Literature DB >> 27537680

How Accurate Are the Minnesota Density Functionals for Noncovalent Interactions, Isomerization Energies, Thermochemistry, and Barrier Heights Involving Molecules Composed of Main-Group Elements?

Narbe Mardirossian1,2, Martin Head-Gordon1,2.   

Abstract

The 14 Minnesota density functionals published between the years 2005 and early 2016 are benchmarked on a comprehensive database of 4986 data points (84 data sets) involving molecules composed of main-group elements. The database includes noncovalent interactions, isomerization energies, thermochemistry, and barrier heights, as well as equilibrium bond lengths and equilibrium binding energies of noncovalent dimers. Additionally, the sensitivity of the Minnesota density functionals to the choice of basis set and integration grid is explored for both noncovalent interactions and thermochemistry. Overall, the main strength of the hybrid Minnesota density functionals is that the best ones provide very good performance for thermochemistry (e.g., M06-2X), barrier heights (e.g., M08-HX, M08-SO, MN15), and systems heavily characterized by self-interaction error (e.g., M06-2X, M08-HX, M08-SO, MN15), while the main weakness is that none of them are state-of-the-art for the full spectrum of noncovalent interactions and isomerization energies (although M06-2X is recommended from the 10 hybrid Minnesota functionals). Similarly, the main strength of the local Minnesota density functionals is that the best ones provide very good performance for thermochemistry (e.g., MN15-L), barrier heights (e.g., MN12-L), and systems heavily characterized by self-interaction error (e.g., MN12-L and MN15-L), while the main weakness is that none of them are state-of-the-art for the full spectrum of noncovalent interactions and isomerization energies (although M06-L is clearly the best from the four local Minnesota functionals). As an overall guide, M06-2X and MN15 are perhaps the most broadly useful hybrid Minnesota functionals, while M06-L and MN15-L are perhaps the most broadly useful local Minnesota functionals, although each has different strengths and weaknesses.

Entities:  

Year:  2016        PMID: 27537680     DOI: 10.1021/acs.jctc.6b00637

Source DB:  PubMed          Journal:  J Chem Theory Comput        ISSN: 1549-9618            Impact factor:   6.006


  29 in total

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Review 2.  Current Status of Quantum Chemical Studies of Cyclodextrin Host-Guest Complexes.

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4.  A GAP-GTPase-GDP-Pi Intermediate Crystal Structure Analyzed by DFT Shows GTP Hydrolysis Involves Serial Proton Transfers.

Authors:  Robert W Molt; Erika Pellegrini; Yi Jin
Journal:  Chemistry       Date:  2019-05-27       Impact factor: 5.236

5.  Stretching of cis-formic acid: warm-up and cool-down as molecular work-out.

Authors:  Katharina A E Meyer; Martin A Suhm
Journal:  Chem Sci       Date:  2019-05-16       Impact factor: 9.825

6.  The halogen bond with isocyano carbon reduces isocyanide odor.

Authors:  Alexander S Mikherdov; Alexander S Novikov; Vadim P Boyarskiy; Vadim Yu Kukushkin
Journal:  Nat Commun       Date:  2020-06-10       Impact factor: 14.919

7.  Comparison of computational chemistry methods for the discovery of quinone-based electroactive compounds for energy storage.

Authors:  Qi Zhang; Abhishek Khetan; Süleyman Er
Journal:  Sci Rep       Date:  2020-12-17       Impact factor: 4.379

8.  Bouncing off walls - widths of exit channels from shallow minima can dominate selectivity control.

Authors:  Mengna Bai; Zhitao Feng; Jun Li; Dean J Tantillo
Journal:  Chem Sci       Date:  2020-08-31       Impact factor: 9.825

9.  Encapsulation of Pollutant Gaseous Molecules by Adsorption on Boron Nitride Nanotubes: A Quantum Chemistry Study.

Authors:  Dolores García-Toral; Raúl Mendoza Báez; Jonatan I Sánchez S; Antonio Flores-Riveros; Gregorio H Cocoletzi; J F Rivas-Silva
Journal:  ACS Omega       Date:  2021-06-03

10.  Performance of Electronic Structure Methods for the Description of Hückel-Möbius Interconversions in Extended π-Systems.

Authors:  Tatiana Woller; Ambar Banerjee; Nitai Sylvetsky; Golokesh Santra; Xavier Deraet; Frank De Proft; Jan M L Martin; Mercedes Alonso
Journal:  J Phys Chem A       Date:  2020-03-13       Impact factor: 2.781

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