Ruggiero Michael T, Korter Timothy M
Department of Chemistry, Syracuse University , 1-014 Center for Science and Technology, Syracuse, New York 13244-4100, United States.
J Phys Chem A. 2016 Jan 21;120(2):227-32. doi: 10.1021/acs.jpca.5b10063. Epub 2016 Jan 11.
Terahertz vibrational spectroscopy has evolved into a powerful tool for the detection and characterization of transition metal sulfate compounds, specifically for its ability to differentiate between various hydrated forms with high specificity. Copper(II) sulfate is one such system where multiple crystalline hydrates have had their terahertz spectra fully assigned, and the unique spectral fingerprints of the forms allows for characterization of multicomponent systems with relative ease. Yet the most commonly occurring form, copper(II) sulfate pentahydrate (CuSO4·5H2O), has proven elusive due to the presence of a broad absorption across much of the terahertz region, making the unambiguous identification of its spectral signature difficult. Here, it is shown that the sub-100 cm(-1) spectrum of CuSO4·5H2O is obscured by absorption from adsorbed water and that controlled drying reveals sharp underlying features. The crystalline composition of the samples was monitored in parallel by X-ray diffraction as a function of drying time, supporting the spectroscopic results. Finally, the terahertz spectrum of CuSO4·5H2O was fully assigned using solid-state density functional theory simulations, helping attribute the additional absorptions that appear after excessive drying to formation of CuSO4·3H2O.
太赫兹振动光谱已发展成为检测和表征过渡金属硫酸盐化合物的强大工具,特别是因其能够高度特异性地区分各种水合形式。硫酸铜(II)就是这样一个系统,其中多种结晶水合物的太赫兹光谱已被完全确定,并且这些形式的独特光谱指纹使得相对容易地表征多组分系统。然而,最常见的形式,即五水合硫酸铜(II)(CuSO4·5H2O),由于在太赫兹区域的大部分范围内存在宽吸收,其光谱特征难以明确识别。在此表明,CuSO4·5H2O在低于100 cm(-1)的光谱被吸附水的吸收所掩盖,而控制干燥揭示了其尖锐的潜在特征。通过X射线衍射作为干燥时间的函数并行监测样品的晶体组成,支持了光谱学结果。最后,使用固态密度泛函理论模拟对CuSO4·5H2O的太赫兹光谱进行了完全归属,有助于将过度干燥后出现的额外吸收归因于CuSO4·3H2O的形成。