Abstract
Recycling of heterogenized gold(I), gold(III), and palladium(II) complexes could be
achieved for Suzuki and Sonogashira cross-coupling reaction between iodo benzene and
arylboronic acids or alkynes. Au(I) and Pd(II) afford selectively nonsymmetrical
biaryl compounds, while gold(III) complexes can only catalyze the arylboronic or alkynes
homocoupling. Recycling occurs without loss of the catalytic activity after several
reaction cycles.
Key words
C-C coupling - gold - Suzuki - Sonogashira - homogeneous catalysis - heterogenized
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Suzuki: the reaction was carried out in a 25 mL vessel, at 130 °C in a time range
of 3-24 h. In a typical run, a mixture of aryl halide (10 mmol), boronic acid (15
mmol), aq K3 PO4 (20 mmol), and catalyst (10-20 mol%) in 3 mL of o -xylene was stirred for the desired time. The solution was allowed to cool, and a
1:1 mixture of Et2 O-H2 O (20 mL) was added. The organic layer was washed, separated, further washed with
another 10 mL portion of Et2 O, dried with anhyd MgSO4 , and filtered. The solvent and volatiles were completely removed under vacuum to
give the crude product which subjected to column chromatographic separation resulted
in pure compounds. The reaction was followed by GC-MS. At the end of the process,
the mixture of reaction was filtered; the residue of support-containing catalyst washed
to completely remove the remains of products and/or reactants and used again.
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Sonogashira: The reaction was carried out in a 25 mL vessel, at 130 °C during 24 h.
In a typical run, a mixture of aryl halide (10 mmol), alkyne (15 mmol), aq K2 CO3 or K3 PO4 (20 mmol) and catalyst (10-20 mol%) in 3 mL of o -xylene was stirred for the desired time. The reaction was followed by GC-MS. At the
end of the process, the mixture of reaction was filtered; the residue of support-containing
catalyst washed to completely remove the remains of products and/or reactants, and
used again.