- Potassium phenoxides bearing bulky yet flexible substituents as highly active catalysts for ring opening polymerization of biobased macrolactone of ethylene brassylate
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- 关键字：HIGH-MOLECULAR-WEIGHT; OMEGA-PENTADECALACTONE; EPSILON-CAPROLACTONE; RAC-LACTIDE; ISOSELECTIVE POLYMERIZATION; DELTA-VALEROLACTONE; BLOCK-COPOLYMERS; FATTY-ACIDS; POLYETHYLENE; (CO)POLYMERIZATION
- 摘要：Well-controlled and efficient ring opening polymerization of biobased ethylene brassylate is of great challenge due to its stainless ring structure that often results in inferior reactivities as well as the presence of two ester groups in the monomer that often lead to extensive intra-/inter- molecular transesterification side reactions. This report discloses a family of potassium phenoxide complexes that bear bulky yet flexible substituents. The bulky nature of the ligand could suppress undesired transesterification reactions, allowing the polymerization proceed in a well controlled manner, as revealed from the detailed kinetic studies that linear relationships between - ln(1x) (x denotes the polymer yield) and the polymerization time and between molecular weights of the obtained polymers and polymer yields. The flexible substituents on the ligand allowed more monomer accessing to the active species, which eventually gave rise to TOFs in a range of 3604-3780 h-1, that were much higher than analogues in previous reports. Moreover, systematic evaluation of the polymerization behaviors demonstrated that the catalytic efficiency of the complexes was closely related to the steric nature of the metal center, increased the steric congestion would give rise to much lower monomer conversions. A plausible mechanism was proposed based on the polymerization results, and such a mechanism was further confirmed by NMR monitoring studies.
- 卷号：211
- 期号：
- 是否译文：否
