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Two-level stochastic search of low-energy conformers for molecular spectroscopy: implementation and validation of MM and QM models

机译:用于分子光谱的低能量符合子的两级随机搜索:MM和QM型号的实现和验证

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摘要

The search for stationary points in the molecular potential energy surfaces (PES) is a problem of increasing relevance in different fields of molecular sciences especially for large, flexible systems characterized by several large-amplitude internal motions leading to shallow minima with comparable energies and separated by small barriers. After structural biology and medicinal chemistry, also high-resolution molecular spectroscopy, which is the focus of our research activity, is nowadays shifting its attention to this kind of molecular systems. In such circumstances, accurate geometrical structures and relative stabilities of all these minima are a mandatory prerequisite for the vis-a-vis comparison between computed and experimental spectra. This task raises, in turn, the problem of the best compromise between accuracy and feasibility. In our opinion, a promising route is offered by a two-level stochastic search in which a relatively inexpensive MM or QM method is used in the initial search, followed by single point energy evaluation at a higher QM level of a relatively large number of low-energy structures in order to select a final short-list of candidates, whose geometries are fully optimized at the higher QM level. Finally, the relative stabilities and properties of the final short-list of energy minima can be computed by a state-of-the-art QM approach. This strategy defines a general two-level search/three-level evaluation approach, which can be finely tuned in terms of the accuracy of the sought results. Setup of the procedure, interface with a general purpose electronic structure code and validation of the most effective low-level methods for some representative molecular systems (three already well characterized and one new) ended up with a general, robust and user-friendly tool, which can be easily used and extended also by non-specialists to aid experimental spectroscopic studies.
机译:搜索分子潜在能量表面(PE)中的静止点是分子科学不同领域的相关性的问题,特别是对于具有几个大幅度内部运动的大型柔性系统,其具有可比能量和分离的浅极限。小障碍。在结构生物学和药用化学之后,也是我们研究活动的重点的高分辨率分子光谱,现在是对这种分子系统的关注。在这种情况下,所有这些最小值的精确的几何结构和相对稳定性是计算和实验光谱之间的Vis-A-Vis比较的强制性先决条件。反过来,这项任务又提出了准确性和可行性之间的最佳折衷问题。在我们看来,在初始搜索中使用了一个有希望的路线,其中使用了相对便宜的MM或QM方法,然后在较高数量的低电平的QM水平下单点能量评估 - 生物结构,以便选择最终的候选者的短期列表,其几何形状在较高的QM级别完全优化。最后,可以通过最先进的QM方法计算最终的能量最小值的相对稳定性和性质。该策略定义了一般的两级搜索/三级评估方法,可以在寻求结果的准确性方面精细调整。设置程序,具有通用电子结构代码的界面和验证一些代表分子系统的最有效的低级方法(三个已经很好的特征,一个新的)最终用了一般,强大,用户友好的工具,这可以通过非专家容易地使用和扩展,以帮助实验性光谱研究。

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