NO-modulated triplet ground state and two-state antiaromaticity in BN-doped cyclobutadienes: a combined DFT and machine learning study.

Abstract

Controlling aromaticity across electronic states is crucial for designing novel species. While aromaticity typically could be achieved in either the lowest singlet state (S₀) or the lowest triplet state (T₁), dual-state aromaticity or antiaromaticity remains less developed. Herein, we demonstrate that NO-substitution uniquely induces antiaromaticity in both S₀ and T₁ states of 1,2-BN-doped cyclobutadiene (1,2-BN-CBD), initially nonaromatic in S₀ and weakly aromatic in T₁. Unlike attachment to nitrogen or carbon, NO bonding to boron (2) induces two-state antiaromaticity, as confirmed by Nucleus-Independent Chemical Shift (NICS), Electron Localization Function (ELF_π), NICS-grid, and Isomerization Stabilization Energy (ISE) analyses. Furthermore, compounds with NO at boron (2 and 10) exhibit triplet ground states. Spin density mainly localizes on NO, driving antiaromaticity in T₁. Principal Interaction Orbital (PIO) and Principal Interacting Spin Orbital (PISO) analyses reveal that exocyclic BN double bond formation enforces planarization and enables localization in the S₀ and T₁ states, leading to two-state antiaromaticity in 2. K-means clustering combined with principal component analysis (one of the most commonly used unsupervised machine learning algorithms) classified BN-doped CBDs based on their electronic and structural properties, uniquely isolating 2 due to its distinct substituent positions and aromaticity behaviors. These findings highlight an important role of the substituent position in tuning electronic and aromatic properties.