A New Class of Conjugated Ionic Polyacetylene. Cyclopolymerization of Dihexyldipropargylammonium Salts by Metathesis Catalysts

Authors
Kang, K.-L.Kim, S.-H.Cho, H.-N.Choi, K.-Y.Choi, S.-K.
Issue Date
1993-01
Citation
Macromolecules, v.26, no.17, pp.4539 - 4543
Abstract
A new class of substituted ionic polyacetylene was synthesized by metathesis polymerization with transition-metal catalysts. The monomers used were dihexyldipropargylammonium salts having bromide and tosylate as counteranions. It was found that MoCl5-based catalyst systems were very effective for the cyclopolymerization of the present ionic monomers. The resulting dark-red polymers exhibited good solubility in polar organic solvents such as methanol, DMSO, DMF, THF, CHCl3, etc., indicative of their ionic nature. Structure of the polymers was confirmed by IR, UV-visible, and 1H and 13C NMR spectroscopy. When doped with an acceptor such as iodine, the polymers exhibited a substantial increase in electrical conductivity (10?3 S/cm) compared to the undoped state (10?9 S/cm). ? 1993, American Chemical Society. All rights reserved.
Keywords
Ammonium compounds; Catalysis; Doping (additives); Electric conductivity; Polymerization; Spectroscopic analysis; Cyclopolymerization; Dihexyldipropargylammonium salts; Metathesis catalysts; Polar organic solvents; Polyacetylenes; Ammonium compounds; Catalysis; Doping (additives); Electric conductivity; Polymerization; Spectroscopic analysis; Cyclopolymerization; Dihexyldipropargylammonium salts; Metathesis catalysts; Polar organic solvents; Polyacetylenes; conjugated; ionic polyacetylene; cyclopolymerization; dihexyldipropargyl ammonium; metathesis catalysts.
ISSN
0024-9297
URI
https://pubs.kist.re.kr/handle/201004/146318
DOI
10.1021/ma00069a019
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KIST Article > Others
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