铀酰
化学
羧酸盐
衰减全反射
质子化
齿合度
红外光谱学
傅里叶变换红外光谱
水溶液
光谱学
红外线的
氨基酸
无机化学
离子
结晶学
分析化学(期刊)
物理化学
立体化学
有机化学
晶体结构
物理
光学
生物化学
量子力学
作者
Astrid Barkleit,Harald Foerstendorf,Karsten Heim,Susanne Sachs,Gert Bernhard
标识
DOI:10.1366/000370208784909607
摘要
Uranyl complexes with phenylalanine and the analogous ligand phenylpropionate were investigated in aqueous solution by attenuated total reflection (ATR) Fourier transform infrared (FT-IR) spectroscopy. The assignment of the observed bands to vibrational modes was accomplished using spectra of the pure ligands recorded at different pH values and spectra of the 15N labeled analogous compounds of the amino acid. The results presented in this work provide a detailed description of the binding states of the uranyl complexes in solution. A bidentate binding of the carboxylate group to the actinide ion was observed by the characteristic shifts of the carboxylate modes. From the spectra the presence of the protonated amino group in the actinide complex can be derived. Due to these findings, contributions of the amino group to the binding to the uranyl ion in the amino acid complex can be ruled out.
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