Gawryszewska P, Sokolnicki J, Dossing A, Riehl J P, Muller G, Legendziewicz J
Faculty of Chemistry, University of Wrocław, 14 F. Joliot-Curie Street, 50-383 Wrocław, Poland.
J Phys Chem A. 2005 May 5;109(17):3858-63. doi: 10.1021/jp0444666.
Absorption, emission, and excitation spectra for solid-state and solution of Tb(III), Dy(III), and Gd(III) complexes with the polypyridine ligand 6,6'-bis[bis(2-pyridylmethyl)-aminomethyl]-2,2'-bipyridine (C36H34N8) are presented. Measurements of excited-state lifetimes and quantum yields in various solvents at room temperature and 77 K are also reported and used to characterize the excited-state energetics of this system. Special attention is given to the characterization of metal-to-ligand energy transfer efficiency and mechanisms. The measurement of circularly polarized luminescence (CPL) from the solution of the Dy(III) complex following circularly polarized excitation confirms the chiral structure of the complexes under study. No CPL is present in the luminescence from the Eu(III) or Tb(III) complex because of efficient racemization. The variation of the magnitude of the CPL as a function of temperature from an aqueous solution of DyL is used for the first time to characterize the solution equilibria between different chiral species.
给出了铽(III)、镝(III)和钆(III)与多吡啶配体6,6'-双[双(2-吡啶甲基)-氨基甲基]-2,2'-联吡啶(C36H34N8)形成的配合物在固态和溶液状态下的吸收光谱、发射光谱和激发光谱。还报道了在室温及77 K下不同溶剂中激发态寿命和量子产率的测量结果,并用于表征该体系的激发态能量学。特别关注了金属到配体的能量转移效率和机制的表征。在圆偏振激发后,对镝(III)配合物溶液的圆偏振发光(CPL)测量证实了所研究配合物的手性结构。由于有效的外消旋作用,铕(III)或铽(III)配合物的发光中不存在CPL。首次利用镝配合物水溶液的CPL强度随温度的变化来表征不同手性物种之间的溶液平衡。