Institute of Organic Chemistry, Johannes Gutenberg-University Mainz, Duesbergweg 10-14, D-55099 Mainz, Germany.
Acc Chem Res. 2010 Jan 19;43(1):129-41. doi: 10.1021/ar900158p.
Dendritic macromolecules with random branch-on-branch topology, termed hyperbranched polymers in the late 1980s, have a decided advantage over symmetrical dendrimers by virtue of typically being accessible in a one-step synthesis. Saving this synthetic effort once had an unfortunate consequence, though: hyperbranching polymerization used to result in a broad distribution of molecular weights (that is, very high polydispersities, often M(w)/M(n) > 5). By contrast, a typical dendrimer synthesis yields a single molecule (in other words, M(w)/M(n) = 1.0), albeit by a labor-intensive, multistep process. But 10 years ago, Sunder and colleagues reported the controlled synthesis of well-defined hyperbranched polyglycerol (PG) via ring-opening multibranching polymerization (ROMBP) of glycidol. Since then, hyperbranched and polyfunctional polyethers with controlled molar mass and low polydispersities (M(w)/M(n) = 1.2-1.9) have been prepared, through various monomer addition protocols, by ROMBP. In this Account, we review the progress in the preparation and application of these uniquely versatile polyether polyols over the past decade. Hyperbranched PGs combine several remarkable features, including a highly flexible aliphatic polyether backbone, multiple hydrophilic groups, and excellent biocompatibility. Within the past decade, intense efforts have been directed at the optimization of synthetic procedures affording PG homo- and copolymers with different molecular weight characteristics and topology. Fundamental parameters of hyperbranched polymers include molar mass, polydispersity, degree of branching, and end-group functionality. Selected approaches for optimizing and tailoring these characteristics are presented and classified with respect to their application potential. Specific functionalization in the core and at the periphery of hyperbranched PG has been pursued to meet the growing demand for novel specialty materials in academia and industry. A variety of fascinating synthetic approaches now provide access to well-defined, complex macromolecular architectures based on polyether polyols with low polydispersity. For instance, a variety of linear-hyperbranched block copolymers has been reported. The inherent attributes of PG-based materials are useful for a number of individual implementation concepts, such as drug encapsulation or surface modification. The excellent biocompatibility of PG has also led to rapidly growing significance in biomedical applications, for example, bioconjugation with peptides, as well as surface attachment for the creation of protein-resistant surfaces.
具有随机支化拓扑结构的树枝状大分子,在 20 世纪 80 年代后期被称为超支化聚合物,由于通常可以通过一步合成得到,因此比对称的树枝状大分子具有明显的优势。不过,节省这一合成步骤曾经带来了不幸的后果:超支化聚合通常会导致分子量分布很宽(也就是说,多分散性非常高,通常 M(w)/M(n) > 5)。相比之下,典型的树枝状大分子合成只能得到单一分子(换句话说,M(w)/M(n) = 1.0),尽管这是一个劳动强度大、多步的过程。但在 10 年前,Sunder 和同事们通过环氧丙烷的开环多支化聚合(ROMBP)报道了具有可控结构的高分子量聚甘油(PG)的可控合成。从那时起,通过各种单体添加方案,通过 ROMBP 制备了具有可控摩尔质量和低多分散性(M(w)/M(n) = 1.2-1.9)的超支化和多功能聚醚。在本综述中,我们回顾了过去十年中这些独特的多功能聚醚多元醇在制备和应用方面的进展。超支化 PG 具有几个显著的特点,包括高度灵活的脂肪族聚醚主链、多个亲水基团和优异的生物相容性。在过去的十年中,人们一直在努力优化合成程序,以获得具有不同分子量特征和拓扑结构的 PG 均聚物和共聚物。超支化聚合物的基本参数包括摩尔质量、多分散性、支化度和端基官能团。介绍了优化和定制这些特性的一些方法,并根据它们的应用潜力进行了分类。在超支化 PG 的核心和外围进行了特定的功能化,以满足学术界和工业界对新型特种材料的日益增长的需求。现在有多种引人入胜的合成方法可以获得基于低多分散性聚醚多元醇的具有良好定义的复杂大分子结构。例如,已经报道了多种线性-超支化嵌段共聚物。PG 基材料的固有属性可用于许多单独的实施概念,例如药物包封或表面改性。PG 的出色生物相容性也使其在生物医学应用中迅速得到重视,例如与肽的生物偶联,以及用于创建抗蛋白表面的表面附着。