Non-innocent P-centers in nonbenzenoid polycyclic aromatic molecules with tunable structures and properties.

Abstract

Implanting heteroatoms into polycyclic aromatic molecules (PAMs) offers a great opportunity to fine-tune their optoelectronic properties. Herein, we report a new type of nonbenzenoid PAM in which the sp2 C atoms are replaced by S and P in the azulene moiety. The synthesis harnessed modular P-chemistry and cyclization chemistry, which afforded the first example of P-azulene-based PAMs with isomeric PN- and PC-type structures. Photophysical and theoretical studies revealed that the P-environments have strong impacts on the structures and properties of the P-PAMs. Different from the electronic structure of azulene with strong π conjugation, the PC derivatives maintained effective σ*-π* hyperconjugation in the frontier molecular orbitals via the P-centers. In particular, the PC derivative with a P(iii)-center showed unexpected room-temperature phosphorescence in solution, which was attributed to the excited-state aromaticity induced structure change at the P-center. Decoration with various aryl groups further modified the photophysical and redox properties in another dimension. Furthermore, bis(triarylamine)-functionalized P-PAMs formed stable radical cations in which the P-environments strongly influenced the mixed-valence state and open-shell characters. As a proof of concept, bis(triarylamine)-functionalized P-PAMs were explored as the hole-transporting layers in perovskite solar cells, and a power conversion efficiency of 14% was achieved. As a new example of nonbenzenoid PAMs with intriguing optoelectronic properties, our P-PAMs are promising building blocks for diverse optoelectronic applications in the future.