Self-Assembled Bimetallic Aluminum-Salen Catalyst for the Cyclic Carbonates Synthesis

Bimetallic bis-urea functionalized salen-aluminum catalysts have been developed for cyclic carbonate synthesis from epoxides and CO2. The urea moiety provides a bimetallic scaffold through hydrogen bonding, which expedites the cyclic carbonate formation reaction under mild reaction conditions. The turnover frequency (TOF) of the bis-urea salen Al catalyst is three times higher than that of a μ-oxo-bridged catalyst, and 13 times higher than that of a monomeric salen aluminum catalyst. The bimetallic reaction pathway is suggested based on urea additive studies and kinetic studies. Additionally, the X-ray crystal structure of a bis-urea salen Ni complex supports the self-assembly of the bis-urea salen metal complex through hydrogen bonding.

Copolymerization of l-lactide and ε-caprolactone catalyzed by mono-and dinuclear salen aluminum complexes bearing bulky 6,6′-dimethylbipheyl-bridge: random and tapered copolymer

Mono- and dinuclear salen aluminum complexes bearing a racemic 6,6′-dimethyl-biphenyl bridge could efficiently catalyze the copolymerization of l-LA and ε-CL in the melt, producing practically random and tapered copolymers, respectively.

Aluminum methyl, alkoxide and α-alkoxy ester complexes supported by 6,6′-dimethylbiphenyl-bridged salen ligands: synthesis, characterization and catalysis for rac-lactide polymerization

A series of mono- and dinuclear salen aluminum complexes could efficiently catalyze the ROP of rac-LA, producing isotactic enriched and atactic PLA, respectively. In solution, the association/dissociation equilibrium of the carbonyl group was found in the model O-lactate complexes.

Bimetallic salen aluminum complexes: cooperation between reactive centers in the ring-opening polymerization of lactides and epoxides

In dinuclear aluminum complexes, opportunely designed to have proximal coordinative pockets, the communication between the two reactive centers allows enhanced catalytic performances.

Hemi-salen aluminum catalysts bearing N, N, O-tridentate type binaphthyl-Schiff-base ligands for the living ring-opening polymerisation of lactide

Hemi-salen aluminum complexes bearing tridentate N, N, O-type binaphthyl-Schiff-base ligands were synthesized and studied as catalysts for living polymerisation of lactide.

Ring-opening polymerization of lactide using chiral salen aluminum complexes as initiators: high productivity and stereoselectivity

Chiral salen aluminum complexes have been synthesized and investigated as initiators for l-lactide and rac-lactide polymerization.