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动作图中的动作:光化学反应的深入见解。

Action Plots in Action: In-Depth Insights into Photochemical Reactivity.

机构信息

School of Chemistry and Physics, Queensland University of Technology (QUT), 2 George Street, Brisbane, Queensland 4000, Australia.

Centre for Materials Science, Queensland University of Technology (QUT), 2 George Street, Brisbane, Queensland 4000, Australia.

出版信息

J Am Chem Soc. 2021 Dec 22;143(50):21113-21126. doi: 10.1021/jacs.1c09419. Epub 2021 Dec 3.

Abstract

Predicting wavelength-dependent photochemical reactivity is challenging. Herein, we revive the well-established tool of measuring action spectra and adapt the technique to map wavelength-resolved covalent bond formation and cleavage in what we term "photochemical action plots". Underpinned by tunable lasers, which allow excitation of molecules with near-perfect wavelength precision, the photoinduced reactivity of several reaction classes have been mapped in detail. These include photoinduced cycloadditions and bond formation based on photochemically generated -quinodimethanes and 1,3-dipoles such as nitrile imines as well as radical photoinitiator cleavage. Organized by reaction class, these data demonstrate that UV/vis spectra fail to act as a predictor for photochemical reactivity at a given wavelength in most of the examined reactions, with the photochemical reactivity being strongly red shifted in comparison to the absorption spectrum. We provide an encompassing perspective of the power of photochemical action plots for bond-forming reactions and their emerging applications in the design of wavelength-selective photoresists and photoresponsive soft-matter materials.

摘要

预测波长相关光化学反应性具有挑战性。在此,我们重新启用了经过充分验证的测量作用光谱的工具,并将该技术进行了适应性改进,以绘制我们所谓的“光化学反应作用图”中波长分辨的共价键形成和断裂。在可调谐激光器的支持下,该激光器可以实现对分子的近乎完美波长精度的激发,我们详细绘制了几种反应类别的光诱导反应性。这些包括基于光化学生成的 - 醌二亚甲基和 1,3-偶极子(如腈亚胺)的光诱导环加成和键形成,以及自由基光引发剂的断裂。按反应类别组织,这些数据表明,在大多数被检查的反应中,紫外/可见光谱不能作为给定波长下光化学反应性的预测指标,与吸收光谱相比,光化学反应性强烈红移。我们提供了光化学反应作用图在形成键反应中的强大功能的全面视角,以及它们在设计波长选择性光致抗蚀剂和光响应软物质材料方面的新兴应用。

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