Hilf Stefan, Grubbs Robert H, Kilbinger Andreas F M
Institut für Organische Chemie, Johannes Gutenberg-Universität Mainz, Duesbergweg 10-14, D-55099 Mainz, Germany.
J Am Chem Soc. 2008 Aug 20;130(33):11040-8. doi: 10.1021/ja8022863. Epub 2008 Jul 23.
The selective placement of a functional group at the chain end of a ring-opening metathesis polymer using ruthenium carbene initiators has been a significant limitation. Here we demonstrate a highly effective and facile end-capping technique for ROMP with living ruthenium carbene chain ends using single-turnover olefin metathesis substrates. Vinylene carbonate and 3H-furanone are introduced as functionalization and termination agents for the ruthenium-initiated ring-opening metathesis polymerization. This leads directly to the formation of functional polymer end groups without further chemical transformation steps. Aldehyde and carboxylic acid end groups can be introduced by this new method which involves the decomposition of acyl carbenes to ruthenium carbides. The high degrees of chain-end functionality obtained are supported by (1)H NMR spectroscopy, MALDI-ToF mass spectrometry, and end-group derivatization.
使用钌卡宾引发剂将官能团选择性地置于开环易位聚合产物的链端一直是一个重大限制。在此,我们展示了一种高效且简便的封端技术,用于具有活性钌卡宾链端的开环易位聚合反应(ROMP),该技术使用单周转烯烃易位底物。碳酸亚乙烯酯和3H-呋喃酮被引入作为钌引发的开环易位聚合反应的官能化和终止剂。这直接导致形成功能性聚合物端基,无需进一步的化学转化步骤。醛基和羧基端基可通过这种新方法引入,该方法涉及酰基卡宾分解为碳化钌。通过核磁共振氢谱(¹H NMR)、基质辅助激光解吸电离飞行时间质谱(MALDI-ToF)和端基衍生化,证实了所获得的高度链端官能化。