Winnacker Malte, Neumeier Michael, Zhang Xiaohan, Papadakis Christine M, Rieger Bernhard
WACKER-Lehrstuhl für Makromolekulare Chemie, Technische Universität München, Lichtenbergstraße 4, 85747, Garching bei München.
Department of Physics, Soft Matter Physics Group, Technische Universität München, James-Franck-Str. 1, 85747, Garching bei München.
Macromol Rapid Commun. 2016 May;37(10):851-7. doi: 10.1002/marc.201600056. Epub 2016 Mar 15.
Polyamides are very important polymers that find applications from commodities up to the automotive and biomedical sectors, and their impact is continuously growing. The synthesis of structurally significant, chiral, and sustainable polyamides is described via a new, convenient, and solvent-free anionic polymerization of a biobased ε-lactam, which is obtained from the renewable terpenoid ketone l-menthone in a one-step synthesis. These polyamides are shown to have outstanding structural and thermal properties, which are thus introduced via the structure and chirality of the natural lactam monomer and which are discussed and compared with those of petroleum-based, established, and commercial polyamide Nylon-6. X-ray data reveal a remarkable degree of crystallinity in these green polymers and emphasize the impact of their structural features on the resulting properties.
聚酰胺是非常重要的聚合物,其应用涵盖从日用品到汽车和生物医学领域,并且其影响力在不断扩大。通过一种新型、便捷且无溶剂的生物基ε-内酰胺阴离子聚合反应,描述了具有重要结构、手性和可持续性的聚酰胺的合成方法,该生物基ε-内酰胺是由可再生萜类酮L-薄荷酮通过一步合成法得到的。这些聚酰胺具有出色的结构和热性能,这些性能通过天然内酰胺单体的结构和手性得以体现,并与石油基、已确立的商业聚酰胺尼龙-6进行了讨论和比较。X射线数据揭示了这些绿色聚合物中显著的结晶度,并强调了其结构特征对所得性能的影响。