1997
DOI: 10.1016/s0376-7388(96)00332-8
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Modeling the degradation kinetics of poly(2-hexyne) membranes via gel permeation chromatography

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Cited by 4 publications
(1 citation statement)
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“…The predominant driving force should be ascribed to the unique properties of substituted polyacetylenes, such as liquid crystallinity, photoluminescence, gas and liquid permeability, and chirality and helicity 4, 5. Despite the great progress in this field, the stability of the synthesized substituted polyacetylenes still seems to be a tough problem, mainly because of the sensitivity of the double bonds in the polymer backbones to oxidation;6, 7 for cis‐rich polyacetylenes, spontaneous cis–trans conformational transformation may be another reason 8, 9. Therefore, some studies have been devoted to the degradation behavior of the involved polymers.…”
Section: Introductionmentioning
confidence: 99%
“…The predominant driving force should be ascribed to the unique properties of substituted polyacetylenes, such as liquid crystallinity, photoluminescence, gas and liquid permeability, and chirality and helicity 4, 5. Despite the great progress in this field, the stability of the synthesized substituted polyacetylenes still seems to be a tough problem, mainly because of the sensitivity of the double bonds in the polymer backbones to oxidation;6, 7 for cis‐rich polyacetylenes, spontaneous cis–trans conformational transformation may be another reason 8, 9. Therefore, some studies have been devoted to the degradation behavior of the involved polymers.…”
Section: Introductionmentioning
confidence: 99%