Corrole

Preparation

Corroles can be prepared by a two-step process, beginning with the condensation reaction of a benzaldehyde with pyrrole. The open-ring product, a bilane (or tetrapyrrane), is cyclized by oxidation, typically with p-chloranil:

Comparison with porphyrins

Corrole and porphyrins differ in several ways. Corroles are triprotic, whereas porphyrins are diprotic. Because of the 3- charge of the triply deprotonated ligand, metallocorroles are formally high-valent. Several are redox-noninnocent, with a corrole radical-dianion ligand. A second difference between corroles and porphyrins is the size of the metal-binding cavity, i.e., 17- vs 18-membered rings. See "Porphyrins and similar compounds" in conjugated systems for more about these side by side images of porphyrin, chlorin, and corrin structures. Due to their lower symmetry, corroles display broader Soret or B-bands and relatively stronger Q-bands, compared to porphyrins. The absorption spectra of corroles in the UV/Visible range tends to be more sensitive towards substituents than in the case of porphyrins.

Coordination complexes

Corroles have been attached to a wide range of transition metals, main group elements, and lanthanides, actinides. and the diprotonated, neutral corrole radical. Additionally, corroles and their metal complexes have been demonstrated to be useful as imaging agents in tumor detection, oxygen sensing, for prevention of heart disease, in synthetic chemistry as oxo, imido, and nitrido transfer agents, and as catalysts for the catalytic reduction of oxygen to water, and hydrogen production form water under aerobic conditions.

Protein-corrole particles have been investigated as carriers of theranostic cargo for tumor targeting.{{cite book|first1=James | last1=Teh

References

References

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3. Ghosh, Abhik. (2017-02-22). "Electronic Structure of Corrole Derivatives: Insights from Molecular Structures, Spectroscopy, Electrochemistry, and Quantum Chemical Calculations". Chemical Reviews.
4. (2010). "Coordination chemistry of corroles with focus on main group elements". Coord. Chem. Rev..
5. (2013). "Lanthanide corroles: a new class of macrocyclic lanthanide complexes". Chem. Commun..
6. (2013). "Synthesis and Characterization of Thorium(IV) and Uranium(IV) Corrole Complexes". J. Am. Chem. Soc..
7. (2015). "The Corrole Radical". Angew. Chem. Int. Ed..
8. (2017). "Fighting Cancer with Corroles". Chemical Reviews.
9. (2016). "Osmium-nitrido corroles as NIR indicators for oxygen sensors and triplet sensitizers for organic upconversion and singlet oxygen generation". Journal of Materials Chemistry C.
10. (2013). "Allosteric inhibitors of HMG-CoA reductase, the key enzyme involved in cholesterol biosynthesis". Chem. Commun..
11. (2012). "Molecular Electronic Structures of Transition Metal Complexes I". Struct. Bond..
12. (2011). "Hangman Corroles: Efficient Synthesis and Oxygen Reaction Chemistry". J. Am. Chem. Soc..