Difluoro-4-bora-3a, 4a-diaza-s-indacene (BODIPY)-based-π-conjugated derivatives are
endowed with extraordinary photonic and electronic properties. The BODIPYs possess …

Fluorophores based on the 4-bora-3a, 4a-diaza-s-indacene (aka boron dipyrromethene,
boron dipyrrin, or BODIPY) platform have found diverse applications in different fields of …

BF2-based fluorophores, such as the well-known BODIPY (4, 4-difluoro-4-bora-3a, 4a-diaza-
s-indacene) dye, are prevalently used in diverse research areas (eg, bioimaging and …

The BODIPYs are a very widely used class of fluorescent dyes, based around a heterocyclic
organic framework, which have found applications across a broad range of research areas …

A fundamental, highly fluorescent, and easily accessible scaffold named BOPPY is reported.
The use of hydrazine as a bridging linkage between pyrrole and N-heteroarenes enables …

Regioselective and stepwise syntheses of a series of functionalized BODIPY dyes through
palladium-catalyzed cross-coupling reactions and direct C–H arylations have been …

Near‐infrared (NIR) fluorophores with characteristics such as deep tissue penetration,
minimal damage to the biological samples, and low background interference, are highly …

Regioselective functionalization of 2, 3, 5, 6, 8-pentachloro-BODIPY 1 produced
unsymmetric BODIPY 5, bearing an isothiocyanate group suitable for conjugation, in only …

A series of push–pull BODIPYs bearing multiple electron-donating and electron-acceptor
groups were synthesized regioselectively from 2, 3, 5, 6, 8-pentachloro-BODIPY, and …

Facile synthetic routes to a new class of red α-benzo-fused BOPHYs with 6, 5, 6, 6, 5, 6-
hexacyclic fused rings and β-thiophene-fused BOPHYs with 5, 5, 6, 6, 5, 5-hexacyclic fused …