Kellner-Rogers Julian S, Hsu Jesse H, Keresztes Ivan, Fors Brett P, Lambert Tristan H
Department of Chemistry and Chemical Biology, Cornell University, 122 Baker Laboratory, Ithaca, New York 14853, USA.
Angew Chem Int Ed Engl. 2024 Dec 20;63(52):e202413093. doi: 10.1002/anie.202413093. Epub 2024 Oct 22.
Materials formed by the ring-opening metathesis polymerization (ROMP) of cyclic olefins are highly valued for industrial and academic applications but are difficult to prepare free of metal contaminants. Here we describe a highly efficient metal-free ROMP of cyclobutenes using hydrazine catalysis. Reactions can be initiated via in situ condensation of a [2.2.2]-bicyclic hydrazine catalyst with an aliphatic or aromatic aldehyde initiator. The polymerizations show living characteristics, achieving excellent control over molecular weight, low dispersity values, and high chain-end fidelity. Additionally, the hydrazine can be used in substoichiometric amounts relative to the aldehyde chain-end while maintaining good control over molecular weight and low dispersity values, indicating that a highly efficient chain transfer mechanism is occurring.
由环烯烃的开环易位聚合(ROMP)形成的材料在工业和学术应用中具有很高的价值,但难以制备不含金属污染物的材料。在此,我们描述了一种使用肼催化的环丁烯高效无金属ROMP。反应可通过[2.2.2] - 双环肼催化剂与脂肪族或芳香族醛引发剂的原位缩合引发。聚合反应具有活性特征,能够出色地控制分子量、实现低分散度值以及高链端保真度。此外,相对于醛链端,肼可以以亚化学计量的量使用,同时保持对分子量的良好控制和低分散度值,这表明发生了高效的链转移机制。