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温度触发的SDS@2β-CD微管与囊泡之间的可逆转变。

Reversible transition between SDS@2β-CD microtubes and vesicles triggered by temperature.

作者信息

Zhou Chengcheng, Cheng Xinhao, Yan Yun, Wang Jide, Huang Jianbin

机构信息

Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory for Structural Chemistry of Unstable and Stable Species, College of Chemistry and Molecular Engineering, Peking University , Beijing 100871, People's Republic of China.

出版信息

Langmuir. 2014 Apr 1;30(12):3381-6. doi: 10.1021/la500010p. Epub 2014 Mar 17.

Abstract

Switching between association and dissociation is the well-known strategy for constructing responsive materials based on the host-guest complexes of cyclodextrins (CDs). In this work, we report that temperature may also trigger self-assembly transition in the supramolecular system composed of sodium dodecyl sulfate (SDS) and β-cyclodextrin (β-CD) at a molar ratio of 1:2. We reported previously that, at this ratio, SDS and β-CD form a channel-type SDS@2β-CD supramolecular unit, which further self-assembles into non-amphiphilic vesicles and microtubes driven by hydrogen bonding. Here, we report that the vesicles and microtubes can be reversibly switched between each other upon decreasing and increasing temperature. Control experiments in heavy water suggest that water molecules play a dominating role in the hydrogen bonding between SDS@2β-CD supramolecular units at lower concentration and higher temperature. Under opposite conditions, the hydrogen bonding between CDs is dominating. Therefore, for the 5% system, we observed a vesicle to microtube transition with a decreasing temperature, whereas for the 10% system, we observed the reverse process. Both processes are reversible. This is not only an example of temperature-triggered responsiveness in non-amphiphilic self-assemblies but also a new mode of responsiveness for the host-guest inclusion systems based on CDs. This temperature-responsive process is anticipated to shed light on the design and development of novel advanced materials.

摘要

在基于环糊精(CD)主客体复合物构建响应性材料时,缔合与解离之间的切换是一种众所周知的策略。在这项工作中,我们报道温度也可能在由十二烷基硫酸钠(SDS)和β-环糊精(β-CD)以1:2摩尔比组成的超分子体系中引发自组装转变。我们之前报道过,在此比例下,SDS和β-CD形成通道型SDS@2β-CD超分子单元,该单元在氢键作用下进一步自组装成非两亲性囊泡和微管。在此,我们报道囊泡和微管在温度降低和升高时可相互可逆切换。在重水中进行的对照实验表明,在较低浓度和较高温度下,水分子在SDS@2β-CD超分子单元之间的氢键中起主导作用。在相反条件下,CD之间的氢键起主导作用。因此,对于5%的体系,我们观察到温度降低时囊泡向微管的转变,而对于10%的体系,我们观察到相反的过程。这两个过程都是可逆的。这不仅是非两亲性自组装中温度触发响应性的一个例子,也是基于CD的主客体包合体系的一种新的响应模式。预计这种温度响应过程将为新型先进材料的设计和开发提供启示。

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