Single-phase block copolymers by cross-metathesis of 1,4-cis-polybutadiene and 1,4-cis-polyisoprene
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Single-phase block copolymers by cross-metathesis of 1,4-cis-polybutadiene and 1,4-cis-polyisoprene

机译:通过1,4-CIS-聚丁二烯和1,4-顺式 - 聚异戊二烯的交叉复分解的单相块共聚物

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AbstractMacromolecular Cross-Metathesis (MCM) reactions on commercial Polybutadiene (PBD) and Polyisoprene (PIP) homopolymers, in the presence of first generation Grubbs and Hoveyda-Grubbs catalysts, are reported.13C-NMR resonances of butadiene(B)/isoprene(I) heterosequences show block-copolymer formation, with blocks longer than a hundred monomer units, even for long reaction times. DSC scans of MCM products show that, with MCM time, PBD crystallinity progressively disappears while the well separated Tgof the two homopolymers merge to an intermediate single Tg. This indicates that PBD and PIP blocks are completely miscible when their lengths are reduced to a few hundred units.13C NMR spectra also show that, for the considered MCM process, double bond isomerizations are definitely more frequent than heterosequence formations.Graphical abstractDisplay OmittedHighlights<
机译:<![CDATA [ 抽象 大分子交叉复分解(MCM)在商业聚丁二烯(PBD)和聚异戊二烯(PIP)均聚物上的反应报道了第一代GRUBBS和HOVEYDA-GRUBBS催化剂。 13> 13 C-NMR共振的丁二烯(B)/异戊二烯(I)异质序列显示嵌段共聚物形成,块长于一百单体单元,即使是长反应时间。 MCM产品的DSC扫描表明,通过MCM时间,PBD结晶度逐渐消失,而两个均聚物的良好分离的T G 合并到中间单个T G 。这表明当它们的长度减少到几百个单元时,PBD和PIP块是完全混溶的。 13 c nmr spectra也表明,对于考虑的MCM过程,双键异构化肯定比异性静脉曲张形成更频繁。 图形摘要 显示省略 突出显示 <

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