Abstract
A series of nickel (II) complexes bearing silicon bridged diphosphines ligands (PNSiP) have been synthesized and characterized. All nickel precatalysts, activated with ethylaluminum dichloride (EtAlCl2), exhibited moderate to high activities for ethylene dimerization to butylene. The in situ nickel precatalysts formed by mixing N-cyclopentyl-N-((diphenylphosphanyl)dimethylsilyl)-1,1-diphenylphosphanamine (L2) with NiBr2(DME) showed high catalytic activity (2.40 × 108 g/(molNi·h)) and high product selectivity (88.6%) towards butene using methylcyclohexane as solvent at 1.0 MPa ethylene pressure and 45°C temperature, no polyethylene(PE) was observed. Ligand backbone tuning of PNSiP-based catalytic systems help in precise understanding of steric bulk variation effects on catalytic performance.
Original language | English |
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Pages (from-to) | 363-368 |
Number of pages | 6 |
Journal | Phosphorus, Sulfur and Silicon and the Related Elements |
Volume | 193 |
Issue number | 6 |
DOIs | |
State | Published - 3 Jun 2018 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2018 Taylor & Francis Group, LLC.
Keywords
- Butene
- ethylaluminum dichloride
- ethylene dimerization
- nickel complexes
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Inorganic Chemistry