论文标题
(3-三甲基二甲丙基丙基)二乙基三亚胺的生长和组织,在二氧化硅上反应性氨基终止的自组装单层中的生长和组织
Growth and organization of (3-Trimethoxysilylpropyl) diethylenetriamine within reactive amino-terminated self-assembled monolayer on silica
论文作者
论文摘要
烷烃链是用于单层制造的最常用的分子。长链用于其强大的范德华相互作用,引起了良好的层组织。胺功能终止的烷基链引起了极大的兴趣,广泛用于进一步的表面功能。由于必须组织此类层以在表面提供胺基部分,因此本研究涉及探索胺终止的SAM形成,以替代通常的氨基丙基烷基硅烷SAM。此外,由于沿链条沿岸的两个NH部分,使用长的NH2端烷基链可以形成氢键。此外,这种氢键使得可以缩短分子长度,同时保留组织良好的单层。为此,我们对使用各种溶剂,相对湿度和温度值对(3-三甲基二甲丙基)二乙基三亚氨基(DETAS)进行了完整研究。通过椭圆测量法和性腺测定法监测移植动力学,并使用AFM和ATR-FTIR光谱法监测了SAM结构和组织。在SAM生长过程和最终完整的SAM中证明了氢键。我们认为,该研究可以更好地控制优质的Detas Sam,以提高其在进一步的表面功能应用中的效率。
Alkane chains are the most commonly used molecules for monolayer fabrication. Long chains are used for their strong van der Waals interactions inducing good layer organization. Amine function-terminated alkyl chains are of great interest and are widely used for further surface functionalization. Since it is mandatory that such layers be organized to provide amine moieties at the surface, the present study deals with exploring amine-terminated SAM formation as an alternative to the usual aminopropylalkylsilane SAM. Additionally, using a long NH2terminated alkyl chain allows the formation of hydrogen bonding thanks to the two NH moieties born along the chain. Furthermore, such hydrogen bonding makes possible to shorten the molecule length while preserving a well-organized monolayer. For this purpose we performed a complete study of the grafting of (3-Trimethoxysilylpropyl) diethylenetriamine (DETAS) on native silicon oxide using various solvents, relative humidity and temperature values. Grafting kinetics was monitored by ellipsometry and goniometry, and SAM structure and organization using AFM and ATR-FTIR spectroscopy. Hydrogen bonding was evidenced within the SAM growth process and in the final complete SAM. We believe such study enables a better control of good quality DETAS SAM in order to improve their efficiency in further surface functionalization applications.