Abstract
Aromaticity is a central concept in chemistry,
pervading areas from biochemistry to materials science. Recently, chemists also
started to exploit intricate phenomena such as the interplay of local and
global (anti)aromaticity or aromaticity in non-planar systems and three
dimensions. These phenomena pose new challenges in terms of our fundamental
understanding and the practical visualisation of aromaticity. To overcome these
challenges, a method for the visualisation of chemical shielding tensors (VIST)
is developed here that allows for a 3D visualisation with quantitative
information about the local variations and anisotropy of the chemical
shielding. After exemplifying the method in different planar hydrocarbons, we
study two non-planar macrocycles to show the unique benefits of the VIST method
for molecules with competing pi-conjugated systems and conclude with a
norcorrole dimer showing clear evidence of through-space aromaticity. We
believe that the VIST method will be a highly valuable addition to the
computational toolbox.
Supplementary materials
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