Extrapolating DFT Toward the Complete Basis Set Limit: Lessons from the PBE Family of Functionals

Author(s):  
Peter Kraus
2011 ◽  
Vol 49 (5) ◽  
pp. 231-236 ◽  
Author(s):  
Teobald Kupka ◽  
Michał Stachów ◽  
Marzena Nieradka ◽  
Jakub Kaminsky ◽  
Tadeusz Pluta ◽  
...  

2020 ◽  
Author(s):  
Ali Amir Khairbek

Standard enthalpies of hydrogenation of 29 unsaturated hydrocarbon compounds were calculated in the gas phase by CCSD(T) theory with complete basis set cc-pVXZ, where X = DZ, TZ, as well as by complete basis set limit extrapolation. Geometries of reactants and products were optimized at the M06-2X/6-31g(d) level. This M06-2X geometries were used in the CCSD(T)/cc-pVXZ//M06-2X/6-31g(d) and cc-pV(DT)Z extrapolation calculations. (MAD) the mean absolute deviations of the enthalpies of hydrogenation between the calculated and experimental results that range from 8.8 to 3.4 kJ mol−1 based on the Comparison between the calculation at CCSD(T) and experimental results. The MAD value has improved and decreased to 1.5 kJ mol−1 after using complete basis set limit extrapolation. The deviations of the experimental values are located inside the “chemical accuracy” (±1 kcal mol−1 ≈ ±4.2 kJ mol−1) as some results showed. A very good linear correlations between experimental and calculated enthalpies of hydro-genation have been obtained at CCSD(T)/cc-pVTZ//M06-2X/6-31g(d) level and CCSD(T)/cc-pV(DT)Z extrapolation levels (SD =2.11 and 2.12 kJ mol−1, respectively).


2019 ◽  
Vol 151 (2) ◽  
pp. 024104 ◽  
Author(s):  
Takuro Nudejima ◽  
Yasuhiro Ikabata ◽  
Junji Seino ◽  
Takeshi Yoshikawa ◽  
Hiromi Nakai

2020 ◽  
Vol 16 (7) ◽  
pp. 4399-4407
Author(s):  
Fabien Bruneval ◽  
Ivan Maliyov ◽  
Clovis Lapointe ◽  
Mihai-Cosmin Marinica

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