| Authors | حسین نعیمی,فاطمه کیانی |
| Journal | J ORGANOMET CHEM |
| Page number | 65 |
| Volume number | 885 |
| IF | 2.066 |
| Paper Type | Full Paper |
| Published At | 2019-01-28 |
| Journal Grade | Scientific - research |
| Journal Type | Electronic |
| Journal Country | Iran, Islamic Republic Of |
| Journal Index | JCR |
Abstract
The Sonogashira cross coupling reaction is an applied method for preparation of diarylethyne compounds
from readily available aryl halide derivatives and phenyl acetylene. The coupling reaction using
nickel complex of N,N0-Bis(2-hydroxyethyl)ethylenediamine onto core shell graphene oxide (GO@SiO2-
BHED-Ni) as a catalyst was studied in this research. This heterogonous catalyst showed good thermal
stability, highly efficiency and recyclability in the reaction. Moreover, the catalyst is simply separated and
can be reused several times without significant loss of catalytic activity. A wide range of aryl halides was
coupled successfully under palladium and phosphine free conditions. The use of this catalyst led to the
formation of substituted aromatic alkynes in excellent yields and short reaction times.