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首页> 外文期刊>The Journal of Chemical Physics >Hydrogen-atom tunneling reactions with methyl formate in solid para-hydrogen: Infrared spectra of the methoxy carbonyl [center dot C(O)OCH3] and formyloxy methyl [HC(O)OCH2 center dot] radicals
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Hydrogen-atom tunneling reactions with methyl formate in solid para-hydrogen: Infrared spectra of the methoxy carbonyl [center dot C(O)OCH3] and formyloxy methyl [HC(O)OCH2 center dot] radicals

机译:用固体对氢气中甲酸甲酯的氢原子隧穿反应:甲氧基羰基[中心点C(O)OCH3]的红外光谱和甲酰氧基甲基[HC(O)OCH2中心点]基团

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摘要

We investigated the reaction of methyl formate, HC(O)OCH3, with hydrogen atoms in solid para-hydrogen (p-H-2) at 1.74 and 3.3 K with infrared absorption spectroscopy. Hydrogen atoms were produced either upon direct photolysis of HC(O)OCH3 at 193 nm or upon irradiation of Cl-2, codeposited with HC(O)OCH3 in p-H-2, with light at 365 nm to produce Cl atoms that react with the p-H-2 host via the reaction Cl + H-2 (v = 1) -> HCl + H induced by subsequent IR irradiation of the p-H-2 matrix. We assigned lines at 1785.2, 1170.6, 1104.6, and 879.4/880.5 cm -1 and five additional weak lines to the methoxy carbonyl radical, center dot C(O)OCH3, and three weak lines at 1751.3, 1152.9, and 994.4/996.8 cm(-1) to the formyloxy methyl radical, HC(O)OCH2 center dot, according to the consideration of possible reactions, correlated variations in intensities after each experimental step, and comparison of observed vibrational wavenumbers and IR intensities with values predicted with the B3LYP/aug-cc-pVTZ method. Unlike most reported H-atom diffusion tunneling reactions, the reaction H + HC(O)OCH3, in solid p-H-2 at 3.3 K was found to diminish rapidly after IR irradiation, but, similar to reactions of H + N2O and H + HC(O)OH, this reaction was reinitiated when the matrix temperature was decreased from 4.0 K to 1.5 K. We confirmed that the method used to generate the mobile H atoms does not affect the subsequent chemistry. A possible reaction mechanism and the role of this reaction in dark interstellar clouds are discussed. Published under license by AIP Publishing.
机译:我们研究了在1.74和3.3K的固体对氢(P-H-2)中与红外吸收光谱的氢原子中甲酯HC(O)OCH3的反应。在193nm处的HC(O)OCH3的直接光解或在Cl-2照射时直接光解氢原子,在pH-2中用HC(O)OCH3,用365nm的光,以产生与之反应的Cl原子通过反应Cl + H-2(v = 1) - > HCl + H诱导的pH-2致铬PH-2宿主。我们在1785.2,1170.6,1104.6和879.4 / 880.5cm -1和五种额外的弱线中分配了9.5厘米,中央点C(o)Och3和3个弱线,1751.3,1152.9和994.4 / 996.8厘米(-1)对甲酰氧基甲基自由基,HC(O)OCH2中心点,根据可能的反应,每个实验步骤后强度相关变化,以及观察到的振动波数和IR强度与B3LYP预测的值的比较/ Aug-CC-PVTZ方法。与大多数报道的H-原子扩散隧穿反应不同,在IR照射后,发现在3.3k下的固体pH-2中的反应H + HC(O)OCH3,但类似于H + N2O和H + HC的反应,迅速减少(o)哦,当基质温度从4.0k降低至1.5k时,将该反应重新产生。我们证实用于产生流动H原子的方法不会影响随后的化学性。讨论了可能的反应机制和这种反应在暗星形云中的作用。通过AIP发布在许可证下发布。

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