铽
发光
镧系元素
部分
铜
微秒
化学
荧光
人口
离子
纳米技术
组合化学
光化学
材料科学
立体化学
光电子学
有机化学
物理
社会学
人口学
量子力学
天文
作者
Manon Isaac,Sergey A. Denisov,Amandine Roux,Daniel Imbert,Gediminas Jonušauskas,Nathan D. McClenaghan,Olivier Sénèque
标识
DOI:10.1002/anie.201505733
摘要
Abstract A prototype luminescent turn‐on probe for Cu + (and Ag + ) is described, harnessing a selective binding site (log K ass =9.4 and 7.3 for Cu + and Ag + , respectively) based on the coordinating environment of the bacterial metallo‐chaperone CusF, integrated with a terbium‐ion‐signaling moiety. Cation–π interactions were shown to enhance tryptophan triplet population, which subsequently sensitized, on the microsecond timescale, the long‐lived terbium emission, offering a novel approach in bioinspired chemosensor design.
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