The Diels‐Alder reaction of biscyclopentadieneones with diacetylenes produces colorless, soluble, phenylated polyphenylenes of high molecular weight (M̄ n ≃ 40,000) in nearly quantitative conversions. The polymers are noncrystalline, form clear films, and are stable in air to 550°C. Under nitrogen, the polymers lost approximately half the phenyl groups attached to the phenylene main chain to give brown‐black insoluble polyphenylenes of very low crystallinity.
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Mukamal et al. (1967) studied this question.
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