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不对称烷基铵盐中的立方中间相。合成与结构模型。

Cubic mesophase in an unsymmetrical alkyl ammonium salt. Synthesis and structural model.

作者信息

Soulié Corinne, Bassoul Pierre, Tournilhac François

机构信息

Ecole Supérieure de Physique et de Chimie Industrielles 10 rue Vauquelin 75231 Paris, France.

出版信息

Chemphyschem. 2002 Dec 16;3(12):1024-30. doi: 10.1002/cphc.200290004.

Abstract

N,N,N-butylethylpentylpropylammonium iodide 4 and related molecules have been selectively synthesised from commercially available aldehydes, amines and alkyl iodides using a reductive alkylation procedure. The crystalline texture of 4 obtained on cooling is optically isotropic between crossed polarisers, indicating a cubic structure. Differential scanning calorimetry (DSC, +10 K min-1) reveals a glass phase transition at -59 degrees C and a melting point at 192 degrees C. The melting entropy (23.9 J mol-1 K-1) indicates a first-order transition between a highly disordered mesophase and the isotropic liquid. Powder X-ray diffraction patterns were indexed in the cubic system (a = 14.08A; Pm3n space group). In this cell, the molecular packing with Z = 6 corresponds to a rather low compactness of 65%. Iodine and tetraalkylammonium ions occupy positions with a 4m2 site symmetry. These highly symmetrical states may be generated by stepwise rotation of the ammonium cation. The same structural model for orientationally disordered crystal (ODIC) phases can be applied to a series of tetraalkylammonium bromides and iodides.

摘要

已使用还原烷基化方法从市售醛、胺和烷基碘中选择性合成了N,N,N-丁基乙基戊基丙基碘化铵4及相关分子。冷却后得到的4的晶体结构在正交偏光镜之间是光学各向同性的,表明为立方结构。差示扫描量热法(DSC,升温速率为10 K min⁻¹)显示在-59℃出现玻璃态转变,熔点为192℃。熔化熵(23.9 J mol⁻¹ K⁻¹)表明在高度无序的中间相和各向同性液体之间存在一级转变。粉末X射线衍射图谱在立方晶系中进行了指标化(a = 14.08Å;空间群为Pm3n)。在这个晶胞中,Z = 6的分子堆积对应于相当低的65%的紧密程度。碘和四烷基铵离子占据具有4m2点群对称性的位置。这些高度对称的状态可能由铵阳离子的逐步旋转产生。相同的取向无序晶体(ODIC)相结构模型可应用于一系列四烷基溴化铵和碘化铵。

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