Abstract

AbstractNovel diruthenium(III) complexes of general formula [RuIII2(μ‐O)‐(μ‐CH3CO2)2(bpy)2L2](PF6)2 (L: tetrahydrothiophene, (3); 4,5‐dihydro‐3(2H)‐thiophenone, (4); thiazole, (5); 4‐methylthiazole, (6); bpy: 2,2’‐bipyridine), which contain sulfur or nitrogen donor ligands at the trans‐to‐oxido sites, have been synthesized. The Ru–S bond distance in 4 is determined by X‐ray crystallography to be 2.447 Å, and the Ru–N(trans‐to‐oxido) length in 5 (2.157 Å) is similar to that of the complex having pyridine as the L ligand, 1. The spectroscopic properties and redox behavior of the complexes bearing sulfur donor ligands have been investigated and compared with those containing nitrogen donor ligands. The potentials of the redox couples of Ru2II,III/Ru2III,III and Ru2III,III/Ru2III,IV for 3 and 4 shift to positive regions compared with those of complexes with nitrogen donor ligands, 1, 5 and 6. The density functional theory (DFT) calculations reveal that the contribution of the trans ligand to the visible absorption is larger in 3 and 4 than in 1, 2 (L: CH3CN), 5 and 6.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.