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Nitranilic acid hexahydrate, a novel benchmark system of the Zundel cation in an intrinsically asymmetric environment: spectroscopic features and hydrogen bond dynamics characterised by experimental and theoretical methods

机译:六水合硝酸镍,本征不对称环境中Zundel阳离子的新型基准体系:通过实验和理论方法表征的光谱特征和氢键动力学

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摘要

Nitranilic acid (2,5-dihydroxy-3,6-dinitro-2,5-cyclohexadiene-l,4-dione) as a strong dibasic acid in acidic aqueous media creates the Zundel cation, H5O2~+. The structural unit in a crystal comprises (H5O2)2~+ (2,5-dihydroxy-3,6-dinitro-l,4-benzoquinonate)~(2-) dihydrate where the Zundel cation reveals no symmetry, being an ideal case for studying proton dynamics and its stability. The Zundel cation and proton transfer dynamics are studied by variable-temperature X-ray diffraction, IR and solid-state NMR spectroscopy, and various quantum chemical methods, including periodic DFT calculations, ab initio molecular dynamics simulation, and quantization of nuclear motion along three fully coupled internal coordinates. The Zundel cation features a short H-bond with the O···O distance of 2.433(2) A with an asymmetric placement of hydrogen. The proton potential is of a single well type and, due to the non-symmetric surroundings, of asymmetric shape. The formation of the Zundel cation is facilitated by the electronegative NO2 groups. The employed spectroscopic techniques supported by calculations confirm the presence of a short H-bond with a complex proton dynamics.
机译:在酸性水性介质中,作为强二元酸的亚硝酸(2,5-二羟基-3,6-二硝基-2,5-环己二烯-1,4-二酮)形成Zundel阳离子H5O2 +。晶体中的结构单元包含(H5O2)2〜+(2,5-二羟基-3,6-二硝基-1,4-苯并奎宁酸酯)〜(2-)二水合物,其中Zundel阳离子没有对称性,是理想情况用于研究质子动力学及其稳定性。 Zundel阳离子和质子转移动力学是通过可变温度X射线衍射,IR和固态NMR光谱学以及各种量子化学方法研究的,包括周期性DFT计算,从头算分子动力学模拟以及沿着三个方向对核运动的量化完全耦合的内部坐标。 Zundel阳离子具有短的H键,O···O距离为2.433(2)A,且氢的位置不对称。质子势是单井型的,并且由于周围环境的不对称性而具有不对称的形状。 Zundel阳离子的形成可通过负电性NO2基团实现。计算所采用的光谱技术证实了短氢键的存在以及质子动力学的复杂性。

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