Capturing Re(i) in an neutral N,N,N pincer Scaffold and resulting enhanced absorption of visible light

Abstract

The organometallic and coordination chemistry of rhenium(I) has been largely restricted to bidentate α-diimine ligation and facial tricarbonyl coordination geometries. The thermal transformation of bidentate bis(imino)pyridine and bidentate terpyridine complexes at 200–240 °C under nitrogen led to a family of Re(I) pincer complexes [κ³-2,6-{ArNCMe}₂(NC₅H₃)]Re(CO)₂X (ArC₆H₅, Me₂C₆H₃, ⁱPr₂C₆H₃; X = Cl, Br) and (κ³-terpy)Re(CO)₂X (X = Cl, Br). The synthesis, single crystal X-ray structural and spectroscopic characterization of these eight species documents their Re coordination geometries and demonstrates the accessibility of such compounds. The basic photophysical features of these compounds show significant elaboration in both number and intensity of the d–π* transitions observed in the UV-vis spectra relative to the bidentate starting materials and these spectra were analyzed using time-dependent DFT computations.