Ring-opening polymerization of six-membered cyclic esters catalyzed by tetrahydroborate complexes of rare earth metals
✍ Scribed by Yuushou Nakayama; Kenta Sasaki; Naoki Watanabe; Zhengguo Cai; Takeshi Shiono
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 341 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0032-3861
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✦ Synopsis
Catalytic behavior of tetrahydroborate complexes of rare earth metals, Ln(BH 4 ) 3 (THF) x (1:
), for ring-opening polymerization (ROP) of six-membered cyclic esters, d-valerolactone (VL) and D,L-lactide (D,L-LA), was studied. The controlled polymerization of VL with 1-6 proceeded in THF at 60 C. The catalytic activities of these complexes for the ROP of VL were observed to be in order of the ionic radii of the metals:
The obtained polymers were demonstrated to be hydroxytelechelic by 1 H NMR and MALDI-TOF MS spectroscopy. The controlled ROP of D,L-LA also proceeded by these complexes. The activities of these complexes for the D,L-LA ROP were also in order of the ionic radii of the metals.
📜 SIMILAR VOLUMES
Lanthanide Schiff-base complexes with the formula [3,5-tBu 2 -2-(O)C 6 H 2 CH=NC 6 H 5 ] 3 Ln(THF) (Ln = Sc, Y, La, Nd, and Gd) were synthesized by the metathesis reaction of anhydrous LnCl 3 with a Schiff-base sodium salt in good yields (> 80%). The complex containing a neodymium center was charact
The polymerization of caprolactone ( 1-CL) was initiated by yttrium triisopropoxide {Y(OP i r ) 3 }, bimetallic isopropoxide of yttrium and aluminum {Y[Al(OP i s ) 4 ] 3 }, yttrium and tin(II) {Y[Sn(OP i r ) 3 ] 3 }, and tin(II) and yttrium {Sn[Y(OP i r ) 4 ] 2 }, respectively. The polymerization wa