Abstract
Embedding techniques allow the efficient description of correlations within localized fragments of large molecular systems while accounting for their environment at a lower level of theory. We introduce FragPT2: a novel embedding framework that addresses multiple interacting active fragments. Fragments are assigned separate active spaces, constructed by localizing canonical molecular orbitals. Each fragment is then solved with a multireference method, self-consistently embedded in the mean field from other fragments. Finally, interfragment correlations are reintroduced through multireference perturbation theory. Our framework provides an exhaustive classification of interfragment interaction terms, offering a tool to analyze the relative importance of various processes such as dispersion, charge transfer, and spin exchange. We benchmark FragPT2 on challenging test systems, including N2 dimers, multiple aromatic dimers, and butadiene. We demonstrate that our method can be successful even for fragments defined by cutting through a covalent bond.
| Original language | English |
|---|---|
| Pages (from-to) | 655-669 |
| Number of pages | 15 |
| Journal | JCTC : Journal of chemical theory and computation |
| Volume | 21 |
| Issue number | 2 |
| Early online date | 10 Jan 2025 |
| DOIs | |
| Publication status | Published - 28 Jan 2025 |
Bibliographical note
Publisher Copyright:© 2025 The Authors. Published by American Chemical Society.
Funding
We thank Dr. Arno Fo\u0308rster, Sarathchandra Khandavilli, and Detlef Hohl for stimulating discussions. We thank Seenivasan Hariharan and Matthias Degroote for useful feedback. We acknowledge support from Shell Global Solutions BV.
| Funders | Funder number |
|---|---|
| Shell Global Solutions BV |