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首页> 外文期刊>Journal of the American Chemical Society >MANGANESE L-EDGE X-RAY ABSORPTION SPECTROSCOPY OF MANGANESE CATALASE FROM LACTOBACILLUS PLANTARUM AND MIXED VALENCE MANGANESE COMPLEXES
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MANGANESE L-EDGE X-RAY ABSORPTION SPECTROSCOPY OF MANGANESE CATALASE FROM LACTOBACILLUS PLANTARUM AND MIXED VALENCE MANGANESE COMPLEXES

机译:扁平乳杆菌和混合价锰配合物锰过氧化氢的锰L-边缘X射线吸收光谱

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摘要

The first Mn L-edge absorption spectra of a Mn metalloprotein are presented in this paper. Both reduced and superoxidized Mn catalase have been examined by fluorescence-detected soft X-ray absorption spectroscopy, and their Mn L-edge spectra are dramatically different. The spectrum of reduced Mn(II)Mn(II) catalase has been interpreted by ligand field atomic multiplet calculations and by comparison to model compound spectra. The analysis finds a 10 Dq value of similar to 1.1 eV, consistent with coordination by predominately nitrogen and oxygen donor ligands. For interpretation of mixed valence Mn spectra, an empirical simulation procedure based on the addition of homovalent model compound spectra has been developed and was tested on a variety of Mn complexes and superoxidized Mn catalase. This routine was also used to determine the oxidation state composition of the Mn in [Ba8Na2ClMn16-(OH)(8)(CO3)(4)L(8)]. 53H(2)O (L = 1,3-diamino-2-hydroxypropane-N,N,N',N'-tetraacetic acid).
机译:本文介绍了锰金属蛋白的第一个Mn L-edge吸收光谱。通过荧光检测的软X射线吸收光谱法已经检查了还原的和过氧化的Mn过氧化氢酶,并且它们的Mn L-边缘光谱显着不同。还原的Mn(II)Mn(II)过氧化氢酶光谱已通过配体场原子多重态计算和与模型化合物光谱的比较得到了解释。分析发现10 Dq值接近1.1 eV,与主要由氮和氧供体配体形成的配位相一致。为了解释混合价锰光谱,已经开发了基于添加等效模型化合物光谱的经验模拟程序,并在多种锰配合物和超氧化锰过氧化氢酶上进行了测试。该程序也用于确定[Ba8Na2ClMn16-(OH)(8)(CO3)(4)L(8)]中Mn的氧化态组成。 53H(2)O(L = 1,3-二氨基-2-羟基丙烷-N,N,N′,N′-四乙酸)。

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