LAUSR

Abstract While copper(I)-bis(diimine) complexes [CuI(L)2]+ are considered as potent substitutes for [RuII(bpy)3]2+, they exhibit low molar extinction coefficients with respect to ruthenium parent analogues. One interesting possibility to improve the light collection ability of [CuI(L)2]+ consists in increasing the length of the Cu-L dipole. In order to achieve this goal, we propose in this contribution to fuse aromatic rings onto the 2,9-di-nbutyl-1,10-phenanthroline core and examine how the properties of the corresponding copper(I) complexes are impacted. Electrochemical, absorption and emission properties are assessed; rewardingly, the envisioned approach was successful since extinction coefficients above 10,000 M−1·cm−1 were measured. All copper(I) complexes remain photoluminescent, with emission maxima greatly varying from 725 to 815 nm, strongly affected by the molecular structures. A rationale to explain the variations of the emission quantum yields is proposed.