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首页> 外文期刊>Journal of physical chemistry letters >Self-Assembly Evolution of N-Terminal Aromatic Amino Acids with Transient Supramolecular Chirality
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Self-Assembly Evolution of N-Terminal Aromatic Amino Acids with Transient Supramolecular Chirality

机译:瞬态超分子手性的N-末端芳族氨基酸的自组装演变

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Deep understanding and fine tailoring of spontaneous structural evolution of self-assembled arrays are pivotal in the rational design of advanced soft materials. However, an indistinct structure-property relationship and pathway complexity in self-assembly lead to a considerable challenge. Herein, we reveal the self-assembly pathway complexity in spontaneous aggregation of several N-terminated aromatic amino acids. By primarily tuning the incubation time, building blocks appended with alanine and serine selectively form 1:1 hydrated clathrates, enabling the microfiber to transition to crystals. The dynamic water intercalation process was studied by incubation time-dependent morphological changes, powder X-ray diffraction, and single-crystal structure analysis. A pronounced amino acid residue effect on the self-assembly evolution was reflected by supramolecular chirality inversion of the building block having the phenylalanine residue, accomplishing dynamic M- to P-helicity transition within a confined time scale.
机译:自动组装阵列的自发结构演变的深度理解和细小剪裁是在先进软材料的合理设计中的关键。然而,自我组装中的模糊结构 - 性质关系和途径复杂程度导致相当大的挑战。在此,我们揭示了几种N封端芳族氨基酸的自发聚集中的自组装途径复杂性。通过主要调整孵化时间,用丙氨酸和丝氨酸含有的构建块选择性地形成1:1水合物的克拉汞,使微纤维能够过渡到晶体。通过孵育时间依赖性形态变化,粉末X射线衍射和单晶结构分析来研究动态水插入过程。对具有苯丙氨酸残基的建筑块的超分子手性转化反映了对自组装演化的明显氨基酸残基效应,在受限时间尺度内完成动态M-至p螺旋性转变。

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