María Menéndez-Herrero , Ángel Martín Pendás , X. Zhang (Editor)
{"title":"Persistence of atoms in molecules: there is room beyond electron densities","authors":"María Menéndez-Herrero , Ángel Martín Pendás , X. Zhang (Editor)","doi":"10.1107/S2052252524000915","DOIUrl":null,"url":null,"abstract":"<div><p>The 3<em>N</em>-dimensional maxima of the square of the wavefunction, the so-called Born maxima, show beyond doubt that the electronic structure of atoms persists in molecules, either in their original ground state or some low-lying excited state. The electron density is only a low-dimensional projection of this much richer landscape.</p></div><div><p>Evidence that the electronic structure of atoms persists in molecules to a much greater extent than has been usually admitted is presented. This is achieved by resorting to <em>N</em>-electron real-space descriptors instead of one- or at most two-particle projections like the electron or exchange-correlation densities. Here, the 3<em>N</em>-dimensional maxima of the square of the wavefunction, the so-called Born maxima, are used. Since this technique is relatively unknown to the crystallographic community, a case-based approach is taken, revisiting first the Born maxima of atoms in their ground state and then some of their excited states. It is shown how they survive in molecules and that, beyond any doubt, the distribution of electrons around an atom in a molecule can be recognized as that of its isolated, in many cases excited, counterpart, relating this fact with the concept of energetic promotion. Several other cases that exemplify the applicability of the technique to solve chemical bonding conflicts and to introduce predictability in real-space analyses are also examined.</p></div>","PeriodicalId":14775,"journal":{"name":"IUCrJ","volume":"11 2","pages":"Pages 210-223"},"PeriodicalIF":2.9000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10916289/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IUCrJ","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052252524000198","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The 3N-dimensional maxima of the square of the wavefunction, the so-called Born maxima, show beyond doubt that the electronic structure of atoms persists in molecules, either in their original ground state or some low-lying excited state. The electron density is only a low-dimensional projection of this much richer landscape.
Evidence that the electronic structure of atoms persists in molecules to a much greater extent than has been usually admitted is presented. This is achieved by resorting to N-electron real-space descriptors instead of one- or at most two-particle projections like the electron or exchange-correlation densities. Here, the 3N-dimensional maxima of the square of the wavefunction, the so-called Born maxima, are used. Since this technique is relatively unknown to the crystallographic community, a case-based approach is taken, revisiting first the Born maxima of atoms in their ground state and then some of their excited states. It is shown how they survive in molecules and that, beyond any doubt, the distribution of electrons around an atom in a molecule can be recognized as that of its isolated, in many cases excited, counterpart, relating this fact with the concept of energetic promotion. Several other cases that exemplify the applicability of the technique to solve chemical bonding conflicts and to introduce predictability in real-space analyses are also examined.
本文提出的证据表明,原子的电子结构在分子中的持续存在程度比通常所承认的要大得多。这是通过使用 N 电子实空间描述符而不是单粒子或最多双粒子投影(如电子或交换相关密度)来实现的。这里使用的是波函数平方的 3N 维最大值,即所谓的博恩最大值。由于晶体学界对这一技术相对陌生,因此采用了基于案例的方法,首先重温了原子基态下的博恩最大值,然后重温了原子的一些激发态。研究表明,它们是如何在分子中存活的,而且毫无疑问,分子中原子周围的电子分布可以被识别为其孤立的(在许多情况下是激发态)对应物的电子分布,并将这一事实与能量促进概念联系起来。此外,还研究了其他一些案例,这些案例说明了该技术在解决化学键冲突和在实际空间分析中引入可预测性方面的适用性。
期刊介绍:
IUCrJ is a new fully open-access peer-reviewed journal from the International Union of Crystallography (IUCr).
The journal will publish high-profile articles on all aspects of the sciences and technologies supported by the IUCr via its commissions, including emerging fields where structural results underpin the science reported in the article. Our aim is to make IUCrJ the natural home for high-quality structural science results. Chemists, biologists, physicists and material scientists will be actively encouraged to report their structural studies in IUCrJ.