Related Experiment Video
Updated: May 29, 2026

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry
Published on: April 8, 2020
On the Equivalence of Two-Point Basis-Set Extrapolations and Robust Parameterization for Coupled-Cluster and
1Computational Chemistry Unit, Department of Chemical Research Support, Weizmann Institute of Science, Rehovot 7610001, Israel.
None:
Basis-set extrapolation (BSE) to the complete basis set (CBS) limit is a cornerstone of several high-accuracy thermochemical computational schemes. In this study, we assess some of the approximations that are commonly made when using BSE. While the extrapolation parameters are typically fitted using coupled-cluster methods, there are cases where these same parameters are applied to other computational methods. While there can be significant differences in the fitted parameters, when applied to two benchmark datasets the difference in performance between the coupled-cluster and method-specific fitted parameters is small. While there are a number of schemes for two-basis-set extrapolations to the CBS limit, it is shown that three common extrapolations─exponential, exponential-square root, and inverse power─reduce to a Schwenke-style correction to the larger basis set of the scaled difference between two sequential basis sets (ECBS = En + f·(En - En-1)). Moreover, this reduction means that the differences between the methods is mathematically meaningless, and given the extrapolation parameter of one scheme one can find both the Schwenke-type extrapolation factor f and the extrapolation factors of the other two schemes and vice versa. Finally, Schwenke-type two-point extrapolation parameters are given for a selection of basis sets for coupled-cluster and selected double-hybrid density functional theory exchange-correlation functionals.
More Related Videos
08:04Excitonic Hamiltonians for Calculating Optical Absorption Spectra and Optoelectronic Properties of Molecular Aggregates and Solids
Published on: May 27, 2020
08:0915N CPMG Relaxation Dispersion for the Investigation of Protein Conformational Dynamics on the µs-ms Timescale
Published on: April 19, 2021
Related Concept Videos
Hybridization of Atomic Orbitals II
¹H NMR: Long-Range Coupling
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene π orbitals.
Hybridization of Atomic Orbitals I
¹H NMR: Interpreting Distorted and Overlapping Signals
As Δν decreases and the signals move closer, the doublets appear increasingly distorted. The intensities of the inner lines increase at the cost of those of the outer lines as the signals are slanted or...
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the involved orbitals. The...
Valence Bond Theory and Hybridized Orbitals
A σ bond (single bond in a Lewis structure) is a covalent bond in which the electron density is...