2000
DOI: 10.1002/(sici)1099-0518(20000515)38:10<1774::aid-pola620>3.0.co;2-f
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Controlled ring-opening polymerization ofL-lactide and 1,5-dioxepan-2-one forming a triblock copolymer
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Cited by 86 publications
(75 citation statements)
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“…The T m of the PLLA blocks is lower than the reported values, due to the rather low molecular weights of the PLLA blocks. The T m and T g values of the triblock copolymers were consistent with earlier reported values for similar triblocks . The multiblock copolymer had higher T g than the triblock copolymers.…”
Section: Resultssupporting
confidence: 90%
“…The T m of the PLLA blocks is lower than the reported values, due to the rather low molecular weights of the PLLA blocks. The T m and T g values of the triblock copolymers were consistent with earlier reported values for similar triblocks . The multiblock copolymer had higher T g than the triblock copolymers.…”
Section: Resultssupporting
confidence: 90%
“…The shortening of the block sequences of the copolymer of CL and DXO, compared with the earlier reported triblocks of LLA and DXO,1, 2 could, as already mentioned, be a result of the transesterifications reaction occuring during copolymerization. It can also be explained by the monomer reactivities; an earlier report on the copolymerization of CL and DXO with a stannous octoate catalyst in bulk at 110 °C gave the reactivities r CL = 0.6 and r DXO = 1.6,7 whereas the reactivity ratios, for the copolymerization of LLA and DXO under similar conditions were r LLA = 10 and r DXO = 0.1 8…”
Section: Resultssupporting
confidence: 50%
“…Efficiencies of the reactions were evaluated by determining the monomer conversions after appropriate time intervals ( Table 1 ). Sn(IV) alkoxide was successfully used for the ROP of l ‐lactide . Reported results presented a fairly good control of reaction and relatively high monomer conversion (>90%) when ROPs are carried out in homogeneous solutions at 60 °C.…”
Section: Resultsmentioning
confidence: 99%
