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Energy Transfer Dynamics in Metal-Organic Frameworks
被引:324
作者:
Kent, Caleb A.
[1
]
Mehl, Brian P.
[1
]
Ma, Liqing
[1
]
Papanikolas, John M.
[1
]
Meyer, Thomas J.
[1
]
Lin, Wenbin
[1
]
机构:
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
基金:
美国国家科学基金会;
关键词:
EXCITED-STATE;
CHARGE-TRANSFER;
MIGRATION DYNAMICS;
ELECTRON-TRANSFER;
COMPLEXES;
PHOTOCHEMISTRY;
RUTHENIUM(II);
(CT)-C-3;
RU(II);
D O I:
10.1021/ja102804s
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Isomorphous metal organic frameworks (MOFs) based on {M[4,4'-(HO2C)(2)-bpy](2)bpy}(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.
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页码:12767 / 12769
页数:3
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