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Tabletop imaging of structural evolutions in chemical reactions demonstrated for the acetylene cation

机译:对乙炔阳离子进行化学反应的结构演变的桌面成像

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摘要

The introduction of femto-chemistry has made it a primary goal to follow the nuclear and electronic evolution of a molecule in time and space as it undergoes a chemical reaction. Using Coulomb Explosion Imaging, we have shot the first high-resolution molecular movie of a to and fro isomerization process in the acetylene cation. So far, this kind of phenomenon could only be observed using vacuum ultraviolet light from a free-electron laser. Here we show that 266 \u2030nm ultrashort laser pulses are capable of initiating rich dynamics through multiphoton ionization. With our generally applicable tabletop approach that can be used for other small organic molecules, we have investigated two basic chemical reactions simultaneously: proton migration and C=C bond breaking, triggered by multiphoton ionization. The experimental results are in excellent agreement with the timescales and relaxation pathways predicted by new and quantitative ab initio trajectory simulations.
机译:毫微微化学的引入使其成为一个主要目标,即随着分子发生化学反应,跟踪其在时间和空间上的核和电子演化。使用库仑爆炸成像,我们拍摄了乙炔阳离子中来回异构化过程的第一个高分辨率分子影片。到目前为止,只有使用来自自由电子激光器的真空紫外线才能观察到这种现象。在这里,我们显示266 u2030nm超短激光脉冲能够通过多光子电离引发丰富的动力学。利用我们可用于其他小有机分子的通用桌面方法,我们同时研究了两个基本化学反应:质子迁移和由多光子电离引发的C = C键断裂。实验结果与新的和定量的从头算轨迹模拟所预测的时标和弛豫途径非常吻合。

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