PPSM, ENS Cachan, CNRS, UniverSUD Paris, F-94230 Cachan, France.
J Phys Chem A. 2010 Mar 11;114(9):3264-9. doi: 10.1021/jp909402k.
The photophysical properties of a complex based on diphenylphosphanoethane (DPPE) fluorescent ligands linked to a europium ion have been investigated by different spectroscopic methods. Upon complexation with europium, the interaction of the phosphane oxide group with europium leads to a red shift of the absorption spectrum and a strong quenching of the ligand emission. The typical sensitized emission of Eu(3+) is observed upon excitation of the ligand with a fluorescence quantum yield of 1%. Time-resolved absorption and emission experiments have been performed in order to investigate the photophysical mechanism involved in this complex. Photophysical studies show that an energy-transfer mechanism occurs from both the first excited singlet and triplet states of the ligand, and the population of the europium ion to the (5)D(1) state takes place, from which the (5)D(0) state is populated. Additionally, electron transfer from the excited singlet state of the ligand to the europium ion appears as a very efficient process.
通过不同的光谱方法研究了基于二苯膦乙烷(DPPE)荧光配体与铕离子连接的配合物的光物理性质。与铕配位后,磷烷氧化物与铕的相互作用导致吸收光谱红移和配体发射强烈猝灭。在配体用荧光量子产率为 1%的光激发时,观察到典型的 Eu(3+)敏化发射。为了研究该配合物中涉及的光物理机制,进行了时间分辨吸收和发射实验。光物理研究表明,能量转移机制发生在配体的第一激发单线态和三线态,并且铕离子的(5)D(1)态的布居发生,其中(5)D(0)态被布居。此外,配体的激发单线态向铕离子的电子转移似乎是一个非常有效的过程。