...
首页> 外文期刊>Inorganica Chimica Acta >Copper and copper-manganese 1D coordination polymers: Synthesis optimization, crystal structure and preliminary studies as catalysts for Baylis-Hillman reactions
【24h】

Copper and copper-manganese 1D coordination polymers: Synthesis optimization, crystal structure and preliminary studies as catalysts for Baylis-Hillman reactions

机译:铜和铜锰1D配位聚合物:合成优化,晶体结构和初步研究作为Baylis-Hillman反应的催化剂

获取原文
获取原文并翻译 | 示例
           

摘要

This work reports the influence of experimental parameters (pH and counter-ion) in the synthesis of the 1D coordination polymer [Cu(IDA)(H2O)(2)](n). (IDA = iminodiacetate), named here Cu-IDA. Copper-manganese bimetallic coordination polymers were also obtained by isomorphic replacement into Cu-IDA structure, with different molar ratio of Cu2+ and Mn2+ ions, denoted here as Cu/Mn-IDA (0.9/0.1; 0.7/0.3 and 0.5/0.5). New coordination polymers are isostructural to Cu-IDA and amounts of manganese atoms inserted into crystalline structure were evaluated by single-crystal X-ray diffraction and Rietveld refinement. All coordination polymers obtained were also characterized by infrared absorption spectroscopy and thermogravimetric analysis. Homometallic and bimetallic compounds were evaluated as catalysts for Baylis-Hillman reaction with yields and reaction times comparable or superior to those in the literature. Compounds containing manganese cations shows higher catalytic performance, especially Cu/Mn-IDA (0.9/0.1) with yield 91% in 5 h of reaction. Results also indicate an important role played by the metallic centre in the catalytic mechanism.
机译:本文报道了合成一维配位聚合物[Cu(IDA)(H2O)(2)](n)的实验参数(pH和反离子)的影响。(IDA=亚氨基二乙酸酯),此处命名为Cu IDA。铜锰双金属配位聚合物也通过同构置换成Cu-IDA结构获得,具有不同的Cu2+和Mn2+离子摩尔比,这里表示为Cu/Mn-IDA(0.9/0.1;0.7/0.3和0.5/0.5)。新的配位聚合物与Cu-IDA是同构的,通过单晶X射线衍射和Rietveld细化评估了插入晶体结构的锰原子数量。通过红外吸收光谱和热重分析对所得配位聚合物进行了表征。均金属和双金属化合物被评价为Baylis-Hillman反应的催化剂,其产率和反应时间与文献中的相当或优于文献中的那些。含锰离子的化合物表现出较高的催化性能,尤其是Cu/Mn-IDA(0.9/0.1),反应5h的产率为91%。结果还表明,金属中心在催化机理中起着重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号