Abstract

Lanthanide(III) complexes with acetylacetonate and meso-tetraalkyltetrabenzoporphyrin (TATBP) having the general formula Ln ( TATBP )acac (where Ln = Tb , Dy , Ho , Er , Tm , Yb ; A = C 12 H 25; Hacac = acetylacetone) are reported. These compexes have been studied by elemental analyses, ultraviolet visible spectra, infrared spectra, molar conductance, 1 H NMR spectra, cyclic voltammetry, surface photovoltage spectroscopy (SPS), and luminescence spectroscopy. The infrared spectral bands of the ligand and complexes were assigned. In dimethylformamide (DMF), 0.1 M tetrabutylammonium perchlorate (TBAP), the synthesized TATBP exhibit two one-electron reversible redox reactions, and Ln(TATBP)acac shows three redox reactions respectively, within the accessible potential window of the solvent. The absorption bands of the complexes appear in the range 431-433 (Soret band), 578-580 (Q band) and 627-631 (Q band) nm. The photovoltaic properties and charge transfer process of these compounds were investigated by surface photovoltage spectroscopy (SPS) and electric-field-induced surface photovoltage spectroscopy (EFISPS) techniques, which reveal that the ligand TATBP and the complexes Er(TATBP)acac are p-type semiconductors. The spectral bands of TATBP correspond to π → π* transitions. Quantum yields of the S 1 → S 0 fluorescence are in the region 0.25-0.27 and the fluorescence lifetimes are in the region 0.014-0.022 ms at room temperature. The phosphorescence bands of the complex at 77 K appears 714 nm.

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