6,6′-Ditriphenylamine-2,2′-bipyridine: Coordination Chemistry and Electrochemical and Photophysical Properties

• Published in: Inorganic chemistry 2021-08, Vol.60 (16), p.11852-11865
• Main Authors: Ross, Daniel A. W, Mapley, Joseph I, Cording, Andrew P, Vasdev, Roan A. S, McAdam, C. John, Gordon, Keith C, Crowley, James D
• Format: Article
• Language: English
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.1c01435

A 2,2′-bipyridine with bulky triphenylamine substituents in the 6 and 6′ positions of the ligand (6,6′-ditriphenylamine-2,2′-bipyridine, 6,6′-diTPAbpy) was generated. Despite the steric bulk, the ligand readily formed bis­(homoleptic) complexes with copper­(I) and silver­(I) ions. Unfortunately, efforts to use the 6,6′-diTPAbpy system to generate heteroleptic [Cu­(6,6′-diTPAbpy)­(bpy)]+ complexes were unsuccessful with only the [Cu­(6,6′-diTPAbpy)2]­(PF6) complex observed. The 6,6′-diTPAbpy ligand could also be reacted with 6-coordinate metal ions that featured small ancillary ligands, namely, the [Re­(CO)3Cl] and [Ru­(CO)2Cl2] fragments. While the complexes could be formed in good yields, the steric bulk of the TPA units does alter the coordination geometry. This is most readily seen in the [(6,6′-diTPAbpy)­Re­(CO)3Cl] complex where the Re­(I) ion is forced to sit 23° out of the plane formed by the bpy unit. The electrochemical and photophysical properties of the family of compounds were also examined. 6,6′-diTPAbpy exhibits a strong ILCT absorption band (356 nm, 50 mM–1 cm–1) which displays a small increase in intensity for the homoleptic complexes ([Cu­(6,6′-diTPAbpy)2]+; 353 nm, 72 mM–1 cm–1, [Ag­(6,6′-diTPAbpy)2]+; 353 nm, 75 mM–1 cm–1), despite containing 2 equiv of the ligand, attributed to an increased dihedral angle between the TPA and bpy moieties. For the 6-coordinate complexes the ILCT band is further decreased in intensity and overlaps with MLCT bands, consistent with a further increased TPA-bpy dihedral angle. Emission from the 1ILCT state is observed at 436 nm (τ = 4.4 ns) for 6,6′-diTPAbpy and does not shift for the Cu, Ag, and Re complexes, although an additional 3MLCT emission is observed for [Re­(6,6′-diTPAbpy)­(CO)3Cl] (640 nm, τ = 13.8 ns). No emission was observed for [Ru­(6,6′-diTPAbpy)­(CO)2Cl2]. Transient absorption measurements revealed the population of a 3ILCT state for the Cu and Ag complexes (τ = 80 ns). All assignments were supported by TD-DFT calculations and resonance Raman spectroscopic measurements.