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Synthesis and Characterization of N-(Arylcarbamothioyl)-cyclohexanecarboxamide Derivatives: The Crystal Structure of N-(Naphthalen-1-ylcarbamothioyl)cyclohexanecarboxamide

机译:N-(芳基氨基甲硫基)-环己烷甲酰胺衍生物的合成与表征:N-(萘-1-基氨基甲硫基硫代酰基)环己烷甲酰胺的晶体结构

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摘要

A number of N-(arylcarbamothioyl)cyclohexanecarboxamide derivatives (aryl substituents: phenyl, 2-chlorophenyl, 3-chlorophenyl, 4-chlorophenyl, o-tolyl, p-tolyl, 3-methoxyphenyl, 4-methoxyphenyl and naphthalen-1yl) have been synthesized. The compounds obtained were characterized by elemental analyses, IR spectroscopy and 1H-NMR spectroscopy. N-(naphthalen-1-ylcarbamothioyl)cyclohexanecarboxamide, >H2L9, was also characterized by a single crystal X-ray diffraction study. This compound, C18H20N2OS, crystallizes in the triclinic space group Pī, with Z = 2, and unit cell parameters a = 6.9921(14) Å, b = 11.002(2) Å, c = 12.381(3) Å, α = 113.28(3)°, β = 99.38(3)°, and γ = 101.85(3)°. The cyclohexane ring adopts a chair conformation. The molecular conformation of the compound is stabilized by an intramolecular (N2-H2•••O1) hydrogen bond which forms a pseudo-six-membered ring.
机译:已经有许多N-(芳基氨基甲硫酰基)环己烷甲酰胺衍生物(芳基取代基:苯基,2-氯苯基,3-氯苯基,4-氯苯基,邻甲苯基,对甲苯基,3-甲氧基苯基,4-甲氧基苯基和萘-1基)。合成的。通过元素分析,红外光谱和 1 1H-NMR光谱对所得化合物进行表征。 N-(萘-1-基氨基甲硫基)环己烷甲酰胺> H2L 9 ,也通过单晶X射线衍射研究表征。该化合物C18H20N2OS在三斜空间群Pī中结晶,Z = 2,晶胞参数a = 6.9921(14)Å,b = 11.002(2)Å,c = 12.381(3)Å,α= 113.28( 3)°,β= 99.38(3)°,γ= 101.85(3)°。环己烷环采用椅子结构。该化合物的分子构象通过形成假六元环的分子内(N2-H2•••O1)氢键稳定。

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