节点文献

SalenAl(OPr)催化CO2和氧化环己烯共聚反应

SALENAl(OPr) CATALYST FOR THE COPOLYMERIZATION OF CO2 AND CYCLOHEXENE OXIDE

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 崔奇张敏徐守萍刘保华陈立班

【Author】 CUI Qi 1,2, ZHANG Min1, XU Shouping 1,2, LIU Baohua1, CHEN Liban1( 1 Guangzhou Institute of Chemistry ,Chinese Academy of Science, Guangzhou 510650 )( 2 Graduate School of the Chinese Academy of Science, Beijing 100039 )

【机构】 中国科学院广州化学研究所中国科学院广州化学研究所 广州510650中国科学院研究生院北京100039广州510650广州510650中国科学院研究生院北京100039

【Abstract】 SalenMX has drawn much attention recently,because it is nonsensitive to moisture and effective for copolymerization of CO2 and epoxides.However,usually expensive organic metal compounds were used.A low cost procedure of SalenMX preparation is described that SalenAl(OPr) can be obtained by using aluminium iso-propoxide reacted with SalenH2 in tetrahydrofuran at room temperature overnight.The catalyst precursor Schiff-base SalenH2 (N,N′-Bis(salicylidene)-1,2-phenylenediamine) was synthesized by refluxing 2 equiv salicylaldehyde and 1 equiv of 1,2-phenylendiamine in methnol for a period of time.SalenH2 and SalenAl(OPr) were characterized by FT-IR,mass Spectroscopy,UV-Vis and 1H-NMR.The copolymerization of carbon dioxide and cyclohexene oxide(CHO) was carried out at 80℃ for a certain period time using 50 mg SalenAl(OPr) as catalyst.SalenAl(OPr) had been shown to be an effective catalyst for the copolymerization of CO2 and CHO along with a small quantity of byproduct cyclic carbonate.The addition of various cocatalysts,including DMAP,N-MeIm,DBU and Bu4NCl or Bu4NBr salts can greatly enhance the rate of copolymerization.The copolymers were produced with >95% carbonate linkages and <5% cyclic carbonates.The highest catalytic efficiency is 190 g copolymer per g catalyst.

【关键词】 CO2氧化环己烯共聚SalenAl(OPr)催化剂
【Key words】 CO2Cyclohexen oxideCopolymerizaitonSalenAl(OPr)Catalyst
【基金】 国家自然科学基金(基金号20274053);江苏省科技攻关项目(项目号BE2003080,BE2003112);广东省工业攻关项目(项目号2003B10505)资助项目
  • 【文献出处】 高分子学报 ,Acta Polymerica Sinica , 编辑部邮箱 ,2006年03期
  • 【分类号】O643.3;O631.3
  • 【被引频次】13
  • 【下载频次】175
节点文献中: 

本文链接的文献网络图示:

本文的引文网络