期刊
DALTON TRANSACTIONS
卷 41, 期 13, 页码 3701-3713出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2dt11954d
关键词
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资金
- NSERC (Canada)
- Canada Foundation for Innovation
- Canada School of Energy and Environment
- GreenCentre Canada
The diastereomerically pure P-stereogenic bis(phosphinimine) ligands 4,6-(ArN=PMePh)(2)dbf [Ar = 4-isopropylphenyl (Pipp): rac-4, meso-4; Ar = 2,6-diisopropylphenyl (Dipp): rac-4a; dbf = dibenzofuran] were synthesised and complexed to zinc using a protonation-alkane elimination strategy. The cationic alkylzinc complexes thus obtained, RZn[4,6-(ArN=PMePh)(2)dbf][B(Ar')(4)] [Ar = Pipp, Ar' = C6H3(CF3)(2): rac-6 (R = Et), meso-6 (R = Et), rac-7 (R = Me) meso-7 (R = Me); Ar = Dipp: rac-6a (R = Et, Ar' = C6H3(CF3)(2)), rac-6b (R = Et, Ar' = C6F5)] were investigated for their competency as initiators for the ring-opening polymerisation of rac-lactide. The formation of polylactide was achieved under relatively mild conditions (40 degrees C, 2-4 h) and the microstructures of the resulting polymers exhibited a slight heterotactic bias [polymer tacticity (P-r) = 0.51-0.63].
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