2019
DOI: 10.13040/ijpsr.0975-8232.10(8).3532-39
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Cited by 3 publications
(1 citation statement)
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“…These peaks decrease dramatically, while the peak assigned to the C-O bond at 1026 cm −1 grows and shifts (−65 shifts). These vibrations [27,31] and shift differentiation support a possible known reaction between HP and thymol to form thymoquinone [32]. Moreover, the weaker C-O bond and stronger -OH stretching signals can indicate the transformation of the thymol phenol into thymoquinone ketone, which is accompanied by a corresponding decrease in the thymoquinone -CH signals (Figure 3).…”
Section: Resultsmentioning
confidence: 70%
“…These peaks decrease dramatically, while the peak assigned to the C-O bond at 1026 cm −1 grows and shifts (−65 shifts). These vibrations [27,31] and shift differentiation support a possible known reaction between HP and thymol to form thymoquinone [32]. Moreover, the weaker C-O bond and stronger -OH stretching signals can indicate the transformation of the thymol phenol into thymoquinone ketone, which is accompanied by a corresponding decrease in the thymoquinone -CH signals (Figure 3).…”
Section: Resultsmentioning
confidence: 70%