Authors | حسین نعیمی,فاطمه کیانی |
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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.
tags: Coupling reaction Diarylethynes Heterogonous catalyst Nickel chloride Graphene oxide