2019
DOI: 10.1016/bs.aihch.2018.12.001
|View full text |Cite
|
Sign up to set email alerts
|

Recent developments in the synthesis of the BODIPY dyes

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
28
0

Year Published

2019
2019
2024
2024

Publication Types

Select...
6
3

Relationship

0
9

Authors

Journals

citations
Cited by 53 publications
(28 citation statements)
references
References 217 publications
0
28
0
Order By: Relevance
“…In this regard, the boron atom is a key position for functionalization of BODIPYs keeping the photophysical properties of the chromophore. Therefore, it has led to easy preparation of dyes with enhanced photostability for lasing, improved water solubility for biological applications, boosted energy-transfer processes for collecting light efficiently, among other valuable applications [7][8][9][10]. BODIPY functionalization at the boron atom has also been used to chirally perturb the inherently achiral BODIPY chromophore towards CPL.…”
Section: Introductionmentioning
confidence: 99%
“…In this regard, the boron atom is a key position for functionalization of BODIPYs keeping the photophysical properties of the chromophore. Therefore, it has led to easy preparation of dyes with enhanced photostability for lasing, improved water solubility for biological applications, boosted energy-transfer processes for collecting light efficiently, among other valuable applications [7][8][9][10]. BODIPY functionalization at the boron atom has also been used to chirally perturb the inherently achiral BODIPY chromophore towards CPL.…”
Section: Introductionmentioning
confidence: 99%
“…The most representative example of dipyrromethene metal complexes are 4,4-difluoro-4-bora-3a,4a-diaza-s-indacenes also known as BODIPYs, which have been successfully used as fluorescent probes in diverse applications [8,9,10]. Other metal complexes have also attracted researchers’ attention, for example, recently, aluminium complexes have been used as catalysts for polymerization reactions [11,12], iron complexes [13] have been used as catalysts for C-H bond amination [14,15], and ruthenium complexes of dipyrromethenes [16,17] were synthetized as precursors of bis(2,2′-bipyridyl)(dipyrrinato)ruthenium(II) complexes.…”
Section: Introductionmentioning
confidence: 99%
“…Herein, bibliographic coverage of the developments on the synthesis of dipyrromethanes since the last reviews in this area [9,30,31,32] is provided (2014–2019). The synthetic strategies have been organized in two main approaches: classical synthetic strategies based on the first report on the synthesis of meso -substituted dipyrromethanes, disclosed in 1974 [33], using acid catalyzed condensation of pyrrole and aldehydes; and recent breakthroughs in dipyrromethane chemistry which allow the synthesis of dipyrromethanes with new substitution patterns.…”
Section: Introductionmentioning
confidence: 99%
“…This chromophore is chemically robust, stable under hard irradiation doses and shows excellent photophysical properties [14][15][16]. Nevertheless, likely its main advantage is the impressive chemical versatility of its boron-dipyrrin backbone, which allows a fine control and tailoring of the photophysical signatures [17,18]. Therefore, a wide assortment of chemical modifications can be applied at the chromophore leading to a vast battery of available functional group [19,20].…”
Section: Introductionmentioning
confidence: 99%