Phosphoraneiminato complexes of transition metals containing the NPR 3 Γ group are known in many coordinationchemical variations [1] as a result of varying bonding modes. In complexes with metal ions in low oxidation states (i, ii) the NPR 3 Γ group acts as m 3 -N bridging ligand, in medium oxidati
Reactivity of Sm(II) compounds as ring-opening polymerization initiators for lactones
β Scribed by Seema Agarwal; Natalia E. Brandukova-Szmikowski; Andreas Greiner
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 64 KB
- Volume
- 20
- Category
- Article
- ISSN
- 1022-1336
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β¦ Synopsis
Successful room temperature ring-opening polymerization (ROP) of e-caprolactone and d-valerolactone has been carried out using SmX 2 (X = I, Br, and cyclopentadienyl (Cp)) catalysts. SmI 2 in the presence of metallic Sm was found to have enhanced reactivity as room temperature ROP initiator for lactones as compared to pure SmI 2 . SmBr 2 and SmCp 2 showed increased reactivity compared with the Sm/SmI 2 system due to their higher reductive power. The catalyst concentration and time of polymerization showed a marked effect on number-average molecular weight (M n ). There was a decrease in M n on increasing reaction time and decreasing catalyst concentration. The initiation mechanism is discussed based on end group analysis of low molecular weight polymers.
π SIMILAR VOLUMES
Ring-opening polymerization of lactone and lactide have been initiated with rare earth organoacid compounds, such as lanthanum acetate in bulk. The polymerization mechanism is in agreement with the "nonionic-coordination-insertion" mechanism, which involves the selective cleavage of the acyl-oxygen
Lithium chloride was found to be an effective and biocompatible catalyst for the ring-opening polymerization of lactide in the presence of hydroxyl-containing compounds. Ethylene glycol (EG) and methyl β£-D-glucopyranoside (MGlc) were used as multifunctional initiators. The polymerization was carried