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通过 X 射线衍射和 13C NMR 光谱研究具有三核和四核核心的棒状介晶的结构特征和分子有序性。

Structural characterization and molecular order of rodlike mesogens with three- and four-ring core by XRD and 13C NMR spectroscopy.

机构信息

Department of Chemistry, S V University, Tirupati, India.

出版信息

J Phys Chem B. 2013 May 9;117(18):5718-29. doi: 10.1021/jp4000126. Epub 2013 Apr 29.

DOI:10.1021/jp4000126
PMID:23627902
Abstract

Structural characterizations using XRD and (13)C NMR spectroscopy of two rodlike mesogens consisting of (i) three phenyl ring core with a polar cyano terminal and (ii) four phenyl ring core with flexible dodecyl terminal chain are presented. The three-ring-core mesogen with cyano terminal exhibits enantiotropic smectic A phase while the four-ring mesogen reveals polymesomorphism and shows enantiotropic nematic, smectic C, and tilted hexatic phases. The molecular organization in the three-ring mesogen is found to be partial bilayer smectic Ad type, and the interdigitation of the molecules in the neighboring layers is attributed to the presence of the polar terminal group. For the four-ring mesogen, the XRD results confirm the existence of the smectic C and the tilted hexatic mesophases. A thermal variation of the layer spacing across the smectic C phase followed by a discrete jump at the transition to the tilted hexatic phase is also observed. The tilt angles have been estimated to be about 45° in the smectic C phase and about 40° in tilted hexatic phase. (13)C NMR results indicate that in the mesophase the molecules are aligned parallel to the magnetic field. From the (13)C-(1)H dipolar couplings determined from the 2D experiments, the overall order parameter for the three-ring mesogen in its smectic A phase has been estimated to be 0.72 while values ranging from 0.88 to 0.44 have been obtained for the four-ring mesogen as it passes from the tilted hexatic to the nematic phase. The orientations of the different rings of the core unit with respect to each other and also with respect to the long axis of the molecule have also been obtained.

摘要

呈现了两种由(i)带有极性氰基末端的三苯环核和(ii)带有柔性十二烷基末端链的四苯环核组成的棒状介晶的 XRD 和(13)C NMR 光谱结构特征。带有氰基末端的三环核介晶表现出热致各向异性近晶 A 相,而四环介晶则呈现多晶型并显示出热致向列相、近晶 C 相和倾斜六方相。发现三环介晶中的分子组织为部分双层近晶 Ad 型,相邻层中分子的互锁归因于极性末端基团的存在。对于四环介晶,XRD 结果证实了近晶 C 相和倾斜六方相的存在。还观察到在向倾斜六方相转变时,近晶 C 相的层间距随温度的变化有一个离散的跳跃。倾斜角在近晶 C 相中约为 45°,在倾斜六方相中约为 40°。(13)C NMR 结果表明,在介晶相中,分子平行于磁场排列。从二维实验确定的(13)C-(1)H 偶极耦合中,三环介晶在近晶 A 相中的整体有序参数估计为 0.72,而当四环介晶从倾斜六方相向向列相转变时,获得的值范围为 0.88 至 0.44。还获得了核心单元的不同环相对于彼此以及相对于分子长轴的取向。

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