首页> 外文学位 >Functional polyester materials with tunable degradability: Investigations into the use of reductive amination, ketoxime ether, and hydrazone linkages for functionalization, covalent stabilization and crosslinking of poly(epsilon-caprolactone) materials.
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Functional polyester materials with tunable degradability: Investigations into the use of reductive amination, ketoxime ether, and hydrazone linkages for functionalization, covalent stabilization and crosslinking of poly(epsilon-caprolactone) materials.

机译:具有可调节降解性的功能性聚酯材料:对还原胺化,酮肟醚和键用于功能化,共价稳定和聚(ε-己内酯)材料交联的研究。

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Aliphatic polyesters represent one class of degradable, polymeric materials that is receiving significant attention in the search for, and design of, biocompatible and bioresorbable synthetic substances. Functional and crosslinked polyesters, having potential biomedical value, are the target of many avenues of current research. This dissertation work expands the utility of a specific aliphatic polyester, poly(epsilon-caprolactone-co-2-oxepane-1,5-dione) (P(CL-co-OPD)), which contains backbone ketone units that can be reacted with various functional, nucleophilic agents. Results presented in this dissertation convey both the successes had and the challenges encountered in the employment of different "iminyl" chemistries for the synthesis of functional and crosslinked materials.; Specifically, the ketone-functionalized polyester was investigated as a general substrate designed to undergo solution-state intramolecular crosslinking and functionalization upon reductive amination with 1,6-hexanediamine and hexylamine, respectively, in the presence of NaCNBH3. Through detailed analysis of the products from these reactions, and simpler systems including small molecule model compounds, the polymeric gamma-keto ester functionality was determined to be incompatible with the reductive amination chemistry, resulting in chain cleavage via intramolecular lactam formation. Subsequent investigation of ketoxime ether formation using synthetic model hydroxylamines, 1-aminooxydodecane and 1,6-bis(aminooxy)hexane, in solution and in the presence of an acid catalyst, resulted in the targeted graft and crosslinked particulate/gel materials, respectively.; With the significant interest in the development of synthetic polymer materials of increasing degrees of complexity, attention has been focused on the efficient and high-yielding conversion of polyesters into multi-functional materials. Facile conjugation of aminooxy- and sulfonyl hydrazide model ligands with P(CL-co-OPD) were also explored by both sequential and single-step approaches. The benefits of the characterization of intermediates in a functionalization sequence were then weighed against the corresponding challenges faced by the establishment of equilibria between coupled and uncoupled species in solution. Additionally, in this dissertation, the advantages of a single-step reaction for the construction of multi-functionalization are stressed. Finally, the synthesis and basic characterization of specific functional materials are highlighted with regard to the preparation of novel ligand-bearing graft and particulate nanostructures, decorated with poly(ethylene oxide), chromophores, fluorophores, and radio-labeled molecules, for potential use in diagnostic imaging and drug delivery.
机译:脂肪族聚酯代表一类可降解的聚合材料,在寻找和设计生物相容性和生物可吸收性合成物质中受到了极大的关注。具有潜在生物医学价值的功能性和交联聚酯是当前研究的许多目标。这项研究工作扩展了特定的脂肪族聚酯聚(ε-己内酯-co-2-环氧庚烷-1,5-二酮)(P(CL-co-OPD))的用途,该化合物包含可以反应的骨架酮单元与各种功能性亲核试剂。本文所提出的结果传达了在使用不同的“亚氨基”化学物质合成功能和交联材料方面所取得的成功和所面临的挑战。具体地,研究了酮官能化的聚酯作为一般底物,该底物设计为在NaCNBH3存在下分别用1,6-己二胺和己胺进行还原胺化时进行溶液状态的分子内交联和官能化。通过对这些反应产物的详细分析,以及包括小分子模型化合物在内的更简单的系统,确定了聚合的γ-酮酯官能团与还原胺化化学不相容,从而导致通过分子内酰胺形成的链断裂。随后在溶液中和在酸催化剂的存在下,使用合成模型羟胺,1-氨基氧基十二烷和1,6-双(氨基氧基)己烷对酮肟醚的形成进行了研究,分别得到了目标接枝和交联的颗粒/凝胶材料。 ;随着对复杂程度日益提高的合成聚合物材料的开发的极大兴趣,人们的注意力已集中在将聚酯高效转化为多功能材料上。通过序贯和单步方法,也探索了氨基氧基酰肼模型和磺酰肼模型配体与P(CL-co-OPD)的简便共轭。然后,权衡了在功能化序列中表征中间体的好处与溶液中偶合和非偶合物种之间建立平衡所面临的相应挑战。另外,在本文中,强调了一步反应用于构建多功能化的优点。最后,着重介绍了特殊功能材料的合成和基本表征,涉及制备新型的带有配体的接枝物和颗粒纳米结构,并用聚环氧乙烷,发色团,荧光团和放射性标记的分子修饰,可潜在地用于诊断成像和药物输送。

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