articleTop 1% cited
The Chemistry of Fluorescent Bodipy Dyes: Versatility Unsurpassed
Angewandte Chemie International Edition · 2007 · Vol. 47(7) · pp. 1184–1201
Gilles UlrichRaymond Ziessel✉(Laboratoire des Matériaux Surfaces et Procédés pour la Catalyse)Anthony Harriman
Abstract
The world of organic luminophores has been confined for a long time to fairly standard biological labeling applications and to certain analytical tests. Recently, however, the field has undergone a major change of direction, driven by the dual needs to develop novel organic electronic materials and to fuel the rapidly emerging nanotechnologies. Among the many diverse fluorescent molecules, the Bodipy family, first developed as luminescent tags and laser dyes, has become a cornerstone for these new applications. The near future looks extremely bright for "porphyrin's little sister".
Luminescence and Fluorescent MaterialsMolecular Sensors and Ion DetectionPorphyrin and Phthalocyanine ChemistryBODIPYFluorescenceNanotechnologyChemistryLuminescencePorphyrinCornerstonePhotochemistryMaterials scienceOptoelectronics
Citations
3,075
FWCI
42.54
field-weighted impact
References
112
Percentile
100%
vs. same field & year
Citations per year
Cited by
BODIPY dyes in photodynamic therapy
Chemical Society Reviews · 2012 · 2,028 citations
Postfunctionalization of the BODIPY Core: Synthesis and Spectroscopy
European Journal of Organic Chemistry · 2015 · 320 citations
Boron dipyrromethene (BODIPY)-based photosensitizers for photodynamic therapy
RSC Advances · 2012 · 623 citations
Photon upconversion based on sensitized triplet–triplet annihilation
Coordination Chemistry Reviews · 2010 · 1,431 citations
Designs of Functional π-Electron Materials based on the Characteristic Features of Boron
Bulletin of the Chemical Society of Japan · 2015 · 250 citations
Tetraphenylethene: a versatile AIE building block for the construction of efficient luminescent materials for organic light-emitting diodes
Journal of Materials Chemistry · 2012 · 848 citations
Twisted Intramolecular Charge Transfer and Aggregation-Induced Emission of BODIPY Derivatives
The Journal of Physical Chemistry C · 2009 · 1,005 citations
A Panchromatic Boradiazaindacene (BODIPY) Sensitizer for Dye-Sensitized Solar Cells
Organic Letters · 2008 · 414 citations
References
Palladium‐Catalyzed Coupling Reactions for the Functionalization of BODIPY Dyes with Fluorescence Spanning the Visible Spectrum
European Journal of Organic Chemistry · 2006 · 255 citations
BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties
Chemical Reviews · 2007 · 5,045 citations
Signaling Recognition Events with Fluorescent Sensors and Switches
Chemical Reviews · 1997 · 6,903 citations
A highly efficient sensor molecule emitting in the near infrared (NIR): 3,5-distyryl-8-(p-dimethylaminophenyl)difluoroboradiaza-s-indacene
New Journal of Chemistry · 2001 · 207 citations
Related articles
Far-red and near infrared BODIPY dyes: synthesis and applications for fluorescent pH probes and bio-imaging
Organic & Biomolecular Chemistry · 2014 · 663 citations
Citation Network
How this paper connects to the literature. Drag to explore, click any node to open that paper.
