A new scaffold for studying photoinduced charge transfer has been constructed by connecting a [Ru(Bpy)3]2+ donor to a bis(8-hydroxyquinolinate)2 copper [CuQ2] acceptor through a peptide nucleic acid (PNA) bridge. The luminescence of the [Ru(Bpy) 3]2+* donor is quenched by electron transfer to the [CuQ2] acceptor. Photoluminescence studies of these donor-bridge-acceptor systems reveal a dependence of the charge transfer on the length and sequence of the PNA bridge and on the position of the donor and acceptor in the PNA. In cases where the [Ru(Bpy)3]2+ can access the base stack at the terminus of the duplex, the luminescence decay is described well by a single exponential; but if the donor is sterically hindered from accessing the base stack of the PNA duplex, a distribution of luminescence lifetimes for the donor [Ru(Bpy)3]2+* is observed. Molecular dynamics simulations are used to explore the donor-PNA-acceptor structure and the resulting conformational distribution provides a possible explanation for the distribution of electron transfer rates. © 2014 American Chemical Society.
CITATION STYLE
Yin, X., Kong, J., De Leon, A., Li, Y., Ma, Z., Wierzbinski, E., … Waldeck, D. H. (2014). Luminescence quenching by photoinduced charge transfer between metal complexes in peptide nucleic acids. Journal of Physical Chemistry B, 118(30), 9037–9045. https://doi.org/10.1021/jp5027042
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