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  2. Phenanthrene - Wikipedia

    en.wikipedia.org/wiki/Phenanthrene

    Phenanthrene is a polycyclic aromatic hydrocarbon (PAH) with formula C 14 H 10, consisting of three fused benzene rings. It is a colorless, crystal-like solid, but can also appear yellow. Phenanthrene is used to make dyes, plastics, pesticides, explosives, and drugs. It has also been used to make bile acids, cholesterol and steroids. [3]

  3. Atoms in molecules - Wikipedia

    en.wikipedia.org/wiki/Atoms_in_molecules

    [6] Furthermore, QTAIM had been used to identify a bond-path network of hydrogen bonds between glucosepane and nearby water molecules. [7] The hydrogen-hydrogen bond is not without its critics. According to one, the relative stability of phenanthrene compared to its isomers can be adequately explained by comparing resonance stabilizations. [8]

  4. Pyrene - Wikipedia

    en.wikipedia.org/wiki/Pyrene

    Pyrene is a polycyclic aromatic hydrocarbon (PAH) consisting of four fused benzene rings, resulting in a flat aromatic system. The chemical formula is C 16 H 10.This yellow-green solid is the smallest peri-fused PAH (one where the rings are fused through more than one face).

  5. Anthracene - Wikipedia

    en.wikipedia.org/wiki/Anthracene

    Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C 14 H 10, consisting of three fused benzene rings. It is a component of coal tar.Anthracene is used in the production of the red dye alizarin and other dyes, as a scintillator to detect high energy particles, as production of pharmaceutical drugs.

  6. Antiaromaticity - Wikipedia

    en.wikipedia.org/wiki/Antiaromaticity

    The analogous cyclic system appears to have even more resonance stabilized, as the negative charge can be delocalized across three carbons instead of two. However, the cyclopropenyl anion has 4 π electrons in a cyclic system and in fact has a substantially higher p K a than 1-propene because it is antiaromatic and thus destabilized. [ 3 ]

  7. Mesomeric effect - Wikipedia

    en.wikipedia.org/wiki/Mesomeric_effect

    In chemistry, the mesomeric effect (or resonance effect) is a property of substituents or functional groups in a chemical compound. It is defined as the polarity produced in the molecule by the interaction of two pi bonds or between a pi bond and lone pair of electrons present on an adjacent atom. [ 1 ]

  8. Phenanthrenequinone - Wikipedia

    en.wikipedia.org/wiki/Phenanthrenequinone

    It has been prepared by oxidation of phenanthrene with chromic acid. [3] It is used as an artificial mediator for electron acceptor/donor in Mo/W containing formate dehydrogenase reduction of carbon dioxide to formate and vice versa. It is a better electron acceptor than the natural nicotinamide adenine dinucleotide (NAD +).

  9. Category:Phenanthrenes - Wikipedia

    en.wikipedia.org/wiki/Category:Phenanthrenes

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