Corroles have come a long way from being a curiosity to being a mainstream research topic.
They are now regularly synthesized in numerous research laboratories worldwide with …

Expanded porphyrins are synthetic analogues of the porphyrins, and differ from these and
other naturally occurring tetrapyrrolic macrocycles by containing a larger central core with a …

The heteroatom-containing porphyrin analogues or core-modified porphyrins that resulted
from the replacement of one or two pyrrole rings with other five-membered heterocycles …

Even though the first expanded porphyrin was reported in the mid-1960s, the advances in its
chemistry are more recent. New and powerful synthetic methods have facilitated the …

Porphyrins and expanded porphyrins have attracted the attention of chemists for a long time
in view of their diverse applications in catalysis; as anion, cation, and neutral substrate …

Abstract Expandierte Porphyrine sind synthetische Analoga der Porphyrine und
unterscheiden sich von diesen und anderen natürlichen makrocyclischen Tetrapyrrolen …

High quantum yields are found for the prototype metallocorrole 1, which is readily prepared
from GaCl3 and tris (pentafluorophenyl) corrole. The crystallographic and electronic …

We have developed a new methodology that affords regioisomerically pure trans-A2B-
corroles. The corrole formation reaction involves the acid-catalyzed condensation of a …

Monoheteroatom substituted porphyrins and diheteroatom substituted porhyrins resulting
from the replacement of one and two nitrogen atoms, respectively, are very stable aromatic …

Porphyrins are tetrapyrrolic 18 π electron conjugated macrocycles with wide applications
that range from materials to medicine. Expanded porphyrins, synthetic analogues of …