1385822-48-9Relevant academic research and scientific papers
Novel sulphur-rich BODIPY systems that enable stepwise fluorescent O-atom turn-on and H2O2 neuronal system probing
Singh, Atul P.,Lee, Kang Mun,Murale, Dhiraj P.,Jun, Taehong,Liew, Hyunjeong,Suh, Yoo-Hun,Churchill, David G.
supporting information; experimental part, p. 7298 - 7300 (2012/08/29)
Bis-arylsulfide BODIPY systems were prepared and studied for multiple O-atom sensing (at 522 nm); 2- and 3-atom loading was optimal (50-fold, "turn on"). Neuronal studies showed greater H2O2 sensitivity than 2′,7′-dichlorofluorescein diacetate. The novel 1,3,6-trimethyl BODIPY formed as a biproduct under Lindsey conditions.
