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  2. Benzocyclooctatetraene - Wikipedia

    en.wikipedia.org/wiki/Benzocyclooctatetraene

    Benzocyclooctatetraene is a polycyclic hydrocarbon with chemical formula C 12 H 10, composed of fused a benzene ring and a cyclooctatetraene ring. Only the benzene ring is aromatic in this compound. Only the benzene ring is aromatic in this compound.

  3. Dibenzocyclooctatetraene - Wikipedia

    en.wikipedia.org/wiki/Dibenzocyclooctatetraene

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  4. Cyclooctatetraene - Wikipedia

    en.wikipedia.org/wiki/Cyclooctatetraene

    1,3,5,7-Cyclooctatetraene (COT) is an unsaturated derivative of cyclooctane, with the formula C 8 H 8. It is also known as [8] annulene . This polyunsaturated hydrocarbon is a colorless to light yellow flammable liquid at room temperature.

  5. Tris(cyclooctatetraene)triiron - Wikipedia

    en.wikipedia.org/wiki/Tris(cyclooctatetraene)triiron

    This suggests that the cyclooctatetraene ligands are highly fluxional and some degree of paramagnetism. [1] Fluxional Ring rotation in Fe 3 (COT) 3 depicted by DeKock et al. [13] COT is known to be a highly fluxional ligand in other compounds too, such compounds being deemed “ring-whizzers” (like the related (cyclooctatetraene)iron ...

  6. Alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene

    Alkylbenzene isomers can be differentiated by observing the position of alkyl substituents on the benzene ring using chemical ionization-proton exchange mass spectrometry. Conventional GC-MS yields limited results because the isomers have identical molecular weight and substituents.

  7. Alkyne trimerisation - Wikipedia

    en.wikipedia.org/wiki/Alkyne_trimerisation

    An alkyne trimerisation is a [2+2+2] cycloaddition reaction in which three alkyne units (C≡C) react to form a benzene ring. The reaction requires a metal catalyst.The process is of historic interest as well as being applicable to organic synthesis. [1]

  8. Template reaction - Wikipedia

    en.wikipedia.org/wiki/Template_reaction

    In the area of homogeneous catalysis, the cyclo-oligomerization of acetylene to cyclooctatetraene at a nickel(II) centre reflects the templating effect of the nickel, where it is supposed that four acetylene molecules occupy four sites around the metal and react simultaneously to give the product. This simplistic mechanistic hypotheses was ...

  9. Cyclodecapentaene - Wikipedia

    en.wikipedia.org/wiki/Cyclodecapentaene

    Computational chemistry suggests a tricyclic[10]annulene derivative with an annulated benzene ring and a full set of cyano substituents would be one of the most acidic compounds known, with a computed pK a in DMSO of −30.4 (compared to for instance −20 for magic acid).