A luminescent cyclometalated gold(III) complex [Au(C^ N^ N-dpp)Cl] (X) (1a, X = C7H7SO3; 1b, X = ClO4; where C^N^N = C-anion of 2,9-diphenyl-1,10-phenanthroline) was prepared and characterized by X-ray crystal analysis. Crystal data for [Au(C24H15N2)Cl](C7H7SO3)‧1/2CH3OH: mol wt 950.97, triclinic, space group [format omited] (No. 2), a = 9.690(3) Å, b = 10.799(2) Å, c = 15.934(3) Å, α = 74.20(1)°, β = 85.59(2)°, γ = 68.72(2)°, V= 1494.6 Å3, Z = 2. In the solid state, two [Au(C^N^N-dpp)Cl]+cations stack on each other with an intermolecular Au‧‧‧Au separation of 3.6 Å. Complexes la and lb are emissive in fluid solutions with quantum yields of ~ 10-4and lifetimes of 0.4–0.7 μs. The emission spectra of 1a and 1b are quite insensitive to solvents (521–670 nm) and display vibrational progression of ~ 1400 cm-1. The small spectral red-shift (1400 cm-1) of the emission of 1a from that of free ligand (dpp) suggests a metal-perturbed intraligand emissive state. The estimated excited state reduction potential E° *(AuIII/II) of 2.2 V (vs NHE) suggests that [Au(C^ N^ N-dpp)Cl]+is a strong photo-oxidant. This photooxidizing property has been demonstrated with the formation of the 1,4-dimethoxybenzene cation radical (DMB•+) upon UV-vis irradiation of an acetonitrile solution of [Au(C^N^N-dpp)Cl]+and DMB and visible light (λ = 406 nm) induced reduction of the gold(III) complex by tetrahydrofuran.
|Number of pages||7|
|Publication status||Published - 1 Mar 1994|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry