1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) was used as organocatalyst to reinvestigate the ring-opening polymerization (ROP) of epsilon-caprolactone (CL) with benzyl alcohol (BnOH) initiator in bulk at 90 degrees C considering the unsuccessful ROP of CL at RT in previously reported publications. Kinetic study indicates that the PCLs could be well-designed with a controlled/living character of polymerization. The use of functional initiators, such as 2hydroxyethyl methacrylate (HEMA), propargyl alcohol (PGA), 6-azido-1-hexanol (AHA) and methoxy poly (ethylene glycol) (mPEG) leads to end-functionalized PCLs. Accordingly, the block copolymerization of CL with delta-valerolactone (VL), trimethylene carbonate (TMC) and lactide (LA) successfully proceeded to give PCL-b-PVL, PCL-b-PTMC and PCL-b-PLA copolymers. Finally, the reaction mechanism was studied with DFT calculations and NMR measurements.
机构:
Univ Paris Est Creteil Val de Marne, CNRS, UMR 7182, ICMPE, F-94320 Thiais, FranceUniv Paris Est Creteil Val de Marne, CNRS, UMR 7182, ICMPE, F-94320 Thiais, France
Boileau, S.
;
Illy, N.
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Univ Paris Est Creteil Val de Marne, CNRS, UMR 7182, ICMPE, F-94320 Thiais, FranceUniv Paris Est Creteil Val de Marne, CNRS, UMR 7182, ICMPE, F-94320 Thiais, France
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Univ Paris Est Creteil Val de Marne, CNRS, UMR 7182, ICMPE, F-94320 Thiais, FranceUniv Paris Est Creteil Val de Marne, CNRS, UMR 7182, ICMPE, F-94320 Thiais, France
Boileau, S.
;
Illy, N.
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h-index: 0
机构:
Univ Paris Est Creteil Val de Marne, CNRS, UMR 7182, ICMPE, F-94320 Thiais, FranceUniv Paris Est Creteil Val de Marne, CNRS, UMR 7182, ICMPE, F-94320 Thiais, France