Superaromaticity

Superaromaticity is used to describe an extra stable nature of some aromatic macrocycle compounds.^[1] These structure contains a number of aromatic rings.

References

↑ Aihara, Jun-ichi (2003), "Hückel-like rule of superaromaticity for charged paracyclophanes", Chemical Physics Letters 381 (1-2): 147–153, doi:10.1016/j.cplett.2003.09.114

External links

Chemical bonds

Intramolecular
("strong")

Covalent bond

By symmetry	Sigma (σ) Pi (π) Delta (δ) Phi (φ)

By multiplicity	1 (single) 2 (double) 3 (triple) 4 (quadruple) 5 (quintuple) 6 (sextuple)

Miscellaneous	Agostic bond Bent bond Dipolar bond Pi backbond Charge-shift bond Hapticity Conjugation Hyperconjugation Antibonding

Resonant bonding	Electron deficiency 3c–2e 4c–2e Hypercoordination 3c–4e Aromaticity möbius super sigma homo spiro σ-bishomo spherical

Metallic bonding

Metal aromaticity

Ionic bonding

Intermolecular
("weak")

van der Waals forces	London dispersion force

Hydrogen bond	Low-barrier Resonance-assisted Symmetric Dihydrogen bonds C–H···O interaction

Other noncovalent	Mechanical bond Halogen bond Aurophilicity Intercalation Stacking Cation–pi bond Anion–pi bond Salt bridge

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Superaromaticity

See also

References

External links