Novel quinonediimines derived from amino acid-like structures 2: Characterization and DFT computational study of N,N′-bis(4′-l-phenylalaninyl)-1,4-quinonediimine

Abstract

Density functional calculations were performed on N,N′-bis(4′-l-phenylalaninyl)-1,4-quinonediimine, a novel substituted aniline “trimer.” This is the second reported symmetric quinonediimine with outer rings derived from amino-acid related structures, the first of which derived from an unmodified, naturally occurring amino acid. Results of the calculations were compared to experimental properties of the herein synthesized trimer. The calculated HOMO levels for isomers of the title compound range from −6.0423 to −6.0178eV, and the LUMO levels from −3.1794 to −3.1772eV. The calculated electron affinities range from 2.1509 to 2.1554eV. The LUMO level is lowest for the syn isomer, and the electron affinity greatest in magnitude for the anti isomer. Compared to the widely-studied amino-capped aniline trimer N,N′-bis(4′-aminophenyl)-1,4-quinonediimine, the title compound has lower LUMO levels and greater electron affinity in both the emeraldine base or emeraldine dihydrochloride (salt) form, suggesting that it might be even more effective in corrosion control applications. Because the outer rings are derived from amino-acid related structures, such molecules, particularly as capping groups for polyanilines, could find use in biomedical applications.