A multi‐descriptor analysis of substituent effects on the structure and aromaticity of benzene derivatives: π‐Conjugation versus charge effects

This work provides a detailed multi-component analysis of aromaticity in monosubstituted (X = CH₃, C <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:mrow><mml:msubsup><mml:mi>H</mml:mi> <mml:mn>2</mml:mn> <mml:mo>-</mml:mo></mml:msubsup> </mml:mrow> </mml:math> , C <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:mrow><mml:msubsup><mml:mi>H</mml:mi> <mml:mn>2</mml:mn> <mml:mo>+</mml:mo></mml:msubsup> </mml:mrow> </mml:math> , NH₂, NH^-, NH⁺, OH, O^-, and O⁺) and para-homodisubstituted (X = CH₃, CH₂, NH₂, NH, OH, and O) benzene derivatives. We investigate the effects of substituents using single-reference (B3LYP/DFT) and multireference (CASSCF/MRCI) methods, focusing on structural (HOMA), vibrational (AI(vib)), topological (ELF_π), electronic (MCI), magnetic (NICS), and stability (S₀-T₁ splitting) properties. The findings reveal that appropriate π-electron-donating and π-electron-accepting substituents with suitable size and symmetry can interact with the π-system of the ring, significantly influencing π-electron delocalization. While the charge factor has a minimal impact on π-electron delocalization, the presence of a p_z orbital capable of interacting with the π-electron delocalization is the primary factor leading to a deviation from the typical aromaticity characteristics observed in benzene.