Improving the ring-opening polymerization ofε-caprolactone andl-lactide using stannous octanoate
✍ Scribed by Chen, Yen-Jen; Fang, Hsin-Jou; Hsu, Sodio C. N.; Jheng, Nai-Yuan; Chang, Hui-Chen; Ou, Siou-Wei; Peng, Wei-Te; Lai, Yi-Chun; Chen, Jia-Yun; Chen, Pao-Lin; Kao, Chien-Han; Zeng, Zhi-Xian; Chen, Jyun-Lin; Chen, Hsuan-Ying
- Book ID
- 115506139
- Publisher
- Springer
- Year
- 2012
- Tongue
- English
- Weight
- 349 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0170-0839
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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
Ring-opening polymerization of -caprolactone (CL) has been initiated with rare earth phenyl compounds in both bulk and solution. These rare earth phenyl initiators can give polycaprolactone (PCL) with high yield and high molecular weight. The polymerization mechanism is through a coordination-deprot
## Ring-opening polymerization of &-caprolactone in the presence of dicarboxylic acids Unfortunately, the second author's name has been misprinted in the above publication.