Carbenaporphyrins: No Longer Missing Ligands in N‐Heterocyclic Carbene Chemistry
Theo Maulbetsch, Doris Kunz
Abstract
macrocyclic framework can be obtained via a 1,3-dipolar cycloaddition ("click-reaction") to form two triazole moieties which were alkylated to the respective triazolium macrocycle. Deprotonation of the ligand precursor with lithium bases to the respective dilithio carbenaporphyrin complex and transmetallation to scandium lead to complexes that exhibit orange fluorescence. Optical property combined with TD-DFT studies verify an aromatic character for each heterocyclic moiety rather than an antiaromatic macrocycle in the ligand precursor as well as in the complexes. While the geometric features of the carbenaporphyrin ligand strongly resemble those of porphyrin, DFT calculations reveal a stronger electron-donating ability of the new ligand.