1354013-66-3Relevant academic research and scientific papers
Tetrathienyl-functionalized red- and NIR-absorbing BODIPY dyes appending various peripheral substituents
Liu, Ping,Gao, Feng,Zhou, Lina,Chen, Yu,Chen, Zhijian
, p. 1393 - 1399 (2017/02/15)
A series of boron-dipyrromethene dyes (BODIPYs) 4a-g with different thienyl moieties at 2,3,5,6-positions of the BODIPY core were synthesized by the Stille cross-coupling reaction. The new compounds were characterized by 1H NMR, 13C
α-fused dithienyl BODIPYs synthesized by oxidative ring closure
Heyer, Elodie,Retailleau, Pascal,Ziessel, Raymond
supporting information, p. 2330 - 2333 (2014/05/20)
Both symmetrical and unsymmetrical α-fused dithienyl-BODIPY dyes have been prepared by oxidative ring closure induced by anhydrous FeCl3. Extension of the π-system in the fused BODIPY leads to a progressive shift to 579 and 665 nm respectively
Synthesis and functionalization of new polyhalogenated BODIPY dyes. Study of their photophysical properties and singlet oxygen generation
Ortiz, Maria J.,Agarrabeitia, Antonia R.,Duran-Sampedro, Gonzalo,Ba?uelos Prieto, Jorge,Lopez, Teresa Arbeloa,Massad, Walter A.,Montejano, Hernán A.,García, Norman A.,Lopez Arbeloa, I?igo
experimental part, p. 1153 - 1162 (2012/02/15)
A theoretical and experimental study on the iodination of BODIPY dyes with different degrees of substitution has been developed. Polyhalogenated BODIPYs synthesized in this work are the first examples of this type of dyes with more than two halogen atoms
