Abstract
Efficient multiple-chromophore coupling in a crystalline metal-organic scaffold was achieved by mimicking a protein system possessing 100 % energy-transfer (ET) efficiency between a green fluorescent protein variant and cytochrome b562. The two approaches developed for ET relied on the construction of coordination assemblies and host-guest coupling. Based on time-resolved photoluminescence measurements in combination with calculations of the spectral overlap function and Förster radius, we demonstrated that both approaches resulted in a very high ET efficiency. In particular, the observed ligand-to-ligand ET efficiency value was the highest reported so far for two distinct ligands in a metal-organic framework. These studies provide important insights for the rational design of crystalline hybrid scaffolds consisting of a large ensemble of chromophore molecules with the capability of directional ET.
| Original language | English |
|---|---|
| Pages (from-to) | 13639-13643 |
| Number of pages | 5 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 54 |
| Issue number | 46 |
| DOIs | |
| State | Published - Nov 1 2015 |
| Externally published | Yes |
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