可控矽烷化：以耐水解甲基丙烯酸酯氮矽三環 於矽基材上作為功能性高分子之構成單元;Controlled Silanization：Hydrolysis Resistance Methacrylate Silatrane as a Building Block for Functional Polymers on Silicon

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Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/89178

Title:	可控矽烷化：以耐水解甲基丙烯酸酯氮矽三環於矽基材上作為功能性高分子之構成單元;Controlled Silanization：Hydrolysis Resistance Methacrylate Silatrane as a Building Block for Functional Polymers on Silicon
Authors:	蔣竣東;Chiang, Chun-Tung
Contributors:	化學工程與材料工程學系
Keywords:	可控矽烷化;甲基丙烯酸酯矽烷官能;非特異性吸附;雙離子材料;氮矽三環類化合物;耐水解;methacrylated silatranes;controlled silanization;zwitterionic materials;antifouling properties;hydrolysis resistance;silatrane
Date:	2022-09-12
Issue Date:	2022-10-04 11:00:23 (UTC+8)
Publisher:	國立中央大學
Abstract:	用於表面修飾的有機矽烷官能基(silane)因為其方便的快速製備、高實用性及對於不同表面材料皆有出色的效果而受到重視。商用的矽烷官能基3-(Trimethoxysilyl)propyl methacrylate (TMSPMA)已廣泛用在製備有機及無機混合材料，該結構的頭基具有三個甲氧基能與金屬表面的羥基反應形成穩定之共價鍵，而在末端官能基則有甲基丙烯酸官能基團能與其他單體進行高分子及交聯反應來形成帶有矽烷之功能性高分子。然而，矽烷官能基容易水解且不易保存的特性導致需要在無水的環境下進行反應，因此傳統的矽烷官能基限制了在工業上應用性。在本研究中，我們合成了具有三環籠狀結構和跨環狀氮矽配位鍵的甲基丙烯酸酯氮矽三環類化合物(Methylacrylate silatrane, MAST)，此結構在水中表現出優異的化學穩定性，此外MAST 能與生物啟發之雙離子材料 2-甲基丙烯醯氧基乙基磷酸膽鹼單體(2-Methacryloyloxyethyl phosphorylcholine, MPC)進行高分子反應並將抗汙性質應用在矽基材的表面。MAST 的化學結構使用了核磁共振光譜學(NMR) 及質譜儀(MS)來佐證其結構，另外利用了核磁共振光譜學、X射線光電子能譜學(XPS)、原子力顯微鏡(AFM)、橢圓偏光儀(Ellipsometry)及水接觸角(Water contact angle)等方法與商用矽烷官能基(TMSPMA)進行在水中的化學穩定性、分子取向、表面粗糙度、薄膜膜厚及潤濕性的比較。此外，抗污的雙離子材料MPC 與MAST 利用傳統自由基聚合成高分子用於玻璃修飾上，其出色的修飾平整性及親水能力，透過細菌及蛋白質的貼附測試來證實。本論文透過發展一種穩定且功能強大之甲基丙烯酸酯氮矽三環類化合物，並具有重複性、可定向性及性質定義明確以達到可控矽烷化的目的，進而推動於矽烷化學的發展。;Organosilicons for surface modification are emphasized for their ease of rapid preparation high availability, and effective modification of different interfacial. The commercial silane 3- (Trimethoxysilyl)propyl methacrylate (TMSPMA) has been widely used in the preparation of organic/inorganic hybrid materials. The silane agent has a trialkoxysilyl group, which reacts with hydroxyl groups on the metal surface and then form Si-O-metal covalent bonds. The methacrylic functional group of the silane agent was firstly polymerized with the other monomers to form a silane-containing functional ploymer. However, TMSPMA is easy to be hydrolyzed, making it inconvenient to store, and requiring an anhydrous solvent for coating. The constrains of conventional metharylic silanes lead to troublesome for industrial implementations. In this study, we synthesized methylacrylate silatrane (MAST) with a tricyclic caged structure and a transannular N → Si dative bond, which shows excellent chemical stability in the presence of water. MAST was applied to co-polymerize with bio-inspired zwitterionic 2-Methacryloyloxyethyl phosphorylcholine (MPC) monomer for antifouling modification on silica surfaces. The chemical structure of the developed MAST was characterized by using nuclear magnetic resonance spectroscopy (NMR), mass spectrometry (MS). The chemical stability in presence of water, molecular orientation, roughness, the film thickness and wettability of methacrylated silatranes were compared with commercially available TMSPMA by using NMR, X-ray photoelectron spectroscopy (XPS), atomic force microscope (AFM), ellipsometry, water contact angle, respectively. In addition, an antifouling zwitterionic MPC monomer was employed for constructing a functional copolymer with MAST by conventional free polymerization for surface deposition on silicon. The functionalities of coatings were verified by treating with hydrogel attachment, protein fouling test, and bacterial adsorption. The thesis contributes the advance of silane chemistry by developing a robust and stable acrylic organolsilane for reproducible, orderly oriented, well defined polymeric coating with an aim for controlled silanization.
Appears in Collections:	[National Central University Department of Chemical & Materials Engineering] Electronic Thesis & Dissertation

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