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利用协变天然框架分析解析分子聚阳离子的顺序和协同碎片化过程。

Disentangling sequential and concerted fragmentations of molecular polycations with covariant native frame analysis.

作者信息

McManus Joseph W, Walmsley Tiffany, Nagaya Kiyonobu, Harries James R, Kumagai Yoshiaki, Iwayama Hiroshi, Ashfold Michael N R, Britton Mathew, Bucksbaum Philip H, Downes-Ward Briony, Driver Taran, Heathcote David, Hockett Paul, Howard Andrew J, Kukk Edwin, Lee Jason W L, Liu Yusong, Milesevic Dennis, Minns Russell S, Niozu Akinobu, Niskanen Johannes, Orr-Ewing Andrew J, Owada Shigeki, Rolles Daniel, Robertson Patrick A, Rudenko Artem, Ueda Kiyoshi, Unwin James, Vallance Claire, Burt Michael, Brouard Mark, Forbes Ruaridh, Allum Felix

机构信息

Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Oxford OX1 3TA, UK.

Department of Physics, Kyoto University, Kyoto, 606-8502, Japan.

出版信息

Phys Chem Chem Phys. 2022 Sep 28;24(37):22699-22709. doi: 10.1039/d2cp03029b.

Abstract

We present results from an experimental ion imaging study into the fragmentation dynamics of 1-iodopropane and 2-iodopropane following interaction with extreme ultraviolet intense femtosecond laser pulses with a photon energy of 95 eV. Using covariance imaging analysis, a range of observed fragmentation pathways of the resulting polycations can be isolated and interrogated in detail at relatively high ion count rates (∼12 ions shot). By incorporating the recently developed native frames analysis approach into the three-dimensional covariance imaging procedure, contributions from three-body concerted and sequential fragmentation mechanisms can be isolated. The angular distribution of the fragment ions is much more complex than in previously reported studies for triatomic polycations, and differs substantially between the two isomeric species. With support of simple simulations of the dissociation channels of interest, detailed physical insights into the fragmentation dynamics are obtained, including how the initial dissociation step in a sequential mechanism influences rovibrational dynamics in the metastable intermediate ion and how signatures of this nuclear motion manifest in the measured signals.

摘要

我们展示了一项实验性离子成像研究的结果,该研究针对1-碘丙烷和2-碘丙烷在与光子能量为95 eV的极紫外飞秒强激光脉冲相互作用后的碎片化动力学。使用协方差成像分析,在相对较高的离子计数率(约每脉冲12个离子)下,可以分离并详细研究所得多阳离子的一系列观察到的碎片化途径。通过将最近开发的本征帧分析方法纳入三维协方差成像过程,可以分离三体协同和连续碎片化机制的贡献。碎片离子的角分布比先前报道的三原子多阳离子研究更为复杂,并且在两种异构物种之间存在显著差异。在对感兴趣的解离通道进行简单模拟的支持下,获得了对碎片化动力学的详细物理见解,包括连续机制中的初始解离步骤如何影响亚稳中间离子的振转动力学,以及这种核运动的特征如何在测量信号中体现。

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