Hydroxypropyl-α-Cyclodextrin-Capped Palladium Nanoparticles: Active Scaffolds for Efficient Carbon-Carbon Bond Forming Cross-Couplings in Water

被引:98
|
作者
Senra, Jaqueline D. [2 ]
Malta, Luiz Fernando B. [1 ]
da Costa, Marcelo E. H. M. [3 ]
Michel, Ricardo C. [4 ]
Aguiar, Lucia C. S. [1 ,2 ]
Simas, Alessandro B. C. [2 ]
Antunes, O. A. C. [1 ,2 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Quim, BR-21941909 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Nucleo Pesquisas Prod Nat, BR-21941614 Rio De Janeiro, Brazil
[3] Pontificia Univ Catolica Chile, Dept Fis, BR-22452970 Rio De Janeiro, Brazil
[4] Univ Fed Rio de Janeiro, Inst Macromol, BR-21945970 Rio De Janeiro, Brazil
关键词
aqueous medium; cross-coupling reactions; cyclodextrins; green chemistry; palladium nanoparticles; SUZUKI-MIYAURA COUPLINGS; CATALYZED HECK REACTION; GOLD NANOPARTICLES; HIGHLY EFFICIENT; ARYL CHLORIDES; METHYLATED CYCLODEXTRINS; SONOGASHIRA REACTION; RECYCLABLE CATALYST; PHENYLBORONIC ACID; ASSISTED SYNTHESIS;
D O I
10.1002/adsc.200900348
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A new approach for the preparation of palladium nanoparticles in water from a renewable source, 2-hydroxypropyl-alpha-cyclodextrin (alpha-HPCD), which acts both as a reductant and capping agent, is presented. The palladium nanoparticles were characterized by using dynamic light scattering (DLS), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS), which revealed the formation of spherical particles in the size range of 2-7 nm. Further analysis by Fourier-transform infrared spectroscopy (FT-IR) and H-1 NMR did not show covalent bonds between cyclodextrins and palladium nanoparticles, suggesting that alpha-HPCD is only physically adsorbed on the nanoparticle surface, presumably through hydrophobic interactions which limit the mutual coalescence of nanoclusters. ne catalytic activity was tested in Suzuki, Heck and Sonogashira reactions in neat water, providing good yields and selectivities of coupling products under very low Pd loadings (0.5-0.0.1 mol%). Remarkably, the nanocatalyst showed significant stability hence the aqueous phase remained active for four subsequent runs. ne combination of a binding site for substrates (the HPCD cavity) and a reactive centre (Pd core) provides a potential to explore functional catalysis in aqueous medium.
引用
收藏
页码:2411 / 2422
页数:12
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