Shuming Dai,Mingqian Wang,Zhiqiang Ding,Honggang Xia,Dongbin Wang,Zhe Ma,Bin Wang
{"title":"6-/7元环碳酸盐与l-丙交酯的序控共聚:共聚物性能的大范围调控","authors":"Shuming Dai,Mingqian Wang,Zhiqiang Ding,Honggang Xia,Dongbin Wang,Zhe Ma,Bin Wang","doi":"10.1021/acs.macromol.6c01662","DOIUrl":null,"url":null,"abstract":"The synthesis of sequence-controlled poly(lactide-carbonate) copolymers via ring-opening copolymerization (ROCOP) of l-lactide (l-LA) with cyclic carbonates under industrially relevant conditions (in bulk and melt) is highly challenging owing to the lack of highly active and thermally stable catalysts. Herein, we systematically investigated the melt and bulk ROCOPs of l-LA with 6-membered trimethylene carbonate (TMC) and 7-membered cyclic 1,4-butylene carbonate (CBC), respectively, using the (amidoalkyl)pyridine–phenolate aluminum methyl complexes as catalysts. The kinetic differentiation and reactivity ratios for l-LA/TMC and l-LA/CBC monomer mixtures were determined in solution polymerization to deeply understand the catalyst-dependent ROCOP behavior. Poly(LA-TMC) and poly(LA-CBC) copolymers with varying comonomer incorporation ratios and tunable sequence length of PLA segments were further synthesized under bulk and melt conditions with different catalysts. The thermal/mechanical properties and degradation behavior of the resulting poly(LA-TMC) and poly(LA-CBC) samples were thoroughly investigated to elucidate the significant effects of comonomer distribution and chain sequences on material properties. Notably, the aluminum complexes exhibited a higher degree of control over the ROCOP process compared with stannous octoate (Sn(Oct)2), affording poly(LA-TMC) and poly(LA-CBC) copolymers with higher molecular weights and superior thermal/mechanical properties under identical conditions. This systematic investigation of the relationships between catalyst/monomer structure, chain composition, and material properties provides valuable insights into the development of high-performance aliphatic copolyesters and the optimization of their practical application performance.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"9 1","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2026-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sequence-Controlled Copolymerization of 6-/7-Membered Cyclic Carbonates with l-Lactide: Wide-Range Regulation of Copolymer Properties\",\"authors\":\"Shuming Dai,Mingqian Wang,Zhiqiang Ding,Honggang Xia,Dongbin Wang,Zhe Ma,Bin Wang\",\"doi\":\"10.1021/acs.macromol.6c01662\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The synthesis of sequence-controlled poly(lactide-carbonate) copolymers via ring-opening copolymerization (ROCOP) of l-lactide (l-LA) with cyclic carbonates under industrially relevant conditions (in bulk and melt) is highly challenging owing to the lack of highly active and thermally stable catalysts. Herein, we systematically investigated the melt and bulk ROCOPs of l-LA with 6-membered trimethylene carbonate (TMC) and 7-membered cyclic 1,4-butylene carbonate (CBC), respectively, using the (amidoalkyl)pyridine–phenolate aluminum methyl complexes as catalysts. The kinetic differentiation and reactivity ratios for l-LA/TMC and l-LA/CBC monomer mixtures were determined in solution polymerization to deeply understand the catalyst-dependent ROCOP behavior. Poly(LA-TMC) and poly(LA-CBC) copolymers with varying comonomer incorporation ratios and tunable sequence length of PLA segments were further synthesized under bulk and melt conditions with different catalysts. The thermal/mechanical properties and degradation behavior of the resulting poly(LA-TMC) and poly(LA-CBC) samples were thoroughly investigated to elucidate the significant effects of comonomer distribution and chain sequences on material properties. Notably, the aluminum complexes exhibited a higher degree of control over the ROCOP process compared with stannous octoate (Sn(Oct)2), affording poly(LA-TMC) and poly(LA-CBC) copolymers with higher molecular weights and superior thermal/mechanical properties under identical conditions. 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Sequence-Controlled Copolymerization of 6-/7-Membered Cyclic Carbonates with l-Lactide: Wide-Range Regulation of Copolymer Properties
The synthesis of sequence-controlled poly(lactide-carbonate) copolymers via ring-opening copolymerization (ROCOP) of l-lactide (l-LA) with cyclic carbonates under industrially relevant conditions (in bulk and melt) is highly challenging owing to the lack of highly active and thermally stable catalysts. Herein, we systematically investigated the melt and bulk ROCOPs of l-LA with 6-membered trimethylene carbonate (TMC) and 7-membered cyclic 1,4-butylene carbonate (CBC), respectively, using the (amidoalkyl)pyridine–phenolate aluminum methyl complexes as catalysts. The kinetic differentiation and reactivity ratios for l-LA/TMC and l-LA/CBC monomer mixtures were determined in solution polymerization to deeply understand the catalyst-dependent ROCOP behavior. Poly(LA-TMC) and poly(LA-CBC) copolymers with varying comonomer incorporation ratios and tunable sequence length of PLA segments were further synthesized under bulk and melt conditions with different catalysts. The thermal/mechanical properties and degradation behavior of the resulting poly(LA-TMC) and poly(LA-CBC) samples were thoroughly investigated to elucidate the significant effects of comonomer distribution and chain sequences on material properties. Notably, the aluminum complexes exhibited a higher degree of control over the ROCOP process compared with stannous octoate (Sn(Oct)2), affording poly(LA-TMC) and poly(LA-CBC) copolymers with higher molecular weights and superior thermal/mechanical properties under identical conditions. This systematic investigation of the relationships between catalyst/monomer structure, chain composition, and material properties provides valuable insights into the development of high-performance aliphatic copolyesters and the optimization of their practical application performance.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.