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

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

    Poly(2,6-diphenyl-p-phenylene oxide) (PPPO) is a porous polymer resin based on oxidative polymerisation of 2,6-diphenylphenol. It is mostly known by its trademark Tenax. It is mostly known by its trademark Tenax.

  3. Polyphenyl ether - Wikipedia

    en.wikipedia.org/wiki/Polyphenyl_ether

    The simplest member of the phenyl ether family is diphenyl ether (DPE), also called diphenyl oxide, the structure of which is provided in Figure 4. Low molecular weight polyphenyl ethers and thioethers are used in a variety of applications, and include high-vacuum devices, optics, electronics, and in high-temperature and radiation-resistant ...

  4. p-Phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/P-Phenylenediamine

    p-Phenylenediamine (PPD) is an organic compound with the formula C 6 H 4 (NH 2) 2. This derivative of aniline is a white solid, but samples can darken due to air oxidation. [1] It is mainly used as a component of engineering polymers and composites like kevlar. It is also an ingredient in hair dyes and is occasionally used as a substitute for ...

  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. Immediately dangerous to life or health - Wikipedia

    en.wikipedia.org/wiki/Immediately_dangerous_to...

    The term immediately dangerous to life or health (IDLH) is defined by the US National Institute for Occupational Safety and Health (NIOSH) as exposure to airborne contaminants that is "likely to cause death or immediate or delayed permanent adverse health effects or prevent escape from such an environment." Examples include smoke or other ...

  7. Diphenyl ether - Wikipedia

    en.wikipedia.org/wiki/Diphenyl_ether

    Diphenyl ether was discovered by Heinrich Limpricht and Karl List in 1855, when they reproduced Carl Ettling's destructive distillation of copper benzoate and separated it from the low-melting oily distillate components ignored by previous researchers. They named the compound phenyl oxide (German: Phenyloxyd) and studied some of its derivatives ...

  8. Phenyl group - Wikipedia

    en.wikipedia.org/wiki/Phenyl_group

    It is often said the resonance stability of phenol makes it a stronger acid than that of aliphatic alcohols such as ethanol (pK a = 10 vs. 16–18). However, a significant contribution is the greater electronegativity of the sp 2 alpha carbon in phenol compared to the sp 3 alpha carbon in aliphatic alcohols.

  9. DPEphos - Wikipedia

    en.wikipedia.org/wiki/DPEphos

    Bis[(2-diphenylphosphino)phenyl] ether, also known as DPEphos, is a wide bite angle diphosphine ligand used in inorganic and organometallic chemistry.The name DPEphos is derived from diphenyl ether (DPE) which makes up the ligand's backbone.