Density Functional Theoretical Studies on Effect of Intramolecular Hydrogen Bonds on Reduction of Nitrophenols

• Published in: Chemical research in Chinese universities 2017-10, Vol.33 (5), p.785-793
• Main Authors: Zhang, Hongmei, Liu, Yan, Ma, Fangping, Qiu, Wei, Lei, Bo, Shen, Jinyou, Sun, Xiuyun, Han, Weiqing, Li, Jiansheng, Wang, Lianjun
• Format: Article
• Language: English
• Subjects: Adiabatic flow; Analytical Chemistry; Chemical bonds; Chemistry; Chemistry and Materials Science; Chemistry/Food Science; Degradation; Density functional theory; Hydrogen bonds; Inorganic Chemistry; Isomers; Mathematical analysis; Nitrophenol; Organic Chemistry; Physical Chemistry; Reduction; Stability analysis; 分子内氢键; 密度泛函理论; 对硝基酚; 理化特性; 电子亲和势; 硝基还原; 计算表; 降解行为
• ISSN: 1005-9040; 2210-3171
• DOI: 10.1007/s40242-017-7066-1

Intramolecular hydrogen bonds（IMHBs） can lead to different physicochemical characteristics of nitro- phenols（NPs） that determine their environmental behavior. In the present work, to reveal the relationship between IMHB and nitrophenol reduction, the effects of IMHB on the molecular geometries and properties of a series of ni- trophenols were investigated with density functional theory（DFT） calculations. The results of the geometry optimiza- tion and atoms-in-molecules（AIM） analysis indicate relatively strong IMHBs in ortho-substituted nitrophenols, whose stability could be significantly improved. In comparing the ELUMO and adiabatic electron affinities（AEA） of the nitrophenol isomers, the presence of IMHBs benefited the reductive degradation of NPs, consistent with a previous study. To gain an insight into the effect mechanism of IMHBs on the reductive degradation behavior of these mole- cules, the condensed electrophilicity Fukui index（f-）, natural charges and Wiberg bond orders of these nitrophenol isomers were calculated. The calculations indicate that the electrophilic reactivity activity of the O atom on the nitro group could be significantly improved due to the formation of IMHBs, which results in the enhanced reductive degradation of ortho-substituted NPs.