Department of Chemistry, CB#3290, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
J Am Chem Soc. 2010 Sep 22;132(37):12767-9. doi: 10.1021/ja102804s.
Isomorphous metal-organic frameworks (MOFs) based on {M4,4'-(HO(2)C)(2)-bpybpy}(2+) building blocks (where M = Ru or Os) were designed and synthesized to study the classic Ru to Os energy transfer process that has potential applications in light-harvesting with supramolecular assemblies. The crystalline nature of the MOFs allows precise determination of the distances between metal centers by X-ray diffraction, thereby facilitating the study of the Ru→Os energy transfer process. The mixed-metal MOFs with 0.3, 0.6, 1.4, and 2.6 mol % Os doping were also synthesized in order to study the energy transfer dynamics with a two-photon excitation at 850 nm. The Ru lifetime at 620 nm decreases from 171 ns in the pure Ru MOF to 29 ns in the sample with 2.6 mol % Os doping. In the mixed-metal samples, energy transfer was observed with an initial growth in Os emission corresponding with the rate of decay of the Ru excited state. These results demonstrate rapid, efficient energy migration and long distance transfer in isomorphous MOFs.
基于{M4,4'-(HO(2)C)(2)-bpybpy}(2+)构筑块的同晶金属-有机骨架(MOFs)(其中 M = Ru 或 Os)被设计和合成,以研究具有在超分子组装中进行光捕获的潜在应用的经典 Ru 到 Os 能量转移过程。MOFs 的晶体性质允许通过 X 射线衍射精确确定金属中心之间的距离,从而促进 Ru→Os 能量转移过程的研究。还合成了具有 0.3、0.6、1.4 和 2.6 mol% Os 掺杂的混合金属 MOFs,以便在 850nm 的双光子激发下研究能量转移动力学。在纯 Ru MOF 中,620nm 处的 Ru 寿命从 171ns 降低到 2.6mol% Os 掺杂样品中的 29ns。在混合金属样品中,观察到能量转移,与 Ru 激发态的衰减速率相对应的 Os 发射初始增长。这些结果表明同晶 MOFs 中存在快速、有效的能量迁移和长距离转移。