Synthesis of novel profluorescent nitroxides as dual luminescent-paramagnetic active probes

被引:10
作者
Coman, Anca G. [1 ]
Paraschivescu, Codruta C. [1 ]
Paun, Anca [1 ]
Diac, Andreea [2 ]
Hadade, Niculina D. [2 ]
Jouffret, Laurent [3 ]
Gautier, Arnaud [3 ]
Matache, Mihaela [1 ]
Ionita, Petre [1 ,4 ]
机构
[1] Univ Bucharest, Dept Organ Chem Biochem & Catalysis, Res Ctr Appl Organ Chem, Fac Chem, 90-92 Panduri St, RO-050663 Bucharest, Romania
[2] Babes Bolyai Univ, Fac Chem & Chem Engn, Supramol Organ & Organometall Chem Ctr, 11 Arany Janos Str, RO-400028 Cluj Napoca, Romania
[3] Univ Clermont Auvergne, CNRS, Sigma Clermont, ICCF, F-63000 Clermont Ferrand, France
[4] Inst Phys Chem Ilie Murgulescu, 202 Splaiul Independentei, Bucharest, Romania
关键词
LIGHT-EMITTING-DIODES; ELECTROPHOSPHORESCENT DEVICES; OXIDATIVE CYCLIZATION; ELECTRON-TRANSPORT; FLUORESCENT-PROBES; 1,3,4-OXADIAZOLES; DERIVATIVES; ACYLHYDRAZONES; RECOGNITION; LIGANDS;
D O I
10.1039/c7nj01698k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe herein the synthesis of new profluorescent nitroxides based on 2,5-disubstituted-1,3,4-oxadiazoles as fluorescent moieties and the 2,2,6,6-tetramethylpiperidine-N-oxyl radical (TEMPO) as paramagnetic probes. The synthesis and optical and electronic properties of the oxadiazole-based precursors of the profluorescent nitroxides, as well as the nitroxides and their reduced forms are also described. Physical investigations (i.e. absorption and emission spectroscopy, cyclic voltammetry) indicate a different luminescence behaviour function to the oxadiazole substituent. A linear response to reducing agents, i.e. sodium ascorbate, monitored by fluorescence spectroscopy, suggests the possibility of using the synthesized compounds as potent active probes in detection of various analytes of interest.
引用
收藏
页码:7472 / 7480
页数:9
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