分子响应特性,电子相关,和量子纠缠

IF 5.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Daniel F. E. Bajac, Andy D. Zapata Escobar and Gustavo A. Aucar*, 
{"title":"分子响应特性,电子相关,和量子纠缠","authors":"Daniel F. E. Bajac,&nbsp;Andy D. Zapata Escobar and Gustavo A. Aucar*,&nbsp;","doi":"10.1021/acs.jctc.4c0148110.1021/acs.jctc.4c01481","DOIUrl":null,"url":null,"abstract":"<p >There is an ever-increasing interest in studying the properties and main characteristics of entangled atomic and molecular quantum states. As a matter of fact, merging two different areas of research like information theory and quantum physics/chemistry gives new insights to understand from a different framework some of the most basic quantum phenomena. In line with this, the calculation and analysis of the electronic origin of some molecular response properties, like the NMR <i>J</i>-coupling, require the consideration of electron correlation (quantum and classical) and the fact that some response properties could arise from nonlocal interactions. In the case of <i>J</i>-couplings, the change of energy due to the flip-flop of one nuclear magnetic dipole moment that is influenced (directly or indirectly) by the flip-flop of another one has its correlate in the NMR spectra. Besides, from a theoretical perspective, this <i>J</i>-coupling interaction is described and calculated using the electronic framework. In the past few years, we started the development of a theory that introduces a new kind of entanglement that occurs among pairs of excitations of molecular orbitals (MOs). In this work, we give the most general expression of such a theory showing that the entanglement is not dependent on the spin-dependence of the external perturbations. We applied this theory to the analysis of vicinal <i>J</i>-couplings between fluorine nuclei in 1,2-difluoroethane, and we show that there is an entanglement between electron-spin-dependent mechanisms (known as FC and SD) and electron-spin-independent mechanisms (PSO). This entanglement remains lightly dependent on the degree of electron correlation considered (up to the higher RPA level), which confirms previous explanations regarding the physical origin of the empirical Karplus rule. Besides, we show new results for the vicinal <i>J</i>(<i>H</i>, <i>H</i>) coupling in ethane that confirm a direct relationship between the Karplus rule and the entanglement among some coupling pathways that contain a couple of excitations of MOs that are close to the coupled nuclei.</p>","PeriodicalId":45,"journal":{"name":"Journal of Chemical Theory and Computation","volume":"21 9","pages":"4674–4687 4674–4687"},"PeriodicalIF":5.5000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular Response Properties, Electron Correlation, and Quantum Entanglement\",\"authors\":\"Daniel F. E. Bajac,&nbsp;Andy D. Zapata Escobar and Gustavo A. Aucar*,&nbsp;\",\"doi\":\"10.1021/acs.jctc.4c0148110.1021/acs.jctc.4c01481\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >There is an ever-increasing interest in studying the properties and main characteristics of entangled atomic and molecular quantum states. As a matter of fact, merging two different areas of research like information theory and quantum physics/chemistry gives new insights to understand from a different framework some of the most basic quantum phenomena. In line with this, the calculation and analysis of the electronic origin of some molecular response properties, like the NMR <i>J</i>-coupling, require the consideration of electron correlation (quantum and classical) and the fact that some response properties could arise from nonlocal interactions. In the case of <i>J</i>-couplings, the change of energy due to the flip-flop of one nuclear magnetic dipole moment that is influenced (directly or indirectly) by the flip-flop of another one has its correlate in the NMR spectra. Besides, from a theoretical perspective, this <i>J</i>-coupling interaction is described and calculated using the electronic framework. In the past few years, we started the development of a theory that introduces a new kind of entanglement that occurs among pairs of excitations of molecular orbitals (MOs). In this work, we give the most general expression of such a theory showing that the entanglement is not dependent on the spin-dependence of the external perturbations. We applied this theory to the analysis of vicinal <i>J</i>-couplings between fluorine nuclei in 1,2-difluoroethane, and we show that there is an entanglement between electron-spin-dependent mechanisms (known as FC and SD) and electron-spin-independent mechanisms (PSO). This entanglement remains lightly dependent on the degree of electron correlation considered (up to the higher RPA level), which confirms previous explanations regarding the physical origin of the empirical Karplus rule. Besides, we show new results for the vicinal <i>J</i>(<i>H</i>, <i>H</i>) coupling in ethane that confirm a direct relationship between the Karplus rule and the entanglement among some coupling pathways that contain a couple of excitations of MOs that are close to the coupled nuclei.</p>\",\"PeriodicalId\":45,\"journal\":{\"name\":\"Journal of Chemical Theory and Computation\",\"volume\":\"21 9\",\"pages\":\"4674–4687 4674–4687\"},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2025-04-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Theory and Computation\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jctc.4c01481\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Theory and Computation","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jctc.4c01481","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

人们对纠缠原子和分子量子态的性质和主要特征的研究日益感兴趣。事实上,将信息理论和量子物理/化学这两个不同的研究领域结合起来,可以从不同的框架中理解一些最基本的量子现象。据此,计算和分析一些分子响应性质的电子起源,如核磁共振j耦合,需要考虑电子相关(量子和经典),以及一些响应性质可能来自非局部相互作用的事实。在j耦合的情况下,由于一个核磁偶极矩的触发器(直接或间接)受到另一个核磁偶极矩触发器的影响而引起的能量变化在核磁共振谱中具有相关性。此外,从理论角度出发,利用电子框架对j耦合相互作用进行了描述和计算。在过去的几年里,我们开始发展一种理论,引入了一种新的纠缠,这种纠缠发生在分子轨道(MOs)的激发对之间。在这项工作中,我们给出了这种理论的最一般的表达,表明纠缠不依赖于外部扰动的自旋依赖性。我们将这一理论应用于1,2-二氟乙烷中氟核之间的邻j耦合分析,并表明在电子自旋依赖机制(称为FC和SD)和电子自旋独立机制(PSO)之间存在纠缠。这种纠缠仍然轻微依赖于所考虑的电子相关程度(直到更高的RPA水平),这证实了先前关于经验Karplus规则的物理起源的解释。此外,我们还展示了乙烷中相邻J(H, H)耦合的新结果,证实了Karplus规则与一些耦合路径之间的纠缠之间的直接关系,这些耦合路径包含一对靠近耦合核的MOs的激发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular Response Properties, Electron Correlation, and Quantum Entanglement

Molecular Response Properties, Electron Correlation, and Quantum Entanglement

There is an ever-increasing interest in studying the properties and main characteristics of entangled atomic and molecular quantum states. As a matter of fact, merging two different areas of research like information theory and quantum physics/chemistry gives new insights to understand from a different framework some of the most basic quantum phenomena. In line with this, the calculation and analysis of the electronic origin of some molecular response properties, like the NMR J-coupling, require the consideration of electron correlation (quantum and classical) and the fact that some response properties could arise from nonlocal interactions. In the case of J-couplings, the change of energy due to the flip-flop of one nuclear magnetic dipole moment that is influenced (directly or indirectly) by the flip-flop of another one has its correlate in the NMR spectra. Besides, from a theoretical perspective, this J-coupling interaction is described and calculated using the electronic framework. In the past few years, we started the development of a theory that introduces a new kind of entanglement that occurs among pairs of excitations of molecular orbitals (MOs). In this work, we give the most general expression of such a theory showing that the entanglement is not dependent on the spin-dependence of the external perturbations. We applied this theory to the analysis of vicinal J-couplings between fluorine nuclei in 1,2-difluoroethane, and we show that there is an entanglement between electron-spin-dependent mechanisms (known as FC and SD) and electron-spin-independent mechanisms (PSO). This entanglement remains lightly dependent on the degree of electron correlation considered (up to the higher RPA level), which confirms previous explanations regarding the physical origin of the empirical Karplus rule. Besides, we show new results for the vicinal J(H, H) coupling in ethane that confirm a direct relationship between the Karplus rule and the entanglement among some coupling pathways that contain a couple of excitations of MOs that are close to the coupled nuclei.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Chemical Theory and Computation
Journal of Chemical Theory and Computation 化学-物理:原子、分子和化学物理
CiteScore
9.90
自引率
16.40%
发文量
568
审稿时长
1 months
期刊介绍: The Journal of Chemical Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere. Papers reporting new theories, methodology, and/or important applications in quantum electronic structure, molecular dynamics, and statistical mechanics are appropriate for submission to this Journal. Specific topics include advances in or applications of ab initio quantum mechanics, density functional theory, design and properties of new materials, surface science, Monte Carlo simulations, solvation models, QM/MM calculations, biomolecular structure prediction, and molecular dynamics in the broadest sense including gas-phase dynamics, ab initio dynamics, biomolecular dynamics, and protein folding. The Journal does not consider papers that are straightforward applications of known methods including DFT and molecular dynamics. The Journal favors submissions that include advances in theory or methodology with applications to compelling problems.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信