Publication | Closed Access
Syntheses and reactions of ferrocene‐containing polymers. III. Cyclopolymerization of 1,1′‐divinylferrocene
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Citations
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References
1970
Year
EngineeringOrganic ChemistryChemistryPolymersMacromolecular EngineeringPolymer ProcessingPolymer ChemistrySynthetic MacromoleculeBf 3Polymer EngineeringPolymer AnalysisRadical PolymerBiomolecular EngineeringRadical PolymersPolymer SciencePolymer CharacterizationPolymerization KineticsPolymer ReactionPolymer Synthesis
Abstract 1,1′‐Divinylferrocene was polymerized with BF 3 OEt 2 and AIBN initiators. Polymers were separated into benzene‐soluble and benzene‐insoluble fractions, the latter probably being crosslinked. The polymers obtained with BF 3 OEt 2 were shown by infrared and NMR spectroscopy to contain both cyclized (70–80%) and uncyclized units, whereas the radical polymer consisted of more than 96% cyclized units. The benzene‐soluble fraction of the cationically obtained polymer softened at temperatures below 150°C, but the insoluble fraction decomposed at 240°C. The radical polymers were stable up to 250–280°C (dec).
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