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Spectroscopic study of cis-to-trans tunneling reaction of HCOOD in rare gas matrices

机译:稀有气体基质中HCOOD的顺式-反式隧穿反应的光谱研究

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The higher energy conformer (cis) of HCOOD is prepared by vibrational excitation of the trans form. The cis conformer decays back to the conformational ground state (trans) via tunneling of deuterium. The tunneling process in HCOOD in rare gas matrices is extremely slow in scale of weeks. We present new measurements of the tunneling rate constants, which characterize the efficiency of the cis-to-trans conversion process in Ne, Ar, Kr, and Xe matrices. The tunneling rates of HCOOD follow the trend kXe kKr kAr kNe, which is anomalous with respect to the reaction barrier of the solvated molecule. We propose a semiempirical energetic scheme of solid state solvation, which is consistent with all experimental observation. The temperature dependence of the tunneling constants rates of HCOOD is very weak compared to HCOOH in all matrices. The fundamental vibrational frequencies of the cis and trans conformers of HCOOD in various matrices are reported.
机译:HCOOD的高能构象异构体(顺式)是通过反式的振动激发制备的。顺式构象异构体通过氘的隧穿退回到构象基态(反式)。在HCOOD中稀有气体基质中的隧穿过程在几周的时间内极其缓慢。我们介绍了隧穿速率常数的新度量,这些度量表征了Ne,Ar,Kr和Xe矩阵中顺式至反式转换过程的效率。 HCOOD的隧穿速率遵循趋势kXe kKr kAr kNe,该趋势相对于溶剂化分子的反应势垒是反常的。我们提出了固态溶剂化的半经验能量方案,与所有实验观察结果一致。与所有矩阵中的HCOOH相比,HCOOD隧穿常数速率的温度依赖性非常弱。报道了在各种基质中HCOOD的顺式和反式构象体的基本振动频率。

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