Directional Electron Transfer in Chromophore-labeled Quantum-sized Au 25 Clusters: Au25 as an Electron Donor
Novel Au25(C6S)17PyS clusters (pyrene-functionalized Au25 clusters) showing interesting electrochemical and optical properties are synthesized and characterized. Significant fluorescence quenching is observed for pyrene attached to Au 25 clusters, suggesting strong excited-state interactions. Time-resolved fluorescence upconversion and transient absorption measurements are utilized to understand the excited-state dynamics and possible interfacial electron- and energy-transfer pathways. Electrochemical investigations suggest the possibility of electron transfer from Au25 clusters to the attached pyrene. Fluorescence upconversion measurements have shown faster luminescence decay for the case of pyrene attached to Au25 clusters pointing toward ultrafast photoinduced electron/energy-transfer pathways. Femtosecond transient absorption measurements have revealed the presence of the anion radical of pyrene in the excited-state absorption, suggesting the directional electron transfer from Au25 clusters to pyrene. The rate of forward electron transfer from the Au25 cluster to pyrene is ultrafast (∼580 fs), as observed with femtosecond fluorescence upconversion and transient absorption. © 2010 American Chemical Society.
M. S. Devadas et al., "Directional Electron Transfer in Chromophore-labeled Quantum-sized Au 25 Clusters: Au25 as an Electron Donor," Journal of Physical Chemistry Letters, American Chemical Society (ACS), Jan 2010.
The definitive version is available at https://doi.org/10.1021/jz100395p
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© 2010 American Chemical Society (ACS), All rights reserved.
01 Jan 2010