Tetraquinolines; four linked quinoline units or porphyrinoids

Tetraquinolines (TEQs) have been recently synthesized and proposed to be a new member of the porphyrinoid family with highly distorted, nonplanar, geometries. In this contribution by studying several molecules, closely related to TEQs, we have suggested that the origin of the nonplanarity of TEQs and their counterparts is a combination of steric strain and the propensity of the molecules to avoid antiaromaticity. The tendency of TEQs to coordinate with doubly charged metal ions can be interpreted in terms of their transition from potential antiaromaticity to nonaromaticity. Even metal-coordinated TEQs do not sustain diatropic ring currents. Although full planarization is not possible because of steric strain, doubly oxidized TEQs and their counterparts sustain moderate global diatropic ring currents and partially planarize. The nature of current density in the molecules is studied in the light of Steiner-Fowler selection rules. 3D current density distribution in TEQ 2+ suggests a transformation from antiaromaticity to aromaticity.