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[Ru(bpy)(3)](2+) 作为瞬态吸收光谱学中的参比物:长寿命 (3)MLCT 激发态形成的差分吸收系数。

[Ru(bpy)(3)](2+) as a reference in transient absorption spectroscopy: differential absorption coefficients for formation of the long-lived (3)MLCT excited state.

机构信息

PCMP, Université Pierre et Marie Curie, F-75005, Paris, France.

出版信息

Photochem Photobiol Sci. 2012 Apr;11(4):632-6. doi: 10.1039/c2pp05333k. Epub 2012 Jan 16.

DOI:10.1039/c2pp05333k
PMID:22246402
Abstract

Transient absorption spectroscopy and other time-resolved methods are commonly used to study chemical reactions and biological processes induced by absorption of light. In order to scale the signal amplitude or to compare results obtained under different conditions, it is advisable to use a reference system, a standard of convenient and well-defined properties. Finding Tris(bipyridine)ruthenium(ii), Ru(bpy)(3), a suitable candidate for a transient-absorption spectroscopy reference due to its favourable photochemical properties, we have determined accurate relative values of differential molar absorption coefficients (Δε) for light-induced formation of the metal-to-ligand charge transfer (MLCT) excited triplet state at several relevant wavelengths (wavelengths of commercially available lasers) in the UV and visible regions. We have also attempted to determine the absolute value of Δε close to the wavelength of maximum bleaching (∼450 nm) and we propose to narrow down the interval of conceivable values for Δε(450) from the broad range of published values (-0.88 × 10(4) M(-1)cm(-1) to -1.36 × 10(4) M(-1)cm(-1)) to -1.1 × 10(4) M(-1)cm(-1)± 15%. Having ourselves successfully applied Ru(bpy)(3) as a standard in a recent time-resolved study of enzymatic DNA repair, we would like to encourage other scientists to use this convenient tool as a reference in their future spectroscopic studies on time scales from picoseconds to hundreds of nanoseconds.

摘要

瞬态吸收光谱学和其他时间分辨方法通常用于研究光吸收诱导的化学反应和生物过程。为了放大信号幅度或比较不同条件下获得的结果,建议使用参考体系,即具有方便且明确性质的标准。我们发现三(联吡啶)钌(ii)[Ru(bpy)(3)](2+)由于其有利的光化学性质,是瞬态吸收光谱参考的合适候选物,因此我们在几个相关波长(商业上可用激光的波长)下确定了光诱导金属-配体电荷转移(MLCT)激发三重态形成的相对差分摩尔吸收系数(Δε)的准确值在 UV 和可见区域。我们还试图确定在最大漂白波长(约 450nm)附近的Δε的绝对值,并提出将 Δε(450)的可想象值的间隔从广泛的发表值(-0.88×10(4)M(-1)cm(-1)至-1.36×10(4)M(-1)cm(-1))缩小到-1.1×10(4)M(-1)cm(-1)±15%。我们最近在酶促 DNA 修复的时间分辨研究中成功地将 [Ru(bpy)(3)](2+)用作标准,我们希望鼓励其他科学家在未来的皮秒到数百纳秒时间尺度的光谱研究中使用此方便的工具作为参考。

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