-
prototypical example of
antiaromaticity, cyclobutadiene, is the
subject of debate, with some
scientists arguing that
antiaromaticity is not a
major factor...
- The lack of
conjugation allows the 8 π
electron molecule to
avoid antiaromaticity, a
destabilizing effect ****ociated with cyclic,
conjugated systems...
-
atoms with p orbitals,
maleic anhydride was long
thought to
exhibit antiaromaticity. However, a
thermochemical study concluded that only 8 kJ/mol of destabilization...
- ****ociated with
aromaticity whereas a
paratropic ring
current signals antiaromaticity. A
similar effect is
observed in three-dimensional fullerenes; in this...
- [4]annulene).
Cyclobutadiene is the only
annulene with
considerable antiaromaticity,
since planarity is unavoidable. With [8]annulene, the
molecule takes...
-
containing 4n π
electrons are
called antiaromatic and are, in general, destabilized.
Molecules that
could be
antiaromatic will tend to
alter their electronic...
-
studies have been
conducted to ****ess the
consequences of
antiaromaticity in boroles.
Their antiaromatic character entails strong electrophilicity of the boron...
-
signals in a 2 to 1 ratio. The
addition of two
electrons removes the
antiaromaticity; it
becomes a
planar 10π-electron
aromatic species and is thus a bicyclic...
- OCLC 642506595. Ayub,
Rabia (2017). "Excited
State Aromaticity and
Antiaromaticity.
Fundamental Studies and Applications" (PDF).
Uppsala University. p...
- atom. The
parent compound, C6H6S is
unstable and is
predicted to be
antiaromatic.
Bulky derivatives have been
isolated and
shown by X-ray crystallography...
