Quantum chemical study of TiO2/dopamine-DNA triads

被引:15
作者
Vega-Arroyo, Manuel
LeBreton, Pierre R.
Zapol, Peter
Curtiss, Larry A.
Rajh, Tijana
机构
[1] Argonne Natl Lab, Div Chem, Argonne, IL 60439 USA
[2] Univ Illinois, Dept Chem, Chicago, IL 60607 USA
[3] Argonne Natl Lab, Div Mat Sci, Argonne, IL 60439 USA
关键词
anatase; nanoparticle; titanium oxide; DNA; photoexcitation; ionization potential; oxidation potential; density functional theory;
D O I
10.1016/j.chemphys.2007.06.037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photoinduced charge separation in triads of DNA covalently linked to an anatase nanoparticle via a dopamine bridge was studied by ab initio calculations of the oxidation potentials of carboxyl-DNA trimers and the TiO2/dopamine complex. Conjugation of dopamine to the TiO2 surface results in a lower oxidation potential of the complex relative to the surface and in localization of photogenerated holes on dopamine, while photogenerated electrons are excited into the conduction band of TiO2. Linking dopamine to the DNA trimers at the 5 ' end of the oligonucleotide may lead to further hole migration to the DNA. Calculations show that for several different sequences hole migration is favorable in double stranded DNA and unfavorable in single-stranded DNA. This extended charge separation was shown to follow from the redox properties of DNA sequence rather than from the modification of DNA's electron donating properties by the dopamine linker, which explains experimental observations. (C) 2007 Published by Elsevier B.V.
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页码:164 / 172
页数:9
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