期刊文献+

醌类化合物催化O_2氧化醛合成羧酸

Catayhtic O_2 Oxidation of Aldehydes to Carboxylic Acids by Quinones
下载PDF
导出
摘要 研究了醌类化合物催化O2氧化醛合成羧酸的催化性能,发现蒽醌的催化活性高于2,3-二氯-5,6-二氰基-1,4-苯醌、四溴对苯醌、苯醌和萘醌,反应温度以及催化剂用量对反应有重要的影响,以5%物质的量(分数)的蒽醌为催化剂,在100℃、0.3 MPa的O2条件下,反应5 h,糠醛的转化率达到26.7%。以1.25%的蒽醌为催化剂,在60℃、0.3 MPa的O2条件下,反应5 h,苯甲醛的转化率达到96%,苯甲酸的分离收率为94%。 The catalytic performance of quinones in the catalytic oxidation of aldehydes to carboxylic acids using O2 as oxidant are studied. The result shows that the catalytic activity of anthraquinone is higher than 2,3 - dichloro - 5,6 - dicyano - benzoquinone, tetrabromo - p - benzoquinone, benzoquinone or naphthaquinone. In addition, the reaction temperature and the amount of catalyst have significant influence on the reaction. Under 0.3 MPa O2, at 100℃, for 5 h,using 5% anthraquinone as catalyst,the conversion of furrural is 26.7 % ; Under 0.3 MPa O2, at 60 ℃, for 5 h, using 1.25 % anthraquinone as catalyst, the conversion of benaldehyde reaches 96%, the isolated yied of bemzouacid is 94%
出处 《河南化工》 CAS 2011年第17期34-36,共3页 Henan Chemical Industry
关键词 醌类化合物 催化 羧酸 quinones catalyst carboxylic acid
  • 相关文献

参考文献1

二级参考文献30

  • 1[29]Shi H,Noguchi N and Niki E.Comparetive study on dynamics of autooxidative action of α-tocopheryl hydroquinone,ubiquinol,and α-tocopherol against lipid peroxidation.Free Radical Bio Med,1999,27(3/4):334-346
  • 2[30]Smart RP,Peelen TJ,Blankespoor RL,et al.Short-lived 1,5-biradicals formed from triplet 1-alkoxy-and 1-(benzyloxy)-9,10-anthraquinones.J Am Chem Soc,1997,119(3):461-465
  • 3[1]Labinger JA and Bercaw JE.Understanding and exploiting C-H bond activation.Nature,2002,417:507-514
  • 4[2]Jia C,Kitamura T and Fujiwara Y.Catalytic functionalization of arenes and alkanes via C-H bond activation.Acc Chem Res,2001,34:633-639
  • 5[3]Periana RA,Mironov O,Taube D,et al.Catalytic,oxidative condensation of CH4 to CH3COOH in one step via CH activation.Science,2003,301(8):814-818
  • 6[4]Sheldon RA and Downing RS.Heterogeneous catalytic transformations for environmentally friendly production.Appl Catal A,1999,189(2):163-183
  • 7[5]Hutchings GJ and Scurrell MS.Designing oxidation catalysts-are we getting better? Cattech,2003,7(3):90-103
  • 8[6]Bard AJ,Whitesides GM,Zare RN,et al.Holy grails in chemistry.Acc Chem Res,1995,28(3):91-91
  • 9[7]Bugg TDH.Dioxygenase enzymes:catalytic mechanisms and chemical models.Tetrahedron,2003,59:7075-7101
  • 10[8]Aboelella NW,Kryatov SV,Gherman BF,et al.Dioxygen activation at a single copper site:structure,bonding,and mechanism of formation of 1∶1 Cu-O2 adducts.J Am Chem Soc,2004,126(51):16896-16911

共引文献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