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Tunable morphology and surface wettability of an amphiphilic azobenzene derivative and its melamine-induced self-assembly

机译:两亲性偶氮苯衍生物及其三聚氰胺诱导的自组装的可调谐形态和表面润湿性

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摘要

Herein, a series of novel hydrogen-bonded complexes derived from 4-[[(dodecyloxy)benz-4-yl]azo]benzoic acid (DBA) and melamine are reported. The morphology and surface wettability of the resulting self-assembled supramolecular architectures can be easily modulated not only by varying the molar ratios of DBA and melamine, but also by external UV irradiation. Based on the results of atomic force microscope, X-ray diffractometer and contact angle measurements, orientation of the coassembled units with different molar ratios of DBA and melamine could be clearly confirmed. Moreover, the effect of photo-isomerisation of the azobenzene units on the wettability of the assemblies has been investigated in detail. As we know, the films derived from the cis-azobenzene derivative usually exhibit a more hydrophilic property than that from the trans-azobenzene derivative. However, the opposite results were obtained for the samples derived from the cis isomers of DBA-melamine (3:1) complexes or DBA. An explanation, based on the surfaces topography, has been proposed.
机译:在此,报道了衍生自4-[[[(十二烷基氧基)苯-4-基]-偶氮]苯甲酸(DBA)和三聚氰胺的一系列新颖的氢键配合物。不仅可以通过改变DBA和三聚氰胺的摩尔比,而且还可以通过外部UV辐照,很容易地调节所得自组装超分子体系的形态和表面润湿性。根据原子力显微镜,X射线衍射仪和接触角测量的结果,可以清楚地确定具有不同摩尔比的DBA和三聚氰胺的共组装单元的取向。此外,已经详细研究了偶氮苯单元的光异构化对组件的润湿性的影响。众所周知,由顺式偶氮苯衍生物衍生的薄膜通常比由反式偶氮苯衍生物衍生的薄膜具有更大的亲水性。但是,从DBA-三聚氰胺(3:1)配合物或DBA的顺式异构体衍生的样品获得了相反的结果。已经提出了基于表面形貌的解释。

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