{"title":"相互关联。","authors":"Francesco A Evangelista","doi":"10.1021/acs.jctc.5c00766","DOIUrl":null,"url":null,"abstract":"<p><p>Quantifying correlation and complexity in quantum many-body states is central to advancing theoretical and computational chemistry, physics, and quantum information science. This work introduces a novel framework, <i>mutual correlation</i>, based on the Frobenius norm squared of the two-body reduced density matrix cumulant. Through systematic partitioning of the cumulant norm, mutual correlation quantifies nonadditive correlations among interacting subsystems. To assess the ability of mutual correlation to identify orbital interactions, we performed benchmark studies on model systems, including H<sub>10</sub>, N<sub>2</sub>, and <i>p</i>-benzyne, and performed a formal and numerical comparison with orbital mutual information. Maximally correlated orbitals, obtained by maximizing a nonlinear cost function of the mutual correlation, are also considered to identify a basis-independent partitioning of correlation. This study suggests that mutual correlation is a broadly applicable metric, useful in active space selection and the interpretation of electronic states.</p>","PeriodicalId":45,"journal":{"name":"Journal of Chemical Theory and Computation","volume":" ","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mutual Correlation.\",\"authors\":\"Francesco A Evangelista\",\"doi\":\"10.1021/acs.jctc.5c00766\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Quantifying correlation and complexity in quantum many-body states is central to advancing theoretical and computational chemistry, physics, and quantum information science. This work introduces a novel framework, <i>mutual correlation</i>, based on the Frobenius norm squared of the two-body reduced density matrix cumulant. Through systematic partitioning of the cumulant norm, mutual correlation quantifies nonadditive correlations among interacting subsystems. To assess the ability of mutual correlation to identify orbital interactions, we performed benchmark studies on model systems, including H<sub>10</sub>, N<sub>2</sub>, and <i>p</i>-benzyne, and performed a formal and numerical comparison with orbital mutual information. Maximally correlated orbitals, obtained by maximizing a nonlinear cost function of the mutual correlation, are also considered to identify a basis-independent partitioning of correlation. This study suggests that mutual correlation is a broadly applicable metric, useful in active space selection and the interpretation of electronic states.</p>\",\"PeriodicalId\":45,\"journal\":{\"name\":\"Journal of Chemical Theory and Computation\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2025-07-29\",\"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://doi.org/10.1021/acs.jctc.5c00766\",\"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://doi.org/10.1021/acs.jctc.5c00766","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Quantifying correlation and complexity in quantum many-body states is central to advancing theoretical and computational chemistry, physics, and quantum information science. This work introduces a novel framework, mutual correlation, based on the Frobenius norm squared of the two-body reduced density matrix cumulant. Through systematic partitioning of the cumulant norm, mutual correlation quantifies nonadditive correlations among interacting subsystems. To assess the ability of mutual correlation to identify orbital interactions, we performed benchmark studies on model systems, including H10, N2, and p-benzyne, and performed a formal and numerical comparison with orbital mutual information. Maximally correlated orbitals, obtained by maximizing a nonlinear cost function of the mutual correlation, are also considered to identify a basis-independent partitioning of correlation. This study suggests that mutual correlation is a broadly applicable metric, useful in active space selection and the interpretation of electronic states.
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.