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Metallophilic interactions in polynuclear Ag(I) complex with 1-methylhydantoin studied by X-ray absorption, electronic and vibrational spectroscopies

机译:X射线吸收,电子和振动光谱研究多核Ag(I)与1-甲基乙内酰脲络合物中的嗜金属相互作用

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摘要

Argentophilic interaction has been studied in silver methylhydantoin complex {[Ag(1-methylhydantoin)] ·0.5H_2O}_n using electronic, Raman and X-ray absorption spectroscopies strengthened theoretically. The EXAFS confirmed coordination number (CN = 3) of complex and metalophilic interactions. The digital filter analysis of electronic spectra revealed that broad bands at ca 38000 cm~(-1) and ca 45000 cm~(-1) observed in the solid state and solutions, respectively, were composed of two transitions, namely L– L(π→π~*) and Ag–Ag tentatively assigned to (4dσ~*→5pσ) in silver ion. The Raman spectroscopy data showed a new band at 83 cm~(-1) assigned to m(Ag2) vibration theoretically supported by DFT.
机译:使用理论上得到加强的电子,拉曼和X射线吸收光谱研究了甲基乙内酰脲银络合物{[Ag(1-甲基乙内酰脲)]·0.5H_2O} _n中的亲银相互作用。 EXAFS确认了复杂和嗜金属相互作用的配位数(CN = 3)。电子光谱的数字滤波器分析表明,在固态和溶液中分别观察到的大约38000 cm〜(-1)和45000 cm〜(-1)的宽带由两个跃迁组成,即L– L( π→π〜*)和Ag-Ag暂时分配给银离子中的(4dσ〜*→5pσ)。拉曼光谱数据表明,在83 cm〜(-1)处有一个新的谱带对应于理论上由DFT支持的m(Ag2)振动。

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