Montero Raúl, Martínez-Martínez Virginia, Longarte Asier, Epelde-Elezcano Nerea, Palao Eduardo, Lamas Iker, Manzano Hegoi, Agarrabeitia Antonia R, López Arbeloa Iñigo, Ortiz Maria J, Garcia-Moreno Inmaculada
SGIKER Laser, Universidad del País Vasco, UPV/EHU , Apartado 644, 48080 Bilbao, Spain.
Departamento de Química Orgánica I, Facultad de CC. Químicas, Universidad Complutense de Madrid , Ciudad Universitaria s/n, 28040 Madrid, Spain.
J Phys Chem Lett. 2018 Feb 1;9(3):641-646. doi: 10.1021/acs.jpclett.7b03074. Epub 2018 Jan 22.
The photodynamics of an orthogonal BODIPY dimer, particularly the formation of triplet states, has been explored by femtosecond and nanosecond transient absorption measurements. The short time scale data show the appearance of transient features of triplet character that, according to quantitative analysis of their intensities, account for more than 100% of the initially excited molecules, which reveals the occurrence of a singlet fission process in the isolated dimers. The formation rate of the triplet correlated state (TT) is found to depend on the solvent polarity, pointing to the mediation of a charge transfer character state. The dissociation of the (TT) state into pairs of individual triplets determines the triplet yield measured in the long time scales. The kinetic model derived from the results provides a comprehensive view of the photodynamics of BODIPY dimers and permits rationalization of the photophysical parameters of these systems.
通过飞秒和纳秒瞬态吸收测量,研究了一种正交硼二吡咯二聚体的光动力学,特别是三重态的形成。短时间尺度的数据显示出具有三重态特征的瞬态特征的出现,根据其强度的定量分析,这些特征占初始激发分子的100%以上,这揭示了在孤立二聚体中发生了单重态裂变过程。发现三重态相关态(TT)的形成速率取决于溶剂极性,表明存在电荷转移特征态的介导作用。(TT)态解离为单个三重态对决定了长时间尺度下测得的三重态产率。从结果推导的动力学模型提供了硼二吡咯二聚体光动力学的全面视图,并使这些系统的光物理参数合理化。