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High resolution spectroscopy of carboxylic acid in the gas phase: Observation of proton transfer in (DCOOH)_2

机译:气相羧酸的高分辨率光谱:(DCOOH)_2中质子转移的观察

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We report the first fully analyzed high resolution spectrum of a carboxylic acid dimer in the gas phase. High resolution spectra in the region of the C-O stretch 1241.7-1250.7 cm~(-1) have been recorded for (DCOOH)_2. The data could be fit within experimental uncertainty to a rigid rotor Watson S reduced Hamiltonian. The vibrational frequency of the C-O stretch in (DCOOH)_2 is determined to be 1244.8461 (2) cm~(-1). Our spectra are the first direct experimental evidence for proton transfer tunneling in formic acid dimer (FAD), with FAD serving as a prototype for double hydrogen bonded organic complexes. Previous theoretical studies predicted proton transfer times covering a range of several orders of magnitude. Our measurements on (DCOOH)_2 established a proton transfer time of 5.8 ns [tunneling splitting of 0.00286 (25) cm~(-1)]. The proton transfer was found to accelerate upon vibrational excitation of the skeleton motion (the vibrational C-O mode), corresponding to a tunneling splitting of 0.00999 (21) cm~(-1). For this state the proton transfer time decreased to 1.7 ns, which corresponds to a vibrationally enhanced proton transfer mechanism. The moments of intertia are in agreement with a C_(2h) structure which indicates a high tunneling barrier. The observed spin statistical weights follow a descritpion of formic acid dimer in the molecular symmetry group G_8, which is isomorphic to the point group D_(2h). Our results suggest an out-of-plane contribution to the proton transfer mechanism for the otherwise planar dimer.
机译:我们报告了在气相中的羧酸二聚体的第一个完全分析的高分辨率光谱。记录了(DCOOH)_2在C-O伸展1241.7-1250.7 cm〜(-1)区域的高分辨率光谱。该数据可以在实验不确定性范围内拟合到刚性转子Watson S简化的哈密顿量。确定在(DCOOH)_2中C-O拉伸的振动频率为1244.8461(2)cm〜(-1)。我们的光谱是在甲酸二聚体(FAD)中质子转移隧穿的第一个直接实验证据,其中FAD用作双氢键有机配合物的原型。先前的理论研究预测质子转移时间涵盖了几个数量级。我们在(DCOOH)_2上的测量确定了5.8 ns的质子传递时间[0.00286(25)cm〜(-1)的隧道分裂)。发现质子传递在骨架运动的振动激发下加速(振动C-O模式),对应于0.00099(21)cm〜(-1)的隧穿分裂。对于此状态,质子传递时间减少到1.7 ns,这对应于振动增强的质子传递机制。中间矩与C_(2h)结构一致,表明存在较高的隧道势垒。观察到的自旋统计权重遵循分子对称群G_8中甲酸二聚体的描述,该分子对称群与点群D_(2h)同构。我们的研究结果表明,平面二聚体对质子转移机制的贡献超出了平面。

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