Abstract
This paper reports the efficient synthesis of the first class of polyisobutylene(PIB)-supported palladium-PEPPSI precatalyst (PEPPSI = pyridine-enhanced precatalyst preparation, stabilization, and initiation). The new complexes are employed in Buchwald–Hartwig amination of aryl chlorides and are found to be reasonably active in the titled cross-coupling reaction. The supported catalysts are tested in polar (1,4-dioxane and 1,2-dimethoxyethane) as well as in aliphatic reaction media (toluene and n-heptane) and display superior activity in the highly lipophilic solvent (n-heptane). The catalytic efficacy of PIB-Pd-PEPPSI precatalyst is measured to be comparable to its nonsupported analog. Pd-leaching is determined by inductively coupled plasma mass spectrometry (ICP-MS) after a simple liquid/liquid extraction and is found to be 2 ppb in the product phase, translating into a recovery of ≈99.8% of the palladium.
| Original language | English |
|---|---|
| Article number | 1700214 |
| Journal | Macromolecular Rapid Communications |
| Volume | 38 |
| Issue number | 15 |
| DOIs | |
| Publication status | Published - Aug 2017 |
| Externally published | Yes |
Keywords
- Buchwald–Hartwig amination
- N-heterocyclic carbenes (NHCs)
- aryl chlorides
- palladium-PEPPSI
- supported catalysts
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