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Catalytically Controlled Ring-Opening Polymerization of 2-Oxo-15-crown-5 for Degradable and Recyclable PEG-Like Polyesters.

Zhitao HuXiaohui CaoXiaohui ZhangBin WuWenjun LuoHuahua HuangLe LiYongming Chen
Published in: ACS macro letters (2022)
Poly(ethylene glycol) (PEG) has been extensively used in diverse applications. However, it is not biodegradable and shows abnormal immune responses. Herein, a fast, controlled, ring-opening polymerization (ROP) of 2-oxo-15-crown-5 (O-15C5) is reported to prepare well-defined PEG-like polyesters, poly(O-15C5). This approach relies on a coordination between the macrocyclic monomer and Na + that increases the electrophilicity of the carbonyl group of O-15C5 and leads to a fast controlled ROP (dispersity, Đ M < 1.2). Both computational and mechanistic studies show that the selective Na + binding to the monomer over poly(O-15C5) allows the ring-opening initiation and propagation to be more energetically favorable than side transesterifications. This is the key to control the challenging entropy-driven ROP of O-15C5. Moreover, with the aid of Na + and organic base, poly(O-15C5) depolymerized readily into O-15C5 in 2 h. Also, it degraded in a buffer of pH 7.4 by hydrolysis.
Keyphrases
  • drug delivery
  • immune response
  • molecularly imprinted
  • multidrug resistant
  • toll like receptor
  • inflammatory response
  • liquid chromatography