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Vibrational Spectra and Dynamics of Anions and Acids in Ionic Liquids

机译:离子液体中阴离子和酸的振动光谱和动力学

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Vibrational spectra and energy relaxation lifetimes are reported for the protonated acidic species hydrazoic acid (HN_3) and the azide (N_3~-), thiocyanate (NCS) and dicyanamide (DCA) anions in imidizolium and phosphonium ionic liquids (ILs). The vibrational spectra and dynamics for the anions in phosphonium tetrafluoroborate and dicyanamide ILs are similar to those previously reported for imidizolium ILs, which resemble the behavior in aprotic molecular solvents such as dimethylsulfoxide. The results are different for hydrazoic acid. In water, methanol and other protic solvents the energy relaxation time is shorter for the azide anion than its protonated and neutral counterpart, hydrazoic acid. In ILs, however, the anion relaxation times are faster than the acid, indicating that the intermolecular interactions are different for acids and anions in ILs compared to conventional molecular solvents.
机译:据报道振动光谱和能量弛豫寿命用于质子化的酸性物质肼(HN_3)和叠氮化物(N_3〜 - ),硫氰酸酯(NCS)和二氰胺(DCA)阴离子(ILS)(ILS)中的质子酸酯(N_3〜 - ),硫氰酸酯(NCS)和二氰胺(DCA)阴离子。磷酸鏻和二氰胺ILS中阴离子的振动光谱和动力学类似于先前报道的咪唑鎓ILS的阴离子,其类似于非质子分子溶剂如二甲基磺酰氧化物的行为。结果对于氮硼酸是不同的。在水中,甲醇和其他质子溶剂的能量松弛时间比其质子化和中性对应物少于其质子化和中性对应的少量氮酸。然而,在ILS中,阴离子弛豫时间比酸快,表明与常规分子溶剂相比,ILS中的分子间相互作用不同于IL的酸和阴离子。

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