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The Difficult Marriage of Triarylcorroles with Zinc and Nickel Ions
Author(s) -
Mario L. Naitana,
W. Ryan Osterloh,
Lorena Di Zazzo,
Sara Nardis,
Fabrizio Caroleo,
Pierluigi Stipa,
KhaiNghi Truong,
Kari Rissanen,
Yuanyuan Fang,
Karl M. Kadish,
Roberto Paolesse
Publication year - 2022
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.2c03099
Subject(s) - corrole , chemistry , free base , tetrapyrrole , zinc , coordination complex , metal ions in aqueous solution , electron paramagnetic resonance , ligand (biochemistry) , metal , nickel , inorganic chemistry , photochemistry , ion , salt (chemistry) , combinatorial chemistry , organic chemistry , biochemistry , physics , receptor , nuclear magnetic resonance , enzyme
The coordination chemistry of corrole has witnessed a great improvement in the past few years and its Periodic Table has been widened to be so large that it is compared with that of porphyrins. However, Ni and Zn ions, commonly used with porphyrins for both synthetic and theoretical purposes, are sparsely reported in the case of corroles. Here, we report synthetic protocols for preparing Ni and Zn triarylcorrole complexes. In the case of Zn, the preliminary oxidation of the free base corrole in DMSO to the neutral corrole radical is a necessary step to obtain the coordination of the metal ion, because the direct reaction led to the formation of an open-chain tetrapyrrole. The Ni complex could be directly obtained by heating the free base corrole and Ni(II) salt to 100 °C in a DMSO solution containing FeCl 3 . The non-innocent nature of the corrole ligand for both complexes has been elucidated by EPR, and in the case of the Zn derivative the first spectroelectrochemical characterization is presented.

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