首页> 外文期刊>Journal of Chemical Crystallography >1-[2-(p-Tolyl)-1-diazenyl]-3-({3-[2-(p-tolyl)-1-diazenyl] perhydrobenzo[d]imidazol-1-yl}methyl)perhydrobenzo[d]imidazole: synthesis,characterization and X-ray crystal structure
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1-[2-(p-Tolyl)-1-diazenyl]-3-({3-[2-(p-tolyl)-1-diazenyl] perhydrobenzo[d]imidazol-1-yl}methyl)perhydrobenzo[d]imidazole: synthesis,characterization and X-ray crystal structure

机译:1- [2-(对甲苯基)-1-二氮烯基] -3-({3- [2-(对甲苯基)-1-二氮烯基]全氢苯并[d]咪唑-1-基}甲基)全氢苯并[d咪唑:合成,表征及X射线晶体结构

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1-[2-(p-Tolyl)-1-diazenyl]-3-({3-[2-(p-tolyl)-1-diazenyl]perhydrobenzo[d]imidazol-1-yl}methyl)perhydrobenzo[d]imidazole(1) has been synthesized by reactionof a mixture of 1,2-diaminocyclohexane and formaldehyde withp-toluene diazonium chloride inaqueous solution. The product has been characterized by IR and NMRspectroscopy and elemental analysis. A crystal grown from solution ina mixed solvent system of ethyl acetate and hexanes was analyzed byX-ray crystallography. The solution of the crystal structure of(1) is important in establishing theconnectivity of this molecule and other compounds of similarstructure. The crystal structure of (1) is compared with the previously reportedstructure of the p-cyano analogue(2). Compounds (1) and (2)differ principally in the relative orientation of the heterocyclicrings; in (1), the molecule has adistinct V-shape, whereas compound (2) adopts a more extended conformation.Significant conjugation within the triazene moieties is evident inboth (1) and (2), as manifested in the N465=N andN–N bond lengths. The conjugation is greater in (2) due to the extended conjugation through tothe nitrile group. The title compound (1){C29H40N8}crystallizes in the monoclinic, space group C2/c, with lattice constants: a = 30.532(6) Å,b =5.9050(12) Å, c= 15.463(3) Å, α = 90°,β = 99.94(3)°, γ = 90°,V =2746.0(10) Å3, Z = 4, D c =1.209 mg m−3,F(000) = 1076, R 1 = 0.0785,wR 2= 0.1877.
机译:1- [2-(对甲苯基)-1-二氮烯基] -3-({3- [2-(对甲苯基)-1-二氮烯基]全氢苯并[d]咪唑-1-基}甲基)全氢苯并[d通过1,2-二氨基环己烷和甲醛的混合物与对甲苯重氮氯化物在水溶液中的反应合成了咪唑(1)。该产物已经通过IR和NMR光谱以及元素分析表征。通过X射线晶体学分析从在乙酸乙酯和己烷的混合溶剂系统中的溶液中生长的晶体。 (1)的晶体结构的溶液对于建立该分子与其他类似结构的化合物的连接性很重要。将(1)的晶体结构与先前报道的对氰基类似物(2)的结构进行比较。化合物(1)和(2)主要在杂环的相对取向上不同;在(1)中,分子具有明显的V形,而化合物(2)具有更扩展的构象。在(1)和(2)中,三氮烯基团之间的显着共轭作用很明显,如N465 = N和N– N键长度。 (2)中的共轭较大,这是由于延伸至腈基的共轭扩展。标题化合物(1){C29 H40 N8 }在单斜空间组C2 / c中结晶,晶格常数为:a = 30.532(6)Å,b = 5.9050( 12)Å,c = 15.463(3)Å,α= 90°,β= 99.94(3)°,γ= 90°,V = 2746.0(10)Å3,Z = 4,D c = 1.209 mg m-3 ,F(000)= 1076,R 1 = 0.0785,wR 2 = 0.1877。

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