Jacques Alexandre, Kirsch-De Mesmaeker Andrée, Elias Benjamin
Institut de la Matière Condensée et des Nanosciences, Université Catholique de Louvain , Place Louis Pasteur 2, Box L4.01.02, B-1348 Louvain-la-Neuve, Belgium.
Inorg Chem. 2014 Feb 3;53(3):1507-12. doi: 10.1021/ic402476b. Epub 2014 Jan 22.
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.
制备并表征了两种含有多吡啶和环金属化配体的双齿铱(III)配合物。研究了它们的光谱和电化学性质,并提出了一个解释其性质的光物理方案。考虑了不同类型的激发态来解释每个配合物中的失活过程。有趣的是,在单核苷酸或多核苷酸存在的情况下,通过发光猝灭实验表明存在从DNA嘌呤碱基(即鸟嘌呤或腺嘌呤)到激发态配合物的光诱导电子转移过程。这项工作首次报道了激发态双齿铱(III)配合物选择性氧化DNA嘌呤碱基的证据。