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Synthesis, Characterization and Cleavage of Surface-Bound Linear Polymers Formed Using Thiol-Ene Photopolymerizations

机译:硫醇-烯光聚合形成的表面结合线性聚合物的合成,表征和裂解

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The formation of linear polymers films using thiol-ene photopolymerizations was investigated by grafting thiol-ene films on the surface with subsequent cleavage and polymer analysis. Silica nanoparticles were first modified with an acrylated silane molecule, and then a dithiol was reacted to this surface using a base catalyzed thiol-acrylate conjugate addition reaction to prepare a uniform surface presenting thiol groups attached to the surface with a cleavable ester linkage. Photopolymerization of difunctional thiol and ene monomers present in various stoichiometric ratios was carried out in the presence of the nanoparticles, and a thiol-ene film was attached to the surface. The polymer film was cleaved from the surface using acid-catalyzed hydrolysis and separated from the particles. It was found that the particle presence does not affect the polymerization of thiol-ene polymers in bulk; however, the presence of surface thiols changes the relative stoichiometry of the thiol and ene monomers at the surface and hence strongly affects the molecular weight of the attached polymer. The number average and the weight average molecular weight of the unattached polymers ranged from 900 to 12,600 g/mol and 1500 to 25,700 g/ml, respectively, as the thiol:ene ratio in the bulk increased from 0.6 to 1. The highest molecular weight of the grafted polymers (M-n = 1600 g/mol, M-w = 2700 g/mol) was achieved when the thiol:ene ratio was close to 0.77:1 in the bulk and decreased monotonically for both higher and lower stoichiometric ratios. When the polymerization rate was decreased and the time scales for reaction increased, the grafted polymer molecular weight increased for stoichiometric thiol-ene monomer mixtures, because the relative effect of surface thiols was decreased.
机译:通过在表面接枝硫醇-烯膜,随后进行裂解和聚合物分析,研究了使用硫醇-烯光聚合形成线性聚合物膜的方法。首先用丙烯酸酯化的硅烷分子对二氧化硅纳米颗粒进行修饰,然后使用碱催化的硫醇-丙烯酸酯共轭加成反应使二硫醇与该表面反应,以制备均匀的表面,该表面具有通过可裂解的酯键连接到表面的硫醇基团。在纳米粒子的存在下进行以各种化学计量比存在的双官能硫醇和烯单体的光聚合,并将硫醇烯膜附着在表面上。使用酸催化的水解从表面切割聚合物膜,并与颗粒分离。已经发现,颗粒的存在不会影响硫醇-烯聚合物的本体聚合。然而,表面硫醇的存在改变了表面上硫醇和烯单体的相对化学计量,因此强烈影响了所连接聚合物的分子量。随着本体中硫醇:烯的比例从0.6增加到1,未连接聚合物的数均分子量和重均分子量分别为900到12600 g / mol和1500到25700 g / ml。当硫醇:烯的比例在本体中接近0.77∶1时,对于较高和较低的化学计量比,接枝聚合物(Mn = 1600g / mol,Mw = 2700g / mol)达到了1%。当降低聚合速率并增加反应时间时,由于表面硫醇的相对作用降低,化学计量的硫醇-烯单体混合物的接枝聚合物分子量增加。

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