Chemical preparation and characterization of new biodegradable aliphatic polyesters end‐capped with diverse steroidal moieties

聚酯纤维 化学 热重分析 高分子化学 凝胶渗透色谱法 烷氧基 聚己内酯 聚合 热稳定性 聚合物 可生物降解聚合物 开环聚合 有机化学 烷基
作者
Jing Yang,Qiaobo Li,Li Yang,Lin Jia,Qiang Fang,Amin Cao
出处
期刊:Journal of Polymer Science Part A [Wiley]
卷期号:44 (6): 2045-2058 被引量:21
标识
DOI:10.1002/pola.21317
摘要

Abstract Novel metal complexes with a single catalytic site and less transesterification seem to provide alternative efficient synthetic approaches to preparing new biodegradable and biologically responsive materials with well‐defined structures. In this study, we rationally designed a new category of aluminum metal complexes bearing a bulky Salen ligand and diverse steroidal alkoxy moieties to synthesize novel biodegradable aliphatic polyesters end‐capped with steroidal building blocks. At first, three new aluminum metal complexes ( 9 – 11 ) were synthesized with good yields of 80–90%, bearing cholesterol and diosgenin derivatives as functional alkoxy moieties. By means of nuclear magnetic resonance (NMR) spectrometry, matrix‐assisted laser desorption/ionization Fourier transform mass spectrometry (MALDI–FTMS), and Fourier transform infrared spectrometry, the molecular structures of 9 – 11 were characterized. Furthermore, new biodegradable aliphatic polyesters, poly(ε‐caprolactone) and poly(δ‐valerolactone) end‐capped with diverse steroidal moieties, were synthesized through the ring‐opening polymerization of ε‐caprolactone and δ‐valerolactone catalyzed by these new metal complexes under 100 °C in toluene, and they were also characterized by gel permeation chromatography, NMR, MALDI–FTMS, differential scanning calorimetry, and thermogravimetric analysis. Very narrow molecular weight distributions were revealed for these new polymer products, and their thermal crystallization and stability strongly depended on the degree of polymerization of the polyester building blocks and the distinct steroidal moieties. Because of the nature of the steroidal moieties, these biodegradable polymers may pave a path to new possibilities as potential biomaterials. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2045–2058, 2006
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