Dual Emission of a Novel (P,N) Re-I Complex: A Computational and Experimental Study on [P,N-{(C6H5)(2)(C5H4N)P}Re(CO)(3)Br]

Pizarro, Nancy; Duque, Mario; Chamorro, Eduardo; Nonell, Santi; Manzur, Jorge; de la Fuente, Julio R.; Gunther, German; Cepeda-Plaza, Marjorie; Vega, Andres

Keywords: molecular-structures, electronic-structure, photophysical properties, rhenium(i) complexes, asymmetric catalysis, diimine complexes, excited singlet, transient-absorption, phosphine-ligands, LIGAND SUBSTITUTION-REACTIONS

Abstract

The spectroscopic, electrochemical, and photophysical properties of the new complex [P,N-{(C6H5)(2)(C5H4N)-P}Re(CO)(3)Br] are reported. The UV-vis spectrum in dichloromethane shows an absorption maximum centered at 315 rim and a shoulder at 350 nm. These absorption bands have been characterized to have MLCT character. Excitation at both wavelengths (maximum and shoulder) leads to an emission band centered at 550 nm. Cyclic voltammetry experiments show two ill-defined irreversible oxidation waves around +1.50 and 1.80 V that are assigned to Re-I/Re-II and Re-II/Re-III couples whereas an irreversible reduction signal centered at 1.80 V is :likewise assigned to a ligand reduction process. These results support the proposal of the MLCT nature of the states implied by the emission of the complex. The luminescent decay fits to a biexponential function, where the lifetimes and emission quantum yields are dependent on the solvent polarity. DFT calculations suggest that d pi -> pi*(pyridine) and d pi -> pi*(phenyl) excited states may account for the existence of two decay lifetimes.

Más información

Título de la Revista: JOURNAL OF PHYSICAL CHEMISTRY A
Volumen: 119
Número: 17
Editorial: AMER CHEMICAL SOC
Fecha de publicación: 2016
Página de inicio: 3929
Página final: 3935
Idioma: en
DOI:

10.1021/jp512614w

Notas: WOS Core Collection ISI, SCOPUS