TY - JOUR
T1 - Bioinspired Approach to Silica Nanoparticle Synthesis Using Amine-Containing Block Copoly(vinyl ethers)
T2 - Realizing Controlled Anisotropy
AU - Sugawara-Narutaki, Ayae
AU - Tsuboike, Sachio
AU - Oda, Yukari
AU - Shimojima, Atsushi
AU - Landenberger, Kira B.
AU - Okubo, Tatsuya
AU - Aoshima, Sadahito
N1 - Funding Information:
The authors thank Prof. Yukio Yamaguchi (The University of Tokyo) for DLS and ζ-potential measurements. They also thank Dr. Junzheng Wang (The University of Tokyo) and Dr. Yu Shinke (Osaka University) for help in FE-SEM observation and polymer synthesis, respectively. This work was supported by a Grant-in-Aid for Scientific Research on the Innovative Areas: “Fusion Materials” (Area no. 2206) from MEXT and by JSPS KAKENHI Grant Numbers 17H03068 and 16K14090, Japan. Part of this work was supported in Nanotechnology Platform Program (Molecule and Material Synthesis), MEXT, Japan, and conducted in Center for Nano Lithography & Analysis, The University of Tokyo and the High Voltage Electron Microscope Laboratory, Nagoya University.
Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/8/20
Y1 - 2019/8/20
N2 - 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-block-isobutyl vinyl ether) (poly(AEVEm-b-IBVEn)) 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 m2 g-1. Among these, silica nanoparticles formed with poly(AEVE115-b-IBVE40) displayed an anisotropy of single openings in the shell. The use of an alternative copolymer, poly(AEVE-b-2-naphthoxyethyl vinyl ether) (poly(AEVE113-b-βNpOVE40)), 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(AEVE115-b-IBVE40) was more deformable during silica deposition than that of poly(AEVE113-b-βNpOVE40) 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.
AB - 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-block-isobutyl vinyl ether) (poly(AEVEm-b-IBVEn)) 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 m2 g-1. Among these, silica nanoparticles formed with poly(AEVE115-b-IBVE40) displayed an anisotropy of single openings in the shell. The use of an alternative copolymer, poly(AEVE-b-2-naphthoxyethyl vinyl ether) (poly(AEVE113-b-βNpOVE40)), 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(AEVE115-b-IBVE40) was more deformable during silica deposition than that of poly(AEVE113-b-βNpOVE40) 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.
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U2 - 10.1021/acs.langmuir.9b01493
DO - 10.1021/acs.langmuir.9b01493
M3 - Article
C2 - 31355647
AN - SCOPUS:85071697514
SN - 0743-7463
VL - 35
SP - 10846
EP - 10854
JO - Langmuir
JF - Langmuir
IS - 33
ER -