Synthesis of amphiphilic V-type silica nanogels and study of their self-assembling at the air-water interface

被引:2
|
作者
Kazakova, V. V. [1 ]
Gorbatsevich, O. B. [1 ]
Malakhova, Yu. N. [2 ,3 ]
Buzin, A. I. [1 ]
Muzafarov, A. M. [1 ,4 ]
机构
[1] Russian Acad Sci, NS Enikolopov Inst Synthet Polymer Mat, 70 Ul Profsoyuznaya, Moscow 117393, Russia
[2] MIREA Russian Technol Univ, MV Lomonosov Inst Fine Chem Technol, 86 Prosp Vernadskogo, Moscow 119571, Russia
[3] Kurchatov Inst, Natl Res Ctr, 1 Pl Akad Kurchatova, Moscow 123182, Russia
[4] Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, 28 Ul Vavilova, Moscow 119991, Russia
基金
俄罗斯科学基金会; 俄罗斯基础研究基金会;
关键词
nanogels; silica nanoparticles; Langmuir-Blodgett films; self-assembly of amphiphilic macromolecules; GOLD NANOPARTICLES; BLOCK-COPOLYMERS; PARTICLES; MICELLES; TRANSITION; MONOLAYERS; EVOLUTION; BRUSHES; LIGANDS;
D O I
10.1007/s11172-018-2333-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The methods for the synthesis of silica nanogels and a modifying agent, as well as related amphiphilic V-type silica nanogels are presented. Self-assembly of the synthesized amphi philic nanogels during the formation of Langmuir monolayers at the air-water interface is considered. Aggregate structures were revealed to form during ordering of the silica V-type nanogels at the air-water interface after collapse of the Langmuir monolayer. For the low-molecular-weight fraction of the silica nanogels, the aggregates do not completely decompose upon the expansion of the Langmuir layer since are formed by mutually penetrating macromolecules. For the highmolecular- weight fraction, they are reversibly formed and decompose in consecutive compression- expansion cycles, which is characteristic of Langmuir layers of nanoparticles.
引用
收藏
页码:2088 / 2097
页数:10
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