Structural and Optical Properties of Metal-Nitrosyl Complexes

• Main Authors: Chantal Daniel, Christophe Gourlaouen
• Format: Article
• Language: English
• Published: MDPI AG 2019-10-01
• Series: Molecules
• Subjects: nitrosyl complexes; electronic structure; conformational isomerism; density functional theory; wavefunction approach
• Online Access: https://www.mdpi.com/1420-3049/24/20/3638

The electronic, structural and optical properties (including Spin−Orbit Coupling) of metal nitrosyl complexes [M(CN)₅(NO)]^2− (M = Fe, Ru or Os) are investigated by means of Density Functional Theory, TD-DFT and MS-CASPT2 based on an RASSCF wavefunction. The energy profiles connecting the N-bound (η¹-N), O-bound (η¹-O) and side-on (η²-NO) conformations have been computed at DFT level for the closed shell singlet electronic state. For each structure, the lowest singlet and triplet states have been optimized in order to gain insight into the energy profiles describing the conformational isomerism in excited states. The energetics of the three complexes are similar—with the N-bound structure being the most stable—with one exception, namely the triplet ground state of the O-bound isomer for the iron complex. The conformation isomerism is highly unfavorable in the S₀ electronic state with the occurrence of two energy barriers higher than 2 eV. The lowest bands of the spectra are assigned to MLCT_NO/LLCT_NO transitions, with an increasing MLCT character going from iron to osmium. Two low-lying triplet states, T1 (MLCT_NO/LLCT_NO) and T2 (MLCT_NO/IL_NO), seem to control the lowest energy profile of the excited-state conformational isomerism.