Periodic B- and N-doped phenalenyl π-aggregates: unexpected nonlinear optical properties by tuning pancake π–π bonding

Abstract

Phenalenyl (PLY) and its derivatives could form one-dimensional π-aggregates through pancake π–π bonding, which would lead to exotic optoelectronic properties. We will highlight the key aspects of the PLY derivatives from the design strategies to exploration of the electronic properties. Here, we primarily construct alternating boron (B)- and nitrogen (N)-doped PLY π-aggregates: dimer[12], trimer[12-1], trimer[12-2], tetramer[12]₂, pentamer[12]₂-1, pentamer[12]₂-2, and hexamer[12]₃. The geometric and electronic structures show that the short intermolecular distances of the π-aggregates drive the formation of pancake π–π bonding. Significantly, the molecular structures show periodic changes in the π-aggregates, but the first hyperpolarizabilities (β_tot) present unexpected changes, which are found to increase sharply with increasing even layer thickness due to intermolecular charge transfer. The β_tot value of hexamer[12]₃ (5.72 × 10⁴ a.u.) is 6.4 times that of tetramer[12]₂ (8.95 × 10³ a.u.), and is 22.4 times that of dimer[12] (2.55 × 10³ a.u.). Thus, constructing π-aggregates can significantly improve the second-order NLO response, which is mainly due to intermolecular charge transfer through pancake π–π bonding of the interlayers.