"Click" Glycodendrimers Containing 27, 81, and 243 Modified Xylopyranoside Termini

被引:48
作者
Camponovo, Jeremy [2 ]
Hadad, Caroline [1 ]
Ruiz, Jaime [2 ]
Cloutet, Eric [3 ]
Gatard, Sylvain [1 ]
Muzart, Jacques [1 ]
Bouquillon, Sandrine [1 ]
Astruc, Didier [2 ]
机构
[1] Univ Reims, CNRS, Inst Chim Mol ICMR, UFR Sci,UMR 6229, F-51687 Reims 2, France
[2] Univ Bordeaux 1, Inst Mol Sci, CNRS,UMR 5255, F-33405 Talence, France
[3] Univ Bordeaux 1, ENSCPB, Lab Chim Polymeres Organ, CNRS,UMR 5629, F-33607 Pessac, France
关键词
BINDING-PROPERTIES; D-XYLOSE; GOLD NANOPARTICLES; ALPHA-THIOSIALODENDRIMERS; BUTADIENE TELOMERIZATION; SELECTIVE RECOGNITION; MOLECULAR ELECTRONICS; STARBURST DENDRIMERS; TRIAZOLE DENDRIMERS; CASCADE MOLECULES;
D O I
10.1021/jo900554b
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of large glycodendrimers containing 27, 81, and 243 terminal modified xylose branches from the first (G(1)-27) to the third generation (G(3)-243) were synthesized from 2'-azidoethyl 2,3,4-tri-O-acetyl-beta-D-xylopyranoside and alkynyl-terminated dendrimers by "click" chemistry that is confirmed to be an excellent method to obtain large glyco-dendtimers exemplified by the use of modified xylose. The dendrimers were first characterized by H-1 NMR, C-13{H-1} NMR, elemental analysis, and IR spectroscopy. The size progression in the series was also demonstrated using both DOSY NMR and size exclusion chromatography (SEC), the latter technique showing the good polydispersity of all the dendrimers. The size measured by dynamic light scattering (DLS) for the dendrimer G(3)-243 is close to that obtained by the DOSY NMR method.
引用
收藏
页码:5071 / 5074
页数:4
相关论文
共 107 条
  • [1] Light-harvesting dendrimers
    Adronov, A
    Fréchet, JMJ
    [J]. CHEMICAL COMMUNICATIONS, 2000, (18) : 1701 - 1710
  • [2] Catalysts based on palladium dendrimers
    Andres, Roman
    de Jesus, Ernesto
    Carlos Flores, Juan
    [J]. NEW JOURNAL OF CHEMISTRY, 2007, 31 (07) : 1161 - 1191
  • [3] [Anonymous], 2001, Dendrimers and Dendrons: Concepts, Synthesis, Applications
  • [4] ARDOIN N, 1995, B SOC CHIM FR, V132, P875
  • [5] Ashton PR, 2002, CHEM-EUR J, V8, P673, DOI 10.1002/1521-3765(20020201)8:3<673::AID-CHEM673>3.0.CO
  • [6] 2-D
  • [7] Dendritic catalysts and dendrimers in catalysis
    Astruc, D
    Chardac, F
    [J]. CHEMICAL REVIEWS, 2001, 101 (09) : 2991 - 3023
  • [8] Metallodendritic catalysis for redox and carbon-carbon bond formation reactions:: A step towards green chemistry
    Astruc, D
    Heuzé, K
    Gatard, S
    Méry, D
    Nlate, S
    Plault, L
    [J]. ADVANCED SYNTHESIS & CATALYSIS, 2005, 347 (2-3) : 329 - 338
  • [9] Dendrimers and gold nanoparticles as exo-receptors sensing biologically important anions
    Astruc, D
    Daniel, MC
    Ruiz, J
    [J]. CHEMICAL COMMUNICATIONS, 2004, (23) : 2637 - 2649
  • [10] Organometallic chemistry at the nanoscale. Dendrimers for redox processes and catalysis
    Astruc, D
    [J]. PURE AND APPLIED CHEMISTRY, 2003, 75 (04) : 461 - 481