Yasir Mohammad, Kilbinger Andreas F M
Department of Chemistry, University of Fribourg, Chemin du Musée 9, CH-1700 Fribourg, Switzerland.
ACS Macro Lett. 2021 Feb 16;10(2):210-214. doi: 10.1021/acsmacrolett.0c00882. Epub 2021 Jan 13.
Norbornene is polymerized extremely fast when reacted with Grubbs' first () or third generation catalyst () because of its very high ring strain energy. Cyclohexene, on the other hand, cannot be polymerized using or due to its very low ring strain energy. Subsequently, the sequence-selective polymerization of these two monomers is extremely challenging. A sequence-selective cascade ring-opening/ring-closing metathesis polymerization of the monomer containing both the norbornene and the cyclohexene ring using or is reported. The polymer structure was analyzed by H NMR, H-H COSY, and H-H ROESY spectroscopy and MALDI-ToF mass spectrometry. Polymers with moderate molecular weight dispersities and good molecular weight control were achieved by varying the ratio between monomer and .
由于降冰片烯具有非常高的环张力能,当它与第一代()或第三代格拉布催化剂()反应时,会极快地发生聚合反应。另一方面,环己烯由于其极低的环张力能,不能使用或进行聚合反应。因此,这两种单体的序列选择性聚合极具挑战性。据报道,使用或对同时含有降冰片烯环和环己烯环的单体进行了序列选择性级联开环/关环易位聚合反应。通过核磁共振氢谱(H NMR)、氢-氢化学位移相关谱(H-H COSY)、氢-氢旋转核 Overhauser 效应谱(H-H ROESY)光谱以及基质辅助激光解吸电离飞行时间质谱(MALDI-ToF)对聚合物结构进行了分析。通过改变单体与之间的比例,获得了具有适度分子量分散度且分子量控制良好的聚合物。