Tetrahedraphene: A Csp<sup>3</sup>‐centered 3D Molecular Nanographene Showing Aggregation‐Induced Emission
Arturo Oró, Fernando Romeo‐Gella, Josefina Perles, Jesús M. Fernández‐García, Inés Corral, Nazario Martı́n
Abstract
Abstract The bottom‐up synthesis of 3D tetrakis(hexa‐peri‐hexabenzocoronenyl)methane, “tetrahedraphene”, is reported. This molecular nanographene constituted by four hexa‐ peri ‐hexabenzocoronene (HBC) units attached to a central sp 3 carbon atom, shows a highly symmetric arrangement of the HBC units disposed in the apex of a tetrahedron. The X‐ray crystal structure reveals a tetrahedral symmetry of the molecule and the packing in the crystal is achieved mostly by CH⋅⋅⋅π interactions since the interstitial solvent molecules prevent the π⋅⋅⋅π interactions. In solution, tetrahedraphene shows the same electrochemical and photophysical properties as the hexa‐ t Bu‐substituted HBC ( t Bu‐HBC) molecule. However, upon water addition, it undergoes a fluorescence change in solution and in the precipitated solid, showing an aggregation induced emission (AIE) process, probably derived from the restriction in the rotation and/or vibration of the HBCs. Time‐Dependent Density Functional Theory (TDDFT) calculations reveal that upon aggregation, the high energy region of the emission band decreases in intensity, whereas the intensity of the red edge emission signal increases and presents a smoother decay, compared to the non‐aggregated molecule. All in all, the excellent correlation between our simulations and the experimental findings allows explaining the colour change observed in the different solutions upon increasing the water fraction.