Abstract
Via ion-pair electrostatic interactions with sulfonate anions, the phosphine-ligated Ru(III) complex cations of [RuIIICl 4(L)2]+ (L = 1-butyl-2-(diphenylphosphino)-3- methylimidazolium) were successfully immobilized into a sulfonated SBA-15 framework, leading to the formation of the cationic Ru(III) complex and anionic sulfonate co-modified SBA-15 material (referred to as Ru-SO3-SBA-15). This material was characterized by powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), N2 adsorption-desorption isotherms, FT-IR, and elemental analysis techniques. As a heterogeneous catalyst, Ru-SO3-SBA-15 exhibited comparable activity and selectivity to the parent homogeneous catalyst [RuIIICl4(L) 2]PF6 in transfer hydrogenation of ketones. However, as a result of the limited durability of Ru-SO3-SBA-15 in strongly alkaline environments at high temperature, the activity of Ru-SO 3-SBA-15 could not be maintained during subsequent recycled uses.
| Original language | English |
|---|---|
| Pages (from-to) | 851-858 |
| Number of pages | 8 |
| Journal | Monatshefte fur Chemie |
| Volume | 144 |
| Issue number | 6 |
| DOIs | |
| State | Published - Jun 2013 |
Keywords
- Green chemistry
- Heterogeneous catalysis
- Hydrogen transfer
- Ion-pair electrostatic interaction
- Ruthenium complexes
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