The use of boron dipyrromethene (BODIPY) in biomedicine is reviewed. To open, its
synthesis and regulatory strategies are summarized, and inspiring cutting‐edge work in post …

Azadipyrromethenes were first described over 70 years ago as blue pigments, but now are
rapidly emerging as a compound class with highly desirable near infrared photophysical …

Abstract Aza-boron-dipyrromethenes (Aza-BODIPYs) are a class of dyes that display
absorption and emission covering visible to NIR region. They can show NIR emission in the …

Aza-BODIPY is an important class of heteroatom-containing BODIPY analogue with strongly
electron-withdrawing nitrogen atom instead of methine carbon atom at the meso-position …

It is commonly accepted that a large π-conjugated system is necessary to realize low-energy
electronic transitions. Contrary to this prevailing notion, we present a new class of light …

BODIPY dyes are well-known for their outstanding features, such as solubility in a wide
range of solvents, useful photophysical properties, and good photochemical and thermal …

Synthesis pathways for the preparation of the BODIPY analogues: aza-BODIPYs, BOPHYs
and some other pyrrole-based acyclic chromophores - Dalton Transactions (RSC Publishing) …

The typical aza-BODIPYs in the dye family are known for bright fluorescence, excellent
stability, and tunable absorption wavelengths. Hence, these dyes are attracting the …

Annularly fused azaBODIPY-based organic fluorophores (HBPs 2) containing up to 13
aromatic ring fusions were synthesized by a Suzuki coupling reaction with …

Three novel π-extended BF2 complexes of β, β-bisphenanthrene-fused azadipyrromethenes
containing nine fused rings have been synthesized on the basis of a tandem Suzuki …