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Oxidation of 17α-ethinylestradiol with Mn(III) and product identification

机译:Mn(III)氧化17α-炔雌醇及产物鉴定

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With increasing concern about the contamination of aquatic environments by estrogenic pollutants, removal of synthetic estrogens such as 17α-ethinylestradiol (EE2) has been widely studied, especially with respect to the treatment methods. However, the degradation products have rarely been identified. The purpose of this study was to identify structurally the oxidation products of EE2. Mn(III) was used as an oxidizing agent. To obtain sufficient oxidation products for HPLC, LC-MS and NMR spectroscopy, a highly concentrated solution of EE2 (1 mM) was prepared in a mixture of water and a water-miscible organic solvent. From HPLC of the reaction products, a single compound (I) was found to be predominant. From LC-MS, its molecular mass was found to be 294, and two hydrogens were believed to have been removed from EE2 (M.W. 296) to form a C=C double bond. The structure of compound I (position of the double bond) was determined using ~1H NMR, ~(13)C NMR, H-H COSY, HSQC and HMBC. As minor products, isomeric dimers (M.W. 590) of EE2, as well as the products (M.W. 588) in which EE2 was coupled to compound I were also formed during the Mn(HI)-mediated oxidation of EE2. ? 2008 Published by Elsevier B.V.
机译:随着越来越多地关注雌激素污染物对水环境的污染,已广泛研究了去除合成雌激素如17α-炔雌醇(EE2)的方法,特别是在治疗方法方面。然而,很少发现降解产物。这项研究的目的是从结构上确定EE2的氧化产物。 Mn(III)用作氧化剂。为了获得用于HPLC,LC-MS和NMR光谱分析的足够的氧化产物,在水和与水混溶的有机溶剂的混合物中制备了高度浓缩的EE2(1 mM)溶液。从反应产物的HPLC中,发现单一化合物(I)是主要的。从LC-MS中,发现其分子量为294,并且认为已经从EE 2(M.W. 296)中除去了两个氢以形成C = C双键。使用〜1H NMR,〜(13)C NMR,H-H COSY,HSQC和HMBC确定化合物I的结构(双键的位置)。作为次要产品,在Mn(HI)介导的EE2氧化过程中,还形成了EE2的异构二聚体(M.W. 590),以及EE2与化合物I偶联的产物(M.W. 588)。 ? 2008年由Elsevier B.V.发行

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