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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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📜 SIMILAR VOLUMES


Polymerization of lactides and lactones.
✍ X. M. Deng; M. L. Yuan; C. D. Xiong; X. H. Li 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 144 KB 👁 1 views

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

Polymerization of lactides and lactones.
✍ Xianmo Deng; Minlong Yuan; Chengdong Xiong; Xiaohong Li 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 153 KB 👁 1 views

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