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作 者:YANGKe-er TONGShan-ling YANYan KANGEn-hua XIAOFeng-shou LIQing CHANGXin FANGChi-guang
机构地区:[1]DepartmentofChemistry,InstituteofAdrancedMaterials,ShantouUniversity,Shantou515063,ChinaP.R. [2]CollegeofChemistry,JilinUniversity,Changchun130023,ChinaP.R. [3]TheSanitationCenterofInspection&TestofJilinProvince,Changchun130012,P.R.China
出 处:《Chemical Research in Chinese Universities》2005年第3期326-333,共8页高等学校化学研究(英文版)
摘 要:In an alkaline 2-propanol solution with 5,10,15,20-tetra(4-methoxyl phenyl) porphyrin iron chloride(TOMPPFeCl) as a catalyst and oxygen as a cheap green oxidant, 2-naphthol was conversed to 2-hydroxy-\{1,4-naphthoquinone(HNQ)\} with a yield of 62.17% and a selectivity of 100%, and the conversion number of TMOPPFeCl catalyst was 8.32/min. The catalytic oxidation products were characterized by means of UV-Vis, IR, GC-MS, ~ 1H NMR and melting point determination. In this catalytic oxidation, the catalytic activity of TMOPPFeCl was researched in detail and the reacting conditions were optimized. A possible reaction mechanism is summarized based on in situ EPR determination.In an alkaline 2-propanol solution with 5,10,15,20-tetra(4-methoxyl phenyl) porphyrin iron chloride(TOMPPFeCl) as a catalyst and oxygen as a cheap green oxidant, 2-naphthol was conversed to 2-hydroxy-\{1,4-naphthoquinone(HNQ)\} with a yield of 62.17% and a selectivity of 100%, and the conversion number of TMOPPFeCl catalyst was 8.32/min. The catalytic oxidation products were characterized by means of UV-Vis, IR, GC-MS, ~ 1H NMR and melting point determination. In this catalytic oxidation, the catalytic activity of TMOPPFeCl was researched in detail and the reacting conditions were optimized. A possible reaction mechanism is summarized based on in situ EPR determination.
关 键 词:Catalytic oxidation NAPHTHOL 2-Hydroxy-1 4-naphthoquinone Molecular oxygen Metalloporphyrin catalyst 2-Propanol
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