Energy Transfer Pathways in Dinuclear Heteroleptic Polypyridyl Complexes: Through-Space vs Through-Bond Interaction Mechanisms
作者:Frances Weldon、Leif Hammarström、Emad Mukhtar、Ronald Hage、Eric Gunneweg、Jaap G. Haasnoot、Jan Reedijk、Wesley R. Browne、Adrian L. Guckian、Johannes G. Vos
DOI:10.1021/ic049896p
日期:2004.7.1
the nature of the bridging ligand allows for an efficient through-bond coupling. The results obtained for the compounds reported here suggest that energy transfer is predominantly taking place via a dipole-dipole, Forster type, mechanism, that may dominate when through-bond coupling is weak. This is in stark contrast to ground state interaction, which is found to be critically dependent on the nature
一系列具有桥接配体1,3-双(5-(2-吡啶基)-1H-1,2,4-三唑-3-基)苯(H(2)的同核和异核钌和多吡啶基配合物报道)和1,4-双(5-(2-吡啶基)-1H-1,2,4-三唑-3-基)苯(H(2)pL)。研究了这些化合物的光物理性质,并特别注意显示出双重发射的异核(RuOs)化合物。这与具有相似金属-金属距离的苯基桥联的聚吡啶Ru-Os络合物相反,在该络合物中,Ru发射被强烈淬灭,因为桥接配体的性质允许有效的键间偶联。从此处报道的化合物获得的结果表明,能量转移主要是通过偶极-偶极,福斯特类型,机理,当键合耦合较弱时,这可能占主导地位。这与基态相互作用形成了鲜明的对比,后者被发现严重取决于所用桥接单元的性质。