Interactions of Metal-Based and Ligand-Based Electronic Spins in Neutral Tripyrrindione ? Dimers.

ABSTRACT: The ability of tetrapyrrolic macrocycles to stabilize unpaired electrons and engage in ?-? interactions is essential for many electron-transfer processes in biology and materials engineering. Herein, we demonstrate that the formation of ? dimers is recapitulated in complexes of a linear tripyrrolic analogue of naturally occurring pigments derived from heme decomposition. Hexaethyltripyrrindione (H3TD1) coordinates divalent transition metals (i.e., Pd, Cu, Ni) as a stable dianionic radical and was recently described as a robust redox-active ligand. The resulting planar complexes, which feature a delocalized ligand-based electronic spin, are stable at room temperature in air and support ligand-based one-electron processes. We detail the dimerization of neutral tripyrrindione complexes in solution through electron paramagnetic resonance (EPR) and visible absorption spectroscopic methods. Variable-temperature measurements using both EPR and absorption techniques allowed determination of the thermodynamic parameters of ? dimerization, which resemble those previously reported for porphyrin radical cations. The inferred electronic structure, featuring coupling of ligand-based electronic spins in the ? dimers, is supported by density functional theory (DFT) calculations.

SUBMITTER: Gautam R 

PROVIDER: S-EPMC5652324 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature