摘要

Adducts of lanthanide beta-diketonates of the general formula LnL(3)(TPTZ) were synthesized and structurally characterized by single crystal X-ray diffraction [Ln = Eu3+, Tb3+, Er3+; L is the conjugate base of dibenzoylmethane (DBM), 1-benzoylacetone (BA), thenoyltrifluoroacetone (TTA), or 4,4,4-trifluoro-1-phenyl-1,3-butanedione (BTFA); TPTZ = 2,4,6-tri(2-pyridyl)-1,3,5-triazine, a rigid Lewis base with a large pi system]. The lanthanide ion in each of these complexes is nonacoordinate with six beta-diketonate oxygen atoms and three TPTZ nitrogen atoms, forming a coordination polyhedron best describable as a monocapped square antiprism. Characteristic red, green, and near infrared luminescence was observed for the Eu3+, Tb3+, and Er3+ complexes, respectively. All complexes showed significantly enhanced luminescence quantum yields when compared with the corresponding aqua analogues, with one of the Eu3+ complexes displaying a quantum yield of 69.7% in chloroform.

  • 出版日期2007-4-11