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Structural determination of a photochemically active diplatinum molecule by time-resolved EXAFS spectroscopy.
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Kinetics of the single-crystal to single-crystal two-photon photodimerization of alpha-trans-cinnamic acid to alpha-truxillic acid.α-反式肉桂酸至α-特鲁酸的单晶到单晶双光子光二聚反应动力学
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Time-resolved X-ray scattering of an electronically excited state in solution. Structure of the 3A(2u) state of tetrakis-mu-pyrophosphitodiplatinate(II).溶液中电子激发态的时间分辨X射线散射。四-μ-焦磷酸二铂酸(II)的³A₂ᵤ态结构。
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极短寿命光致分子物种的时间分辨同步加速器衍射及理论研究

Time-resolved synchrotron diffraction and theoretical studies of very short-lived photo-induced molecular species.

作者信息

Coppens Philip, Benedict Jason, Messerschmidt Marc, Novozhilova Irina, Graber Tim, Chen Yu-Sheng, Vorontsov Ivan, Scheins Stephan, Zheng Shao-Liang

机构信息

Chemistry Department, University at Buffalo, State University of New York, Buffalo, NY 14260-3000, USA.

出版信息

Acta Crystallogr A. 2010 Mar;66(Pt 2):179-88. doi: 10.1107/S0108767309055342. Epub 2010 Feb 18.

DOI:10.1107/S0108767309055342
PMID:20164641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2824528/
Abstract

Definitive experimental results on the geometry of fleeting species are at the time of writing still limited to monochromatic data collection, but methods for modifications of the polychromatic Laue data to increase their accuracy and their suitability for pump-probe experiments have been implemented and are reviewed. In the monochromatic experiments summarized, excited-state conversion percentages are small when neat crystals are used, but are higher when photoactive species are embedded in an inert framework in supramolecular crystals. With polychromatic techniques and increasing source brightness, smaller samples down to tenths of a micrometre or less can be used, increasing homogeneity of exposure and the fractional population of the excited species. Experiments described include a series of transition metal complexes and a fully organic example involving excimer formation. In the final section, experimental findings are compared with those from theoretical calculations on the isolated species. Qualitative agreement is generally obtained, but the theoretical results are strongly dependent on the details of the calculation, indicating the need for further systematic analysis.

摘要

在撰写本文时,关于瞬态物种几何结构的确切实验结果仍仅限于单色数据收集,但已实施并综述了修改多色劳厄数据以提高其准确性及其适用于泵浦-探测实验的方法。在总结的单色实验中,使用纯晶体时激发态转化率较小,但当光活性物种嵌入超分子晶体的惰性框架中时转化率较高。随着多色技术的发展和光源亮度的提高,可以使用小至十分之一微米或更小的样品,从而提高曝光的均匀性和激发物种的分数丰度。所描述的实验包括一系列过渡金属配合物和一个涉及准分子形成的全有机实例。在最后一部分,将实验结果与对孤立物种的理论计算结果进行了比较。总体上获得了定性一致,但理论结果强烈依赖于计算细节,这表明需要进一步进行系统分析。