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Rovibrational bound states of SO2 isotopologues. I: Total angular momentum J=0-10

机译:SO2同位素的鲁释结合状态。 I:总角度j = 0-10

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Isotopic variation of the rovibrational bound states of SO2 for the four stable sulfur isotopes S-32-34,S-36 is investigated in comprehensive detail. In a two-part series, we compute the low-lying energy levels for all values of total angular momentum in the range J = 0-20. All rovibrational levels are computed, to an extremely high level of numerical convergence. The calculations have been carried out using the ScalIT suite of parallel codes. The present study (Paper I) examines the J = 0-10 rovibrational levels, providing unambiguous symmetry and rovibrational label assignments for each computed state. The calculated vibrational energy levels exhibit very good agreement with previously reported experimental and theoretical data. Rovibrational energy levels, calculated without any Coriolis approximations, are reported here for the first time. Among other potential ramifications, this data will facilitate understanding of the origin of mass-independent fractionation of sulfur isotopes in the Archean rock record-of great relevance for understanding the "oxygen revolution''. (C) 2015 Elsevier B.V. All rights reserved.
机译:在综合细节中研究了四个稳定的硫同位素S-32-34,S-36的SO2的振动结合状态的同位素变化。在两部分系列中,我们计算j = 0-20范围内的总角动量的所有值的低位能量水平。所有振动水平都被计算为极高的数值趋同。已经使用Scalit Suite的并行代码进行了计算。本研究(纸张I)检查了j = 0-10 rovibriation水平,为每个计算状态提供明确的对称性和rovibriation标签分配。计算出的振动能量水平与先前报道的实验和理论数据表现出非常良好的一致性。在没有任何科里奥利近似的情况下计算的振动能量水平在此首次报告。在其他潜在的影响之外,这种数据将促进在Archean Rock记录中对硫磺同位素的群体同位素的群众分级的起源 - 了解“氧气革命”。(c)2015年Elsevier B.V.保留所有权利。

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