期刊文献+

一种绿色简便制备富勒醇的方法

A Simple and Green Method of Preparing Fullerenol
在线阅读 下载PDF
导出
摘要 为了解决富勒烯在水中溶解性差的问题,该文以富勒烯多氧化物为原料,在50℃下,将富勒烯多氧化物置于H2O2中水解,H2O2可以将富勒烯多氧化物进行二次氧化,成功制备了富勒醇。产品在水中溶解度可达59.8g/L。通过FTIR、UV-Vis、MALDI-TOF对产品进行了表征和分析。该文提供了一种制备富勒醇的简便方法,为其制备提供了借鉴。 In order to solve the problem of the poor solubility of fullerene in water, a method of preparing water-soluble fullerenol has been realized based on the fullerene oxides in this paper. In detail, the fullerene oxides were further oxidized and hydrolyzed by H202 to form more hydroxyl groups on fullerene cage under 50 ℃ to successfully synthesize fullerenol. The solubility of fullerenol is 59. 8 g/L. The target product was characterized by FTIR, UV-Vis and MALDI-TOF. Such a novel method of preparing fullerenol provides a new reference for the preparation methods of fullerenol. Key words:
出处 《精细化工》 EI CAS CSCD 北大核心 2014年第1期129-131,共3页 Fine Chemicals
关键词 富勒醇 富勒烯多氧化物 高水溶性 精细化工中间体 fullerenol fullerene oxides highly water-soluble fine chemical intermediates
  • 相关文献

参考文献11

  • 1Friedman S H,Decamp D L,Sijbesma R P,e( al. Inhibition of theHiv - 1 protease by fullerene derivatives-model-building studiesand experimental-verification [ J ]. J Am Chem Soc, 1993, 115(15):6506 -6509.
  • 2Chiang L Y,Swirczewski J W,Hsu C S,et al. Multihydroxyadditions onto C - 60 fullerene molecules [ J ]. J Chem Soc ChemComm ,1992 (24) :1791 -1793.
  • 3Chiang L Y,Upasani R B,Swirczewski J W. Versatile nitroniumchemistry for C - 60 fullerene functionalization [ J ]. J Am ChemSoc,1992,114(26) :10154 -10157.
  • 4Schneider N S,Darwish A D,Kroto H W,ei al. Formation offullerols via hydroboration of fullerene - C - 60 [ J ]. J Chem SocChem Comm, 1994(4) :463 -464.
  • 5Chiang L Y,Wang L Y,Swirczewski J W,et al. Efficient synthesisof polyhydroxylated fullerene derivatives via hydrolysis ofpolycyclosulfated precursors[ J]. J Org Chem, 1994,59( 14) :3960-3968.
  • 6Chiang L Y,Bhonsle J B,Wang LY,et al. Efficient one-flasksynthesis of water-soluble [60] fullerenols[ J ]. Tetrahedron,1996,52(14) :4963 -4972.
  • 7Kokubo K,Matsubayashi K,Tategaki H,et al. Facile synthesis ofhighly water-soluble fullerenes more than half-covered by hydroxylgroups[ J]. ACS Nano,2008,2(2) :327 -333.
  • 8Ken Kokubo,Shogo Shirakawa,Naoki Kobayashi,Hisae Aoshima,Takumi Oshima.Facile and Scalable Synthesis of a Highly Hydroxylated Water-Soluble Fullerenol as a Single Nanoparticle[J].Nano Research,2011,4(2):204-215. 被引量:5
  • 9张晓敏,邓波,李景烨,姚思德.紫外光氧化法制备水溶性富勒醇[J].辐射研究与辐射工艺学报,2010,28(1):1-4. 被引量:3
  • 10Haufler R E,Conceicao J,Chibante L P F,e. a/. Efficientproduction of C60 ( Buckminsterfullerene ),C60h36,and thesolvated buckide ion[ J]. J Phys Chem - Us ,1990,94(24) :8634-8636.

二级参考文献16

  • 1孙大勇,刘子阳,郭兴华,佘益民,周雨,刘淑莹.C_(60)(OH)_x的简便合成及性质[J].高等学校化学学报,1996,17(1):19-20. 被引量:15
  • 2Gottlieb H E, Kotlyar V, Nudelman A. J Org Chem, 1997, 62:7512-7515.
  • 3Ken Kokubo, Kenji Matsubayashi, Hiroshi Tategaki. ACS NANO, 2008, 2:327-333.
  • 4Kratchmer W, Lamb Lowell D, Fostiropoulos K, et al. Nature, 1990, 347 (6291): 354-358.
  • 5Hwang K C, Mauzerall D. Nature, 1993, 361:138.
  • 6Friedman S H, Decamp D L, Sijbesma R P, et al. J Am Chem Soc, 1993(115): 6506.
  • 7LI J, TAKEU CHIA, OZAWAM, et al. J Chem Soc Chem Commun, 1993, 23:1784-1785.
  • 8CHEN Boy Hom, HUANG Jen Pang, WANG Li Y, et al. J Chem Soc, Perkin Trans I, 1998, 7:1171-1173.
  • 9Andrievsky G V, Kosevich M V, Vock O M, et al. Chem Commun, 1995, 12:1281-1282.
  • 10Andrievsky G V, Klochkov V K, Mchedlov-Petrossyan N O, et al. Chem Phys Lett, 1999, 300-392.

共引文献8

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