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用于光控客体分子结合与释放的含葫芦[8]脲多层膜

Cucurbit[8]uril-Containing Multilayer Films for the Photocontrolled Binding and Release of a Guest Molecule.

作者信息

Nicolas Henning, Yuan Bin, Zhang Xi, Schönhoff Monika

机构信息

Institute of Physical Chemistry, University of Muenster , Corrensstrasse 28/30, 48149 Münster, Germany.

Key Laboratory of Organic Optoelectronics & Molecular Engineering, Department of Chemistry, Tsinghua University , Beijing 100084, P. R. China.

出版信息

Langmuir. 2016 Mar 15;32(10):2410-8. doi: 10.1021/acs.langmuir.6b00128. Epub 2016 Feb 26.

Abstract

The powerful host-guest chemistry of cucurbit[8]uril (CB[8]) was employed to obtain photoresponsive polyelectrolyte multilayer films for the reversible and photocontrolled binding and release of an organic guest molecule. For this purpose, we designed and synthesized a polyelectrolyte with azobenzene side groups. Then, CB[8] was associated with the azo side group to obtain a supramolecular host-guest complex that was further used as building block in order to prepare photoresponsive and CB[8]-containing polyelectrolyte multilayer films. Ultraviolet spectroscopy and a dissipative quartz crystal microbalance are employed to monitor the formation of the host-guest complex and the layer-by-layer self-assembly of the multilayer films, respectively. We demonstrate that the photoresponsive properties of the azo side groups are maintained before and after host-guest complexation with CB[8] in solution and within the multilayer films, respectively. A guest molecule was then specifically included as second binding partner into the CB[8]-containing multilayer films. Subsequently, the release of the guest was performed by UV light irradiation due to the trans-cis isomerization of the adjacent azo side groups. Re-isomerization of the azo side groups was achieved by VIS light irradiation and enabled the rebinding of the guest into CB[8]. Finally, we demonstrate that the photocontrolled binding and release within CB[8]-containing multilayer films can reliably and reversibly be performed over a period of more than 2 weeks with constant binding efficiency. Therefore, we expect such novel type of photosensitive films to have promising future applications in the field of stimuli-responsive nanomaterials.

摘要

利用葫芦[8]脲(CB[8])强大的主客体化学性质,制备了光响应性聚电解质多层膜,用于有机客体分子的可逆光控结合与释放。为此,我们设计并合成了一种带有偶氮苯侧基的聚电解质。然后,将CB[8]与偶氮侧基结合,得到超分子主客体复合物,并将其进一步用作构建单元,以制备含CB[8]的光响应性聚电解质多层膜。分别采用紫外光谱和耗散石英晶体微天平监测主客体复合物的形成以及多层膜的逐层自组装过程。我们证明,在溶液中以及多层膜内,与CB[8]进行主客体络合前后,偶氮侧基的光响应特性均得以保持。随后,将一种客体分子作为第二个结合伙伴特异性地引入含CB[8]的多层膜中。接着,由于相邻偶氮侧基的反式-顺式异构化,通过紫外光照射实现客体的释放。通过可见光照射实现偶氮侧基的重新异构化,使客体能够重新结合到CB[8]中。最后,我们证明,含CB[8]的多层膜内的光控结合与释放能够在超过2周的时间内以恒定的结合效率可靠且可逆地进行。因此,我们期望这种新型的光敏膜在刺激响应纳米材料领域具有广阔的应用前景。

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