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Interplay between electronic correlation and metal-ligand delocalization in the spectroscopy of transition metal compounds: case study on a series …

A new interesting article has been published in J Chem Theory Comput. 2018 Oct 22. doi: 10.1021/acs.jctc.8b00591. [Epub ahead of print] and titled:

Interplay between electronic correlation and metal-ligand delocalization in the spectroscopy of transition metal compounds: case study on a series …

Authors of this article are:

Giner E, Tew D, Garniron Y, Alavi A.

A summary of the article is shown below:

We present a comprehensive theoretical study of the physical phenomena that determine the relative energies of three of the lowest electronic states of each of the square-planar copper complexes $cucl$, $cunh$ and $cuwater$, and present a detailed analysis of the extent to which truncated configuration interaction (CI) and coupled cluster (CC) theories succeed in predicing the excitation energies. We find that ligand-metal charge transfer (CT) single excitations play a crucial role in the correct determination of the properties of these systems, even though the first impact of these CT on the energetics of these systems appears at fourth order in perturbation theory. We provide a minimal selected CI space for describing these systems with multi-reference theories and use a high-order perturbation theory analysis within this space to derive a simple and general physical picture for the LMCT process. We find that CCSD energy differences agree very well with near full CI values even though the $D_1$ diagnostics are large, which casts doubt on the usefulness of singles-amplitude based multi-reference diagnostics. CISD severely underestimates the excitation energies and the failure is a direct consequence of the size-inconsisency errors in CISD. Finally, we present reference values for the energy differences computed using explicitly correlated CCSD(T) and BCCD(T) theory.

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