Non-Covalent Interactions Atlas Benchmark Data Sets 3: Repulsive Contacts

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F21%3A00541366" target="_blank" >RIV/61388963:_____/21:00541366 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00216208:11310/21:10442261

Výsledek na webu

<a href="https://doi.org/10.1021/acs.jctc.0c01341" target="_blank" >https://doi.org/10.1021/acs.jctc.0c01341</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/acs.jctc.0c01341" target="_blank" >10.1021/acs.jctc.0c01341</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Non-Covalent Interactions Atlas Benchmark Data Sets 3: Repulsive Contacts

Popis výsledku v původním jazyce

The new R739×5 data set from the Non-Covalent Interactions Atlas series (www.nciatlas.org) focuses on repulsive contacts in molecular complexes, covering organic molecules, sulfur, phosphorus, halogens, and noble gases. Information on the repulsive parts of the potential energy surface is crucial for the development of robust empirically parametrized computational methods. We use the new data set of highly accurate CCSD(T)/CBS interaction energies to test selected density functional theory (DFT) and semiempirical quantum-mechanical methods. The double-hybrid functionals were the best performing, with the revDSD-PBEP86-D3 being the most accurate DFT method, followed by the range-separated ωB97X functionals. Out of semiempirical methods, GFN2-xTB yielded the best results. On the example of the PM6 method, we analyze the source of error and its relation to the difficulties in the description of conformational energies, and we also devise an immediately applicable correction that fixes the most serious uncorrected issues previously encountered in practical calculations.

Název v anglickém jazyce

Non-Covalent Interactions Atlas Benchmark Data Sets 3: Repulsive Contacts

Popis výsledku anglicky

The new R739×5 data set from the Non-Covalent Interactions Atlas series (www.nciatlas.org) focuses on repulsive contacts in molecular complexes, covering organic molecules, sulfur, phosphorus, halogens, and noble gases. Information on the repulsive parts of the potential energy surface is crucial for the development of robust empirically parametrized computational methods. We use the new data set of highly accurate CCSD(T)/CBS interaction energies to test selected density functional theory (DFT) and semiempirical quantum-mechanical methods. The double-hybrid functionals were the best performing, with the revDSD-PBEP86-D3 being the most accurate DFT method, followed by the range-separated ωB97X functionals. Out of semiempirical methods, GFN2-xTB yielded the best results. On the example of the PM6 method, we analyze the source of error and its relation to the difficulties in the description of conformational energies, and we also devise an immediately applicable correction that fixes the most serious uncorrected issues previously encountered in practical calculations.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10403 - Physical chemistry

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2021

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of Chemical Theory and Computation

ISSN

1549-9618

e-ISSN

1549-9626

Svazek periodika

17

Číslo periodika v rámci svazku

3

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

14

Strana od-do

1548-1561

Kód UT WoS článku

000629135700022

EID výsledku v databázi Scopus

2-s2.0-85101810630