期刊
ACS MACRO LETTERS
卷 5, 期 6, 页码 766-771出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsmacrolett.6b00342
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资金
- Ghent University
- Flanders Innovation and Entrepeneurship
- Belgian State, the Prime Minister's office [P7/05]
The ultrafast and additive-free triazolinedione-click reaction with electron rich (di)enes is a powerful method for the ultrafast ligation of polymer segments. A versatile method is described for the introduction of dickable TAD end groups in various polymer segments, using reversible addition-fragmentation chain transfer polymerization. These triazolinedione-functionalized prepolymers were subsequently used for macromolecular functionalization with a low molecular weight diene and block copolymer synthesis of different types within seconds, at ambient conditions, through the coupling with diene-functionalized polymers such as poly(ethylene glycol) and poly(isobornyl acrylate).
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