期刊
CCS CHEMISTRY
卷 3, 期 1, 页码 620-630出版社
CHINESE CHEMICAL SOC
DOI: 10.31635/ccschem.020.202000232
关键词
organocatalyst; ring-opening polymerization; polyester; sustainable polymer; recyclability
资金
- National Natural Science Foundation of China [21801151]
- Shandong Provincial Natural Science Foundation, China [ZR2018BEM029]
- 111 Project [D17004]
- Taishan Scholars Constructive Engineering Foundation [tsqn20161031]
This study presents the successful development of an organocatalytic chemoselective ROP of MBL to produce functional unsaturated polyester, showcasing delicate chemoselectivity control through temperature and urea catalyst selection. The obtained polyester can be fully recycled back to its monomer through mild chemolysis, and experimental and theoretical calculations support the mechanistic insights of the kinetically favored ROP pathway using urea with stronger acidity at low temperatures.
Despite the great potential of biorenewable alpha-methylene-gamma-butyrolactone (MBL) to produce functional, recyclable polyester, the ring-opening polymerization (ROP) of MBL remains a challenge due to the competing polymerization of the highly reactive exocyclic double bond and low-strained five-membered ring. In this contribution, we present the first organocatalytic chemoselective ROP of MBL to exclusively produce functional unsaturated polyester by utilizing a phosphazene base/urea binary catalyst. We show that delicate chemoselectivity can be realized by controlling the temperature and using selected urea catalysts. The obtained polyester can be completely recycled back to its monomer by chemolysis under mild conditions. Experimental and theoretical calculations provide mechanistic insights and indicate that the ROP pathway is kinetically favored by using urea with stronger acidity at low temperatures.
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