首页> 外文会议>IUPAC International conference on novel materials and their synthesis >SYNTHESIS OF POLYCARBONATES BY COPOLYMERIZATION OF CARBON DIOXIDE AND CYCLOHEXENE OXIDE USING SCHIFF BASE COMPLEX AS CATALYST
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SYNTHESIS OF POLYCARBONATES BY COPOLYMERIZATION OF CARBON DIOXIDE AND CYCLOHEXENE OXIDE USING SCHIFF BASE COMPLEX AS CATALYST

机译:使用Schiff碱基复合物作为催化剂共聚合成二氧化碳和环己烯的共聚

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Chemical fixation of CO_2 is a very attractive subject not only from the viewpoint of carbon resource utilization, but also from increasing environmental concerns. One of the most promising green reactions in this area is the alternating copolymerization of CO_2 with epoxides to generate biodegradable polycarbonates, which was first reported by Inoue using ZnEt_2/H_2O catalyst in 1969. Since then, there have been many catalysts so far developed for the alternating copolymerization. Among all the catalysts reported, the Schiff base complexes catalysts are known to produce high molecular weight polycarbonate at mild conditions. Herein, we report the synthesis of a novel Schiff base Zn complex and its catalytic behavior for the coupling reactions of carbon dioxide and cyclohexene oxide. The ligand was prepared by the reaction of 2-thiophenecarboxaldehy and o-phenylenediamine, and the catalyst was synthesized by the coordination of the ligand and ZnEt_2. The catalytic behavior of the catalyst for the copolymerization of CO_2 with epoxides was investigated. TON of 421.1 and 1.85 ×10~4g·mol~(-1) for the copolymer were achieved. This work was supported by Foundation of He'nan Educational Committee (14A150016); This work was also supported by Doctoral Fund of Henan Polytechnic University (B2012-052).
机译:Co_2的化学固定是一种非常有吸引力的对象,不仅是碳资源利用的观点,而且来自越来越多的环境问题。该领域中最有前景的绿色反应之一是Co_2与环氧化物的交替共聚,以产生可生物降解的聚碳酸酯,其首先在1969年使用Znet_2 / H_2O催化剂首先报道。从那时起,迄今为止已经为此开发了许多催化剂交替的共聚。在报道的所有催化剂中,已知席夫碱基复合物催化剂在温和条件下生产高分子量聚碳酸酯。在此,我们报告了一种新型席夫碱Zn络合物的合成及其催化行为,用于二氧化碳和环己烯的偶联反应。通过2-噻吩甲基甲醛和O-苯二胺的反应制备配体,通过配体和Znet_2的配位合成催化剂。研究了用环氧化物的CO_2共聚催化剂的催化作用。实现共聚物的421.1和1.85×10〜4g·mol〜(-1)。这项工作得到了何安安教育委员会(14A150016)的基础支持;该工作也得到河南理工大学博士基金(B2012-052)的支持。

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