Sugawara-Narutaki Ayae, Tsuboike Sachio, Oda Yukari, Shimojima Atsushi, Landenberger Kira B, Okubo Tatsuya, Aoshima Sadahito
Department of Materials Chemistry , Nagoya University , Furo-cho , Chikusa-ku, Nagoya 464-8603 , Japan.
Department of Chemical System Engineering , The University of Tokyo , Hongo , Bunkyo-ku, Tokyo 113-8656 , Japan.
Langmuir. 2019 Aug 20;35(33):10846-10854. doi: 10.1021/acs.langmuir.9b01493. Epub 2019 Aug 12.
Core-shell polymer-silica hybrid nanoparticles smaller than 50 nm in diameter were formed in the presence of micelles of poly(2-aminoethyl vinyl ether--isobutyl vinyl ether) (poly(AEVE--IBVE)) through the hydrolysis and polycondensation of alkoxysilane in aqueous solution at a mild pH and temperature. The size of the nanoparticles as well as the number and size of the core parts were effectively controlled by varying the molecular weight of the copolymers. The polymers could be removed by calcination to give hollow silica nanoparticles with Brunauer-Emmett-Teller surface areas of more than 500 m g. Among these, silica nanoparticles formed with poly(AEVE--IBVE) displayed an anisotropy of single openings in the shell. The use of an alternative copolymer, poly(AEVE--2-naphthoxyethyl vinyl ether) (poly(AEVE--βNpOVE)), yielded core-shell nanoparticles with less pronounced anisotropy. These results showed that the degree of anisotropy could be controlled by the rigidity of micelles; the micelle of poly(AEVE--IBVE) was more deformable during silica deposition than that of poly(AEVE--βNpOVE) in which aromatic interactions were possible. This bioinspired, environmentally friendly approach will enable large-scale production of anisotropic silica nanomaterials, opening up applications in the field of nanomedicine, optical materials, and self-assembly.
在温和的pH值和温度条件下,通过烷氧基硅烷在水溶液中的水解和缩聚反应,在聚(2-氨基乙基乙烯基醚-异丁基乙烯基醚)(聚(AEVE-IBVE))胶束存在下形成了直径小于50 nm的核壳聚合物-二氧化硅杂化纳米颗粒。通过改变共聚物的分子量,可以有效地控制纳米颗粒的尺寸以及核部分的数量和尺寸。通过煅烧可以除去聚合物,从而得到具有超过500 m²/g的Brunauer-Emmett-Teller表面积的中空二氧化硅纳米颗粒。其中,由聚(AEVE-IBVE)形成的二氧化硅纳米颗粒在壳层中显示出单孔的各向异性。使用另一种共聚物聚(AEVE-2-萘氧基乙基乙烯基醚)(聚(AEVE-βNpOVE)),得到的核壳纳米颗粒各向异性不太明显。这些结果表明,各向异性程度可以通过胶束的刚性来控制;在二氧化硅沉积过程中,聚(AEVE-IBVE)的胶束比可能存在芳族相互作用的聚(AEVE-βNpOVE)的胶束更易变形。这种受生物启发的环保方法将能够大规模生产各向异性二氧化硅纳米材料,为纳米医学、光学材料和自组装领域开辟应用前景。