文献类型：期刊文献

英文题名：Magnesium complexes containing biphenyl-based tridentate imino-phenolate ligands for ring-opening polymerization of rac-lactide and α-methyltrimethylene carbonate

作者：Yi, Wei;Ma, Haiyan[1]

机构：[1]E China Univ Sci & Technol, Shanghai Key Lab Funct Mat Chem, Shanghai 200237, Peoples R China; E China Univ Sci & Technol, Lab Organometall Chem, Shanghai 200237, Peoples R China

年份：2014

卷号：43

期号：13

起止页码：5200

外文期刊名：DALTON TRANSACTIONS

收录：;EI(收录号：20141217472283);WOS:【SCI-EXPANDED(收录号:WOS:000332475300033)】；

基金：This work was subsidized by the National Natural Science Foundation of China (NNSFC, 20604009, 21074032), the Program for New Century Excellent Talents in University (for H. Ma, NCET-06-0413) and the Fundamental Research Funds for the Central Universities (WD1113011, WK1214048). All the financial supports are gratefully acknowledged. H. Ma also acknowledges the very kind donation of a Braun glove-box by AvH Foundation.

语种：英文

外文关键词：Ligands - Oxygen - Nuclear magnetic resonance spectroscopy - Magnesium compounds - Catalyst activity

摘要：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).