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  2. Cyclooctatetraene - Wikipedia

    en.wikipedia.org/wiki/Cyclooctatetraene

    This polyunsaturated hydrocarbon is a colorless to light yellow flammable liquid at room temperature. Because of its stoichiometric relationship to benzene, COT has been the subject of much research and some controversy. Unlike benzene, C 6 H 6, cyclooctatetraene, C 8 H 8, is not aromatic, although its dianion, C 8 H 2− 8 (cyclooctatetraenide ...

  3. Antiaromaticity - Wikipedia

    en.wikipedia.org/wiki/Antiaromaticity

    An antiaromatic compound may demonstrate its antiaromaticity both kinetically and thermodynamically. As will be discussed later, antiaromatic compounds experience exceptionally high chemical reactivity. Being highly reactive is not "indicative" of an antiaromatic compound, but merely suggests that the compound could be antiaromatic.

  4. Cyclooctadecanonaene - Wikipedia

    en.wikipedia.org/wiki/Cyclooctadecanonaene

    The 1 H NMR of this compound exhibits hallmarks of a system with an aromatic ring current, with the 12H signal of exterior hydrogens at 9.25 ppm, while 6H signal of interior hydrogens resonates at a remarkable −2.9 ppm in THF-d 8 at −60 °C. On the other hand, a single signal at 5.45 ppm (weighted average of two individual signals) is ...

  5. Cyclooctatetraenide anion - Wikipedia

    en.wikipedia.org/wiki/Cyclooctatetraenide_anion

    In chemistry, the cyclooctatetraenide anion or cyclooctatetraenide, more precisely cyclooctatetraenediide, is an aromatic species with a formula of [C 8 H 8] 2− and abbreviated as COT 2−. It is the dianion of cyclooctatetraene. Salts of the cyclooctatetraenide anion can be stable, e.g., Dipotassium cyclooctatetraenide or disodium ...

  6. Photophosphorylation - Wikipedia

    en.wikipedia.org/wiki/Photophosphorylation

    This word is taken from two Greek words, photos, which means light, and synthesis, which in chemistry means making a substance by combining simpler substances. So, in the presence of light, synthesis of food is called 'photosynthesis'. Noncyclic photophosphorylation through light-dependent reactions of photosynthesis at the thylakoid membrane.

  7. Organic photochemistry - Wikipedia

    en.wikipedia.org/wiki/Organic_photochemistry

    However, the intensity of light drops rapidly with the distance to the light source due to adsorption by the reactants. [12] The influence of the radiation on the reaction rate can often be represented by a power law based on the quantum flow density, i.e. the mole light quantum (previously measured in the unit einstein) per area and time. One ...

  8. Homoaromaticity - Wikipedia

    en.wikipedia.org/wiki/Homoaromaticity

    Homoaromaticity, in organic chemistry, refers to a special case of aromaticity in which conjugation is interrupted by a single sp 3 hybridized carbon atom. Although this sp 3 center disrupts the continuous overlap of p-orbitals, traditionally thought to be a requirement for aromaticity, considerable thermodynamic stability and many of the spectroscopic, magnetic, and chemical properties ...

  9. Light-dependent reactions - Wikipedia

    en.wikipedia.org/wiki/Light-dependent_reactions

    Light-dependent reactions of photosynthesis at the thylakoid membrane. Light-dependent reactions are certain photochemical reactions involved in photosynthesis, the main process by which plants acquire energy. There are two light dependent reactions: the first occurs at photosystem II (PSII) and the second occurs at photosystem I (PSI).