Magnesium complexes containing biphenyl-based tridentate imino-phenolate ligands for ring-opening polymerization of rac-lactide and alpha-methyltrimethylene carbonate

作者：Yi, Wei; Ma, Haiyan^*

来源：Dalton Transactions, 2014, 43(13): 5200-5210.

DOI：10.1039/c3dt53513d

• EARTH-METAL-COMPLEXES
• ZINC-COMPLEXES
• TRIMETHYLENE CARBONATE
• EPSILON-CAPROLACTONE
• CYCLIC ESTERS
• STRUCTURAL-CHARACTERIZATION
• COORDINATION CHEMISTRY
• ALUMINUM COMPLEXES
• CATALYTIC-ACTIVITY
• IMMORTAL ROP

A series of racemic 2-[(2'-(dimethylamino)biphenyl-2-ylimino) methyl]-4-R2-6-R1-phenols ((LH)-H-1-(LH)-H-4) were reacted with {Mg[N(SiMe3)(2)](2)}(2) to provide four heteroleptic magnesium complexes (L1-4)MgN-(SiMe3)(2).(THF)(n) (1, R-1 = Bu-t, R-2 = Me, n = 1; 2, R-1 = R-2 = CMe2Ph, n = 0; 3, R-1 = CPh3, R-2 = tBu, n = 1; 4, R-1 = Br, R-2 = tBu, n = 0), which have been fully characterized. X-ray structural determination shows that complex 1 possesses a monomeric structure, but complex 4 is dimeric with C2-symmetry where the two metal centers are bridged by two phenolate oxygen atoms of the ligands. The coordination geometry around the magnesium center in these complexes can be best described as a distorted tetrahedral geometry. The heteroleptic complexes 1-4 efficiently initiate the ring-opening polymerization of rac-lactide and alpha-methyltrimethylene carbonate (alpha-MeTMC) and the polymerizations are better controlled in the presence of 2-propanol. In general, the introduction of a bulky ortho-substituent on the phenoxy unit results in increases of both the catalytic activity and the stereo-or regioselectivity of the corresponding magnesium complex. Microstructure analyses of the resulting PLAs revealed that Pr values range from 0.46 to 0.81, depending on the catalyst and the polymerization conditions. For racemic alpha-MeTMC, detailed analyses using 1H and 13C NMR spectroscopy indicated the preferential ring-opening of alpha-MeTMC at the most hindered oxygen-acyl bond (X-reg = 0.65-0.86).

• 出版日期2014
• 单位华东理工大学