aromaticity's Usage Examples:

In chemistry, aromaticity is a property of cyclic (ring-shaped), planar (flat) structures with pi bonds in resonance (those containing delocalized electrons).

Thus, it does not exhibit appreciable aromaticity.

exhibit aromaticity, aliphatic compounds lack this delocalization.

The term "aromatic" was assigned before the physical mechanism determining aromaticity was.

In organic chemistry, Möbius aromaticity is a special type of aromaticity believed to exist in a number of organic molecules.

pi-systems that obey Hückel's rule are instead considered to demonstrate aromaticity.

Metal aromaticity is the concept of aromaticity, found in many organic compounds, extended to metals.

In organic chemistry, spherical aromaticity is formally used to describe an unusually stable nature of some spherical compounds such as fullerenes, polyhedral.

needed] Spiroaromaticity in organic chemistry refers to a special case of aromaticity in which conjugation is interrupted by a single spiroatom.

values indicate aromaticity and positive values antiaromaticity.

Yet another method called the harmonic oscillator model of aromaticity (HOMA) is defined.

Homoaromaticity, in organic chemistry, refers to a special case of aromaticity in which conjugation is interrupted by a single sp3 hybridized carbon atom.

2017 experimental evidence was reported for bicycloaromaticity (dual aromaticity) to exist in a bicyclic porphyrinoid.

In other words, aromaticity should be required for this interaction to occur.

Porphyrinoid macrocycles can show variable aromaticity.

Its aromaticity makes it relatively stable; however, it is only weakly basic.

Arsole is only moderately aromatic, with about 40% the aromaticity of pyrrole.

been a number of computational and experimental analyses of borazine's aromaticity.

Möbius–Hückel concept Möbius aromaticity Baird, N.

Resonance and aromaticity in the lowest 3ππ* state of.

The stability of this π electron system is referred to as aromaticity.