期刊文献+

两种碱土金属甲基磺酸盐的结构和催化性能研究 被引量:1

Study on the structure and catalytic performance of two alkaline earth methanesulfonates
下载PDF
导出
摘要 以甲基磺酸和两种碱土金属氧化物为原料,合成了两个金属配合物[Mg(H_2O)_6](CH_3SO_3)_2·6H_2O(1)和Ca(CH_3SO_3)_2(2),通过X-射线单晶衍射和热重分析确定了配合物的晶体结构和热分解过程.结果表明,甲基磺酸镁含有12个结晶水,属于三方晶系,R 3空间群,a=9. 3230 (7)?,b=9. 3230 (7)?,c=21. 2017 (12)?,α=90°,β=90°,γ=180°,V=1595. 93(19)?~3,Z=3.甲基磺酸钙不含结晶水,属于正交晶系,Pbca空间群,a=10. 1298 (6)?,b=9. 2202 (5)?,c=17. 3274 (10)?,α=90°,β=90°,γ=90°,V=1618. 36 (16)?~3,Z=8.采用Biginelli作为探针反应研究其催化性能,证明甲基磺酸镁的催化性能优于甲基磺酸钙. Two metal complexes [ Mg( H2 O)6 ] ( CH3803 )2 ·6H2O ( 1 ) and Ca ( CH3 SO3 )2 (2) were syn- thesized by methanesultbnic acid and two alkaline earth metal oxides. The crystal structure and thermal decompo- sition of them were determined by X - ray single crystal diffraction technique and thermogravimetric analysis. The results show that the magnesium methanesulfonate has twelve crystal waters and belongs to the trigonal system, R 3space group, a=9.3230 (7) A, b=9.3230 (7) A, c=21.2017 (12) A, α =90°, β= 90°, γ=180°, V= 1595.93 ( 19 ) A, Z = 3. The calcium methanesulfonate has no crystal water and belongs to orthorhombic sys- tem, Pbca space group, a = 10. 1298 (6) A, b =9. 2202 (5) A,c = 17. 3274 (10) A, α =90°,β =90°,γ= 90°, V= 1618.36 (16) A3, Z = 8. Their catalytic performance was studied by using Biginelli as a probe reac- tion. The resuhs indicated that the catalytic activity of magnesium methanesulfonate is better than that of calcium methanesulfonate.
作者 宋志国 张皜昊 张顺 王敏 SONG Zhiguo;ZHANG Haohao;ZHANG Shun;WANG Min(Center of Experimental Management,Bohai University,Jinzhou 121013,China;College of Chemistry and Chemical Engineering,Bohai University,Jinzhou 121013,China)
出处 《渤海大学学报(自然科学版)》 CAS 2018年第3期198-203,共6页 Journal of Bohai University:Natural Science Edition
基金 辽宁省自然科学基金项目(No:2015020201) 辽宁省高等学校优秀人才支持计划(No:LJQ2015002) 国家自然科学基金项目(No:21406016)
关键词 甲基磺酸盐 晶体结构 BIGINELLI反应 催化性能 methanesulfonates crystal structure Biginelli reaction catalytic performance
  • 相关文献

参考文献3

二级参考文献27

  • 1J.WJ.Bosco,A.K.Saikia,Synth.Commun.38(2008)77.
  • 2A.Saini,S.Kumar,J.S.Sandhu,Synth.Commun.38(2008)106.
  • 3A.K.Bhattacharya,M.Mujahid,A.A.Natu,Synth.Commun.38(2008)128.
  • 4A.V.Reddy,K.Ravinder,V.L.N.Reddy,et al.Synth.Commun.33(2003)1531.
  • 5S.C.Roy,B.Banerjee,Synlett(2002)1677.
  • 6R.Fazaeli,S.Tangestaninejad,H.Aliyan,Appl.Catal.A:Gen.318(2007)218.
  • 7J.R.Satam,R.V.Jayaram,Catal.Commun.8(2007)1414.
  • 8A.R.Hajipour,A.Zarei,A.E.Ruoho,Tetrahedron Lett.48(2007)2881.
  • 9M.Wang,Z.C.Wang,Z.L.Sun,et al.React.Kinet.Catal.Lett.84(2005)223.
  • 10M.Wang,Z.G.Song,H.Gong,et al.Prep.Biochem.Biotechnol.38(2008)105.

共引文献10

同被引文献7

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部