Timbart Laurianne, Renard Estelle, Langlois Valérie, Guerin Philippe
LRP, UMR 7581, Université Paris XII, 2 à 8, rue H. Dunant, 94 320 Thiais, France.
Macromol Biosci. 2004 Nov 20;4(11):1014-20. doi: 10.1002/mabi.200400104.
Novel biodegradable polyester block copolymers have been synthesized by using well-defined poly(3-hydroxyoctanoate) (PHO) oligomers having a hydroxyl end group and an ester end group with M(n) values of 800, 2,500, 5,300, 8,000, or 20,000 as an elastomeric soft segment and poly(epsilon-caprolactone) as a more crystalline segment. These PHO oligomers prepared by methanolysis were subjected to block copolymerization with epsilon-caprolactone. The chemical structure of the copolymers was confirmed by (1)H NMR and (13)C NMR spectroscopy. All the copolyesters are semi-crystalline and two T(g) were observed by differential scanning calorimetry when the molecular weight of the PHO block is about 20,000.
通过使用具有羟基端基和酯端基、数均分子量(M(n))分别为800、2500、5300、8000或20000的明确的聚(3-羟基辛酸酯)(PHO)低聚物作为弹性体软段,以及聚(ε-己内酯)作为更具结晶性的段,合成了新型可生物降解聚酯嵌段共聚物。通过甲醇解制备的这些PHO低聚物与ε-己内酯进行嵌段共聚。通过(1)H NMR和(13)C NMR光谱确认了共聚物的化学结构。当PHO嵌段的分子量约为20000时,所有共聚酯都是半结晶的,并且通过差示扫描量热法观察到两个玻璃化转变温度(T(g))。