A series of free-base and metalated isocorroles represented as (TT-n-iso-Cor)H2 and (TT-n-iso-Cor)MII, where n = 5 or 10 and M = Ni or Cu, were synthesized and characterized by electrochemistry and spectroelectrochemistry in CH2Cl2 containing 0.1 M tetra-n-butylammonium perchlorate. The metalation of the free-base macrocycles with CoII, MnIII, or ZnII was also attempted but was unsuccessful. Six isocorroles were isolated and shown to undergo two stepwise oxidations to give π-cation radicals and dications in CH 2Cl2, with the most stable products being obtained in the case of the 10-substituted derivatives. The same isocorroles could also be reduced by one or two electrons, but the initial one-electron addition products are unstable and undergo a rapid chemical reaction giving a reduced corrole or corrole-like product, which could be reoxidized to the corresponding (TTCor)M at a controlled positive potential. This series of reactions effectively illustrates an isocorrole to corrole conversion upon reduction and reoxidation and was monitored by both electrochemistry and thin-layer spectroelectrochemistry. © 2010 American Chemical Society.

Synthesis and characterization of free-base, copper, and nickel isocorroles / Pomarico, Giuseppe; Xiao, Xiao; Nardis, Sara; Paolesse, Roberto; Fronczek, Frank R.; Smith, Kevin M.; Fang, Yuanyuan; Ou, Zhongping; Kadish, Karl M.. - In: INORGANIC CHEMISTRY. - ISSN 0020-1669. - 49:12(2010), pp. 5766-5774. [10.1021/ic100730j]

Synthesis and characterization of free-base, copper, and nickel isocorroles

Pomarico, Giuseppe
Primo
;
2010

Abstract

A series of free-base and metalated isocorroles represented as (TT-n-iso-Cor)H2 and (TT-n-iso-Cor)MII, where n = 5 or 10 and M = Ni or Cu, were synthesized and characterized by electrochemistry and spectroelectrochemistry in CH2Cl2 containing 0.1 M tetra-n-butylammonium perchlorate. The metalation of the free-base macrocycles with CoII, MnIII, or ZnII was also attempted but was unsuccessful. Six isocorroles were isolated and shown to undergo two stepwise oxidations to give π-cation radicals and dications in CH 2Cl2, with the most stable products being obtained in the case of the 10-substituted derivatives. The same isocorroles could also be reduced by one or two electrons, but the initial one-electron addition products are unstable and undergo a rapid chemical reaction giving a reduced corrole or corrole-like product, which could be reoxidized to the corresponding (TTCor)M at a controlled positive potential. This series of reactions effectively illustrates an isocorrole to corrole conversion upon reduction and reoxidation and was monitored by both electrochemistry and thin-layer spectroelectrochemistry. © 2010 American Chemical Society.
2010
isocorrole; corrole complexes; oxidation
01 Pubblicazione su rivista::01a Articolo in rivista
Synthesis and characterization of free-base, copper, and nickel isocorroles / Pomarico, Giuseppe; Xiao, Xiao; Nardis, Sara; Paolesse, Roberto; Fronczek, Frank R.; Smith, Kevin M.; Fang, Yuanyuan; Ou, Zhongping; Kadish, Karl M.. - In: INORGANIC CHEMISTRY. - ISSN 0020-1669. - 49:12(2010), pp. 5766-5774. [10.1021/ic100730j]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1708380
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