丙交酯
序列(生物学)
表征(材料科学)
高分子化学
材料科学
化学
共聚物
有机化学
聚合物
纳米技术
生物化学
作者
Louise Kuehster,Michael S. Bingham,Jingyi Dai,Young Kuk Jhon,Yan Wang,Bin Qin,William C. Smith,Xiaoming Xu,Feng Zhang,Nathaniel A. Lynd
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-04-03
卷期号:58 (8): 3886-3897
被引量:2
标识
DOI:10.1021/acs.macromol.4c02895
摘要
Established methods of characterizing repeat unit sequence by measuring changes in comonomer concentration during copolymerization and inferring the resulting copolymer sequence are inapplicable to poly(lactide-co-glycolide) due to reverse and transesterification reactions. In this case, measurement of repeat unit sequences must be based on direct measurement on the copolymer. Here, the assignment of the 13C NMR spectrum of the glycolyl methylene of poly(lactide-co-glycolide) to specific compositional ester tetrads is reported using insights provided by a stochastic model regression analysis of experimental reversible transesterification copolymerization data. The relative integrals of the deconvoluted compositional tetrad signals can be interpreted within the context of a model for repeat unit clustering that describes the cumulative population of homosequences with at least nG adjacent glycolyl esters, including the resonant glycolyl ester. The decay of the relative population of homosequence length nG is described by an exponential decay f(n) = e(1–n)/σb with the parameter σb describing the degree of clustering of glycolyl ester units. An empirical model describes the time-evolution of σb as a function of reaction time, which evolves due to comonomer reversibility and copolymer transesterification.
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