Half a century after the synthesis of the first subporphyrinoid, the study of tripyrrole and
trisoindole porphyrin analogues constitutes a fervent and rapidly expanding research area …

A 1, 1, 4, 4-tetracyanobuta-1, 3-diene (TCBD)–aniline moiety has been introduced, for the
first time, at the axial position of two subphthalocyanines (SubPcs) peripherally substituted …

Porphyrins are widely used in anticancer photodynamic therapy (PDT). However, low
physiological solubility and lack of selectivity towards cancer cells are the main limitations of …

Two subphthalocyanines (SubPcs) decorated at their peripheral (SubPc 1) or peripheral and
axial (SubPc 2) positions with tetracyanobuta-1, 3-diene (TCBD)–aniline moieties have …

Boron subphthalocyanines bearing a wide range of functional groups were tested as
prospective photosensitizers and fluorophores. Synthetic protocols to novel 4 …

The efficient harvesting and transport of visible light by electronic energy transfer (EET) are
critical to solar energy conversion in both nature and molecular electronics. In this work, we …

Subphthalocyanine has been incorporated into a robust metal–organic framework having
amino groups as binding sites. The resulting SubPc@ MIL-101 (Cr)-NH2 composite has a …

An efficient post-macrocyclization strategy to new octaphenoxy-substituted zinc
pyrazinoporphyrazine has been developed. This approach allows avoiding the template …

Phenyl and phenoxy-substituted boron subphthalocyanines were decorated by non-
steroidal anti-inflammatory drug diclofenac using axial exchange reaction. Target complexes …

Quantum-chemical calculation of the molecular structures of potential isomeric (NNNN)-
donoratomic macrocyclic tetradentate ligands, cis-and trans-di [benzo] porphyrazines, was …