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芳基偶氮吡唑在玻璃和氧化硅上的自组装单分子层:光异构化和光响应润湿性

Self-Assembled Monolayers of Arylazopyrazoles on Glass and Silicon Oxide: Photoisomerization and Photoresponsive Wettability.

作者信息

Arndt Niklas B, Schlüter Friederike, Böckmann Marcus, Adolphs Thorsten, Arlinghaus Heinrich F, Doltsinis Nikos L, Ravoo Bart Jan

机构信息

Center for Soft Nanoscience and Organic Chemistry Institute, Westfälische Wilhelms-Universität Münster, Busso-Peus Straße 10, 48149 Münster, Germany.

Center for Soft Nanoscience and Institute of Solid State Theory, Westfälische Wilhelms-Universität Münster, Wilhelm-Klemm-Straße 10, 48149 Münster, Germany.

出版信息

Langmuir. 2022 Jan 18;38(2):735-742. doi: 10.1021/acs.langmuir.1c02651. Epub 2022 Jan 6.

Abstract

Surface coatings that respond to external influences and change their physical properties upon application of external stimuli are of great interest, with light being a particularly desirable choice. Photoswitches such as azobenzenes have been employed in a range of photoresponsive coatings. One striking change in physical property of many photoresponsive coatings is their responsive wettability upon illumination. In this work, we present photoswitchable self-assembled monolayers based on arylazopyrazoles (AAPs). In solution, AAPs offer significant improvements in terms of the photostationary state, thermal stability, and fatigue resistance. The AAP photoswitch is coupled to triethoxysilanes for an easy, one-step functionalization of glass and silicon oxide surfaces. We show the synthesis of AAP-based silanes and the successful surface functionalization, and we confirm the excellent photoswitchability of the AAPs in a self-assembled monolayer upon alternating irradiation with UV (365 nm) and green (520 nm) light. The self-assembled monolayers are investigated by UV/vis spectroscopy, X-ray photoelectron spectroscopy (XPS), time-of-flight secondary ion mass spectrometry (ToF-SIMS), and contact angle goniometry. We furthermore investigate the effect of substitution of the AAPs on the photoresponsive wetting behavior and compare this with density functional theory (DFT) calculations of the dipole moments of the AAPs.

摘要

能够响应外部影响并在施加外部刺激时改变其物理性质的表面涂层备受关注,其中光尤其是一种理想的选择。诸如偶氮苯之类的光开关已被应用于一系列光响应涂层中。许多光响应涂层的一个显著物理性质变化是其在光照下的响应润湿性。在这项工作中,我们展示了基于芳基偶氮吡唑(AAPs)的光开关自组装单分子层。在溶液中,AAPs在光稳态、热稳定性和抗疲劳性方面有显著改善。AAP光开关与三乙氧基硅烷偶联,以便对玻璃和氧化硅表面进行简便的一步功能化。我们展示了基于AAP的硅烷的合成以及成功的表面功能化,并通过用紫外线(365纳米)和绿光(520纳米)交替照射,证实了自组装单分子层中AAPs具有出色的光开关性。通过紫外可见光谱、X射线光电子能谱(XPS)、飞行时间二次离子质谱(ToF-SIMS)和接触角测角法对自组装单分子层进行了研究。我们还研究了AAPs取代对光响应润湿行为的影响,并将其与AAPs偶极矩的密度泛函理论(DFT)计算结果进行了比较。

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