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The single donator-single acceptor hydrogen bonding structure in water probed by Raman spectroscopy

机译:拉曼光谱探测水中单供体-单受体氢键结构

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In this work, the Raman spectra of aqueous C_(12)E_5 solutions are recorded and utilized to demonstrate the existence of single donator-single acceptor (DA) hydrogen bonding in water. From Raman OH stretching bands of aqueous C_(12)E_5 solutions, the relative intensity of 3430 cm~(-1) subband increases with C_(12)E_5 concentrations. For confined water, the DA hydrogen bonding can be expected to be the important hydrogen bonding species. Therefore, the 3430 cm~(-1) component can be ascribed to OH vibration engaged in DA hydrogen bonding. This is in agreement with our recent explanation on Raman OH stretching band of water. For water at ambient conditions, the double donor-double acceptor (DDAA) and DA should be the dominant hydrogen bonding species, the ratio of DDAA to DA can be approximately to be 0.75:1, and the mean hydrogen bonding can be determined to be 2.75.
机译:在这项工作中,记录了C_(12)E_5水溶液的拉曼光谱,并将其用于证明水中存在单个供体-单受体(DA)氢键。在C_(12)E_5水溶液的拉曼OH拉伸带中,随着C_(12)E_5浓度的增加,3430 cm〜(-1)子带的相对强度增加。对于承压水,可以预期DA氢键是重要的氢键物种。因此,3430 cm〜(-1)的成分可以归因于DA氢键结合的OH振动。这与我们最近对拉曼OH拉伸水带的解释是一致的。对于环境条件下的水,双供体-双受体(DDAA)和DA应该是主要的氢键键合物种,DDAA与DA的比率可以约为0.75:1,并且可以确定平均氢键键为2.75。

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