Rational Functionalization of a C Buckybowl To Enable a C:Buckybowl Cocrystal for Organic Semiconductor Applications.

Fullerene fragments, referred to as buckybowls, are garnering interest due to their distinctive molecular shapes and optoelectronic properties. Here, we report the synthesis and characterization of a novel C subunit, diindeno[4,3,2,1-:4',3',2',1'-]perylene, that is substituted with either triethylsilyl(TES)-ethynyl or 2,4,6-triisopropylphenyl groups at the -positions. The resulting compounds ( and ) display a bowl-to-bowl inversion at room temperature. Notably, the substituent groups on the -positions alter both the geometric and the electronic properties as well as the crystal packing of the buckybowls. In contrast to the 2,4,6-triisopropylphenyl groups in , the TES-ethynyl groups in lead to enhanced bond length alternation, resulting in weaker aromaticity of the six-membered rings of the buckybowl skeleton. forms one-dimensional (1D) concave-in-convex stacking columns, and when is blended with C, the buckybowls encapsulate C and result in two-dimensional cocrystals. Organic field-effect transistor (OFET) measurements demonstrate that displays a hole mobility of 0.31 cm V s, and the -C cocrystal exhibits ambipolar transport characteristics with electron and hole mobilities approaching 0.40 and 0.07 cm V s, respectively. This work demonstrates the potential of buckybowls for the development of organic semiconductors.