Synthesis of BODIPY dyes through postfunctionalization of the boron dipyrromethene core

N Boens, B Verbelen, MJ Ortiz, L Jiao… - Coordination Chemistry …, 2019 - Elsevier
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 …

Structural modification strategies for the rational design of red/NIR region BODIPYs

H Lu, J Mack, Y Yang, Z Shen - Chemical Society Reviews, 2014 - pubs.rsc.org
This review focuses on classifying different types of long wavelength absorbing BODIPY
dyes based on the wide range of structural modification methods that have been adopted …

Fluorescent indicators based on BODIPY

N Boens, V Leen, W Dehaen - Chemical Society Reviews, 2012 - pubs.rsc.org
This critical review covers the advances made using the 4-bora-3a, 4a-diaza-s-indacene
(BODIPY) scaffold as a fluorophore in the design, synthesis and application of fluorescent …

Postfunctionalization of the BODIPY core: synthesis and spectroscopy

N Boens, B Verbelen, W Dehaen - European Journal of …, 2015 - Wiley Online Library
In this review we describe the various new methodologies for synthetic postmodification of
the BODIPY core designed and developed by our research groups, as well as their …

Establishing design principles for emissive organic SWIR chromophores from energy gap laws

HC Friedman, ED Cosco, TL Atallah, S Jia, EM Sletten… - Chem, 2021 - cell.com
The rational design of bright near and shortwave infrared (NIR: 700–1,000; SWIR: 1,000–
2,000 nm) emitters remains an open question with applications spanning imaging and …

Geometry relaxation-induced large Stokes shift in red-emitting borondipyrromethenes (BODIPY) and applications in fluorescent thiol probes

Y Chen, J Zhao, H Guo, L Xie - The Journal of organic chemistry, 2012 - ACS Publications
2-Thienyl and 2, 6-bisthienyl BODIPY derivatives (BS-SS and BS-DS) were prepared that
show intense absorption (ε= 65000 M–1 cm–1 at 507 nm) and a large Stokes shift (96 nm) …

Singlet oxygen generation by novel NIR BODIPY dyes

SG Awuah, J Polreis, V Biradar, Y You - Organic Letters, 2011 - ACS Publications
Five novel near-infrared BODIPY dyes were prepared for improved singlet oxygen
generation using thiophene and bromine. Theoretical, optical, photostable, and singlet …

Halogenated boron-dipyrromethenes: synthesis, properties and applications

V Lakshmi, MR Rao, M Ravikanth - Organic & Biomolecular Chemistry, 2015 - pubs.rsc.org
Boron-dipyrromethene dyes (BODIPYs) containing halogens at pyrrole carbons are very
useful synthons for the synthesis of a variety of BOIDPYs for a wide range of applications …

A highly selective red-emitting FRET fluorescent molecular probe derived from BODIPY for the detection of cysteine and homocysteine: an experimental and …

J Shao, H Sun, H Guo, S Ji, J Zhao, W Wu, X Yuan… - Chemical …, 2012 - pubs.rsc.org
A red-emitting BODIPY-based fluorescent-resonance-energy-transfer (FRET) molecular
probe 1 for selective detection of cysteine and homocysteine was designed. The …

Design, synthesis and functionalization of BODIPY dyes: applications in dye-sensitized solar cells (DSSCs) and photodynamic therapy (PDT)

IS Yadav, R Misra - Journal of Materials Chemistry C, 2023 - pubs.rsc.org
In recent years, BODIPY dyes have emerged as a valuable category of luminogens for
optoelectronic applications because of their spectacular properties, such as good …