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  2. Cation–π interaction - Wikipedia

    en.wikipedia.org/wiki/Cation–π_interaction

    Benzene, the model π system, has no permanent dipole moment, as the contributions of the weakly polar carbon–hydrogen bonds cancel due to molecular symmetry.However, the electron-rich π system above and below the benzene ring hosts a partial negative charge.

  3. Hückel method - Wikipedia

    en.wikipedia.org/wiki/Hückel_method

    [1] [2] [3] It provides the theoretical basis for Hückel's rule that cyclic, planar molecules or ions with + π-electrons are aromatic. It was later extended to conjugated molecules such as pyridine, pyrrole and furan that contain atoms other than carbon and hydrogen (heteroatoms). [4]

  4. Charge-transfer complex - Wikipedia

    en.wikipedia.org/wiki/Charge-transfer_complex

    In chemistry, charge-transfer (CT) complex, or electron donor-acceptor complex, describes a type of supramolecular assembly of two or more molecules or ions. The assembly consists of two molecules that self-attract through electrostatic forces, i.e., one has at least partial negative charge and the partner has partial positive charge, referred ...

  5. Pi-interaction - Wikipedia

    en.wikipedia.org/wiki/Pi-interaction

    In chemistry, π-effects or π-interactions are a type of non-covalent interaction that involves π systems.Just like in an electrostatic interaction where a region of negative charge interacts with a positive charge, the electron-rich π system can interact with a metal (cationic or neutral), an anion, another molecule and even another π system. [1]

  6. Hückel's rule - Wikipedia

    en.wikipedia.org/wiki/Hückel's_rule

    Hückel's rule can also be applied to molecules containing other atoms such as nitrogen or oxygen. For example, pyridine (C 5 H 5 N) has a ring structure similar to benzene, except that one -CH- group is replaced by a nitrogen atom with no hydrogen. There are still six π electrons and the pyridine molecule is also aromatic and known for its ...

  7. Delocalized electron - Wikipedia

    en.wikipedia.org/wiki/Delocalized_electron

    In the simple aromatic ring of benzene, the delocalization of six π electrons over the C 6 ring is often graphically indicated by a circle. The fact that the six C-C bonds are equidistant is one indication that the electrons are delocalized; if the structure were to have isolated double bonds alternating with discrete single bonds, the bond would likewise have alternating longer and shorter ...

  8. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Benzene is an organic chemical compound with the molecular formula C 6 H 6. The benzene molecule is composed of six carbon atoms joined in a planar hexagonal ring with one hydrogen atom attached to each. Because it contains only carbon and hydrogen atoms, benzene is classed as a hydrocarbon.

  9. Sigma complex - Wikipedia

    en.wikipedia.org/wiki/Sigma_complex

    In the halogenation of benzene, the sigma complex comprises the six carbon atoms of the benzene ring, each bonded to a hydrogen atom. An additional halogen atom is bonded to one of the carbon atoms, which is sp 3-hybridized, while the other carbons remain sp 2-hybridized.