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The Nature of Interactions and UV-Induced Response within α-Zirconium Phosphate Intercalation Compounds with Azobenzenes

机译:α-磷酸锆与偶氮苯的嵌入化合物中的相互作用性质和UV诱导的响应

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摘要

Azobenzenes immobilization on a solid support enables the usage of their trans-cis isomerization ability for preparation of functional materials. The behavior of azobenzenes in the interlayer space of α-zirconium phosphate (ZrP) upon the UV–Vis irradiation was investigated. Two experimental approaches were performed: (1) co-intercalation of benzylalkylammonium surfactants and azobenzene in the interlayers of ZrP (ZBCnA), and (2) intercalation of p-aminoazobenzene (ZpA). The materials were characterized with XRD, FTIR, UV–Vis, CHN analysis, and the molecular modeling. The molecules in ZBCnA samples were sparsely packed and held by weak hydrophobic interactions. Conversely, the molecules in ZpA sample were strongly H-bonded to the ZrP, well-ordered, and densely packed. These structural features determined the samples’ photoresponsive behavior. Low density of molecules in the ZBCnA samples, allowed the effective, fast, and reversible isomerization of azobenzene. Whereas the ZpA sample did not react to the UV irradiation because of the steric hindrance of tightly packed molecules.
机译:将偶氮苯固定在固体载体上可以利用其反式-顺式异构化能力制备功能材料。研究了紫外线-可见光照射下α-磷酸锆(ZrP)层间空间中偶氮苯的行为。进行了两种实验方法:(1)在ZrP(ZBCnA)的中间层中共插入苄基烷基铵表面活性剂和偶氮苯,以及(2)对-氨基偶氮苯(ZpA)的插入。通过XRD,FTIR,UV-Vis,CHN分析和分子建模对材料进行了表征。 ZBCnA样品中的分子稀疏地堆积并通过弱疏水相互作用保持。相反,ZpA样品中的分子牢固地与ZrP形成氢键,排列整齐并紧密堆积。这些结构特征决定了样品的光响应行为。 ZBCnA样品中分子的低密度可实现偶氮苯的有效,快速和可逆的异构化。而ZpA样品由于紧密堆积的分子的位阻而对UV辐射没有反应。

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