Literature DB >> 25594728

Halogenated boron-dipyrromethenes: synthesis, properties and applications.

Vellanki Lakshmi1, Malakalapalli Rajeswara Rao, Mangalampalli Ravikanth.   

Abstract

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. Among the functional groups, halogens are the functional groups which can be regiospecifically introduced at any desired pyrrole carbon of the BODIPY framework by adopting appropriate synthetic strategies. The halogenated BODIPYs can undergo facile nucleophilic substitution reactions to prepare several interesting BODIPY based compounds. This review describes the synthesis, properties and potential applications of halogenated BODIPYs containing one to six halogens at the pyrrole carbons of the BODIPY core as well as properties and applications of some of the substituted BODIPYs derived from halogenated BODIPYs.

Entities:  

Year:  2015        PMID: 25594728     DOI: 10.1039/c4ob02293a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  13 in total

1.  Synthesis of BODIPY-Peptide Conjugates for Fluorescence Labeling of EGFR Overexpressing Cells.

Authors:  Ning Zhao; Tyrslai M Williams; Zehua Zhou; Frank R Fronczek; Martha Sibrian-Vazquez; Seetharama D Jois; M Graça H Vicente
Journal:  Bioconjug Chem       Date:  2017-04-28       Impact factor: 4.774

2.  BCl3-Activated Synthesis of COO-BODIPY Laser Dyes: General Scope and High Yields under Mild Conditions.

Authors:  César Ray; Christopher Schad; Florencio Moreno; Beatriz L Maroto; Jorge Bañuelos; Teresa Arbeloa; Inmaculada García-Moreno; Cassie Villafuerte; Gilles Muller; Santiago de la Moya
Journal:  J Org Chem       Date:  2020-03-17       Impact factor: 4.354

3.  Spectroscopic and 1O2 Sensitization Characteristics of a Series of Isomeric Re(bpy)(CO)3Cl Complexes Bearing Pendant BODIPY Chromophores.

Authors:  Andrea M Potocny; Justin J Teesdale; Alize Marangoz; Glenn P A Yap; Joel Rosenthal
Journal:  Inorg Chem       Date:  2019-04-03       Impact factor: 5.165

4.  Carbazole Substituted BODIPYs: Synthesis, Computational, Electrochemical and DSSC Studies.

Authors:  Praseetha E Kesavan; Raghu Nath Behera; Shigeki Mori; Iti Gupta
Journal:  J Fluoresc       Date:  2017-08-14       Impact factor: 2.217

5.  Stepwise Polychlorination of 8-Chloro-BODIPY and Regioselective Functionalization of 2,3,5,6,8-Pentachloro-BODIPY.

Authors:  Ning Zhao; Sunting Xuan; Frank R Fronczek; Kevin M Smith; M Graça H Vicente
Journal:  J Org Chem       Date:  2015-07-28       Impact factor: 4.354

6.  Synthesis and regioselective functionalization of perhalogenated BODIPYs.

Authors:  Ning Zhao; Sunting Xuan; Brandon Byrd; Frank R Fronczek; Kevin M Smith; M Graça H Vicente
Journal:  Org Biomol Chem       Date:  2016-06-02       Impact factor: 3.876

Review 7.  Boron chemistry in a new light.

Authors:  Guillaume Duret; Robert Quinlan; Philippe Bisseret; Nicolas Blanchard
Journal:  Chem Sci       Date:  2015-07-31       Impact factor: 9.825

8.  Light-Activated Carbon Monoxide Prodrugs Based on Bipyridyl Dicarbonyl Ruthenium(II) Complexes.

Authors:  Stepan Geri; Tereza Krunclova; Olga Janouskova; Jiri Panek; Martin Hruby; Daniel Hernández-Valdés; Benjamin Probst; Roger A Alberto; Constantin Mamat; Manja Kubeil; Holger Stephan
Journal:  Chemistry       Date:  2020-08-13       Impact factor: 5.236

Review 9.  Design of BODIPY dyes as triplet photosensitizers: electronic properties tailored for solar energy conversion, photoredox catalysis and photodynamic therapy.

Authors:  Elena Bassan; Andrea Gualandi; Pier Giorgio Cozzi; Paola Ceroni
Journal:  Chem Sci       Date:  2021-04-14       Impact factor: 9.825

10.  Targeting EGFR Overexpression at the Surface of Colorectal Cancer Cells by Exploiting Amidated BODIPY-Peptide Conjugates.

Authors:  Tyrslai M Williams; Zehua Zhou; Sitanshu S Singh; Martha Sibrian-Vazquez; Seetharama D Jois; Maria da Graça Henriques Vicente
Journal:  Photochem Photobiol       Date:  2020-04-16       Impact factor: 3.421

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