School of Chemistry and Biochemistry, Georgia Institute of Technology, 901 Atlantic Drive NW, Atlanta, Georgia 30332, United States.
J Am Chem Soc. 2020 Jul 29;142(30):12942-12947. doi: 10.1021/jacs.0c06045. Epub 2020 Jul 20.
Ruthenium alkoxymethylidene complexes have rarely been demonstrated as active species in metathesis reactions and are frequently regarded as inert. Herein, we highlight the ability of these Fischer-type carbenes to participate in cascade alternating ring-opening metathesis polymerization through their efficient alkyne addition reactions. When enyne monomers are combined with low-strain cyclic vinyl ethers, a controlled chain-growth copolymerization occurs that exhibits high degrees of alternation (>90% alternating diads) and produces degradable poly(vinyl ether) materials with low dispersities and targetable molecular weights. This new method is amenable to the synthesis of alternating diblock polymers that can be degraded to small-molecule fragments under aqueous acidic conditions. This work furthers the potential of Fischer-type ruthenium alkylidenes in polymerization strategies and presents new avenues for the generation of functional metathesis materials.
钌烷氧基甲叉络合物很少被证明是复分解反应中的活性物种,通常被认为是惰性的。在此,我们强调了这些费歇尔型卡宾通过其有效的炔烃加成反应参与级联开环复分解聚合的能力。当烯炔单体与低应变环状乙烯基醚结合时,会发生可控的链增长共聚反应,具有高的交替度(>90%交替二联体),并产生可降解的聚(乙烯基醚)材料,具有低分散度和目标分子量。这种新方法适用于合成可在水性酸性条件下降解为小分子片段的交替嵌段聚合物。这项工作进一步推动了费歇尔型钌亚烷基在聚合策略中的潜力,并为功能性复分解材料的生成开辟了新途径。