2017
DOI: 10.13040/ijpsr.0975-8232.8(12).4909-29
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Cited by 2 publications
(1 citation statement)
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“…Finally, spectroscopic characterization by 13 C NMR shows chemical shifts for the benzothiazole without substituents at 155 ppm (C2), 123 pm (C4), 126 ppm (C5), 125 ppm (C6), 122 ppm (C7), 153 ppm (C3a) and 134 ppm (C7a). Ultraviolet-visible spectroscopy (UV-Vis) shows a more complex electronic absorption with λ max of 217, 251 nm, (ε = 18,620 L mol −1 cm −1 , 5500 L mol −1 cm −1 ), 285 nm (ε = 1700 L mol −1 cm −1 ) and 295 nm (ε = 1350 L mol −1 cm −1 ) [60][61][62].…”
Section: Synthesis and Characterization Of Benzothiazolesmentioning
confidence: 99%
“…Finally, spectroscopic characterization by 13 C NMR shows chemical shifts for the benzothiazole without substituents at 155 ppm (C2), 123 pm (C4), 126 ppm (C5), 125 ppm (C6), 122 ppm (C7), 153 ppm (C3a) and 134 ppm (C7a). Ultraviolet-visible spectroscopy (UV-Vis) shows a more complex electronic absorption with λ max of 217, 251 nm, (ε = 18,620 L mol −1 cm −1 , 5500 L mol −1 cm −1 ), 285 nm (ε = 1700 L mol −1 cm −1 ) and 295 nm (ε = 1350 L mol −1 cm −1 ) [60][61][62].…”
Section: Synthesis and Characterization Of Benzothiazolesmentioning
confidence: 99%