Reference Vertical Excitation Energies for Transition Metal Compounds

To enrich and enhance the diversity of the $\text{textsc}quest$ database of highly-accurate excitation energies [\href{https://doi.org/10.1002/wcms.1517}{Véril $\mathit{\text{et}}\mathit{\text{al.}}$, $\mathit{\text{WIREs}}\mathit{\text{Comput.}}\mathit{\text{Mol.}}\mathit{\text{Sci.}}$~$\mathbf{\text{11}}$, e1517 (2021)}], we report vertical transition energies in transition metal compounds. Eleven diatomic molecules with singlet or doublet ground state containing a fourth-row transition metal (\ce{CuCl}, \ce{CuF}, \ce{CuH}, \ce{ScF}, \ce{ScH}, \ce{ScO}, \ce{ScS}, \ce{TiN}, \ce{ZnH}, \ce{ZnO}, and \ce{ZnS}) are considered and the corresponding excitation energies are computed using high-level coupled-cluster (CC) methods, namely CC3, CCSDT, CC4, and CCSDTQ, as well as multiconfigurational methods such as CASPT2 and NEVPT2. In some cases, to provide more comprehensive benchmark data, we also provide full configuration interaction estimates computed with the $\mathit{\text{"Configuration}}\mathit{\text{Interaction}}\mathit{\text{using}}\mathit{\text{a}}\mathit{\text{Perturbative}}\mathit{\text{Selection}}\mathit{\text{made}}\mathit{\text{Iteratively"}}$ (CIPSI) method. Based on these calculations, theoretical best estimates of the transition energies are established in both the aug-cc-pVDZ and aug-cc-pVTZ basis sets. This allows us to accurately assess the performance of CC and multiconfigurational methods for this specific set of challenging transitions. Furthermore, comparisons with experimental data and previous theoretical results are also reported.