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首页> 外文期刊>International journal of mass spectrometry >Reactions between neutral molecules and cation-radicals in the gas-phase: Can protonation occur without proton transfer?
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Reactions between neutral molecules and cation-radicals in the gas-phase: Can protonation occur without proton transfer?

机译:气相中性分子与阳离子自由基之间的反应:如果没有质子转移,质子化会发生吗?

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Gas-phase collisions of Gly and Ala with free electrons were employed to form positive ions at well determined energies. At elevated molecular vapor pressure, protonated [Gly+H](+) and [Ala+H](+) ions were also observed. The appearance energies of [Gly+H](+) and [Ala+H](+) were both determined as 0.30 +/- 0.14 eV higher than the ionization energies of their M-center dot* congeners. Quantum chemical calculations predict proton transfer reactions rather than hydrogen atom abstraction reactions as the likely [M+H](+) forming method in our experiment. Microcanonical rate coefficient calculations using B3LYP/6-311++G(2d,p) frequencies and rotational constants, support abstraction of a C-alpha proton for glycine, whereas the C-terminal proton abstraction mechanism was found as being more favorable for alanine. Additionally, substantial immonium ion formation was observed at experimental energies identical to either the protonated product or cation radical for glycine and alanine, respectively. Theoretical barriers to M-center dot cation radical fragmentation to HRCNH2+ indicate that they are product-limited and that the glycine barriers are generally larger than those for alanine. (C) 2015 Elsevier B.V. All rights reserved.
机译:Gly和Ala与自由电子的气相碰撞被用来以确定的能量形成正离子。在升高的分子蒸气压下,还观察到质子化的[Gly + H](+)和[Ala + H](+)离子。 [Gly + H](+)和[Ala + H](+)的出现能均被确定为比其M中心点*同系物的电离能高0.30 +/- 0.14 eV。量子化学计算预测质子转移反应,而不是氢原子提取反应,这是我们实验中可能的[M + H](+)形成方法。使用B3LYP / 6-311 ++ G(2d,p)频率和旋转常数的微规范速率系数计算,支持甘氨酸的C-α质子的抽象,而C末端质子的抽象机理被认为对丙氨酸更有利。另外,在与甘氨酸和丙氨酸的质子化产物或阳离子自由基相同的实验能量下观察到大量的铵离子形成。 M-中心点阳离子自由基断裂为HRCNH2 +的理论壁垒表明它们是产物受限的,并且甘氨酸壁垒通常比丙氨酸壁垒更大。 (C)2015 Elsevier B.V.保留所有权利。

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