| Autor: |
Chengang Cao, Yang Zhai, Fakhre Alam, Haonan Fan, Jingyi Zhang, Tao Jiang |
| Jazyk: |
angličtina |
| Rok vydání: |
2022 |
| Předmět: |
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| Zdroj: |
Catalysts, Vol 12, Iss 9, p 944 (2022) |
| Druh dokumentu: |
article |
| ISSN: |
2073-4344 |
| DOI: |
10.3390/catal12090944 |
| Popis: |
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. |
| Databáze: |
Directory of Open Access Journals |
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