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首页> 外文期刊>Turkish journal of chemistry >Peripherally 1,2-dinaphthyl ethanediol substituted phthalocyanine complexes: synthesis, characterization, aggregation, and application in benzyl alcohol oxidation at room temperature
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Peripherally 1,2-dinaphthyl ethanediol substituted phthalocyanine complexes: synthesis, characterization, aggregation, and application in benzyl alcohol oxidation at room temperature

机译:外围1,2-二萘基乙二醇取代的酞菁配合物:合成,表征,聚集及其在室温下苯甲醇氧化中的应用

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In this study, the synthesis of a novel 1,2-dinaphthyl ethanediol substituted phthalonitrile (2 ) together with tetra-substituted zinc(II) phthalocyanine (Pc) (3 ) and cobalt(II) Pc (4 ) bearing 1,2-dinaphthyl ethanediol at peripheral positions was described. The aggregation behaviors of metallophthalocyanines 3 and 4 in solution were investigated by carrying out Beer-Lambert experiments at different concentrations. In addition, the catalytic activity of new cobalt(II) Pc 4 was investigated for benzyl alcohol oxidation. Benzyl alcohol was converted to benzaldehyde using cobalt(II) Pc 4 as a catalyst by a conversion of 99% with selectivity of 100% at room temperature in 1 h. Several spectroscopic techniques such as FT-IR, UV-Vis, $^{1}$H and $^{13}$C NMR, and MALDI-TOF MS were used for the characterization of the newly synthesized compounds.
机译:在这项研究中,合成了一种新的1,2-二萘基乙二醇取代的邻苯二甲腈( 2)与四取代的锌(II)酞菁(Pc)( 3)和钴(II)Pc(< b> 4)描述了在周边位置带有1,2-二萘基乙二醇的化合物。通过在不同浓度下进行Beer-Lambert实验研究了金属酞菁 3和 4在溶液中的聚集行为。另外,研究了新的钴(II)Pc 4对苄醇氧化的催化活性。使用钴(II)Pc b 4作为催化剂,将苄醇在室温下在1小时内以99%的转化率和100%的选择性转化为苯甲醛。几种光谱技术(例如FT-IR,UV-Vis,$ ^ {1} $ H和$ ^ {13} $ C NMR和MALDI-TOF MS)用于表征新合成的化合物。

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