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SYNTHESIS AND CHARACTERIZATION OF CARBOXYLIC SUBSTITUTED BINUCLEAR IRON PHTHALOCYANINES

机译:羧基取代的双核晶硅酞菁的合成与表征

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Phthalocyanine compounds is a kind of organic functional dyes, which has good optical, thermal and chemical stability. Such compounds has broad application prospects in the optical conductivity, optical storage, catalytic oxidation, and other high-tech fields. However, its solubiliey in water and organic solvents is very little, which restrict the application in many fields[1]. Carboxylic substituted phthalocyanines had not only a good solubility in water ,but excellent catalytic properties in many appilication fields. They were used as effective catalysts for oxidation of thiols and hydrosulfides by dioxygen. They have found wide application in the catalytic oxidation of mercaptans in the oil fractions. The oxidation of thiols or alkali sulfides catalyzed by metalophthalocyanine complexes is not complete, the end products being disulfides, sulfer and thiosulfates, respectively.
机译:酞菁化合物是一种有机官能染料,具有良好的光学,热和化学稳定性。这些化合物具有光导率,光学储存,催化氧化和其他高科技领域的广泛应用前景。然而,它的溶解在水和有机溶剂中很少,这限制了许多领域的应用[1]。羧基取代的酞菁在水中不仅具有良好的溶解度,而且在许多安抚场中具有优异的催化性能。它们被用作通过二恶英氧化硫醇和氢硫化物的有效催化剂。它们在油分中的硫醇催化氧化方面发现了广泛的应用。由金属酞菁配合物催化的硫醇或碱硫化物的氧化不完整,最终产物分别是二硫化,蚕丝和硫代硫酸盐。

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