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  2. Zylon - Wikipedia

    en.wikipedia.org/wiki/Zylon

    Zylon (IUPAC name: poly(p-phenylene-2,6-benzobisoxazole)) is a trademarked name for a range of thermoset liquid-crystalline polyoxazole. This synthetic polymer material was invented and developed by SRI International in the 1980s and manufactured by Toyobo. [2] In generic usage, the fiber is referred to as PBO. [3]

  3. Poly(p-phenylene) - Wikipedia

    en.wikipedia.org/wiki/Poly(p-phenylene)

    Poly(p-phenylene) (PPP) is made of repeating p-phenylene units, which act as the precursor to a conducting polymer of the rigid-rod polymer family. The synthesis of PPP has proven challenging, but has been accomplished through excess polycondensation with the Suzuki coupling method.

  4. Poly (2,6-diphenylphenylene oxide) - Wikipedia

    en.wikipedia.org/wiki/Poly(2,6-diphenylphenylene...

    Poly(2,6-diphenylphenylene oxide) reacts with oxidising agents such as chlorine, ozone, nitrogen oxides and sulfur oxides forming acetophenone, benzaldehyde and phenol. Therefore, control of blanks is essential and storage time of samples on poly(2,6-diphenylphenylene oxide) is less than a month.

  5. Poly(p-phenylene oxide) - Wikipedia

    en.wikipedia.org/wiki/Poly(p-phenylene_oxide)

    Poly(p-phenylene oxide) (PPO), poly(p-phenylene ether) (PPE), poly(oxy-2,6-dimethyl-1,4-phenylene), often referred to simply as polyphenylene oxide, is a high-temperature thermoplastic with the general formula (C 8 H 8 O) n. It is rarely used in its pure form due to difficulties in processing.

  6. Category:Phenylene compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Phenylene_compounds

    4-Hydroxyphenyl compounds (1 C, 153 P) I. 2-Iodophenyl compounds (6 P) ... Cyclobis(paraquat-p-phenylene) D. Dactolisib; Diethynylbenzene dianion; 1,3 ...

  7. Polyphenyl ether - Wikipedia

    en.wikipedia.org/wiki/Polyphenyl_ether

    With respect to volatilities, p-derivatives have the lowest volatilities, and the o-derivatives have the highest volatilities. The opposite is true for flash points and fire points. Spontaneous ignition temperatures of polyphenyl ethers lie between 550 and 595 °C (1,022 and 1,103 °F), alkyl substitution reduces this value by ~50 °C (122 °F).

  8. Phenylene group - Wikipedia

    en.wikipedia.org/wiki/Phenylene_group

    In organic chemistry, the phenylene group (−C 6 H 4 −) is based on a di-substituted benzene ring . For example, poly(p-phenylene) is a polymer built up from para-phenylene repeating units. [1] The phenylene group has three structural isomers, based on which hydrogens are substituted: para-phenylene, meta-phenylene, and ortho-phenylene.

  9. Poly(p-phenylene vinylene) - Wikipedia

    en.wikipedia.org/wiki/Poly(p-phenylene_vinylene)

    Poly(p-phenylene vinylene) (PPV, or polyphenylene vinylene) is a conducting polymer of the rigid-rod polymer family. PPV is the only polymer of this type that can be processed into a highly ordered crystalline thin film. PPV and its derivatives are electrically conducting upon doping.