共 50 条
Access to Photoreactive Core-Shell Nanomaterials by Photoinitiated Polymerization-Induced Self-Assembly
被引:7
|作者:
Molle, Edgar
[1
,2
]
Le, Dao
[1
,2
]
Abbariki, Tannaz Norizadeh
[1
]
Akdemir, Meryem S.
[1
,2
]
Takamiya, Masanari
[1
]
Miceli, Enrico
[1
,2
]
Kassel, Olivier
[1
]
Delaittre, Guillaume
[1
,2
,3
,4
]
机构:
[1] KIT, ITG, Hermann von Helmholtz Pl 1, D-76244 Eggenstein Leopoldshafen, Germany
[2] KIT, Inst Chem Technol & Polymer Chem ITCP, Engesserstr 18, D-76131 Karlsruhe, Germany
[3] Univ Appl Sci Aachen, Inst Appl Polymer Chem, Heinrich Mussmann Str 1, D-52428 Julich, Germany
[4] Deutsch Textilforschungszentrum Nord West DTNW gG, Adlerstr 1, D-47798 Krefeld, Germany
来源:
关键词:
dipolar cycloaddition;
dispersion polymerization;
lambda orthogonality;
photopolymerization;
photoreactivity;
AQUEOUS DISPERSION POLYMERIZATION;
COPOLYMER NANO-OBJECTS;
PHOTOCLICK CHEMISTRY;
MORPHOLOGICAL TRANSITIONS;
IN-VIVO;
NANOPARTICLES;
LIGHT;
CYCLOADDITIONS;
ORTHOGONALITY;
VESICLES;
D O I:
10.1002/cptc.201900216
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
We report the straightforward synthesis of photoreactive nanoobjects exhibiting various colloidal morphologies by photoinitiated polymerization-induced self-assembly (PISA). Poly(oligoethylene glycol methyl ether methacrylate) copolymers with pendent UV-activatable diaryl tetrazole moieties were employed as macromolecular chain-transfer agents in water for the dispersion photopolymerization of 2-hydroxypropyl methacrylate under visible light. This led to the in situ formation of amphiphilic block copolymers, driving the self-assembly into core-shell nanoparticles, nanofibers, and nano/microvesicles. The tetrazole group present in the shell of the nanoobjects permitted functionalization with various functional molecules and polymers via UV-triggered nitrile imine-mediated tetrazole-ene cycloaddition (NITEC), enabling the alteration of surface properties of the nanomaterials (fluorescence, charge, hydrophilicity).
引用
收藏
页码:1084 / 1089
页数:6
相关论文