{"title":"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。","authors":"Ryan J Anderson, Takuya Akiyama, Ian A Tonks","doi":"10.1039/d5fd00034c","DOIUrl":null,"url":null,"abstract":"<p><p>Herein, we report ring-opening polymerizations and copolymerizations of substituted δ-lactones derived from isoprene, butadiene, and CO<sub>2</sub>. While the telomerization of CO<sub>2</sub> with butadiene to form a disubstituted δ-lactone is well-established, the similar telomerization of isoprene with CO<sub>2</sub>-or cotelomerization of isoprene and butadiene with CO<sub>2</sub>-has been less studied. Our initial efforts focused on identifying the factors that govern yield and selectivity in the cotelomerization of isoprene, butadiene, and CO<sub>2</sub>. 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-2<i>H</i>-pyran-2-one (EtPeP), and 3-ethyl-6-methyl-6-vinyltetrahydro-2<i>H</i>-pyran-2-one (EtVMeP) and the butadiene homocoupled lactone, 3-ethyl-6-vinyltetrahydro-2<i>H</i>-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 EtPeP<i>via</i> 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 CO<sub>2</sub>-based copolymers with molar masses (<i>M</i><sub>n</sub>) ranging from 5.5 to 12.7 kDa and narrow dispersities (<i>Đ</i> = 1.3). Increasing the proportion of EtPeP relative to EtVP led to a notable increase in the glass transition temperature (<i>T</i><sub>g</sub>) 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 EtPeP<i>via</i> cotelomerization of butadiene and isoprene with CO<sub>2</sub>.</p>","PeriodicalId":76,"journal":{"name":"Faraday Discussions","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and ring-opening (co)polymerization of lactones derived from the cotelomerization of isoprene, butadiene, and CO<sub>2</sub>.\",\"authors\":\"Ryan J Anderson, Takuya Akiyama, Ian A Tonks\",\"doi\":\"10.1039/d5fd00034c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Herein, we report ring-opening polymerizations and copolymerizations of substituted δ-lactones derived from isoprene, butadiene, and CO<sub>2</sub>. While the telomerization of CO<sub>2</sub> with butadiene to form a disubstituted δ-lactone is well-established, the similar telomerization of isoprene with CO<sub>2</sub>-or cotelomerization of isoprene and butadiene with CO<sub>2</sub>-has been less studied. Our initial efforts focused on identifying the factors that govern yield and selectivity in the cotelomerization of isoprene, butadiene, and CO<sub>2</sub>. 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-2<i>H</i>-pyran-2-one (EtPeP), and 3-ethyl-6-methyl-6-vinyltetrahydro-2<i>H</i>-pyran-2-one (EtVMeP) and the butadiene homocoupled lactone, 3-ethyl-6-vinyltetrahydro-2<i>H</i>-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 EtPeP<i>via</i> 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 CO<sub>2</sub>-based copolymers with molar masses (<i>M</i><sub>n</sub>) ranging from 5.5 to 12.7 kDa and narrow dispersities (<i>Đ</i> = 1.3). Increasing the proportion of EtPeP relative to EtVP led to a notable increase in the glass transition temperature (<i>T</i><sub>g</sub>) 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 EtPeP<i>via</i> cotelomerization of butadiene and isoprene with CO<sub>2</sub>.</p>\",\"PeriodicalId\":76,\"journal\":{\"name\":\"Faraday Discussions\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Faraday Discussions\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5fd00034c\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Faraday Discussions","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5fd00034c","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
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.