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Photochromic spiropyran- and spirooxazine-homopolymers in mesoporous thin films by surface initiated ROMP

机译:表面引发ROMP在中孔薄膜中的光致变色螺吡喃和螺恶嗪均聚物

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摘要

The control of ionic permselectivity in porous films is an interesting aspect in the context of lab-on-chip devices and m-electronics. Especially, visible light triggered ionic permselectivity control is of relevance because control by light can be maintained externally without changing internal system parameters. In addition, light is a sustainable energy source if sunlight is used. Here, we present the first mesoporous films modified with two different photochromic homopolymers by surface-initiated ring opening metathesis polymerization (SI-ROMP). Spiropyran-and spirooxazine functionalized norbornene monomers and the corresponding ROMP homopolymers are synthesized in solution and in mesopores and compared concerning their optical properties such as photochromic conversion kinetics, photostability, and the ratio of converted molecules. Optical properties are investigated using UV/VIS spectroscopy and H-1-NMR spectroscopy. Especially, spirooxazine, whose surface functionalization has not been studied in detail, shows fast switching properties and higher ratios of photochromically interconverted molecules. After grafting spiropyran- and spirooxazine norbornene homopolymers into mesopores, a slightly faster photochromic interconversion of polymers located inside the mesopores is observed compared to the solution polymers.
机译:在芯片实验室设备和m电子学的背景下,控制多孔膜中离子渗透性是一个有趣的方面。尤其是,可见光触发的离子渗透选择性控制非常重要,因为可以在不更改内部系统参数的情况下从外部维护光控制。另外,如果使用阳光,光是可持续的能源。在这里,我们介绍通过表面引发的开环复分解聚合反应(SI-ROMP)用两种不同的光致变色均聚物改性的第一介孔膜。在溶液和中孔中合成了螺吡喃和螺恶嗪官能化的降冰片烯单体以及相应的ROMP均聚物,并比较了它们的光学性质,例如光致变色转化动力学,光稳定性和转化分子的比例。使用UV / VIS光谱和H-1-NMR光谱研究光学性质。特别地,尚未详细研究表面官能化的螺恶嗪显示出快速的开关性能和较高比例的光致变色互变分子。将螺并吡喃和螺并恶嗪降冰片烯均聚物接枝到中孔中之后,与溶液聚合物相比,观察到位于中孔内部的聚合物的光致变色反应快一些。

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