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Solvent effects in positronium complex formation and the bubble model

机译:正电子配合物形成中的溶剂效应和气泡模型

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The formation of positronium-acceptor complexes (Ps-Ac) with nitro aromatics and quinone has attracted much attention. The dependence of such reactions on temperature and on the nature of the solvent is sometimes discussed within the ambit of the bubble model of Ps in liquids. However, the description generally adopted is that of a sharp bubble boundary which is not only unrealistic as a liquid interface but has also been shown recently, through a series of papers by the present authors, to be in contradiction with experimental observations. An explanation is sought for the observed occurrence of both Arrhenius and anti-Arrhenius temperature dependence in the reaction rate for Ps-Ac complex formation seen over different temperature regimes in terms of the Kramers' turnover in the context of the improved version of the bubble model.
机译:与硝基芳香族化合物和醌形成正电子受体复合物(Ps-Ac)引起了广泛关注。有时在液体中Ps气泡模型的范围内讨论这种反应对温度和溶剂性质的依赖性。然而,通常采用的描述是尖锐的气泡边界,其不仅作为液体界面是不现实的,而且最近在本作者的一系列论文中已经表明与实验观察相矛盾。寻求一种解释,即在改进的气泡模型的背景下,根据克雷默斯的周转率,在不同温度范围内观察到的Ps-Ac配合物形成反应速率中观察到的阿伦尼乌斯和反阿伦尼乌斯温度依赖性的发生。

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