Thiol ligand capped quantum dot as an efficient and oxygen tolerance photoinitiator for aqueous phase radical polymerization and 3D printing under visible light

被引:32
|
作者
Zhu, Yifan [1 ]
Ramadani, Emira [1 ]
Egap, Eilaf [1 ,2 ]
机构
[1] Rice Univ, Dept Mat Sci & Nanoengn, Houston, TX 77005 USA
[2] Rice Univ, Dept Chem & Biomol Engn, Houston, TX 77005 USA
关键词
PET-RAFT; PHOTOREDOX CATALYSIS; SEMICONDUCTOR NANOCRYSTALS; CATIONIC-POLYMERIZATION; GRAPHITIC CARBON; ENE; CDS; PHOTOCATALYSIS; PHOTOPOLYMERIZATION; NANOCOMPOSITES;
D O I
10.1039/d1py00705j
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report here a rapid visible-light-induced radical polymerization in aqueous media photoinitiated by only ppm level thiol ligand capped cadmium selenide (CdSe) quantum dots (QDs). Simple ligand exchange procedures with various bifunctional thiol ligands facilitate the dispersion of CdSe QDs in water, thus expanding the scope of aqueous photocatalysts. The polymerization showcased excellent oxygen tolerance, giving a low dispersity (D) of 1.27. Additive thiol molecules were proposed to act as the coinitiating species, oxidized by photoexcited CdSe QDs to form thiyl radicals and further initiate the polymerization. More importantly, successful thiol-ene click reactions were achieved by scaling up the thiol to olefin ratio to 1, suggesting the thiol ligand coinitiating mechanism and meanwhile demonstrating the great potential of QD photocatalysts in organic transformations. Furthermore, the photoinitiation system using CdSe QDs could be readily employed for photo 3D printing of photocurable resin poly(ethylene glycol) diacrylates, opening up vast opportunities for fabricating advanced polymer-inorganic hybrid materials.
引用
收藏
页码:5106 / 5116
页数:11
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