Lewis Frederick D, Zhu Huihe, Daublain Pierre, Sigmund Karsten, Fiebig Torsten, Raytchev Milen, Wang Qiang, Shafirovich Vladimir
Department of Chemistry, Northwestern University, Evanston, IL 60201, USA.
Photochem Photobiol Sci. 2008 May;7(5):534-9. doi: 10.1039/b719715b. Epub 2008 Mar 13.
The mechanism and dynamics of charge separation and charge recombination in synthetic DNA hairpins possessing a stilbenedicarboxamide linker and a single guanine-cytosine base pair have been reinvestigated. The combination of femtosecond broad-band pump probe spectroscopy, nanosecond transient absorption experiments, and picosecond fluorescence decay measurements permits analysis of the formation and decay of the stilbene anion radical. Reversible hole injection resulting in the formation of the stilbene-adenine contact radical ion pair is found to occur on the picosecond time scale. The mechanism for charge separation across two or more base pairs is revised from single step superexchange to a multi-step process: hole injection followed by hole transport and hole trapping. The mechanism of charge recombination remains assigned to a superexchange process.
对含有二苯乙烯二甲酰胺连接体和单个鸟嘌呤 - 胞嘧啶碱基对的合成DNA发夹中电荷分离和电荷复合的机制及动力学进行了重新研究。飞秒宽带泵浦探测光谱、纳秒瞬态吸收实验和皮秒荧光衰减测量相结合,使得对二苯乙烯阴离子自由基的形成和衰减进行分析成为可能。发现导致二苯乙烯 - 腺嘌呤接触自由基离子对形成的可逆空穴注入发生在皮秒时间尺度上。跨两个或更多碱基对的电荷分离机制从单步超交换修正为多步过程:空穴注入,随后是空穴传输和空穴捕获。电荷复合机制仍被认为是超交换过程。