作者: Malte S. Mikus , Sebastian Torker , Amir H. Hoveyda
关键词: Ruthenium 、 Polymer chemistry 、 Ring-opening metathesis polymerisation 、 Isomerization 、 Monomer 、 Tacticity 、 Polymerization 、 Metathesis 、 Chemistry 、 ROMP
摘要: Readily accessible and easy-to-handle Ru complexes capable of generating all-Z polynorbornene polynorbornadiene by ring-opening metathesis polymerization (ROMP) with controllable selectivity, ranging from ≈50 to ≥95 % syndiotactic, are introduced. It is demonstrated that the rate non-metathesis based polytopal isomerization levels syndiotacticity may be fine-tuned adjustment monomer concentration catalyst's steric electronic characteristics.