Zhang Shiping, Yang Jing, Liu Xiaoyun, Chang Jianhua, Cao Amin
Polymer Materials Lab, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Street, People's Republic of China.
Biomacromolecules. 2003 Mar-Apr;4(2):437-45. doi: 10.1021/bm0201183.
A new biodegradable copolyester, poly(butylene succinate-co-butylene malate) P(BS-co-BM), has been preliminarily prepared with optically active centers and lateral hydroxyl functional groups via a four-step synthetic strategy. First, an optically active benzyl-protected dimethyl malate was synthesized from a starting material of (S)-dimethyl malate and purified with good yield. Then, copolyester poly(butylene succinate-co-benzyl-protected butylene malate), P(BS-co-BBM), was prepared through a skilled condensation copolymerization of the benzyl-protected dimethyl malate, dimethyl succinate, and 1,4-butanediol in the presence of titanium tetraisopropoxide as the catalyst. Finally, a Pd/C catalyzed hydrogenation was applied to eliminate the benzyl protection group in a mixed solution of THF and methanol; thus the target copolyester P(BS-co-BM) was attained. On the other hand, physical properties of the synthesized copolyesters were systematically characterized by means of nuclear magnetic resonance spectrometer, Fourier transformed infrared spectrometer, gel permeation chromatography, optical polarimeter, quantitative hydroxyl titration, and thermal analytical instruments. The experimental evidence demonstrated a successful construction of the product P(BS-co-BM) bearing lateral hydroxyl functional groups. It was also revealed that the lower BBM unit content was in the benzyl-protected optically active P(BS-co-BBM) copolyester, the higher melting point T(m), crystallinity, the broader molecular distribution, and the lower glass transition temperature T(g) would be detected, and these results can be accounted for the presence of bulky lateral benzyl moieties. In contrast, the deprotected product P(BS-co-55 mol % BM) showed a higher T(m), crystallinity and lower T(g) than its counterpart P(BS-co-55 mol % BBM). Interestingly, a thermal stability as high as that of the linear PBS was observed for P(BS-co-55 mol % BM) while a strong BBM unit content dependence of thermal stability was detected for the benzyl-protected copolyester P(BS-co-BBM)s. Therefore, these results may be beneficial for the new optically active P(BS-co-BM) bearing hydrophilic hydroxyl functional groups as a potential biomaterial.
一种新型可生物降解共聚酯,聚(丁二酸丁二醇酯 - 共 - 苹果酸丁二醇酯)P(BS - co - BM),已通过四步合成策略初步制备而成,其具有光学活性中心和侧链羟基官能团。首先,由(S)-苹果酸二甲酯起始原料合成了具有光学活性的苄基保护的苹果酸二甲酯,并以良好产率进行了纯化。然后,在四异丙醇钛作为催化剂存在的情况下,通过苄基保护的苹果酸二甲酯、丁二酸二甲酯和1,4 - 丁二醇的熟练缩聚反应制备了共聚酯聚(丁二酸丁二醇酯 - 共 - 苄基保护的苹果酸丁二醇酯),P(BS - co - BBM)。最后,在四氢呋喃和甲醇的混合溶液中应用钯/碳催化氢化以消除苄基保护基团;从而得到目标共聚酯P(BS - co - BM)。另一方面,通过核磁共振光谱仪、傅里叶变换红外光谱仪、凝胶渗透色谱仪、旋光仪、定量羟基滴定和热分析仪器系统地表征了合成共聚酯的物理性质。实验证据表明成功构建了带有侧链羟基官能团的产物P(BS - co - BM)。还发现苄基保护的光学活性P(BS - co - BBM)共聚酯中BBM单元含量越低,熔点T(m)、结晶度越高,分子分布越宽,玻璃化转变温度T(g)越低,这些结果可归因于庞大的侧链苄基部分的存在。相比之下,脱保护产物P(BS - co - 55 mol % BM)比其对应物P(BS - co - 55 mol % BBM)表现出更高的T(m)、结晶度和更低的T(g)。有趣的是,对于P(BS - co - 55 mol % BM)观察到了与线性PBS一样高的热稳定性,而对于苄基保护的共聚酯P(BS - co - BBM)s检测到热稳定性强烈依赖于BBM单元含量。因此,这些结果对于新型带有亲水性羟基官能团的光学活性P(BS - co - BM)作为潜在生物材料可能是有益的。