Hidden excimer formation in the gas-phase photodynamics of a BN-doped phenanthrene

Abstract

Replacing CC units by isoelectronic BN motifs provides a powerful strategy to tune the electronic structure and excited-state chemistry of polycyclic aromatic hydrocarbons (PAHs). Here, we combine multiphoton ionization spectroscopy, time-resolved photoelectron imaging, ion velocity-map imaging, and quantum-chemical calculations to disentangle the monomer and dimer photophysics of 4a,4b-azaboraphenanthrene. The monomer exhibits a structured S$_1 \leftarrow$ S$_0$ spectrum with an origin at $22880 \pm 15\,\mathrm{cm}^{-1}$, corresponding to $2.837 \,\mathrm{eV}$, and pronounced activity in low-wavenumber deformation modes. Photoelectron spectroscopy yields an adiabatic ionization energy of $7.18 \pm 0.02\,\mathrm{eV}$. While the structured spectrum, high fluorescence quantum yield, small computed geometry changes, and weak spin-orbit couplings all point to a long-lived monomer S$_1$ state, time-resolved photoelectron images reveal an additional picosecond component. Ion imaging shows that this component originates from dissociative ionization of the molecular dimer, which projects dimer excited-state dynamics into the monomer mass channel. Computations identify the initially excited dimer state as a bright H-aggregate-like exciton, followed by ultrafast S$_2 \rightarrow$ S$_1$ internal conversion and subsequent structural relaxation toward an excimeric S$_1$ minimum. The experimentally observed $\approx 15\,\mathrm{ps}$ time constant is therefore assigned to excimer formation in the neutral dimer.