Related Experiment Video
Updated: Jan 20, 2026
Cationic Chain-Growth Polymerization: Mechanism
Effects of Ether on the Cationic Polymerization of Isobutylene Catalyzed by AlCl3
Shan Zhu1, Kai Wang1, Yangcheng Lu1
1State Key Laboratory of Chemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.
Abstract:
In this work, we prepared different initiator solutions containing ether and AlCl3 by changing the addition sequence of ingredients, studied the interactions between ether and AlCl3 from the evolution of the Fourier transform infrared (FTIR) spectra by comparison, and investigated the catalytic performances of AlCl3 affected by ether for isobutylene polymerization. We observed that different preparation methods of initiator solutions could lead to two kinds of interactions between ether and H2O/AlCl3 in hexane. The strong interaction could stabilize carbenium ions and seriously decrease the catalytic performance, whereas the weak interaction could promote isomerization and proton elimination. Moreover, we found that the preparation method of initiator solutions was not a critical factor in CH2Cl2. Finally, a universal mechanism based on the AlCl3-involved interactions in different solvents was proposed to understand the effects of ether on the cationic polymerization catalyzed by AlCl3 thoroughly.
Related Concept Videos
Cationic Chain-Growth Polymerization: Mechanism
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Structure and Nomenclature of Ethers
Ethers are organic compounds with an ether functional group which is characterized by an oxygen atom connected to two — identical or different — alkyl, aryl, or vinyl groups. The C–O–C linkage in dimethyl ether — the simplest ether — has an approximately tetrahedral bond angle of 110.3 degrees. The oxygen atom is sp3- hybridized, with the C–O distance being about 140 pm.
Classification of Ethers
Based on their attached substituent...
Crown Ethers
Polymerization
Polymers are made from macromolecules, which are composed of repeating units (the so called monomeric units). In our modern world, polymers play an important role. One of the first important polymers was nylon, which is a polyamide. It found widespread application in tooth brushes and...
Physical Properties of Ethers
An ether molecule has a net dipole moment due to the polarity of C–O bonds. Subsequently, boiling points of ethers are lower than those of alcohols of comparable molecular weight and slightly higher than those of hydrocarbons of comparable molecular weight (Table 1).
Ethers can act as hydrogen bond acceptors, making them more water-soluble than hydrocarbons, but since ethers cannot act as hydrogen bond donors, they are much less soluble in water than alcohols. Ethers are considered...
