The electrochemical polymerization of cyclohexylvinylether has been investigated in 1,2dichloroethane solution using various tetrabutylammonium salts, viz. tri-iodide, iodide, tetrafluoroborate and perchlorate, as supporting electrolytes in reaction ceils with two platinum electrodes. The first two
Electro-initiated cationic polymerizations—III: Polymerization of anethole in the presence of tetra-alkylammonium perchlorates
✍ Scribed by P. Cerrai; G. Guerra; M. Tricoli
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 330 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0014-3057
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✦ Synopsis
The electro-polymerization of trans-anethole in 1,2-dichloroethane solution with tetraethyland tetrabutylammonium perchlorates as supporting electrolytes was studied: the dependences of pobmerization rates and molecular weight on some experimental parameters were determined.
To investigate the electrolytic formation of initiating species, the anolyte from the electrolysis of the supporting salt in the absence of monomer was examined; the presence of electrolytically produced perchloric acid was ascertained unequivocally. However, owing to the polarographic behaviour of anethole, which shows an oxidation wave at lower anodic potential than the solvent salt couple, it was not possible to postulate any reaction mechanism based on a single initiation reaction.
The fact that the polymerizations were carried out without control of the anodic potential and some of the kinetic results indicate that two parallel initiation reactions (direct monomer oxidation and 9rotonation by electrolytically formed perchloric acid) can occur.
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