首页> 外文期刊>Macromolecules >Formation of and Coalescence from the Inclusion Complex of a Biodegradable Block Copolymer and #alpha#-Cyclodiextrin: A Novel Means To Modify the Phase Structure of Biodegradable Block Copolymers
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Formation of and Coalescence from the Inclusion Complex of a Biodegradable Block Copolymer and #alpha#-Cyclodiextrin: A Novel Means To Modify the Phase Structure of Biodegradable Block Copolymers

机译:从可生物降解的嵌段共聚物和#alpha#-环糊精的包合物的形成和合并:修改可生物降解的嵌段共聚物的相结构的新手段

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摘要

A well-defined biodegradable block copolymer (PCL-b-PLLA, M_n = 1.72 x 10~4, M_w/M_n = 1.37) of poly(#epsilon#-caprolactone) (PCL) and poly(L-lactide) (PLLA) was synthesized by a two-step ring-opening polymerization of #epsilon#-caprolactone and L-lactide. Furthermore, we found that #alpha#-cyclodextrin (#alpha#-CD) molecules may simultaneously thread onto both PLLA and PCL blocks of PCL-b-PLLA to form an inclusion complex (IC). Washing the copolymer-#alpha#-CD with hot water removed the #alpha#-CD, and the copolymer chains were coalesced. Very interestingly, the coalesced copolymer sample shows a great suppression in microphase separation, compared with the as-synthesized copolymer. In contrast to the significant decrease in crystallinity of ca. 50% and up to 79% for PCL and PLLA blocks, respectively, the melting points (T_m's) and the cold crystallization temperautres (T_(cc)'s) of both PCL and PLLA blocks of the coalesced sample increased in DSC measurements. These results may imply that only small amounts of more extended crystals, with less chain folding, were produced during the process of copolymer coalescence. Fourier transform infrared (FTIR) spectra, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and wide-angle X-ray diffraction (WAXD) measurements were employed to demonstrate formation of the block copolymer-#alpha#-CD IC as well as to gauge the suppression of the microphase separation in the coalesced sample.
机译:聚(ε-己内酯)(PCL)和聚(L-丙交酯)(PLLA)的定义明确的可生物降解的嵌段共聚物(PCL-b-PLLA,M_n = 1.72 x 10〜4,M_w / M_n = 1.37)通过ε-己内酯和L-丙交酯的两步开环聚合反应合成α-己内酰胺。此外,我们发现#alpha#-环糊精(#alpha#-CD)分子可以同时穿线到PCL-b-PLLA的PLLA和PCL嵌段上,形成包合物(IC)。用热水洗涤共聚物-α-CD,除去α-CD,并将共聚物链聚结。非常有趣的是,与合成后的共聚物相比,聚结的共聚物样品在微相分离方面表现出极大的抑制作用。与此相反,钙的结晶度显着降低。对于PCL和PLLA嵌段,分别达到50%和高达79%,在DSC测量中,聚结样品的PCL和PLLA嵌段的熔点(T_m's)和冷结晶温度(T_(cc)')均增加。这些结果可能暗示在共聚物聚结过程中仅产生少量具有较少链折叠的更多延伸的晶体。使用傅立叶变换红外(FTIR)光谱,差示扫描量热法(DSC),热重分析(TGA)和广角X射线衍射(WAXD)测量来证明嵌段共聚物-#alpha#-CD IC的形成以及衡量对聚结样品中微相分离的抑制作用。

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