Abstract
Phenylene–salalens—sequential tetradentate dianionic {ONNO}-type ligands that include an ortho-phenylene group bridging between an imine and amine internal donors bound to phenol arms with a broad variety of substitution patterns are described. Zirconium and hafnium complexes of the type [{ONNO}M(O-tBu)2] were formed as single diastereomers, which, according to crystallographic structures, featured the fac(around the amine)-mer(around the imine) wrapping mode. The reactivity and stereoselectivity in rac-lactide (rac-LA) polymerizations were found to depend on the substitution pattern: complexes featuring small groups on the imine-side phenol and bulky groups on the amine-side phenol exhibited the favorable combination of high activity and high isoselectivity (Pm≤0.91). Isotactic stereoblock copolymers of high molecular weights were prepared. The polymers crystallized in the stereocomplex phase according to thermal (differential scanning calorimetry) and crystallographic analysis.
| Original language | English |
|---|---|
| Pages (from-to) | 11540-11548 |
| Number of pages | 9 |
| Journal | Chemistry - A European Journal |
| Volume | 23 |
| Issue number | 48 |
| DOIs | |
| State | Published - 25 Aug 2017 |
Keywords
- hafnium
- isotacticity
- lactide
- poly(lactic acid)
- zirconium
ASJC Scopus subject areas
- Catalysis
- Organic Chemistry
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