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Examination of the Magneto-Structural Effects of Hangman Groups on Ferric Porphyrins by EPR

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Nehrkorn,  Joscha Paul
Research Department DeBeer, Max Planck Institute for Chemical Energy Conversion, Max Planck Society;

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Bonke,  Shannon A.
Research Department DeBeer, Max Planck Institute for Chemical Energy Conversion, Max Planck Society;

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Schnegg,  Alexander
Research Department DeBeer, Max Planck Institute for Chemical Energy Conversion, Max Planck Society;

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Citation

Nehrkorn, J. P., Bonke, S. A., Aliabadi, A., Schwalbe, M., & Schnegg, A. (2019). Examination of the Magneto-Structural Effects of Hangman Groups on Ferric Porphyrins by EPR. Inorganic Chemistry, 58(20), 14228-14237. doi:10.1021/acs.inorgchem.9b02348.


Cite as: https://hdl.handle.net/21.11116/0000-0006-5B3A-4
Abstract
Ferric hangman porphyrins are bioinspired models for haem hydroperoxidase enzymes featuring an acid/base group in close vicinity to the metal center, which results in improved catalytic activity for reactions requiring O-O bond activation. These functional biomimics are examined herein with a combination of EPR techniques to determine the effects of the hanging group on the electronics of the ferric center. These results are compared to those for ferric octaethylporphyrin chloride [Fe(OEP)Cl], tetramesitylporphyrin chloride [Fe(TMP)Cl], and the pentafluorophenyl derivative [Fe(TPFPP)Cl], which were also examined herein to study the electronic effects of various substituents. Frequency-domain Fourier-transform THz-EPR com- bined with field domain EPR in a broad frequency range from 9.5 to 629 GHz allowed the determination of zero-field splitting parameters, revealing minor rhombicity E/D and D values in a narrow range of 6.24(8) to 6.85(5) cm(-1). Thus, the hangman porphyrins display D values in the expected range for ferric porphyrin chlorides, though D appears to be correlated with the Fe-Cl bond length. Extrapolating this trend to the ferric hangman porphyrin chlorides, for which no crystal structure has been reported, indicates a slightly elongated Fe-Cl bond length compared to the non-hangman equivalent.