Chromium Catalysts Based on Unsymmetrical PNP Ligands for Selective Ethylene Tri-/Tetramerization: Effect of Electron-Withdrawing/Donating Substituents on Catalytic Performance

Abstract

The in situ formation and activation of Cr(III) catalysts based on unsymmetrical PNP ligands yield efficient catalytic systems for selective ethylene tri-/tetramerization. The electronic nature (electron-withdrawing or electron-donating) and position (para or meta) of the substituents over the phenyl rings of the PNP, the nature of cocatalyst (DMAO/AlEt3 and MMAO-3A), and reaction conditions have been observed to have a marked impact on catalytic performance, particularly catalytic activity. Ligand L2, bearing 4-(trifluoromethyl)phenyl substituents, yielded 33.6 kg(product).g(Cr)−1·h−1 catalytic activity with 57.7% C8 selectivity under optimal conditions. Ligand L4, having para-tolyl substituents, yielded 43.3 kg(product).g(Cr)−1·h−1 with 59.0% C8 selectivity under optimum conditions. Changing the positions of both the electron-withdrawing and electron-donating substituents from para to meta over the phenyls of the PNP may lead to both catalytic systems exhibiting poor performance.

Keywords

• chromium catalysts
• unsymmetrical PNP ligands
• ethylene tri-/tetramerization
• 1-hexene/1-octene