2020
DOI: 10.1134/s1061934820060131
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Sensors Based on Single- and Double-Layer Plasticized Membranes for the Potentiometric Determination of Mefenamic and Phenylanthranylic Acids

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Cited by 5 publications
(3 citation statements)
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“…Yield: 93.93% (0.78 mmol, 0.31 g), FT-IR (KBr) cm −1 : 3413 (broad OH), 2900−2800 (CH 2 ), 1633 (−C = N), 1468, 1437 (C−C), 1267, 1112 (C−O). 1 H NMR (500 MHz, CDCl 3 ): δ (ppm) 0.89 (3H, t, H 23 ), 1.62 (2H, sex, H 22 ), 2.23 (3H, s, H 16 ), 3.45 (2H, td, H 21 ), 3.69 (2H, s, H 12 ), 3.78 (2H, s, H 1 ), 3.80 (2H, s, H 6 ), 6.86 (1H, s, H 14 ), 6.88 (1H, dd, 4 J = 1.5, 3 J = 5 Hz, H 4 ), 7.04 (1H, dd, 4 J = 1.5, 3 J = 5 Hz, H 3 ), 7.14 (1H, dd, 4 J = 1.5, 3 J = 5 Hz, H 10 ), 7.19 (1H, s, H 17 ), 7.36 (1H, d, 3 J = 2, H 5 ), 7.58 (1H, td, 4 J = 2, 3 J = 7.5, H 9 ), 7.62 (1H, d, 3 J = 7.5, H 8 ), 8.19 (1H, s, H 19 ), 8.41 (1H, d, 3 J = 5, H 11 ); 13…”
Section: Synthesis Of Model Compound (Model Schiff Base)mentioning
confidence: 99%
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“…Yield: 93.93% (0.78 mmol, 0.31 g), FT-IR (KBr) cm −1 : 3413 (broad OH), 2900−2800 (CH 2 ), 1633 (−C = N), 1468, 1437 (C−C), 1267, 1112 (C−O). 1 H NMR (500 MHz, CDCl 3 ): δ (ppm) 0.89 (3H, t, H 23 ), 1.62 (2H, sex, H 22 ), 2.23 (3H, s, H 16 ), 3.45 (2H, td, H 21 ), 3.69 (2H, s, H 12 ), 3.78 (2H, s, H 1 ), 3.80 (2H, s, H 6 ), 6.86 (1H, s, H 14 ), 6.88 (1H, dd, 4 J = 1.5, 3 J = 5 Hz, H 4 ), 7.04 (1H, dd, 4 J = 1.5, 3 J = 5 Hz, H 3 ), 7.14 (1H, dd, 4 J = 1.5, 3 J = 5 Hz, H 10 ), 7.19 (1H, s, H 17 ), 7.36 (1H, d, 3 J = 2, H 5 ), 7.58 (1H, td, 4 J = 2, 3 J = 7.5, H 9 ), 7.62 (1H, d, 3 J = 7.5, H 8 ), 8.19 (1H, s, H 19 ), 8.41 (1H, d, 3 J = 5, H 11 ); 13…”
Section: Synthesis Of Model Compound (Model Schiff Base)mentioning
confidence: 99%
“…These bands disappeared in the case of FCDs@ SiO 2 -TPA due to the formation of an azomethinic bond and new vibrational bands were observed at 794 cm −1 (Si−O−Si symmetric stretching), 963 cm −1 (Si−O symmetric stretching), 1074 cm −1 (Si−O−Si asymmetric stretching), and 1634 cm −1 (C�N) (Figure 1a). The 1 H NMR spectrum of TPA in CDCl 3 exhibited a singlet at 10.15 ppm due to the aldehydic proton (H 19 ), which shifted upfield to 8.41 ppm in the case of the model Schiff base compound due to azomethine bond formation with n-propylamine. 13 Thermogravimetric analysis (TGA) of FCDs revealed a mass loss of 98.60% when the the temperature was increased from room temperature to approximately 80 °C.…”
Section: Characterization Studiesmentioning
confidence: 99%
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