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 …

Subphthalocyanines (SubPcs) have undergone extensive research activity because of their
unique properties, rich chemistry, and tremendous applicability. Over decades, researchers …

Eighteen boron subphthalocyanines (BsubPcs) axial derivatives were synthesized through
axial exchange reactions with Br-BsubPc under relatively mild conditions to systematically …

A sub-group of the phthalocyanine family, the boron subphthalocyanines (BsubPcs), have
robust chemistry and can be readily modified at the axial and peripheral positions to tune …

Boron subphthalocyanines (SubPcs) are cone shaped π-conjugated molecules comprised
of three azomethine-bridged isoindole units and a central boron atom with an axial …

A novel and straightforward strategy for boron functionalization in boron dipyrromethenes
(BODIPYs) is developed. In particular, this synthetic strategy provides new possibilities for …

“Homoleptic” tetracoordinate boron compounds, in which the central boron atom links to four
identical atoms, are a special and important family of boron compounds. During the past …

Chiral conjugated materials with curved topologies hold significant promise for advanced
optoelectronic applications. Among these, bowl-shaped subphthalocyanine (SubPc) …

Boron subphthalocyanines comprised of three isoindole units bridged by aza‐linkages are
attractive light harvesters on account of their intense low‐energy absorptions. Herein, we …

Although a wide variety of boron-based “scorpionate” ligands have been implemented, a
modular route that offers facile access to different substitution patterns at boron has yet to be …