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A facile and rapid synthesis of unsubstituted polythiophene with high electrical conductivity using binary organic solvents

โœ Scribed by Sang Soo Jeon; Soo Jung Yang; Kee-Jung Lee; Seung Soon Im


Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
1013 KB
Volume
51
Category
Article
ISSN
0032-3861

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โœฆ Synopsis


Dichloromethane and acetonitrile containing thiophene and oxidant, respectively, were adopted as a binary organic solvent for oxidative synthesis of unsubstituted polythiophene (UPTh) under various conditions, i.e., oxidant/monomer molar ratio, polymerization temperature, and reaction time. We also investigated the effects of polymerization medium on the chemical and physical properties of the UPTh. The electrical conductivities of the UPThs polymerized in only acetonitrile or aqueous medium were 1.0 ร‚ 10 ร€4 Scm ร€1 and zero, respectively. However, the UPTh obtained in binary organic solvent system exhibited the highest electrical conductivity of 20.1 Scm ร€1 without post-doping process under an oxidant/monomer molar ratio of 5:1 and a reaction time of 0.2 h at 0 C. Furthermore, it showed an enhanced crystalline structure, thermal stability, and longer p-conjugation length than those in acetonitrile or aqueous medium. We also found that the presence of water as a polymerization medium inevitably gave rise to the incorporation of hydroxyl and carbonyl groups into the UPTh main chains by nucleophilic attack of water molecules. Therefore, these undesired structures broke the conjugated structures, resulting in UPTh with an electrically non-conducting property. The morphology of UPTh prepared in binary organic solvent appeared to be an aggregate of nanoparticles (50e200 nm). The combination of organic solvents should provide another systematic approach to the facile and rapid synthesis of UPThs with high conductivity.


๐Ÿ“œ SIMILAR VOLUMES


Chemical synthesis at solid interfaces.
โœ J.F. Pilard; G. Marchand; J. Simonet ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 684 KB

Electrogenerated polythiophenes were evaluated as Merrifield-like resins for the anchoring of amine functions together with deprotection processes. Suitable linkers were terminated with a fully regenerable aromatic sulfonamide moiety. The S-N bond was cleaved to liberate the amine with high selectiv