Abstract
A bis-C (cage)-substituted o-carborane 1,2-bis (3-butenyl)-1,2-dicarba- closo-dedocaborane is successfully synthesized via cross-coupling reaction of carboranyl Grignard reagent with allyl bromide in the presence of copper (I) salt as catalyst. The optimization of this cross-coupling reaction reveals that the copper (I) salts have high catalytic activity for the formation of the corresponding dialkenyl-substituted o-carborane, especially in the presence of 1-phenyl-1-propyne as additive, whereas the palladium and nickel complexes containing triphenylphosphine ligands favor the formation of mono-substituted alkenylcarborane.
| Original language | English |
|---|---|
| Pages (from-to) | 321-323 |
| Number of pages | 3 |
| Journal | Inorganic Chemistry Communications |
| Volume | 15 |
| DOIs | |
| State | Published - Jan 2012 |
Keywords
- Alkenylcarborane
- Copper catalyzed
- Cross-coupling
- Optimization
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