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环氧丙烷与生物可再生萜烯基环酐的交替共聚:一种可持续合成具有高玻璃化转变温度的脂肪族聚酯的方法。

Alternating copolymerization of propylene oxide with biorenewable terpene-based cyclic anhydrides: a sustainable route to aliphatic polyesters with high glass transition temperatures.

机构信息

Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, NY 14853-1301 (USA).

出版信息

Angew Chem Int Ed Engl. 2015 Feb 23;54(9):2665-8. doi: 10.1002/anie.201410641. Epub 2015 Jan 21.

Abstract

The alternating copolymerization of propylene oxide with terpene-based cyclic anhydrides catalyzed by chromium, cobalt, and aluminum salen complexes is reported. The use of the Diels-Alder adduct of α-terpinene and maleic anhydride as the cyclic anhydride comonomer results in amorphous polyesters that exhibit glass transition temperatures (Tg ) of up to 109 °C. The polymerization conditions and choice of catalyst have a dramatic impact on the molecular weight distribution, the relative stereochemistry of the diester units along the polymer chain, and ultimately the Tg of the resulting polymer. The aluminum salen complex exhibits exceptional selectivity for copolymerization without transesterification or epimerization side reactions. The resulting polyesters are highly alternating and have high molecular weights and narrow polydispersities.

摘要

报道了由铬、钴和铝席夫碱配合物催化的环氧丙烷与萜烯基环状酸酐的交替共聚。使用α-松油烯和马来酸酐的 Diels-Alder 加合物作为环状酸酐共聚单体,得到无定形聚酯,其玻璃化转变温度(Tg)高达 109°C。聚合条件和催化剂的选择对分子量分布、聚合物链上二酯单元的相对立体化学以及最终聚合物的 Tg 有显著影响。铝席夫碱配合物表现出对共聚反应的优异选择性,没有酯交换或差向异构化副反应。所得聚酯具有高度交替性、高分子量和较窄的多分散性。

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