Due to enthralling applications in various fields and augmenting fundamental wisdom, π-
conjugated macrocycles in general and porphyrin systems in particular are constantly …

This Review discusses the recent developments in the field of synthetic chemistry of PAH–
porphyrin hybrids, emphasizing phenanthrene‐embedded carbaporphyrinoids and related …

Dual-cavity macrocycles with extended π-conjugation are synthetically challenging yet
attractive targets, exhibiting intriguing topologies and functional properties. In this work, a …

Stable and nonaromatic phenothiazinophyrins which resulted from the replacement of one
of the pyrrole rings of porphyrin with a phenothiazine unit were synthesized by condensing …

Unprecedented nonaromatic stable phenothiazine-embedded porphyrinoids were
synthesized by incorporating phenothiazine subunits into the hexaphyrin framework. The …

A series of new stable dibenzothiophene embedded heteroporphyrins were synthesized in 6–
7% yields by condensing 1 equiv of dibenzothiophene-based tripyrrane with 1 equiv of four …

A tetra-functionalized pyrene precursor 4b is prepared using the Suzuki–Miyaura coupling of
1, 3, 6, 8-tetrabromopyrene with N-Boc-2-pyrroleboronic acid. 4b displayed a blue emission …

The one-and two-photon absorption (1PA and 2PA) properties of three expanded
aceneporphyrinoids, 28-thia-, 28-selena-and 28-tellura-2, 7-naphthiporphyrin, have been …

A new type of expanded dibenzothiophene-containing thiacarbaporphyrinoid containing
one dibenzothiophene, two p-phenylene, one thiophene, and two pyrrole rings connected …

The synthesis of a new class of carbazole based macrocycles via [3+ 1] acid-catalyzed
condensation is reported. Spectroscopic investigations and computational studies imply that …