Isocyanate-, Isothiocyanate-, Urea-, and Thiourea-Substituted Boron Dipyrromethene Dyes as Fluorescent Probes

2006 ◽  
Vol 71 (8) ◽  
pp. 3093-3102 ◽  
Author(s):  
Raymond Ziessel ◽  
Laure Bonardi ◽  
Pascal Retailleau ◽  
Gilles Ulrich
Keyword(s):  
Fluorescent Probes ◽  
Boron Dipyrromethene

Pyrrolopyrrole aza boron dipyrromethene based two-photon fluorescent probes for subcellular imaging

2018 ◽  
Vol 6 (35) ◽  
pp. 5570-5581 ◽  
Author(s):  
Yimin Zhou ◽  
Chao Ma ◽  
Nengyue Gao ◽  
Qiong Wang ◽  
Pui-Chi Lo ◽  
...  
Keyword(s):  
Fluorescent Probes ◽  
Two Photon ◽  
Boron Dipyrromethene ◽  
Subcellular Imaging

A series of two-photon-absorbing pyrrolopyrrole aza boron dipyrromethenes have been prepared which can serve as fluorescent probes for subcellular imaging.

Development of 2,6-carboxy-substituted boron dipyrromethene (BODIPY) as a novel scaffold of ratiometric fluorescent probes for live cell imaging

2009 ◽  
pp. 7015 ◽  
Author(s):  
Toru Komatsu ◽  
Yasuteru Urano ◽  
Yuuta Fujikawa ◽  
Tomonori Kobayashi ◽  
Hirotatsu Kojima ◽  
...  
Keyword(s):  
Fluorescent Probes ◽  
Live Cell Imaging ◽  
Cell Imaging ◽  
Live Cell ◽  
Boron Dipyrromethene ◽  
Novel Scaffold

Spectroscopic characterization of synthetic heteroatom-functionalized fluorescent probes for bioimaging / Sentetik heteroatom-fonksiyonelize floresans probların biyogörüntüleme uygulamaları için spektroskopik karakterizasyonu

2015 ◽  
Vol 40 (5) ◽  
Author(s):  
Özlem Dilek
Keyword(s):  
Fluorescent Probes ◽  
Emission Spectra ◽  
Spectroscopic Characterization ◽  
Spectroscopic Properties ◽  
Absorption Bands ◽  
Broad Absorption ◽  
Cellular Environment ◽  
Boron Dipyrromethene ◽  
Biological Labeling

AbstractObjective: Fluorescent probes are essential tools for monitoring biological systems in cellular environment. Several boron dipyrromethene (BODIPY) derived fluorescent probe derivatives have been synthesized by nucleophilic substitution reaction and their spectroscopic properties have also been determined.Methods: Initial BODIPY dye framework was prepared from the reaction of pyrrole-2-carbaldehyde and benzaldehyde and then readily reacted with heteroatom-based nucleophiles at 3- and 5- position of BODIPY core. The spectroscopic properties of these new molecules have been reported.Results: Amine based nucleophiles tend to produce broad absorption bands on the spectra. Our studies indicated that heteroatom-based nucleophiles on the BODIPY core resulted in a red shift on the absorption and emission spectra.Conclusion: The synthesized fluorophores can therefore be potentially used as imaging agents for biological labeling.

Boron-Dipyrromethene-Functionalized Hemilabile Ligands as “Turn-On” Fluorescent Probes for Coordination Changes in Weak-Link Approach Complexes

2013 ◽  
Vol 52 (9) ◽  
pp. 5484-5492 ◽  
Author(s):  
Alejo M. Lifschitz ◽  
Chad M. Shade ◽  
Alexander M. Spokoyny ◽  
Jose Mendez-Arroyo ◽  
Charlotte L. Stern ◽  
...  
Keyword(s):  
Fluorescent Probes ◽  
Weak Link ◽  
Hemilabile Ligands ◽  
Turn On ◽  
Boron Dipyrromethene

Boronic Acid Functionalized Boron Dipyrromethene Fluorescent Probes: Preparation, Characterization, and Saccharides Sensing Applications

2012 ◽  
Vol 84 (23) ◽  
pp. 10214-10220 ◽  
Author(s):  
Jingying Zhai ◽  
Ting Pan ◽  
Jingwei Zhu ◽  
Yanmei Xu ◽  
Juan Chen ◽  
...  
Keyword(s):  
Fluorescent Probes ◽  
Boronic Acid ◽  
Sensing Applications ◽  
Boron Dipyrromethene
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