Literature DB >> 22515199

Electrochemistry and electrogenerated chemiluminescence of BODIPY dyes.

Alexander B Nepomnyashchii1, Allen J Bard.   

Abstract

BODIPY (boron dipyrromethene) dyes are unique materials with spectroscopic and electrochemical properties comparable to those of aromatic hydrocarbons. Electrochemical studies are useful in understanding the redox properties of these materials and finding structure-stability relations for the radical ions; along with spectroscopy, these studies help researchers design novel compounds with desired properties. This Account represents our attempt at a full description of the electrochemical and electrogenerated chemiluminescence (ECL) properties of the BODIPY dyes. When the dyes are completely substituted with alkyl or other groups, the radical ions of BODIPY dyes are highly stable. But if they include unsubstituted positions, the radical ions can undergo dimerization or other reactions. BODIPY dyes also show unusually large separations, ~1.0 V, between the first and second cyclic voltammetric (CV) waves for both oxidation and reduction half-reactions. Alkyl-substituted BODIPY dyes show good photoluminescence (PL) quantum efficiencies, and radical ion electron transfer annihilation in these molecules produces electrogenerated chemiluminescence (ECL), the intensity of which depends on the structure of the dye. The large separation between waves and the presence of strong ECL signals are both important in the design of stable ECL-based materials. The ECL spectra provide a fast method of monitoring the electrochemical formation of dimers and aggregates from the monomers. BODIPY dyes are particularly good systems for studying stepwise electron transfer in their chemically synthesized oligomers and polymers because of the small separation between the first oxidation and first reduction waves, generally about 2.0-2.4 V, and their relative ease of reduction compared with many other aromatic compounds. The larger separation between consecutive waves for oxidation compared with reduction is noticeable for all BODIPY dimers and trimers. We also observe a more difficult addition or extraction of a third electron compared with the second for the trimers, signaling the importance of electrostatic interactions. In general, BODIPY dyes combine interesting electrochemical and spectroscopic properties that suggest useful analytical applications.

Entities:  

Year:  2012        PMID: 22515199     DOI: 10.1021/ar200278b

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  25 in total

1.  Synthesis and Spectroscopic Investigation of a Series of Push-Pull Boron Dipyrromethenes (BODIPYs).

Authors:  Sunting Xuan; Ning Zhao; Xiangyi Ke; Zehua Zhou; Frank R Fronczek; Karl M Kadish; Kevin M Smith; M Graça H Vicente
Journal:  J Org Chem       Date:  2017-02-16       Impact factor: 4.354

2.  Synthesis, Photophysics, Electrochemistry and Electrogenerated Chemiluminescence of PEG-Modified BODIPY dyes in Organic and Aqueous Solutions.

Authors:  Alexander B Nepomnyashchii; Allen J Pistner; Allen J Bard; Joel Rosenthal
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2013-03-21       Impact factor: 4.126

3.  Photocatalytic Conversion of CO2 to CO using Rhenium Bipyridine Platforms Containing Ancillary Phenyl or BODIPY Moieties.

Authors:  Gabriel A Andrade; Allen J Pistner; Glenn P A Yap; Daniel A Lutterman; Joel Rosenthal
Journal:  ACS Catal       Date:  2013-08-02       Impact factor: 13.084

4.  Redox switchable catalysis utilizing a fluorescent dye.

Authors:  Brena L Thompson; Casey R Simons; Zachariah M Heiden
Journal:  Chem Commun (Camb)       Date:  2019-09-19       Impact factor: 6.222

5.  A BODIPY-Based Water-Soluble Fluorescent Probe for Naked Eye Detection of pH.

Authors:  Xianjiao Meng; Duanlin Cao; Zhiyong Hu; Zhichun Li; Xinghua Han; Wenbing Ma
Journal:  J Fluoresc       Date:  2019-11-22       Impact factor: 2.217

6.  Design, Synthesis, Characterization and Electrochemical Properties of BODIPY Dyes Containing Mono, Bis-2-Naphthyloxyhexyloxy and 4-(Benzyloxy)Phenoxyhexyloxy Groups.

Authors:  Zekeriya Biyiklioglu; Turgut Keleş
Journal:  J Fluoresc       Date:  2016-09-03       Impact factor: 2.217

7.  Reversible Absorption and Emission Responses of Nile Blue and Azure A Derivatives in Extreme Acidic and Basic Conditions.

Authors:  Xiu-Li Wang; Ru Sun; Wei-Jin Zhu; Xin-Long Sha; Jian-Feng Ge
Journal:  J Fluoresc       Date:  2017-02-06       Impact factor: 2.217

8.  Ground State and Excited State Tuning in Ferric Dipyrrin Complexes Promoted by Ancillary Ligand Exchange.

Authors:  Claudia Kleinlein; Shao-Liang Zheng; Theodore A Betley
Journal:  Inorg Chem       Date:  2017-04-24       Impact factor: 5.165

9.  Synthesis, electrochemistry, and electrogenerated chemiluminescence of two BODIPY-appended bipyridine homologues.

Authors:  Honglan Qi; Justin J Teesdale; Rachel C Pupillo; Joel Rosenthal; Allen J Bard
Journal:  J Am Chem Soc       Date:  2013-08-27       Impact factor: 15.419

Review 10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.