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Ultrafast photofragment ion spectroscopy of the Wolff rearrangement in 5-diazo Meldrum's acid

机译:5-重氮Meldrum酸中Wolff重排的超快光碎片离子光谱

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摘要

We investigate the gas-phase photochemistry of 5-diazo Meldrum's acid (DMA), a photoactive compound used in lithography, by femtosecond photofragment ion spectroscopy. Transient-absorption studies in solution had revealed an ultrafast intramolecular Wolff rearrangement to a ketene after UV excitation, followed by reactions which also involve the solvent. Due to the absence of solvent molecules in this gas-phase study, we are able to focus purely on the photochemistry of the Wolff rearrangement and subsequent reaction steps. The observation of the time-resolved photofragment ion signals allows us to discriminate the dynamics of ketene and carbene products. By identification of the different possible molecular origins for a certain fragment ion signal, the time scale of the Wolff rearrangement and the lifetime of the ketene product are inferred. We further identified experimental signatures of a second Wolff rearrangement emanating from the carbene product, as had been conjectured indirectly for this molecule from pyrolysis studies.
机译:我们通过飞秒光碎裂离子光谱研究了5-重氮Meldrum酸(DMA)的气相光化学,该酸是一种用于光刻的光敏化合物。溶液中的瞬态吸收研究表明,紫外线激发后,分子内的沃尔夫夫超快重排成乙烯酮,随后反应也涉及溶剂。由于在该气相研究中不存在溶剂分子,因此我们能够将重点纯粹放在Wolff重排的光化学和后续反应步骤上。时间分辨的光碎裂离子信号的观察使我们能够区分乙烯酮和卡宾产物的动力学。通过确定某个片段离子信号的不同可能分子起源,可以推断出沃尔夫夫重排的时间尺度和烯酮产物的寿命。我们进一步确定了从卡宾产物中产生的第二个Wolff重排的实验特征,正如热解研究间接推测的那样。

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