Demetallation of <i>meso</i>-substituted porphyrins

A mild and efficient method for the acid-promoted demetallation of functionalized metalloporphyrins is described. In contrast to the normally harsh conditions required, a variety of Cu porphyrins were rapidly demetallated in excellent yields using methanesulfonic acid in a chlorinated hydrocarbon solvent at room temperature or under microwave heating. Some Co, Ni, and Ag porphyrins could also be efficiently demetallated. Notably, the presence of a small amount of a coordinating solvent in the reaction mixture either completely inhibited the demetallation or significantly slowed it down. Electron withdrawing functionality also slowed down the demetallation time.

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Publication Details

Journal
Journal of Porphyrins and Phthalocyanines
Published
2025-02-01
DOI
https://doi.org/10.1142/s1088424625500257
Citations
1
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
Field-Weighted Citation Impact
0.52
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article

Demetallation of meso-substituted porphyrins

David L. Officer, Ashley Walker, Paweł Wagner
1 citations
Journal of Porphyrins and Phthalocyanines
Porphyrin and Phthalocyanine Chemistry
0.52
article

Demetallation of meso-substituted porphyrins

David L. Officer, Ashley Walker, Paweł Wagner
article en
1 citations

Abstract

A mild and efficient method for the acid-promoted demetallation of functionalized metalloporphyrins is described. In contrast to the normally harsh conditions required, a variety of Cu porphyrins were rapidly demetallated in excellent yields using methanesulfonic acid in a chlorinated hydrocarbon solvent at room temperature or under microwave heating. Some Co, Ni, and Ag porphyrins could also be efficiently demetallated. Notably, the presence of a small amount of a coordinating solvent in the reaction mixture either completely inhibited the demetallation or significantly slowed it down. Electron withdrawing functionality also slowed down the demetallation time.

Journal of Porphyrins and PhthalocyaninesVol. 29(01n02)
University of Wollongong (AU), ARC Centre of Excellence for Electromaterials Science (AU)
Openalex Percentile: Top 42%
Porphyrin and Phthalocyanine Chemistry
0.52
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