2015
DOI: 10.1016/j.jelechem.2014.12.014
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Electrochemistry and electrogenerated chemiluminescence of benzoxazole derivatives in nonaqueous media

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Cited by 7 publications
(6 citation statements)
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“…The electrochemical investigations were similar with that in Ref. [38]. A typical three-electrode setup with a platinum disk working electrode (2.0 mm diameter), a Pt auxiliary electrode, and a quasi-reference silver wire electrode was used for electrochemical experiment.…”
Section: Apparatusmentioning
confidence: 80%
“…The electrochemical investigations were similar with that in Ref. [38]. A typical three-electrode setup with a platinum disk working electrode (2.0 mm diameter), a Pt auxiliary electrode, and a quasi-reference silver wire electrode was used for electrochemical experiment.…”
Section: Apparatusmentioning
confidence: 80%
“…Although the first report of porphyrins ECL by Bader dates back to 1972, there had been rare research on the ECL of porphyrins. Porphyrinic Zr metal–organic framework (MOF) PCN-224 is a kind of porous structure nanomaterial that is composed of Zr 6 cluster and TCPP with good biocompatibility and excellent stability in a physiological environment, where porphyrins are used for light harvesting as well as in energy and electron transfer. In recent years, PCN-224 has been used in a photo-electrochemical sensor, fluorescence sensor, photodynamic therapy, and so on. ,, However, the ECL property of PCN-224 has never been studied previously.…”
Section: Introductionmentioning
confidence: 99%
“…Among a wide range of compounds [6][7][8][9][10][11][12][13] and materials [14][15][16][17][18][19] that have shown utility as ECL emitters are boron difluoride (BF 2 ) formazanate complexes such as 1ac, which can be prepared from formazans 2 [20][21] using straightforward and cost-effective syntheses. This makes BF 2 formazanate complexes attractive alternatives to the more commonly studied BODIPY complexes for ECL application.…”
Section: Introductionmentioning
confidence: 99%
“…1 H NMR (399.8 MHz, CDCl 3 ): δ 8.03 (d, 3 J HH = 9 Hz, 2H, aryl CH), 7.85 (d, 3 J HH = 9 Hz, 4H, aryl CH), 7.00−6.95 (m, 6H, aryl CH), 3.87 (s, 3H, OCH 3 ), 3.86 (s, 6H, OCH 3 ) ppm. 13 C NMR (100.5 MHz, CDCl 3 ): δ 160.8, 160.7, 137.9, 137.8, 127.1, 127.0, 125.2 (t, 4 J CF = 3 Hz), 114.6, 114.3, 55.9, 55.7 ppm. 11 B NMR (128.3 MHz, CDCl 3 ): δ −0.5 (t, 1 J BF = 29 Hz) ppm.…”
Section: ■ Introductionmentioning
confidence: 99%
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