期刊文献+

Salen Co(Ⅱ)配合物催化氧化百里酚制备百里醌的研究

Catalytic oxidation of thymol to prepare thymoquinone by Salen Co(Ⅱ) complex
下载PDF
导出
摘要 使用Salen Co(Ⅱ)配合物催化氧化百里酚制备百里醌,考察了不同的反应条件对催化体系的影响。确定该合成工艺的最佳条件为以氧气为氧化剂,10%mol Salen Co(Ⅱ)配合物为催化剂,在DMF溶液中30℃反应9h,收率可达99.1%。该工艺具有反应选择性好、反应条件温和、收率高和后处理操作简单等特点,适合于工业化生产。 Thymoquinone was prepared from catalytic oxidation of thymol by Salen Co (Ⅱ) complex. The best reaction oxidation conditions of thymol were optimized by investigating the effect of different reaction conditions on the catalytic system. The reaction was carried on 9 hours in the DMF solution under 30 ℃, oxygen as oxidant and 10% mol Salen Co (Ⅱ) complex as catalyst. This method was suitable for industrial production because it prossessed some advantages such as high selectivity, mild reaction conditions, high efficiency and simple to operate.
出处 《黑龙江大学工程学报》 2013年第2期38-41,共4页 Journal of Engineering of Heilongjiang University
基金 哈尔滨市科技创新人才研究专项资金项目(RC2012XK001005)
关键词 SALEN Co(Ⅱ)配合物 催化氧化 百里酚 百里醌 Salen Co(Ⅱ) complex catalytic oxidation thymol thymoquinone
  • 相关文献

参考文献16

  • 1Banerjee S,Kaseb A 0, Wang Z,et al. Antitumor ac-tivity of gemcitabine and oxaliplatin is augmented bythymoquinone in pancreatic cancer [J]. Cancer Res.,2009, 69 (13): 5 575-5 583.
  • 2Jafri S H, Glass J,Shi R,Prince M. et al. Kleiner-Hancock H. , Thymoquinone and cisplatin as a thera-peutic combination in lung cancer: In vitro and in vivo[J]. J Exp. Clin. Cancer Res.,2010,29: 87-89.
  • 3Kremers E,Wakeman N, Hixon R M. Thymoquinone[J]. Org. Syn.,1941,1: 511-512.
  • 4Egusquiza M G,Romanelli G P,Cabello C,et al. Are-ne and phenol oxidation with hydrogen peroxide using sandwich- type substituted polyoxometalates as catalysts[J]. Catal. Commun.,2008,9 (1): 45-50.
  • 5Noyori R, Aoki M, Sato K, et al. Green oxidation withaqueous hydrogen peroxide [J]. Chem. Commua,2003,(18): 1 977-1 986.
  • 6Omura K. Rapid conversion of phenols to p-benzoquino-nes under acidic conditions with lead dioxide [J]. Syn-thesis. ,1998, (9): 1 145-1 148.
  • 7Punniyamurthy T,Velusamy S,Iqbal J,Recent ad-vances in transition metal catalyzed oxidation of organicsubstrates with molecular oxygen [J]. Chem. Rev.,2005, 105 (6): 2 329-2 364.
  • 8Liotta D,Arbiser J,Short J W,Simple, inexpensiveprocedure for the large-scale production of alkyl qui-nones [J]. J. Org. Cherru,1983,48 (17): 2 932-2 933.
  • 9臧树良,岳爽.新型高效催化剂——甲基三氧化铼(MTO)的研究发展[J].当代化工,2007,36(6):551-556. 被引量:3
  • 10Meunier B,Metalloporphyrins as versatile catalysts foroxidation reactions and oxidative DNA cleavage [J].Chem. Rev.,1992,92 (6): 1 411-1 456.

二级参考文献33

  • 1Ana Santos. Rhenium and Molybdenum Oxo Complexes: Synthesis and Catalytic Application for Olcfin Epoxidation, Ph. D Thesis, Page 8.
  • 2I. R. Beattie, P.J. Jones. Methyltrioxorhenium. An Air - Stable Compound Containing a Carbon - Rhenium Bond [ J ]. Inorg. Chem., 1979, 18:2318-2319.
  • 3W. A. Herrmann, J. G.Kuchhr, J. K. Felixberger,et al. Methylrhenium Oxides: Synthesis from R207 and Catalytic Activity in Olefin Metathesis[J]. Angew. Chem.Int. Ed. Engl, 1988, 27: 394 - 396.
  • 4W. A. Herrmann, F. E.Kuhn, R.W. Fischer, et al. Multiple Bond between Transition Metals and Main - Group Elements.124.^1 Structures and Reactivity of Acylperrhenates[ J]. Inorg. Chem, 1992. 31. :4431 -4432.
  • 5J. Jacob, J. H. Espenson. Selective C - H Bond Activation of Arenes Catalyzed by Methylrhenium Trioxide [ J]. Inorg. Chim. Acta, 1998, 270(1,2): 55-59.
  • 6W. A. Herrmarm, R. M. Kratzer. R. W. Fischer, Alkylrhenium Oxides from Perrhenates: A New Economical Access to Organometallie Oxide Catalysts[J]. Angew. Chem. Int. Ed Engl., 1997, 36 (23) : 2652 - 2654.
  • 7W. A. Herrmann, J. G. Kuchler, G. Weichselbaumer, et al. Multiple Bonds between main Group Elements and Transition Metals LⅩⅣ Methyl (trioxo) rhenium Base Adduets and Base Reactions Crystal Structure of Sodium(ben = 20 - 15 - crocon - 5) Perhenate[ J ]. Organomet. Chem, 1989, 372 ( 3 ) : 351 - 370.
  • 8W. A. Herrmann, G. Weiehselbaumer, E. Herdtweck. Multiple Bond between mainGroup Elements and Transition Metal LⅩⅧ The "metal acid" Methyl(tri - oxo)rhenium Adduct Formation with Amine Base and Aromaties. The Structure of Anline Complex CH3ReO3H2NC6H5 [J]. Organomet. Chem, 1989, 372 ( 3 ) : 371 - 389.
  • 9E.Fritz, Kuhn,M. Ana, Santos, W.Peter, Roesky, et al. Trigonal - Bipyramidal Lewis Base Adducts of Methyltrioxorhenium (vii) and Their Bisperoxo Congeners: Characterization, Application in Catalytic Epoxidation, and Density Functional Mechanistic Study[J]. Chem. Eur, 1999, 5 (12):3603-615.
  • 10Paula Ferreira, Wen- Mei Xue, Elva Bencze, E,et al. Bidentate Lewis Base Adducts of Methyltrioxorhenium and Their Application in Catalytic Expoxoidation[J] .Inorg. Chem, 2001, 40:5834 - 5841.

共引文献38

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