Electronic Structure of Corrole Derivatives: Insights from Molecular Structures, Spectroscopy, Electrochemistry, and Quantum Chemical Calculations

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Abstract
Presented herein is a comprehensive account of the electronic structure of corrole derivatives. Our knowledge in this area derives from a broad range of methods, including UV–vis–NIR absorption and MCD spectroscopies, single-crystal X-ray structure determination, vibrational spectroscopy, NMR and EPR spectroscopies, electrochemistry, X-ray absorption spectroscopy, and quantum chemical calculations, the latter including both density functional theory and ab initio multiconfigurational methods. The review is organized according to the Periodic Table, describing free-base and main-group element corrole derivatives, then transition-metal corroles, and finally f-block element corroles. Like porphyrins, corrole derivatives with a redox-inactive coordinated atom follow the Gouterman four-orbital model. A key difference from porphyrins is the much wider prevalence of noninnocent electronic structures as well as full-fledged corrole•2– radicals among corrole derivatives. The most common orbital pathways mediating ligand noninnocence in transition-metal corroles are the metal(dz2)–corrole(“a2u”) interaction (most commonly observed in Mn and Fe corroles) and the metal(dx2–y2)–corrole(a2u) interaction in coinage metal corroles. Less commonly encountered is the metal(dπ)–corrole(“a1u”) interaction, a unique feature of formal d5 metallocorroles. Corrole derivatives exhibit a rich array of optical properties, including substituent-sensitive Soret maxima indicative of ligand noninnocence, strong fluorescence in the case of lighter main-group element complexes, and room-temperature near-IR phosphorescence in the case of several 5d metal complexes. The review concludes with an attempt at identifying gaps in our current knowledge and potential future directions of electronic–structural research on corrole derivatives.
Funding Information
  • Norges Forskningsr?d (231086)

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