Ring-opening polymerization of ω-pentadecalactone catalyzed by phosphazene superbases
KAUST DepartmentChemical Science Program
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division
Polymer Synthesis Laboratory
Permanent link to this recordhttp://hdl.handle.net/10754/622906
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AbstractA fast and living ring-opening polymerization (ROP) of ω-pentadecalactone (PDL), a representative monomer of macrolactones, was achieved using a primary alcohol as the initiator and t-BuP or t-octP as the catalyst. The use of t-BuP instead of the t-BuP superbase slows down the polymerization rate. The ROP of PDL proceeds to high conversion not only at 80 °C in bulk but also at room temperature and in dilute solution. The synthesized PDL homopolymers and block copolymers with poly(ethylene glycol) were characterized by high-temperature GPC (HT-GPC), H NMR and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). Melting temperatures, determined by differential scanning calorimetry, are also reported.
CitationLadelta V, Bilalis P, Gnanou Y, Hadjichristidis N (2017) Ring-opening polymerization of ω-pentadecalactone catalyzed by phosphazene superbases. Polym Chem 8: 511–515. Available: http://dx.doi.org/10.1039/c6py01983h.
SponsorsThis research was supported by King Abdullah University of Science and Technology (KAUST).
PublisherRoyal Society of Chemistry (RSC)