduction mechanisms and to explain the effect of axial coordination on their redox properties.
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