Room-Temperature Near-Infrared Phosphorescence from C Nanographene Tetraimide by π-Stacking Complexation with Platinum Porphyrin.

Near-Infrared (NIR) phosphorescence at room temperature is challenging to achieve for organic molecules due to negligible spin-orbit coupling and a low energy gap leading to fast non-radiative transitions. Here, we show a supramolecular host-guest strategy to harvest the energy from the low-lying triplet state of C nanographene tetraimide 1. H NMR and X-ray analysis confirmed the 1 : 2 stoichiometric binding of a Pt(II) porphyrin on the two π-surfaces of 1. While the free 1 does not show emission in the NIR, the host-guest complex solution shows NIR phosphorescence at 77 K. Further, between 860-1100 nm, room temperature NIR phosphorescence (λ=900 nm, τ=142 μs) was observed for a solid-state sample drop-casted from a preformed complex in solution. Theoretical calculations reveal a non-zero spin-orbit coupling between isoenergetic S and T of π-stacked [1 ⋅ Pt(II) porphyrin] complex. External heavy-atom-induced spin-orbit coupling along with rigidification and protection from oxygen in the solid-state promotes both the intersystem crossing from the first excited singlet state into the triplet manifold and the NIR phosphorescence from the lowest triplet state of 1.