Spectroscopic signatures of ligand field states in {Ru(II)(imine)} complexes

• Published in: Dalton transactions : an international journal of inorganic chemistry Vol. 45; no. 13; pp. 5464 - 5475
• Main Authors: Cadranel, Alejandro, Pieslinger, German E, Tongying, Pornthip, Kuno, Masaru K, Baraldo, Luis M, Hodak, José H
• Format: Journal Article
• Language: English
• Published: England 01.01.2016
• Subjects: Absorption; Ligands; Pyridines; Ruthenium; Signatures; Spectroscopy; Thiocyanates
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/c5dt04332h

Ligand field (LF) states have been present in discussions on the photophysics and photochemistry of ruthenium-iminic chromophores for decades, although there is very little documented direct evidence of them. We studied the picosecond transient absorption (TA) spectroscopy of four {Ru(II)(imine)} complexes that respond to the formula trans-[Ru(L)4(X)2], where L is either pyridine (py) or 4-methoxypyridine (MeOpy) and X is either cyanide or thiocyanate. Dicyano compounds behave as most ruthenium polypyridines and their LF states remain silent. In contrast, in the dithiocyanate complexes we found clear spectroscopic evidence of the participation of LF states in the MLCT decay pathway. These states are of donor and acceptor character simultaneously and this is manifested in the presence of MLCT and LMCT transient absorption bands of similar energy. Spectroelectrochemical techniques supported the interpretation of the absorption features of MLCT states, and DFT methods helped to assign their spectroscopic signatures and provided strong evidence on the nature of LF states.