Synthesis and characterization of poly(1,8-diethynylnaphthalene)

Authors
Cho, H.N.Kim, S.H.Kim, C.Y.
Issue Date
1995-01
Publisher
Springer-Verlag
Citation
Polymer Bulletin, v.34, no.2, pp.125 - 132
Abstract
The cyclopolymerization of 1,8-diethynylnaphthalene(DEN) and its copolymerization with diethyl dipropargylmalonate(DEDPM) were carried out by various transition metal catalysts. MoCl5-based catalyst was found to be very effective and gave almost a quantitative polymer yield. The resulting dark-brown homopolymer(PDEN) was partially soluble in chloroform, tetrahydrofuran, and dimethyl sulfoxide, whereas copolymer (1:1) with number avaerage molecular weight {Mathematical expression} of 2.1x104 by GPC showed good solubility in those solvents. The structure of the polymers was analysed by IR, NMR, and UV-VIS spectroscopies. From the spectral and solubility data, it is proposed that cyclized products with the conjugated system are formed. Room temperature conductivities of the I2-doped homo and copolymer were found to be about 7.5x10-3 and 5.1x10-3 S/cm, respectively. ? 1995 Springer-Verlag.
Keywords
Catalysts; Copolymerization; Gel permeation chromatography; Infrared spectroscopy; Molecular weight; Nuclear magnetic resonance spectroscopy; Solubility; Structure (composition); Synthesis (chemical); Thermal conductivity; Ultraviolet spectroscopy; Conjugated systems; Cyclopolymerization; Diethyl dipropargy malmonate; Diethynylnaphthalene; Quantitative polymer yield; Transition metal catalysts; Organic polymers; Catalysts; Copolymerization; Gel permeation chromatography; Infrared spectroscopy; Molecular weight; Nuclear magnetic resonance spectroscopy; Solubility; Structure (composition); Synthesis (chemical); Thermal conductivity; Ultraviolet spectroscopy; Conjugated systems; Cyclopolymerization; Diethyl dipropargy malmonate; Diethynylnaphthalene; Quantitative polymer yield; Transition metal catalysts; Organic polymers; synthesis
ISSN
0170-0839
URI
https://pubs.kist.re.kr/handle/201004/145413
DOI
10.1007/BF00316386
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KIST Article > Others
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