116821-45-5Relevant articles and documents
A simple access to ω-aminoalkyltrialkoxysilanes: Tunable linkers for self-organised organosilicas
Pichon, Beno?t P.,Wong Chi Man, Michel,Bied, Catherine,Moreau, Jo?l J.E.
, p. 1126 - 1130 (2006)
A simple route to ω-aminoalkyltriethoxysilanes with variable alkylene chain lengths, (EtO)3Si(CH2)nNH2 (n = 5, 11) is described. These silyl linkers have been used to prepare urea-based compounds with H-bonding and hydrophobic interactions which enable the self-assembly of the molecules. These molecular precursors are suitable for the obtention of nano-structured hybrid silicas.
Maleic imide base three ethoxy silane series compound synthesis and self-assembly film preparation method
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, (2019/06/26)
Among various factors influencing performances of organic electronic components, interfacial property is the most important one influencing the performance of the whole component. In the invention, a series of maleimidotriethoxy silane-series compounds are synthesized, wherein a monomolecular film layer is formed on a surface of an oxide substrate through a self-assembling method, thereby modifying the substrate. Dicyclopentadiene platinum chloride is employed as a catalyst to perform hydrosilylation. Nuclear magnetism is carried out for representation. A test result proves that the catalyst allows catalytic addition to a compound having an amino group to be carried out high-efficiently, and furthermore, silicone on a silanoethoxyl group is connected to a position of a terminal group of a double bond before addition. A self-assembling method is utilized to form the monomolecular film layer on the surface of the oxide substrate. A Young contact angle instrument and XPS is employed for representation, which proves that a flat monomolecular film layer is formed on the surface of the oxide substrate.
