Journal
JOURNAL OF COMPUTATIONAL CHEMISTRY
Volume 42, Issue 10, Pages 688-698Publisher
WILEY
DOI: 10.1002/jcc.26489
Keywords
benchmark study; chalcogen bonds; coupled‐ cluster; density functional calculations; noncovalent interactions
Categories
Funding
- Conselho Nacional de Desenvolvimento Cientifico e Tecnologico
- Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior
- Fundacao de Amparo a Pesquisa do Estado de Minas Gerais
- Netherlands Organization for Scientific Research
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The study conducted a hierarchical benchmark and performance analysis of selenium bonds using ab initio and DFT methods. The results indicated that M06-2X, B3LYP, and M06 were the top-performing functionals, while BLYP-D3(BJ) and PBE showed poorer performance.
We have performed a hierarchical ab initio benchmark and DFT performance study of D(2)Ch center dot center dot center dot A(-) chalcogen bonds (Ch = S, Se; D, A = F, Cl). The ab initio benchmark study is based on a series of ZORA-relativistic quantum chemical methods [HF, MP2, CCSD, CCSD(T)], and all-electron relativistically contracted variants of Karlsruhe basis sets (ZORA-def2-SVP, ZORA-def2-TZVPP, ZORA-def2-QZVPP) with and without diffuse functions. The highest-level ZORA-CCSD(T)/ma-ZORA-def2-QZVPP counterpoise-corrected complexation energies (Delta E-CPC) are converged within 1.1-3.4 kcal mol(-1) and 1.5-3.1 kcal mol(-1) with respect to the method and basis set, respectively. Next, we used the ZORA-CCSD(T)/ma-ZORA-def2-QZVPP (Delta E-CPC) as reference data for analyzing the performance of 13 different ZORA-relativistic DFT approaches in combination with the Slater-type QZ4P basis set. We find that the three-best performing functionals are M06-2X, B3LYP, and M06, with mean absolute errors (MAE) of 4.1, 4.2, and 4.3 kcal mol(-1), respectively. The MAE for BLYP-D3(BJ) and PBE amount to 8.5 and 9.3 kcal mol(-1), respectively.
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