Synthesis of mid-chain functional macrophotoinitiators of poly(D,L-lactide) homopolymer and tetrablock poly(D,L-lactide)-poly(ε-caprolactone) copolymer by ring-opening polymerization
Autor: | Mustafa Degirmenci, Tuba Urun, Mustafa Durgun, Esra Barım |
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Přispěvatelé: | Tunceli Meslek Yüksekokulu |
Rok vydání: | 2015 |
Předmět: |
chemistry.chemical_classification
Materials science Polymers and Plastics General Chemical Engineering macrophotoinitiator block copolymer General Chemistry Polymer Ring-opening polymerization poly(D L-lactide) chemistry.chemical_compound Monomer chemistry Polymerization Polymer chemistry Materials Chemistry Copolymer ring-opening polymerization (ROP) Caprolactone Prepolymer Photoinitiator poly(ε-caprolactone) |
Zdroj: | Designed Monomers and Polymers. 18:669-677 |
ISSN: | 1568-5551 |
Popis: | We have synthesized novel biobased and environmental friendly mid-chain functional macrophotoinitiators of poly(D,L-lactide) homopolymer (PDLLA-PI-PDLLA) and tetrablock poly(D,L-lactide)-poly(ε-caprolactone) copolymer (PDLLA-PCL-PI-PCL-PDLLA) with controlled molecular weights and narrow molecular weight distributions via ring-opening polymerization (ROP). Mid-chain functional poly(D,L-lactide) (PDLLA-PI-PDLLA) macrophotoinitiator was prepared by ROP of D,L-lactide (DLLA) monomer using a dihydroxy-functional photoinitiator (HO-PI-OH) as the initiator and stannous-2-ethyl hexanoate (Sn(Oct)2) as the catalyst. Tetrablock poly(D,L-lactide)-poly(ε-caprolactone) copolymer (PDLLA-PCL-PI-PCL-PDLLA) with a mid-chain photofunctional group was synthesized via sequential ROP of ε-caprolactone and D,L-lactide using Sn(Oct)2 as the catalyst. The resultant polymers were fully characterized by means of 1H NMR, FTIR, UV–vis, Fluorescence, and GPC techniques. The obtained macrophotoinitiators were used as a prepolymer in photoinitiated free radical polymerization for obtaining AB-type diblock copolymer and ABC-type triblock terpolymer. |
Databáze: | OpenAIRE |
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