Abstract
The response of a molecule to an applied external magnetic field can be evaluated by a graphical representation of the induced magnetic field. We have applied this technique to four representative, cyclic organic molecules, that is, to aromatic (C6H6, D6h), anti-aromatic (C4H4, D2h) and non-aromatic (C 4H8, D4h, and C6H12, D3d) molecules. The results show that molecules that contain a π system possess a long-range magnetic response, while the induced magnetic field is short-range for molecules without π systems. The induced magnetic field of aromatic molecules shields the external field. In contrast, the anti-aromatic molecules increase the applied field inside the ring. Aromatic, anti-aromatic, and non-aromatic molecules can be characterized by the appearance of the magnetic response. We also show that the magnetic response is directly connected to nucleus-independent chemical shifts (NICS).
Original language | English |
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Pages (from-to) | 4367-4371 |
Number of pages | 5 |
Journal | Chemistry - A European Journal |
Volume | 10 |
Issue number | 17 |
DOIs | |
Publication status | Published - 2004 Sept 6 |
All Science Journal Classification (ASJC) codes
- Catalysis
- Organic Chemistry