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Synthesis of Telechelic Polyisoprene via Ring-Opening Metathesis Polymerization in the Presence of Chain Transfer Agent

机译:存在链转移剂的开环复分解聚合法合成远螯聚异戊二烯

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摘要

Telechelic polyisoprene was synthesized via the ring-opening metathesis polymerization (ROMP) of 1,5-dimethyl-1,5-cyclooctadiene (DMCOD) in the presence of cis-1,4-diacetoxy-2-butene as a chain transfer agent (CTA). This method afforded telechelic polymer in excellent yield, and the acetoxy groups were successfully removed to yield α,ω-hydroxy end-functionalized polyisoprene with potential for subsequent reactions. Efficient, quantitative incorporation of CTA was achieved, and NMR spectroscopy was utilized to confirm the chemical identity of the polymer end groups. Polymerization of discrete DMCOD monomer generated polyisoprene with excellent regioregularity in the polymer backbone. Successful ROMP of sterically challenging DMCOD in the presence of a CTA for chain end-functionalization was borne out through screening of a variety of Ru-based olefin metathesis catalysts.
机译:远螯聚异戊二烯是在顺式1,4-二乙酰氧基-2-丁烯作为链转移剂的存在下,通过1,5-二甲基-1,5-环辛二烯(DMCOD)的开环复分解聚合(ROMP)合成的(号召性文字)。该方法以优异的收率提供了遥螯聚合物,并且成功地除去了乙酰氧基,以产生具有后续反应潜力的α,ω-羟基末端官能化的聚异戊二烯。实现了CTA的高效定量掺入,并利用NMR光谱法确认了聚合物端基的化学特性。离散DMCOD单体的聚合反应生成的聚异戊二烯在聚合物主链中具有极好的区域规则性。通过筛选各种Ru基烯烃复分解催化剂,可以证明在具有CTA的CTA存在下,具有空间挑战性的DMCOD的成功ROMP。

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  • 年度 2010
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  • 正文语种 {"code":"en","name":"English","id":9}
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