化学
烷基
中间相
吡啶
结晶学
热致晶体
晶体结构
镍
离子键合
液晶
碳氢化合物
相(物质)
离子
立体化学
药物化学
有机化学
液晶
物理
光学
作者
Hai‐Bao Duan,Shanshan Yu,Jian-Lan Liu,Zhengfang Tian,Xiao‐Ming Ren
出处
期刊:Polyhedron
[Elsevier]
日期:2014-02-01
卷期号:69: 251-261
被引量:6
标识
DOI:10.1016/j.poly.2013.12.007
摘要
Eight metal–dithiolene compounds, [Cn-Apy][Ni(mnt)2] (Cn-Apy+ = 1-alkyl-4-aminopyridinium with n = 2–5 and 7–10; mnt2− = maleonitriledithiolate), were synthesized and characterized, amongst which the crystal structures were determined for six compounds (n = 3, 5, 7–10). The anions and cations form alternatively layered arrangement. The anion layer is built from the irregular stacks, the neighboring stacks are aligned along the long molecular axis direction of anions, and the alignment pattern is related to hydrocarbon chain length in 1-alkyl-4-aminopyridinium. Seven compounds exhibit the thermotropic liquid crystalline behaviors with the smetic A phase fingerprints. The mesophase observed in a propyl chain compound is uncommon compared with the suggested rule that a dodecyl hydrocarbon chain is necessary at least in the pyridinium-based ionic liquid crystals. The [Cn-Apy][Ni(mnt)2] compounds showed distinct magnetic behaviors. This is due to the magnetic couplings between anions being achievable through pathways of weakly intermolecular interactions.
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