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Conformational transition of a non-associative fluorinated amphiphile in aqueous solution. II. Conformational transition vs. supramolecular assembly

机译:非缔合氟化两亲物在水溶液中的构象转变。二。构象转变与超分子组装

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Unlike many known amphiphiles, the fluorinated amphiphilic dendrimer studied in this work demonstrated a concentration-dependent conformational transition rather than micellization or assembly. Hydrophobic and hydrophilic interactions with water were suggested as the most probable driving force of this transition. This assumption was consistent with the observed ~(19) F chemical shift changes of the dendrimer compared to a known micelle-forming fluorinated amphiphile. Since water is an important factor in the process, trends of the concentration-dependent changes in water proton transverse relaxation rate served as an indicator of structural changes and/or supramolecular assembly. The conformational transition process was also confirmed by ion-mobility mass-spectrometry. We suggested that structural features, namely, steric hindrances, prevented the micellization/assembly of the dendrimer of this study. This conclusion might inform the approach to develop novel unconventional amphiphiles.
机译:与许多已知的两亲物不同,在这项工作中研究的氟化两亲树状聚合物表现出浓度依赖性构象转变,而不是胶束化或组装。与水的疏水和亲水相互作用被认为是这种转变的最可能驱动力。与已知的形成胶束的氟化两亲物相比,该假设与观察到的树枝状聚合物的〜(19)F化学位移变化一致。由于水是该过程中的重要因素,因此水质子横向弛豫速率的浓度依赖性变化趋势可作为结构变化和/或超分子组装的指标。构象转变过程也通过离子迁移质谱法证实。我们建议结构特征,即位阻,阻止了这项研究的树状聚合物的胶束化/组装。这一结论可能会为开发新型非常规两亲物的方法提供参考。

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