Akerele Oluwatoyin, Lemmerer Andreas
Jan Boeyens Structural Chemistry Laboratory, Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand, Private Bag 3, Johannesburg, 2050, South Africa.
Acta Crystallogr C Struct Chem. 2025 Jun 1;81(Pt 6):310-318. doi: 10.1107/S205322962500378X. Epub 2025 May 13.
Aminocarb [4-(dimethylamino)-3-methylphenyl N-methylcarbamate, CHNO], a synthetic pesticide, was crystallized and characterized by single-crystal and powder X-ray diffraction. In the solid state, the molecules have a strong chain N-H...O hydrogen bond with a strength of -29.37 kJ mol and a short C-H...π contact that build a wave-like three-dimensional structure. The structural stability and intermolecular interaction of Aminocarb were investigated using differential scanning calorimetry (DSC) and density functional theory (DFT). The results show that the compound is chemically stable, and the two dominating interactions are electrostatic and dispersion energies. An electrostatic potential map reveals the binding sites of the molecules for reactivity. The understanding of the structural stability and interactions in Aminocarb provided in this study could be used to design new compounds with improved solubility and bioavailability. The dimethylamino group and the methyl group on the carbamate could be modified with other alkyl groups, which might reduce the Aminocarb toxicity, thereby leading to the development of safe, efficient and cost-effective compounds.
涕灭威[4-(二甲氨基)-3-甲基苯基N-甲基氨基甲酸酯,CHNO]是一种合成农药,通过单晶和粉末X射线衍射对其进行了结晶和表征。在固态中,分子具有强度为-29.37 kJ mol的强链状N-H...O氢键和形成波浪状三维结构的短C-H...π接触。使用差示扫描量热法(DSC)和密度泛函理论(DFT)研究了涕灭威的结构稳定性和分子间相互作用。结果表明该化合物化学稳定,两种主要相互作用是静电能和色散能。静电势图揭示了分子的反应活性结合位点。本研究中对涕灭威结构稳定性和相互作用的理解可用于设计具有改善溶解性和生物利用度的新化合物。氨基甲酸酯上的二甲氨基和甲基可以用其他烷基进行修饰,这可能会降低涕灭威的毒性,从而开发出安全、高效且经济高效的化合物。