异戊二烯、丁二烯和CO2共端粒生成内酯的合成和开环(共)聚合。

IF 3.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
Ryan J Anderson, Takuya Akiyama, Ian A Tonks
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引用次数: 0

摘要

本文报道了异戊二烯、丁二烯和CO2衍生的开环聚合和共聚取代δ-内酯。虽然二氧化碳与丁二烯的端粒化形成二取代的δ-内酯已经被证实,但异戊二烯与二氧化碳的类似端粒化或异戊二烯和丁二烯与二氧化碳的共端粒化的研究却很少。我们最初的努力集中在确定影响异戊二烯、丁二烯和CO2共端粒化产率和选择性的因素。最有效的共端粒/加氢反应顺序被放大,得到两个异戊二烯-丁二烯偶联内酯,3-乙基-6-(丙-1-烯-2-基)四氢- 2h -吡喃-2- 1 (EtPeP)和3-乙基-6-甲基-6-乙烯基四氢- 2h -吡喃-2- 1 (EtVMeP)和丁二烯均偶联内酯,3-乙基-6-乙烯基四氢- 2h -吡喃-2- 1 (EtVP)的混合物。这三种内酯的比例取决于端粒化条件和所采用的纯化方法。通过交替路线,逐步合成了纯EtVMeP和etpepp。用三氮杂环癸烯(TBD)对纯内酯和内酯混合物进行有机催化开环聚合(ROP),得到了摩尔质量(Mn)在5.5 ~ 12.7 kDa之间,分散度(Đ = 1.3)较窄的co2基共聚物。增加EtPeP相对于EtVP的比例,共聚物的玻璃化转变温度(Tg)显著升高,达到-20.5℃。虽然EtPeP进行了成功的开环聚合,但与EtVMeP的反应导致聚合终止,因为形成了非亲核叔烷醇链端。因此,少量的EtVMeP可以对共端粒化产生的内酯混合物的共聚产生有害影响。这些研究结果激发了通过丁二烯和异戊二烯与CO2共端粒化选择性合成etpep5的进一步发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and ring-opening (co)polymerization of lactones derived from the cotelomerization of isoprene, butadiene, and CO2.

Herein, we report ring-opening polymerizations and copolymerizations of substituted δ-lactones derived from isoprene, butadiene, and CO2. While the telomerization of CO2 with butadiene to form a disubstituted δ-lactone is well-established, the similar telomerization of isoprene with CO2-or cotelomerization of isoprene and butadiene with CO2-has been less studied. Our initial efforts focused on identifying the factors that govern yield and selectivity in the cotelomerization of isoprene, butadiene, and CO2. The most effective cotelomerization/hydrogenation reaction sequence was scaled-up, leading to mixtures of two isoprene-butadiene coupled lactones, 3-ethyl-6-(prop-1-en-2-yl)tetrahydro-2H-pyran-2-one (EtPeP), and 3-ethyl-6-methyl-6-vinyltetrahydro-2H-pyran-2-one (EtVMeP) and the butadiene homocoupled lactone, 3-ethyl-6-vinyltetrahydro-2H-pyran-2-one (EtVP). The ratios of these three lactones varied depending on the telomerization conditions and purification methods employed. Stepwise syntheses of pure EtVMeP and EtPePvia alternate routes were also carried out. The pure lactones as well as lactone mixtures were subjected to organocatalyzed ring-opening (co)polymerization (ROP) using triazabicyclodecene (TBD), yielding CO2-based copolymers with molar masses (Mn) ranging from 5.5 to 12.7 kDa and narrow dispersities (Đ = 1.3). Increasing the proportion of EtPeP relative to EtVP led to a notable increase in the glass transition temperature (Tg) of the copolymers, reaching -20.5 °C. While EtPeP underwent successful ring-opening polymerization, reactions with EtVMeP resulted in termination of the polymerization owing to the formation of a non-nucleophilic tertiary alkoxide chain end. Thus, small amounts of EtVMeP can have a deleterious effect on copolymerizations of lactone mixtures derived from cotelomerization. These results motivate further development in the selective synthesis of EtPePvia cotelomerization of butadiene and isoprene with CO2.

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来源期刊
Faraday Discussions
Faraday Discussions 化学-物理化学
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期刊介绍: Discussion summary and research papers from discussion meetings that focus on rapidly developing areas of physical chemistry and its interfaces
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