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Communication: Frequency shifts of an intramolecular hydrogen bond as a measure of intermolecular hydrogen bond strengths

机译:通讯:分子内氢键的频移,作为分子间氢键强度的量度

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Infrared-ultraviolet double resonance spectroscopy has been applied to study the infrared spectra of the supersonically cooled gas phase complexes of formic acid, acetic acid, propionic acid, formamide, and water with 9-hydroxy-9-fluorenecarboxylic acid (9HFCA), an analog of glycolic acid. In these complexes each binding partner to 9HFCA can function as both proton donor and acceptor. Relative to its frequency in free 9HFCA, the 9-hydroxy (9OH) stretch is blue shifted in complexes with formic, acetic, and propionic acids, but is red shifted in the complexes with formamide and water. Density functional calculations on complexes of 9HFCA to a variety of H bonding partners with differing proton donor and acceptor abilities reveal that the quantitative frequency shift of the 9OH can be attributed to the balance struck between two competing intermolecular H bonds. More extensive calculations on complexes of glycolic acid show excellent consistency with the experimental frequency shifts.
机译:红外-紫外线双共振光谱法已用于研究甲酸,乙酸,丙酸,甲酰胺和水与类似物9-羟基-9-芴羧酸(9HFCA)的超声冷却气相复合物的红外光谱乙醇酸。在这些复合物中,每个9HFCA的结合伴侣都可以充当质子供体和受体。相对于游离9HFCA中的频率,在与甲酸,乙酸和丙酸形成的络合物中,9-羟基(9OH)呈蓝色移,而在与甲酰胺和水形成的复合物中呈红色移。对9HFCA与具有不同质子供体和受体能力的各种H键合伙伴的复合物进行的密度泛函计算表明,9OH的定量频移可归因于两个竞争性分子间H键之间的平衡。乙醇酸配合物的更广泛的计算表明与实验频率偏移具有极好的一致性。

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