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| Content Provider | Springer Nature Link |
|---|---|
| Author | Nie, Kun Feng, Tao Song, FengKui Zhang, Yong Sun, HongMei Yuan, Dan Yao, YingMing Shen, Qi |
| Copyright Year | 2014 |
| Abstract | A series of neutral bimetallic lanthanide aryloxides p-C$_{6}$H$_{4}$[OLnL(THF)$_{ n }$]$_{2}$ [Ln = Y (1), Yb (2), Sm (3) (n = 1) and La (4) (n = 2), L = Me$_{2}$NCH$_{2}$CH$_{2}$N{CH$_{2}$-(2-O-C$_{6}$H$_{2}$-$^{ t }$Bu$_{2}$-3,5)}$_{2}$] and alkoxides p-C$_{6}$H$_{4}$CH$_{2}$[OLnL(THF)]$_{2}$ [Ln = Y (5), Yb (6)] supported by an amine-bridged bis(phenolate) ligand have been synthesized through one-pot reactions of Ln(C$_{5}$H$_{5}$)$_{3}$(THF), LH$_{2}$ with p-benzenediol and 1,4-benzenedimethanol, respectively. All complexes have been fully characterized by elemental analyses, single-crystal X-ray diffraction analysis, and IR and multi-nuclear NMR spectroscopy (in the cases of 1, 4 and 5). Study of their catalytic behavior revealed that, in general, all complexes are efficient initiators for the polymerization of rac-lactide (LA) and rac-β-butyrolactone (BBL), except for 3 and 4 in the case of BBL. The influence imposed by lanthanides of different ionic radii and initiating groups of different structures on the activity, controllability, and stereoselectivity of polymerization were systematically studied and compared. Highly heterotactic PLA (P $_{r}$ up to 0.99) and syndiotactic PHB (P $_{r}$ ≈ 0.81) with high molecular weight and narrow polydispersity formed and were automatically capped with hydroxyl functionality at both ends. |
| Starting Page | 1106 |
| Ending Page | 1116 |
| Page Count | 11 |
| File Format | |
| ISSN | 16747291 |
| Journal | Science in China Series B: Chemistry |
| Volume Number | 57 |
| Issue Number | 8 |
| e-ISSN | 18691870 |
| Language | English |
| Publisher | Science China Press |
| Publisher Date | 2014-06-27 |
| Publisher Place | Heidelberg |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | amine-bridged bis(phenolate) ligand bimetallic lanthanide aryloxides and alkoxides ring-opening polymerization stereoselectivity Chemistry/Food Science |
| Content Type | Text |
| Resource Type | Article |
| Subject | Chemistry |
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