Tallavaara Pekka, Telkki Ville-Veikko, Jokisaari Jukka
NMR Research Group, Department of Physical Sciences, University of Oulu, PO Box 3000, FIN-90014 University of Oulu, Finland.
J Phys Chem B. 2006 Nov 2;110(43):21603-12. doi: 10.1021/jp064222g.
The behavior of nematic liquid crystal (LC) Merck Phase 4 confined to controlled pore glass (CPG) materials was investigated using 129Xe nuclear magnetic resonance (NMR) spectroscopy of xenon gas dissolved in the LC. The average pore diameters of the materials varied from 81 to 2917 A, and the measurements were carried out within a wide temperature range (approximately 185-370 K). The spectra contain lots of information about the effect of confinement on the phase of the LC. The theoretical model of shielding of noble gases dissolved in liquid crystals on the basis of pairwise additivity approximation was applied to the analysis of the spectra. When pore diameter is small, smaller than approximately 150 A, xenon experiences on average an isotropic environment inside the pore, and no nematic-isotropic phase transition is observed. When the size is larger than approximately 150 A, nematic phase is observed, and the LC molecules are oriented along pore axis. The orientational order parameter of the LC, S, increases with increasing pore size. In the largest pores, the orientation of the molecules deviates from the pore axis direction to magnetic field direction, which implies that the size of the pores (approximately 3000 A) is close to magnetic coherence length. The decrease of magnetic coherence length with increasing temperature is clearly seen from the spectra. When the sample is cooled rapidly by immersing it in liquid nitrogen, xenon atoms do not squeeze out from the solid, as they do during gradual freezing, but they are occluded inside the solid lattice, and their chemical shift is very sensitive to crystal structure. This makes it possible to study the effect of confinement on the solid phases. According to the measured 129Xe NMR spectra, possibly three different solid phases are observed from bulk liquid crystal in the used temperature region. The same is also seen from the samples containing larger pores (pore size larger than approximately 500 A), and the solid-solid phase-transition temperatures are the same. However, no first-order solid-solid phase transitions are observed from the smaller pores. Melting point depression, that is, the depression of solid-nematic transition temperature observed from the pores as compared with that in bulk LC, is seen to be very sensitive to the pore size, and it can be used for the determination of pore size of an unknown material.
利用溶解在向列型液晶(LC)中的氙气的129Xe核磁共振(NMR)光谱,研究了限制在可控孔径玻璃(CPG)材料中的默克4相向列型液晶的行为。材料的平均孔径在81至2917 Å之间变化,测量在很宽的温度范围(约185 - 370 K)内进行。光谱包含了许多关于限制对液晶相影响的信息。基于成对加和近似的溶解在液晶中的稀有气体屏蔽理论模型被用于光谱分析。当孔径较小时,小于约150 Å,氙在孔内平均经历各向同性环境,未观察到向列 - 各向同性相变。当尺寸大于约150 Å时,观察到向列相,且液晶分子沿孔轴取向。液晶的取向序参数S随孔径增大而增加。在最大的孔中,分子的取向从孔轴方向偏离到磁场方向,这意味着孔的尺寸(约3000 Å)接近磁相干长度。从光谱中可以清楚地看到磁相干长度随温度升高而减小。当将样品快速浸入液氮中冷却时,氙原子不像在逐渐冷冻过程中那样从固体中挤出,而是被封闭在固体晶格内,并且它们的化学位移对晶体结构非常敏感。这使得研究限制对固相的影响成为可能。根据测得的129Xe NMR光谱,在所用温度区域内,从本体液晶中可能观察到三种不同的固相。在含有较大孔径(孔径大于约500 Å)的样品中也观察到同样的情况,且固 - 固相变温度相同。然而,在较小的孔中未观察到一级固 - 固相变。熔点降低,即与本体液晶相比,从孔中观察到的固 - 向列相变温度降低,被发现对孔径非常敏感,并且可用于测定未知材料的孔径。