The Chemical Space of B, N-substituted Polycyclic Aromatic Hydrocarbons: Combinatorial Enumeration and High-Throughput First-Principles Modeling

Abstract

Combinatorial introduction of heteroatoms in the two-dimensional framework of aromatic hydrocarbons opens up possibilities to design compound libraries exhibiting desirable photovoltaic and photochemical properties. Exhaustive enumeration and first-principles characterization of this chemical space provide indispensable insights for rational compound design strategies. Here, for the smallest seventy-seven Kekulean-benzenoid polycyclic systems, we reveal combinatorial substitution of C atom pairs with the isosteric and isoelectronic B, N pairs to result in 7,453,041,547,842 (7.4 tera) unique molecules. We present comprehensive frequency distributions of this chemical space, analyze trends and discuss a symmetry-controlled selectivity manifestable in synthesis product-yield. Furthermore, by performing high-throughput ab initio density functional theory calculations of over thirty-three thousand (33k) representative molecules, we discuss quantitative trends in the structural stability and inter-property relationships across heteroarenes. Our results indicate a significant fraction of the 33k molecules to be electronically active in the 1.5-2.5 eV region, encompassing the most intense region of the solar spectrum, indicating their suitability as potential light-harvesting molecular components in photo-catalyzed solar cells.

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Cited by in corpus (1)

• Deep learning for molecular design - a review of the state of the art