Cisbio Bioassays, Parc Marcel Boiteux, BP 84175, 30204 Bagnols-sur-Cèze Cedex, France.
Inorg Chem. 2011 Jun 6;50(11):4987-99. doi: 10.1021/ic200227b. Epub 2011 May 9.
Two europium complexes with bis(bipyridine) azamacrocyclic ligands featuring pendant arms with or without π-conjugated donor groups are synthesized and fully characterized by theoretical calculations and NMR spectroscopy. Their photophysical properties, including two-photon absorption, are investigated in water and in various organic solvents. The nonfunctionalized ligand gives highly water-stable europium complexes featuring bright luminescence properties but poor two-photon absorption cross sections. On the other hand, the europium complex with an extended conjugated antenna ligand presents a two-photon absorption cross section of 45 GM at 720 nm but is poorly luminescent in water. A detailed solvent-dependent photophysical study indicates that this luminescence quenching is not due to the direct coordination of O-H vibrators to the metal center but to the increase of nonradiative processes in a protic solvent induced by an internal isomerization equilibrium.
合成了两种具有双(联吡啶)氮杂大环配体的铕配合物,这些配体带有或不带有π-共轭给电子基团的侧臂,并通过理论计算和 NMR 光谱进行了全面表征。研究了它们在水和各种有机溶剂中的光物理性质,包括双光子吸收。非功能化配体给出了具有高稳定性和明亮发光性质但双光子吸收截面较差的铕配合物。另一方面,具有扩展共轭天线配体的铕配合物在 720nm 处的双光子吸收截面为 45GM,但在水中的发光性较差。详细的溶剂依赖性光物理研究表明,这种发光猝灭不是由于 O-H 振动器与金属中心的直接配位,而是由于质子溶剂中内部互变异构平衡引起的非辐射过程的增加。