Abstract
A series of asymmetric formamidine ligands bearing different substituents with various steric and electronic properties on the nitrogen of the N-C-N motif were synthesized. Group 4 bis(formamidinate) dimethylamido, chloride, and benzyl complexes were studied using these asymmetric ligands and their solid-state structures and their behavior in solution were determined. These complexes were activated with MAO (methylalumoxane) or a combination of cocatalysts and tested in the polymerization of ethylene and propylene. A noticeable influence of the formamidine nitrogen substituents on the activity of the catalyst and properties of the obtained polymers was observed. Further, a plausible mechanism for the polymerization of propylene is presented derived from a combination of ESR-C60 and MALDI-TOF trapping experiments which shed light on the nature of the active catalytic species.
| Original language | English |
|---|---|
| Pages (from-to) | 3119-3136 |
| Number of pages | 18 |
| Journal | Organometallics |
| Volume | 33 |
| Issue number | 12 |
| DOIs | |
| State | Published - 23 Jun 2014 |
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
Fingerprint
Dive into the research topics of 'Asymmetric bis(formamidinate) group 4 complexes: Synthesis, structure and their reactivity in the polymerization of α-olefins.'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver