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  2. Triphenylmethanol - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethanol

    Triphenylmethanol (also known as triphenylcarbinol and TrOH) is an organic compound. It is a white crystalline solid that is insoluble in water and petroleum ether, but well soluble in ethanol, diethyl ether, and benzene. In strongly acidic solutions, it produces an intensely yellow color, due to the formation of a stable "trityl" carbocation ...

  3. (E)-Stilbene - Wikipedia

    en.wikipedia.org/wiki/(E)-Stilbene

    (E)-Stilbene, commonly known as trans-stilbene, is an organic compound represented by the condensed structural formula C 6 H 5 CH=CHC 6 H 5.Classified as a diarylethene, it features a central ethylene moiety with one phenyl group substituent on each end of the carbon–carbon double bond.

  4. Triphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethane

    Triphenylmethane or triphenyl methane (sometimes also known as Tritan), is the hydrocarbon with the formula (C 6 H 5) 3 CH. This colorless solid is soluble in nonpolar organic solvents and not in water.

  5. Triphenylene - Wikipedia

    en.wikipedia.org/wiki/Triphenylene

    white Density: 1.308 g/cm 3 [2] Melting point: 198 °C; 388 °F; 471 K ... triphenylene has attracted attention as the core of discotic mesogen in liquid crystalline ...

  6. Triphenylmethyl chloride - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethyl_chloride

    Triphenylmethyl chloride is commercially available. It may be prepared by the reaction of triphenylmethanol with acetyl chloride, or by the Friedel–Crafts alkylation of benzene with carbon tetrachloride to give the trityl chloride-aluminium chloride adduct, which is then hydrolyzed. [3]

  7. Triphenylmethyl hexafluorophosphate - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethyl_hexafluoro...

    Triphenylmethyl hexafluorophosphate (also triphenylcarbenium hexafluorophosphate, trityl hexafluorophosphate, or tritylium hexafluorophosphate) is an organic salt with the formula [(C 6 H 5) 3 C] + [PF 6] −, consisting of the triphenylcarbenium cation [(C 6 H 5) 3 C] + and the hexafluorophosphate anion [PF 6] −.

  8. Triphenylmethyl radical - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethyl_radical

    The radical was discovered by Moses Gomberg in 1900 at the University of Michigan. [9] [10] [11] He tried to prepare hexaphenylethane from triphenylmethyl chloride and zinc in benzene in a Wurtz reaction and found that the product, based on its behaviour towards iodine and oxygen, was far more reactive than anticipated.

  9. Triphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine

    Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C 6 H 5) 3 and often abbreviated to P Ph 3 or Ph 3 P. It is versatile compound that is widely used as a reagent in organic synthesis and as a ligand for transition metal complexes, including ones that serve as catalysts in organometallic chemistry.