期刊文献+

固载脯氨酸的毛发状纳米粒子的合成及其应用研究 被引量:1

Synthesis and application research of hairy nanoparticle supported proline
下载PDF
导出
摘要 毛发状粒子表面的聚合物链是一个具有一定流动性的动态体系,其负载的催化剂综合了均相和非均相负载催化剂的优点,为手性催化剂的负载和实用化提供了一条新的途径。本文利用Si O2纳米粒子表面修饰制得的功能基,通过表面RAFT聚合,并经过氨基去保护后制得负载脯氨酸的毛发状纳米粒子。通过热重、红外和透射电镜对毛发状二氧化硅纳米粒子的结构进行表征,并将获得的毛发状纳米粒子作为催化剂直接催化不对称Aldol反应。 The polymer brushes on the surface of hairy nanoparticles are a dynamic system possessing a certain degree of mobility,so hairy particles supported catalysts can combine the advantages of both homogeneous catalysts and heterogeneous catalysts,andprovide a new and practical way for chiral catalyst load. Based on above,the hairy nanoparticles supported proline were synthesizedby surface-initiated RAFT polymerization from silica initiator particles. The structure and composition of the hairy nanoparticles obtainedwere characterized by Fourier transform infrared spectrum(FTIR),thermogravimetric analyzer(TGA)and transmission electronmicroscope(TEM). Futhermore,the achieved hairy nanoparticles were used in asymmetric direct Aldol reaction as catalysts.
出处 《化学研究与应用》 CAS CSCD 北大核心 2014年第11期1758-1763,共6页 Chemical Research and Application
基金 国家自然科学基金(21204019)资助 国家博士后基金(2012M521398)资助 河南省国际科技合作项目(134300510055)资助 河南省重点科技攻关项目(112102310086)资助 河南师范大学青年基金
关键词 毛发状纳米粒子 RAFT聚合 脯氨酸 ALDOL反应 hairy nanoparticle RAFT proline Adol reaction
  • 相关文献

参考文献30

  • 1List B,Lerner R A,Barbas III C F. Proline-Catalyzed DirectAsymmetric Aldol Reactions[J]. J. Am. Chem. Soc. ,2000,122(10):2395-2396.
  • 2Gruttadauria M,Giacalone F,Noto R. Supported prolineand proline-derivatives as recyclable organocatalysts[J].Chem. Soc. Rev. 2008,37(8):1666-1688.
  • 3Huang J,Zhang X. T,Armstrong D. W. Highly EfficientAsymmetric Direct Stoichiometric Aldol Reactions on/ inWater[J]. Angew Chem. Int Ed. ,2007,46(47):9073-9077.
  • 4Bergbreiter D E,Tian J. H,Hongfa C. Using Soluble PolymerSupports To Facilitate Homogeneous Catalysis[J].Chem. Rev. ,2009,109(2):530-582.
  • 5Simon M O,Li C. J. Green chemistry oriented organic synthesisin water[J]. Chem. Soc. Rev. ,2012,41(4):1415-1427.
  • 6Wang Z,Chen G,Ding K. Self-Supported Catalysts[J].Chem. Rev. ,2009,109(2):322-359.
  • 7Zhao,B. ;Zhu,L. Mixed Polymer Brush-grafted Particles:A New Class of Environmentally Responsive NanostructuredMaterials[J]. Macromol,2009,42(24):9369-9383.
  • 8Goel V,Pietrasik J,Dong H. C,et al. Structure of PolymerTethered Highly Grafted Nanoparticles [J]. Macromol,2011,44(20):8129-8135.
  • 9Wang B. B,Li B,Dong B,et al. Homo-and Hetero-ParticleClusters Formed by Janus Nanoparticles with BicompartmentPolymer Brushes [J]. Macromol,2010,43 (22):9234-9238.
  • 10Li D. J,Sheng X,Zhao B. Environmentally Responsive“Hairy” Nanoparticles:Mixed Homopolymer Brushes onSilica Nanoparticles Synthesized by Living Radical PolymerizationTechniques[J]. J. Am. Chem. Soc. ,2005,127(17):6248-6256.

二级参考文献2

共引文献5

同被引文献21

  • 1List B,Lerner R A, Barbas III C F. Proline-Catalyzed Di- rect Asymmetric Aldol Reactions [J]. J. Am. Chem. Soc. ,2000,122(10) :2395-2396.
  • 2Millet R, Traff A M, Petrus M L, et al. Enantioselective Synthesis of syn-and anti-l, 3-Aminoalcohols via beta- Aminoketones and Subsequent Reduction/Dynamic Kinetic Asymmetric Transformation[J]. J. Am. Chem. Soc. ,2010, 132(43) :15182-15184.
  • 3Albrecht L, Jiang H, Diekmeiss G, et al. Asymmetric For- real trans-Dihydroxylation and trans-Aminohydroxylation of or, β-Unsaturated Aldehydes via an Organoeatalytie Reac- tion Cascade [J]. J. Am. Chem. Soc., 2010, 132 ( 26 ) : 9188-9196.
  • 4Hayashi Y, Gotoh H, Honma M, et al. Organocatalytic, En- antioselective Intramolecular[6+2] Cycloaddition Reaction for the Formation of Ttleyelopentanoids and Insight on Its Mechanism from a Computational Study[J]. J. Am. Chem. Soc. ,2011,133 (50) :20175-20185.
  • 5Notz W, Tanaka F, Watanabe S, et al. The direct organo- catalytic asymmetric Mannich reaction: Unmodified alde- hydes as nueleophiles [J]. J. Org. Chem. , 2003,68 ( 25 ) : 9624-9634.
  • 6List B, Pojarliev P, Castello C. Proline-eatalyzed asymmet- fie aldol reactions between ketones and alpba-unsubstitut- ed aldehydes[J]. Org. Lett. ,2001,3(4) :573-575.
  • 7Mase N, Thayumanavan R, Tanaka F, et al. Direct asym- mettle organoeatalytie Michael reactions of alpha, alpha- disubstituted aldehydes with beta-nitrostyrenes for the syn- thesis of quaternary carbon-containing products [J]. Org. Lett. ,2004,6( 15 ) :2527-2530.
  • 8Torii H, Nakadai M, Ishihara K, et al. Asymmetric direct aldol reaction assisted by water and a proline-derived tet- razole catalyst [J]. Angew. Chem. Int. Ed. , 2004, 43 ( 15 ) : 1983-1986.
  • 9Mase N, Barbas III C F. In water, on water, and by water: mimicking nature's aldolases with organocatalysis and wa- ter[J]. Org. Biomol. Chem. ,2010,8 ( 18 ) :4043-4050.
  • 10Sakthivel K, Notz W, Bui T, et al. Amino acid catalyzed direct asymmetric aldol reactions:A bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reac- tions[J]. J. Am. Chem. Soc., 2001, 123 ( 22 ) : 5260- 5267.

引证文献1

二级引证文献3

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