Harville Payten A, Moss Olivia C, Rana Abhijit, Snowden Elizabeth A, Johnson Mark A
Sterling Chemistry Laboratory, Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States.
J Phys Chem A. 2024 Sep 12;128(36):7714-7719. doi: 10.1021/acs.jpca.4c04283. Epub 2024 Aug 28.
We demonstrate a method to determine the structures of the primary photodissociation products from a cryogenically cooled parent ion. In this approach, a target ion is cooled by a pulse of buffer gas and tagged in a 20 K Paul trap. The cold ion is then photodissociated by pulsed (∼5 ns) UV laser excitation, and the ionic products are trapped, cooled, and tagged by introduction of a second buffer gas pulse in the same trap. The tagged fragments are then ejected into a triple focusing, UV/vis/IR time-of-flight photofragmentation mass spectrometer which yields vibrational and electronic spectra of the mass-selected photofragments. These methods are demonstrated by application to the 266 nm photodissociation of the Rhodamine 6G cation to yield the R575 fragment ion based on loss of ethene as well as to a weaker secondary fragment arising from loss of / 43.
我们展示了一种确定低温冷却母离子初级光解离产物结构的方法。在这种方法中,目标离子通过缓冲气体脉冲冷却,并在20K的保罗阱中进行标记。然后,通过脉冲(约5ns)紫外激光激发使冷离子发生光解离,通过在同一阱中引入第二个缓冲气体脉冲来捕获、冷却并标记离子产物。然后将标记的碎片喷射到三重聚焦的紫外/可见/红外飞行时间光解离质谱仪中,该仪器可产生质量选择光碎片的振动和电子光谱。通过将这些方法应用于罗丹明6G阳离子在266nm处的光解离,以基于乙烯的损失产生R575碎片离子,以及应用于因损失/43而产生的较弱二级碎片,对这些方法进行了验证。