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钾碰撞中电子转移诱导的氟烷选择性键断裂

Selective bond breaking of halothane induced by electron transfer in potassium collisions.

作者信息

Lozano A I, Maioli L S, Pamplona B, Romero J, Mendes M, Ferreira da Silva F, Kossoski F, Probst M, Süβ D, Bettega M H F, García G, Limão-Vieira P

机构信息

Atomic and Molecular Collisions Laboratory, CEFITEC, Department of Physics, Universidade NOVA de Lisboa, 2829-516 Caparica, Portugal.

出版信息

Phys Chem Chem Phys. 2020 Nov 7;22(41):23837-23846. doi: 10.1039/d0cp02570d. Epub 2020 Oct 19.

DOI:10.1039/d0cp02570d
PMID:33073277
Abstract

We present novel experimental results of negative ion formation of halothane (CHBrClF) upon electron transfer from hyperthermal neutral potassium atoms (K°) in the collision energy range of 8-1000 eV. The experiments were performed in a crossed molecular beam setup allowing a comprehensive analysis of the time-of-flight (TOF) mass negative ions fragmentation pattern and a detailed knowledge of the collision dynamics in the energy range investigated. Such TOF mass spectra data show that the only negative ions formed are Br, Cl and F, with a strong energy dependence in the low-energy collision region, with the bromine anion being the most abundant and sole fragment at the lowest collision energy probed. In addition, potassium cation (K) energy loss spectra in the forward scattering direction were obtained in a hemispherical energy analyser at different K° impact energies. In order to support our experimental findings, ab initio quantum chemical calculations have been performed to help interpret the role of the electronic structure of halothane. Potential energy curves were obtained along the C-X (X = Br, Cl) coordinate to lend support to the dissociation processes yielding anion formation.

摘要

我们展示了在8 - 1000 eV碰撞能量范围内,超热中性钾原子(K°)进行电子转移时,氟烷(CHBrClF)形成负离子的全新实验结果。实验在交叉分子束装置中进行,可对飞行时间(TOF)质谱负离子碎裂模式进行全面分析,并详细了解所研究能量范围内的碰撞动力学。此类TOF质谱数据表明,形成的唯一负离子是Br、Cl和F,在低能碰撞区域具有强烈的能量依赖性,在所探测的最低碰撞能量下,溴阴离子是最丰富且唯一的碎片。此外,在不同K°碰撞能量下,利用半球形能量分析仪获得了前向散射方向的钾阳离子(K)能量损失谱。为支持我们的实验结果,已进行了从头算量子化学计算,以帮助解释氟烷电子结构的作用。沿着C - X(X = Br、Cl)坐标获得了势能曲线,以支持产生阴离子形成的解离过程。

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