Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/23284
Title: An experimental and computational study of antioxidant activity of N-phenylthiourea and N-phenylselenourea analogues
Authors: Dinh, Quy Huong
Tran, Duong
Pham, Cam Nam
Keywords: N-phenylthiourea
N-phenylselenourea
Antioxidant
DPPH* radical scavenging ability
Lonization energy
Bond dissociation energy
Potential energy surlace
Issue Date: 2019
Series/Report no.: Vietnam Journal of Chemistry;No 57(04) .- Page.469-479
Abstract: The antioxidant performance of N-phenylthiourea has been expenmentally studied via the half maximal inhibitory concentration value (IC₅₀) in combination with quantum calculations. In the experimental part, DPPH* (1,1-diphenyl-2-picrylhydrazyl) radical scavenging ability of N-phenylthiourea (IC₅₀) was measured to be 4.82.10⁻⁴ M. Based on three antioxidant mechanisms being hydrogen atom transter (HAT), single electron transfer followed by proton transfer (SETPT) and sequential proton loss electron transfer (SPLET), the essential thermoparameters of N-phenylthiourea derivatives were carried out at ROB3LYP/6-311++G(2df.2p)//B3LYP/6-311G(d,p) in both gas phase and ethanol in order to evaluate their antioxidant capacity. For the sake of comparison, N-phenylselenourea derivatives were also taken into account. The computational results indicated that the antioxidant of N-phenylsclenourea is better than that of N-phenulthiourea. Besides, potential energy surfaces of N-phenylselenourea derivatives and HOO* radical were investigated. All the reactions were thermodynamically favored. The derivatives containing the electron donating group at the para position of N-phenylselenourea considerably enhanced their antioxidant capacity. As a result, para- N(CH₃)₂-C₆H₄-NH-CSe-MH₂ was the best potential antioxidant in the studied compounds.
URI: http://dspace.ctu.edu.vn/jspui/handle/123456789/23284
ISSN: 2525-2321
Appears in Collections:Vietnam Journal of Chemistry

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