Abstract
The steric and electronic properties of aryl substituents in monoaryl borohydrides (Li[ArBH3]) and dihydroboranes were systematically varied and their reactions with [Ru(PCy3)2HCl(H2)] (Cy: cyclohexyl) were studied, resulting in bis(σ)-borane or terminal borylene complexes of ruthenium. These variations allowed for the investigation of the factors involved in the activation of dihydroboranes in the synthesis of terminal borylene complexes. The complexes were studied by multinuclear NMR spectroscopy, mass spectrometry, X-ray diffraction analysis, and density functional theory (DFT) calculations. The experimental and computational results suggest that the ortho-substitution of the aryl groups is necessary for the formation of terminal borylene complexes.
| Original language | English |
|---|---|
| Pages (from-to) | 13566-13571 |
| Number of pages | 6 |
| Journal | Chemistry - A European Journal |
| Volume | 25 |
| Issue number | 59 |
| DOIs | |
| Publication status | Published - 22 Oct 2019 |
| Externally published | Yes |
Keywords
- boranes
- borohydrides
- borylenes
- sigma boranes
- steric effects
ASJC Scopus subject areas
- Catalysis
- General Chemistry
- Organic Chemistry