SGIker Laser Facility, UPV/EHU, Sarriena, s/n, Leioa 48940, Spain.
Phys Chem Chem Phys. 2019 Feb 6;21(6):3098-3105. doi: 10.1039/c8cp06416d.
We have investigated the relaxation, following excitation in the 290-235 nm region, of neutral aniline homoclusters (An)n formed in a supersonic expansion by femtosecond time resolved ionization. The applied method permits isolation of the dynamics of the dimer from that originated in bigger species of the generated distribution. Interestingly, and differently from the monomer and (An)n≥3 clusters, the dimer does not present a N-H dissociative 1πσ* channel. This fact can be explained in terms of the symmetric structure adopted, in which each molecule establishes two N-Hπ interactions, destabilizing the H dissociation channel. The observations permit relating the photophysics to the interactions established by the aniline units and confirming previous observations and theoretical predictions on the structure of aniline aggregates.
我们通过飞秒时间分辨电离研究了在 290-235nm 区域激发后中性苯胺同核簇(An)n 的弛豫,这些同核簇是在超音速膨胀中形成的。所应用的方法允许将二聚体的动力学与源自所生成分布中大物种的动力学区分开来。有趣的是,与单体和(An)n≥3 簇不同,二聚体没有呈现 N-H 离解 1πσ*通道。这一事实可以根据所采用的对称结构来解释,其中每个分子建立两个 N-Hπ相互作用,使 H 离解通道失稳。这些观察结果使我们能够将光物理与苯胺单元建立的相互作用联系起来,并证实了先前关于苯胺聚集体结构的观察和理论预测。