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Angew Chem Int Ed Engl ; 59(37): 15897-15901, 2020 Sep 07.
Artigo em Inglês | MEDLINE | ID: mdl-32449826

RESUMO

A copper complex of a heterocorrole analogue with an N-N linkage, 1,19-diaza-21,24-dicarbadibenzocorrole (Cu-5), was successfully synthesized via oxidative metalation-cyclization of a tetrapyrrolic precursor. The N-N linkage in the skeleton of Cu-5, which serves as a mediator of π-electron delocalization, features an 18π aromatic system. The electronic structure of Cu-5 is best described as a ground-state singlet species stabilized by the distinct NNCC coordination core. This finding shows how the ligand's design can be used to modulate the Cu 3 d x 2 - y 2 orbital energy, thereby making such compounds invaluable for copper-based catalytic applications.

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