A series of free-base and metalated isocorroles represented as (TT-n-iso-Cor)H(2) and (TT-n-iso-Cor)M(II), where n = 5 or 10 and M = Ni or Cu, were synthesized and characterized by electrochemistry and spectroelectrochemistry in CH(2)Cl(2) containing 0.1 M tetra-n-butylammonium perchlorate. The metalation of the free-base macrocycles with Co(II), Mn(III), or Zn(II) was also attempted but was unsuccessful. Six isocorroles were isolated and shown to undergo two stepwise oxidations to give pi-cation radicals and dications in CH(2)Cl(2), 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.
A series of free-base and n class="Chemical">metalated isocorroles represented as (TT-n-iso-Cor)H(2) and (TT-n-iso-Cor)M(II), where n = 5 or 10 and M = Ni or Cu, were synthesized and characterized by electrochemistry and spectroelectrochemistry in CH(2)Cl(2) containing 0.1 M tetra-n-butylammonium perchlorate. The metalation of the free-base macrocycles with Co(II), Mn(III), or Zn(II) was also attempted but was unsuccessful. Six isocorroles were isolated and shown to undergo two stepwise oxidations to give pi-cation radicals and dications in CH(2)Cl(2), with the most stable products being obtained in the case of the 10-substituted derivatives. The same isocorrolescould 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 corroleconversion upon reduction and reoxidation and was monitored by both electrochemistry and thin-layer spectroelectrochemistry.
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