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Electron Spin Relaxation in Solvated Manganese(II) Ion Solutions

机译:溶剂化锰(II)离子溶液中的电子自旋弛豫

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Electron spin resonance (ESR) spectra were obtained for solutions of manganese(II) perchlorate in dimethylformamide (DMF), diethylformamide (DEF), dimethylsulfoxide (DMSO), and water. Variation of line shape with solvent and temperature was obtained and interpreted at low temperatures in terms of a model in which solvent fluctuations about the solvated ion modulate the ligand field and relax the electron spin through spin—orbit interaction. Relaxation times for Dgr;ms=1 transitions of theS=52system were calculated using a semiclassical density‐matrix formalism. In DMF, DEF, and DMSO solutions another contribution to relaxation was observed at high temperatures which may be attributable to ligand exchange or to internal motion in the complex ion. The high‐temperature process was not observed in aqueous manganese(II) solutions.
机译:获得了高氯酸锰(II)在二甲基甲酰胺(DMF)、二乙基甲酰胺(DEF)、二甲基亚砜(DMSO)和水中溶液的电子自旋共振(ESR)谱图。在低温下,获得了线形随溶剂和温度的变化,并用一个模型进行了解释,其中溶剂离子周围的溶剂波动调节配体场并通过自旋-轨道相互作用松弛电子自旋。使用半经典密度&连字符矩阵形式计算了 &Dgr;ms=1 的 S=52 系统的弛豫时间。在 DMF、DEF 和 DMSO 溶液中,观察到在高温下对弛豫的另一种贡献,这可能归因于配体交换或络合离子中的内部运动。在锰(II)水溶液中未观察到高温过程。

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