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Azide-water intermolecular coupling measured by two-color two-dimensional infrared spectroscopy

机译:二维二维红外光谱法测定叠氮化物-水分子间的耦合

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We utilize two-color two-dimensional infrared spectroscopy to measure the intermolecular coupling between azide ions and their surrounding water molecules in order to gain information about the nature of hydrogen bonding of water to ions. Our findings indicate that the main spectral contribution to the intermolecular cross-peak comes from population transfer between the asymmetric stretch vibration of azide and the OD-stretch vibration of D_2O. The azide-bound D2O bleach/stimulated emission signal, which is spectrally much narrower than its linear absorption spectrum, shows that the experiment is selective to solvation shell water molecules for population times up to ~500 fs. The waters around the ion are present in an electrostatically better defined environment. Afterwards, ~1 ps, the sample thermalizes and selectivity is lost. On the other hand, the excited state absorption signal of the azide-bound D2O is much broader. The asymmetry in spectral width between bleach/stimulated emission versus excited absorption has been observed in very much the same way for isotope-diluted ice Ih, where it has been attributed to the anharmonicity of the OD potential.
机译:我们利用二维二维红外光谱法测量叠氮化物离子与其周围水分子之间的分子间偶联,以获取有关水与离子之间氢键键合性质的信息。我们的发现表明,对分子间交叉峰的主要光谱贡献来自叠氮化物的不对称拉伸振动与D_2O的OD拉伸振动之间的种群转移。叠氮键结合的D2O漂白剂/受激发射信号在光谱上比线性吸收光谱要窄得多,这表明该实验对溶剂化壳水分子的选择性高达〜500 fs。离子周围的水存在于静电条件更好的环境中。此后,约1 ps,样品发生热化,选择性丧失。另一方面,叠氮化物结合的D 2 O的激发态吸收信号要宽得多。对于同位素稀释的冰Ih,已经以几乎相同的方式观察到了漂白/受激发射与受激吸收之间的谱宽不对称性,这归因于OD电位的不谐和性。

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