Selective DNA Purine Base Photooxidation by Bis-terdentate Iridium(III) Polypyridyl and Cyclometalated Complexes

被引:21
作者
Jacques, Alexandre [1 ]
Kirsch-De Mesmaeker, Andree [1 ]
Elias, Benjamin [1 ]
机构
[1] Catholic Univ Louvain, Inst Mat Condensee & Nanosci, B-1348 Louvain, Belgium
关键词
ELECTRON-TRANSFER; PHOTOPHYSICAL PROPERTIES; COORDINATION-COMPOUNDS; METAL-COMPLEXES; AXIAL SYMMETRY; REDUCTION; PHOTOCHEMISTRY; RUTHENIUM(II); SPECTROSCOPY; FAMILY;
D O I
10.1021/ic402476b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two bis-terdentate iridium(III) complexes with polypyridyl and cyclometalated ligands have been prepared and characterized. Their spectroscopic and electrochemical properties have been studied, and a photophysical scheme addressing their properties is proposed. Different types of excited states have been considered to account for the deactivation processes in each complex. Interestingly, in the presence of mono- or polynucleotides, a photoinduced electron-transfer process from a DNA purine base (i.e., guanine or adenine) to the excited complex is shown through luminescence quenching experiments. For the first time, this work reports evidence for selective DNA purine bases oxidation by excited iridium(III) bis-terdentate complexes.
引用
收藏
页码:1507 / 1512
页数:6
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