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首页> 外文期刊>Journal of Macromolecular Science. Physics >Fiber diffraction as a useful supplement to single-crystal electron diffraction data in the direct three-dimensional structure analysis of polymers
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Fiber diffraction as a useful supplement to single-crystal electron diffraction data in the direct three-dimensional structure analysis of polymers

机译:纤维衍射在聚合物的直接三维结构分析中作为单晶电子衍射数据的有用补充

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摘要

When zonal electron diffraction data from chain-folded lamellae are combined with the three-dimensional (3-D) information from a microfiber, it is possible to determine a polymer crystal structure by direct methods to visualize the atomic arrangement in the unit cell. An analysis of the poly(ethylene sulfide) structure (space group Pbcn, a = 8.51,b = 4.94, c = 6.69 Angstrom) is presented as an example of such a determination. The crystallographic phases-including 17 of 20 unique zonal hk0 data collected earlier from chain-folded lamellae, as well as two other phases permitted for origin definition in three dimensions - served as a basis set for extension into three dimensions by the Sayre equation. The phase extension into the 3-D indices of the fiber diffraction set (39 unique amplitudes including 32 estimated from 14 overlapped maxima) was quite accurate, especially for the most intense reflections. Combination of these phases with amplitude values to generate the three-dimensional potential map allowed direct visualization of the atomic distribution in the unit cell. The structure could then be refined by a match of a chain model to the observed potential distribution, after optimizing the bonding geometry. These results demonstrate that, with the use of fiber data as a supplement, alternative experimental approaches to true three-dimensional structure determinations exist in polymer electron crystallography, even if epitaxial crystallization methods cannot provide the necessary orthogonal orientation of the chain packing. By this approach, the ''missing cone'' problem for goniometry in the electron microscope can be largely overcome.
机译:当将来自链折叠薄片的区域电子衍射数据与来自微纤维的三维(3-D)信息相结合时,可以通过直接方法确定聚合物晶体结构,以可视化晶胞中的原子排列。聚(亚乙基硫醚)结构(空间群Pbcn,a = 8.51,b = 4.94,c = 6.69埃)的分析作为这种测定的一个例子。晶体学阶段-包括较早从链折叠薄层中收集的20个独特的hk0纬向hk0数据中的17个,以及允许在三个维度上定义原点的其他两个阶段-充当了Sayre方程扩展为三个维度的基础。到光纤衍射装置的3-D索引中的相位扩展(39个独特的振幅,包括从14个重叠的最大值估计的32个)是非常准确的,尤其是对于最强烈的反射。这些相位与振幅值的组合以生成三维电势图,可以直接观察晶胞中的原子分布。在优化键合几何形状之后,可以通过链模型与观察到的电势分布的匹配来优化结构。这些结果表明,利用纤维数据作为补充,即使外延结晶方法不能提供必要的正交堆积方向,在聚合物电子晶体学中也存在用于确定真正的三维结构的替代实验方法。通过这种方法,可以极大地克服电子显微镜中测角法的“缺失锥”问题。

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