“…The respective 1 H peaks were shifted to lower frequency by ca 0.6–1.3 ppm (LL bpy ) or ca 0.9–1.55 ppm (LL phen ), either in cases when exact Δ 1H coord coordination shifts could be determined (i.e. when the δ 1H chemical shifts for the complex and the ligand concerned the same solvent: [Fe(4,4 ′ ‐dimethoxy‐bpy) 3 ] 2+ ,48 [Fe(5,5 ′ ‐diamino‐bpy) 3 ] 2+ ,49, 50 [Ru(4,4 ′ ‐dimethyl‐bpy) 3 ] 2+ ,2 [Ru(5,5 ′ ‐dimethyl‐bpy) 3 ] 2+ ,2 [Ru(bpy‐4,4′‐dicarboxylate) 3 ] 4− ,51, 52 [Ru(bpy‐5,5 ′ ‐dicarboxylate) 3 ] 4− ,53 [Ru(bpy‐4,4 ′ ‐disulfonate) 3 ] 4− ,54 [Os(bpy‐4,4 ′ ‐dicarboxylate) 3 ] 4− 52 and [Fe(4,7‐diphenyl‐phen) 3 ] 2+ ,55 [Ru(4,7‐diphenyl‐phen) 3 ] 2+ 56) or when they were evaluated only approximately (due to the change of solvent: [Fe(4,4 ′ ‐dimethyl‐bpy) 3 ] 2+ ,57 [Ru(4,4 ′ ‐di‐ tert ‐butyl‐bpy) 3 ] 2+ ,29, 58 [Ru(4,4 ′ ‐dichloro‐bpy) 3 ] 2+ ,29 [Ru(4,7‐dichloro‐phen) 3 ] 2+ ,59 [Os(4,7‐dimethyl‐phen) 3 ] 2+ ,31 [Os(5,6‐dimethyl‐phen) 3 ] 2+ 31).…”