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通过水诱导的形状转变树枝状两亲分子的构象有序化来消除软Frank-Kasper相的对称性破缺

Deactivating Symmetry Breaking of a Soft Frank-Kasper Phase via Water-Induced Conformational Ordering of a Shapeshifting Dendritic Amphiphile.

作者信息

Wang Chien-Lung, Chuang Wei-Tsung, Lee Mu-Tzu, Wang Yong-Rui, Chen Shih-Yong, Huang Hung-Ju, Liu Shao-Yuan, Lin Jhih-Min, Chen Chun-Yu, Lee Yao-Chang, Jeng U-Ser

机构信息

Department of Chemistry, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd, Taipei 10617, Taiwan.

National Synchrotron Radiation Research Center, 101 Hsin-Ann Road, Hsinchu 30076, Taiwan.

出版信息

ACS Appl Mater Interfaces. 2025 May 28;17(21):31403-31410. doi: 10.1021/acsami.5c04140. Epub 2025 May 13.

DOI:10.1021/acsami.5c04140
PMID:40358738
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12123561/
Abstract

Water guides biomolecules to their native conformations in a high-dimensional conformational space. To explore a similar role in synthetic self-assembly, a wedge-shaped, shape-shifting dendron (SD) was studied. Cooling from the isotropic melt trapped SD in a metastable Frank-Kasper σ phase with symmetry breaking due to high conformational freedom. In situ SAXS, microbeam SAXS, and ATR-FTIR confirmed that water vapor disrupts supramolecular micelles in the σ phase and unfolds some cone-shaped SD molecules, facilitating improved chain-chain packing and inducing the low-symmetry σ phase to transition into a more symmetric hydrated lamellar () phase. The water-induced conformational ordering of the SD thus enables a rare σ → phase transition, initially blocked by the SD's hydrophilic volume fraction. Spectroscopy results also illustrated that during the conformational ordering, water molecules are encapsulated into the hydrophilic domains of the ordered phases, enhancing the phase stability of the phase and the hydrated quasicrystalline DDQC and σ phases that evolved from the phase. These findings reveal a novel self-assembly pathway for the wedge-shaped amphiphile that deactivates the symmetry breaking in the Frank-Kasper σ phase and emphasize the role of water in guiding synthetic molecules to their optimal supramolecular structures, echoing the self-assembly principles in nature.

摘要

在高维构象空间中,水引导生物分子形成其天然构象。为了探索水在合成自组装中发挥的类似作用,研究了一种楔形、可变形的树枝状分子(SD)。从各向同性熔体冷却时,由于构象自由度高,SD被困在具有对称性破缺的亚稳Frank-Kasper σ相中。原位小角X射线散射(SAXS)、微束SAXS和衰减全反射傅里叶变换红外光谱(ATR-FTIR)证实,水蒸气破坏了σ相中的超分子胶束,并使一些锥形SD分子展开,促进了链间堆积的改善,并诱导低对称性的σ相转变为对称性更高的水合层状()相。因此,水诱导的SD构象有序化实现了罕见的σ→相转变,该转变最初因SD的亲水体积分数而受阻。光谱结果还表明,在构象有序化过程中,水分子被包裹在有序相的亲水区中,增强了相以及从相演变而来的水合准晶DDQC和σ相的相稳定性。这些发现揭示了楔形两亲分子的一种新型自组装途径,该途径消除了Frank-Kasper σ相中的对称性破缺,并强调了水在引导合成分子形成其最佳超分子结构中的作用,这与自然界中的自组装原理相呼应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91ba/12123561/07be902d6629/am5c04140_0007.jpg
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本文引用的文献

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