“…Furthermore, the electronic properties of both metal center and substituents onto the coordinated ligands allow easy addressable modulation of both redox and emission properties with luminescence colors adjustable over the entire visible spectrum and beyond. 2,8,9 Also, for derivatives based on the second and third row of the transition metal block, such as d 6 Ir(III), Ru(II), Os(II), and Re(I), as well as d 8 Pt(II) and Au(III), 18,19 and d 10 Au(I), 20,21 the sizeable spinorbit coupling effect induced by the heavy atom promotes fast and efficient intersystem crossing process between singletand triplet-manifold electronic states, yielding triplet excited states with radiative rate constants (k r ) capable of efficiently competing with the radiationless deactivation pathways (k nr ).…”