Laboratoire Francis Perrin, CEA/DSM/IRAMIS/SPAM-CNRS URA 2453, CEA/Saclay, 91191 Gif-sur-Yvette, France.
J Am Chem Soc. 2010 Sep 1;132(34):11834-5. doi: 10.1021/ja102800r.
The fluorescence of calf thymus DNA is studied by steady-state and time-resolved spectroscopy combining fluorescence upconversion and time-correlated single photon counting. The fluorescence spectrum is very similar to that of a stoichiometric mixture of monomeric chromophores, arising from bright pi pi* states, and contrasts with the existing picture of exciplex emission in natural DNA. Yet, the DNA fluorescence decays span over five decades of time, with 98% of the photons being emitted at times longer than 10 ps. These findings, in association with recent studies on model duplexes, are explained by the involvement of dark states, possibly related to charge separation, serving as a reservoir for the repopulation of the bright pi pi* states.
通过稳态和时间分辨光谱学结合荧光上转换和时间相关单光子计数,研究了小牛胸腺 DNA 的荧光。荧光光谱与来自明亮的ππ态的单体发色团的化学计量混合物的光谱非常相似,与天然 DNA 中存在的激基复合物发射的现有图像形成对比。然而,DNA 荧光衰减跨越五个数量级的时间,98%的光子在 10 ps 以上的时间发射。这些发现与最近对模型双链体的研究相关,解释为涉及暗态(可能与电荷分离有关)作为重新填充明亮的ππ态的储库。