47367-75-9Relevant articles and documents
Phenoxazine-based Near-infrared Fluorescent Probes for the Specific Detection of Copper (II) Ions in Living Cells
Shen, Yang,Zheng, Wubin,Yao, Yusi,Wang, Dongmei,Lv, Guanglei,Li, Chunxia
, p. 2864 - 2867 (2020)
Abstract: It is well known that copper ions play a critical role in various physiological processes. However, a variety of human diseases are tightly correlated with copper overload. Although there are numerous fluorescent probes capable of detecting copper ions, most of them are “turn-off” probes owing to copper (II) ions fluorescence quenching effect, resulting in poor sensitivity. Herein, a novel “turn-on” near-infrared (NIR) fluorescent probe PZ-N based on phenoxazine was designed and synthesized for the selective detection of copper (II) ions (Cu2+). Upon the addition of Cu2+, the probe could quickly react with Cu2+ and emit strong fluorescence, along with colour change from colourless to obvious blue. Moreover, the probe PZ-N showed good water solubility, high selectivity, and excellent sensitivity with low limit of detection (1.93 nM) towards copper (II) ions. More importantly, PZ-N was capable of effectively detecting Cu2+ in living cells.
The near-infrared fluorescent probes based on phenoxazine for the rapid detection of hypochlorous acid
Hao, Shiyou,Li, Chunxia,Lv, Guanglei,Shen, Yang,Yang, Jiajia,Yao, Yusi,Zheng, Wubin
, (2020)
Hypochlorous acid (HOCl) is tightly related with a series of diseases, and plays an important part in biological processes. Herein, we designed and synthesized two “turn-on” near-infrared (NIR) probes (BC-2 and BC-3) based on phenoxazine to sense and imag
Synthesis and radiation sensitivity of phenoxazine type color formers including thiol ester protective group
Tachikawa, Tatsuya,Sato, Yohei,Tokita, Sumio
, p. 161/[461]-166/[466] (2007/10/03)
3,7-Bis(N,N-diethylamino)-10-(phenylthio)carbonylphenoxazine (1a) and its analogs (1b-f) were synthesized and the color change after γ irradiation was investigated. The color change of acetonitrile solutions of 1a ([1a] 0 = 1.0 × 10-3 M) after γ irradiation was identified by naked eyes at the dose of 20 Gy. Phenylthio-substituted compound la showed more significant absorbance increase than phenoxy-substituted compound, 3,7-bis(N,N-diethylamino)-10-phenoxycarbonylphenoxazine (2a). The C-S cleavage in la by γ irradiation was revealed to occur more easily than the C-O cleavage in 2a. The sensitivity of the color formers 1a-f) to γ rays was correlated with the stability of the thiyl radicals generated in the reaction.