We then found that the degree of macrocyclic aromaticity is very sensitive to the way of oligomerization: Revision history

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30 April 2024

  • curprev 04:2204:22, 30 April 2024‎ Copyplane5 talk contribs‎ 5,318 bytes +5,318‎ Created page with "In general, it is markedly suppressed by linkage or substitution at meso positions but is fairly insensitive to direct edge-to-edge fusion. These predictions are consistent with observed chemical shifts of protons attached to the porphyrin macrocycles. Antiaromatic circuits are created in doubly- and triply-linked porphyrin oligomers. These circuits must be the origin of paramagnetic currents induced around the naphthalene-like junction zones in triply-linked oligomers...."
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