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Efficient one-pot synthesis of propargylamines catalysed by gold nanocrystals stabilized on montmorilloniteElectronic supplementary information (ESI) available. See DOI: 10.1039/c4cy00666f
Size selective Au 0 -nanoparticles were generated in situ in the nanopores of modified montmorillonite. The modification of montmorillonite was carried out with HCl under controlled conditions for generating nanopores (less than 8 nm) in the matrix and these nanopores acted as "hosts" for...
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Summary: | Size selective Au
0
-nanoparticles were generated
in situ
in the nanopores of modified montmorillonite. The modification of montmorillonite was carried out with HCl under controlled conditions for generating nanopores (less than 8 nm) in the matrix and these nanopores acted as "hosts" for the
in situ
generation of Au
0
-nanoparticles. The synthesis consisted of impregnation of the acid-activated montmorillonite with HAuCl
4
aqueous solution followed by reduction with NaBH
4
. The synthesised Au
0
-nanoparticles crystallized in the face centred cubic lattice were single crystals with a preferential growth direction along the (111) plane. A N
2
adsorption-desorption study revealed specific surface areas of 327-579 m
2
g
−1
, large specific pore volumes ~0.7 cm
3
g
−1
, and pore diameters of 0-10 nm of the support. TEM, FESEM and X-ray studies indicate that Au
0
-nanoparticles of 0-10 nm were evenly distributed on the support which then serves as an efficient green catalyst for the one-pot, three-component coupling of an aldehyde, an amine and an alkyne
via
C-H alkyne-activation to synthesize propargylamines with 82-94% yield and 100% selectivity under mild reaction conditions. The nanocatalysts can be recycled and reused several times without significant loss of their catalytic activity.
Size selective Au
0
-nanoparticles were generated
in situ
in the nanopores of montmorillonite and applied in the one-pot, three-component coupling of an aldehyde, an amine and an alkyne to synthesize propargylamines. |
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ISSN: | 2044-4753 2044-4761 |
DOI: | 10.1039/c4cy00666f |