1189166-60-6Relevant academic research and scientific papers
A highly selective turn-on fluorescent chemodosimeter for Cr(vi) and its application in living cell imaging
Ye, Jia-Hai,Wang, Yixin,Bai, Yang,Zhang, Wenchao,He, Weijiang
, p. 2989 - 2992 (2014)
A BODIPY-based fluorescent probe, functionalized with an aminomaleonitrile was synthesized as a turn-on fluorescent chemodosimeter for Cr(vi) in aqueous solution based on the Cr(vi) promoted oxidation reaction. Moreover, it can fluorescently respond to Cr(vi) in living cells.
A colorimetric and highly sensitive and selective chemodosimeter for Cu2+ and its application in live cell imaging
Ye, Jia-Hai,Xu, Jing,Chen, Huachao,Bai, Yang,Zhang, Wenchao,He, Weijiang
, p. 6269 - 6273 (2014)
A new BODIPY (4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene)-based colorimetric and fluorescent chemodosimeter 1 has been designed and synthesized. Specific turn-on fluorescence response of 1 for Cu2+ was investigated in CH3CN-H2O (1:1, v/v) solution, which can be deduced to a reaction of Cu2+ promoted selectively hydrolysis of CN bond to generate formyl-BODIPY. The chemodosimeter 1 can selectively recognize Cu2+ rather than other metal ions in aqueous solution. Confocal fluorescence imaging of cells for detecting Cu2+ in vivo was carried out successfully. The favorable features of chemodosimeter 1 toward Cu2+ include significant fluorescence enhancement (1340-fold), high selectivity, and low detection limit (0.2 μM).
Cell membrane targeted BODIPY type organic photosensitizer and application
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Paragraph 0023; 0032; 0040-0042, (2021/06/26)
The invention belongs to the field of tumor photodynamic therapy application, and particularly relates to a cell membrane targeted BODIPY type organic photosensitizer and application. The BODIPY type organic dye molecule provided by the invention has the advantages of cell membrane targeting, AIE characteristic, high ROS generation efficiency, capability of realizing fluorescence imaging guided tumor photodynamic therapy and the like.
β-formyl-BODIPYs from the Vilsmeier-Haack reaction
Jiao, Lijuan,Yu, Changjiang,Li, Jilong,Wang, Zhaoyun,Wu, Min,Hao, Erhong
supporting information; experimental part, p. 7525 - 7528 (2010/01/06)
(Chemical Equation Presented) A series of β-formyl-BODIPYs 2 were synthesized in high yields from tetramethyl-BODIPYs 1 via the Vilsmeier-Haack reaction and were further functionalized using a Knoevenagel condensation to generate novel BODIPYs 3 and 4. 20
