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Intramolecular electron transfer in DNA and ruthenium(II) systems

Johan Olofsson (Institutionen för kemi och biovetenskap)
Göteborg : Chalmers University of Technology, 2004. ISBN: 91-7291-456-4.

When ruthenium(II) complexes with heteroaromatic ligands absorb light, an electron is pushed from the metal ion out into one of the ligands, a process called metal-to-ligand-charge-transfer (MLCT). The resulting excited state can be used to initiate further electron transfer processes, or it can decay relatively slow back into the ground state with the emission of light.

In the first paper we used the ruthenium complex [Ru(phen)2dppz]2+ to study the distance dependence for electron transfer in DNA, and concluded from luminescence measurements of the system that no efficient long range electron transfer was present over distances corresponding to more than a few base pairs.

We further performed a theoretical study of electron hole-transfer mediated by DNA, and suggested that the transfer can normally be understood as step-wise hopping between guanine (G) sites. Another conclusion from the calculation is that intrastrand transfer is predicted to be more efficient than interstrand transfer.

The Ru(II) complexes studied within this thesis are luminescent when binding to DNA and in non-aqueous solution, but the luminescence is extremely low in water. The last four papers of the thesis contributes to a photophysical characterization of this “light-switch”-effect. By studying resonance Raman spectra of the excited state species we observed significant differences in the different environments of acetonitril, water and DNA, and, very interestingly, also an evolution of the excited state spectrum with time in water.

Picosecond time-resolved measurements in glycerol showed that at least three excited states species of MLCT character are involved in the decay, and further that the populations are sensitive to hydrogen bonding which gives rise to an anomalous change in quantum yield with temperature.

A spectroscopical study of the deactivation process in four different polyol solvents showed that the same excited states are involved in all solvents, and that a dark state, assigned to a double hydrogen-bonded species, had to be involved.

Different methyl substituted complexes was studied, and we found that the effect of the methyl groups on the deactivation process was mainly steric, rather than electronic.

Nyckelord: dppz, solvent relaxation, light switch effect, electron transfer and hydrogen bond

Denna post skapades 2006-08-29. Senast ändrad 2013-09-25.
CPL Pubid: 1223


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