化学
DNA
立体化学
荧光
结晶学
物理
生物化学
量子力学
作者
Qianxiong Zhou,Wanhua Lei,Yi Sun,Jingrong Chen,Chao Li,Yuanjun Hou,Xuesong Wang,Baowen Zhang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2010-04-29
卷期号:49 (11): 4729-4731
被引量:45
摘要
The sequential replacement of a bpy ligand (bpy = 2,2′-bipyridine) by a dpb ligand (dpb = 2,3-bis(2-pyridyl) benzoquinoxaline) in the series [Ru(bpy)3−n(dpb)n]2+ (n = 1−3) leads to a remarkable increase of the excited state lifetime, the 1O2 quantum yield, and the binding affinity toward dsDNA, rendering both [Ru(bpy)(dpb)2]2+ and [Ru(dpb)3]2+ efficient DNA photocleavage activities upon red light irradiation (≥600 nm).
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