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Spherical Aromaticity inIh Symmetrical Fullerenes: The 2(N+1)2 Rule
426
Citations
15
References
2000
Year
Organic Charge-transfer CompoundEngineeringPhysicsNatural SciencesNmr Chemical ShiftsFullereneOrganic ChemistryPhysical ChemistryMaximal Spherical AromaticityQuantum ChemistryChemistrySpherical Charge Distribution
The maximal spherical aromaticity of an icosahedral fullerene such as C202+ (see picture) can only be achieved with 2(N+1)2 π electrons. There is clear evidence for this rule from the magnetic behavior of the endohedral He complexes on the basis of 3He NMR chemical shifts and it is ascribed to the spherical charge distribution.
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