𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Ring opening polymerization of 2-ethyl-2-oxazoline

✍ Scribed by B. L. Rivas; S. I. Ananías


Publisher
Springer
Year
1987
Tongue
English
Weight
190 KB
Volume
18
Category
Article
ISSN
0170-0839

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Acetyl Halide Initiator Screening for th
✍ Renzo M. Paulus; C. Remzi Becer; Richard Hoogenboom; Ulrich S. Schubert 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 316 KB

## Abstract Kinetic investigations on the cationic ring‐opening polymerization of 2‐ethyl‐2‐oxazoline were conducted using acetyl chloride, acetyl bromide, and acetyl iodide as initiators. Various polymerization temperatures ranging from 80 to 220 °C were applied under microwave irradiation. The re

Scale-up of Microwave-Assisted Polymeriz
✍ Richard Hoogenboom; Renzo M. Paulus; Åke Pilotti; Ulrich S. Schubert 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 203 KB

## Abstract **Summary:** The use of microwave heating in polymer science is a rapidly growing field of research leading to faster and cleaner polymerization procedures. However, the majority of the investigations are performed at small scales (≈1 mL), which is far away from potential commercial app

Scale-Up of Microwave-Assisted Polymeriz
✍ Renzo M. Paulus; Tina Erdmenger; C. Remzi Becer; Richard Hoogenboom; Ulrich S. S 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 282 KB

## Abstract Microwave‐assisted polymerizations is a growing field of interest because the use of microwave irradiation instead of thermal heating was demonstrated to result in faster, cleaner, and higher yielding reactions. To overcome the one‐at‐a‐time nature of preparing polymerizations in single

2-Perbromomethyl-2-oxazoline: a novel tr
✍ Tushar Kanti Bera; Swaminathan Sivaram 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 348 KB

Polymerization of 2-methyl-2-oxazoline was carried out using a trifunctional initiator, 2-perbromomethyl-2-oxazoline. The degree of polymerization (DP) of the resulting polymer was very close to the feed mole ratio of the monomer to initiator. The number-average molecular weight a, increased linearl