Abstract
A variety of phthalocyanine analogues with a seven-membered ring unit in place of a five-membered ring unit were synthesized from aromatic dicarbonitriles bearing cyano groups at 1,4-separate positions. Based on the spectroscopic analyses and theoretical calculations, tetraazachlorine-like electronic structures of these novel compounds stemming from severe twist of the conjugation system at the seven-membered ring unit have been revealed.
Original language | English |
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Pages (from-to) | 579-581 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 53 |
Issue number | 5 |
DOIs | |
Publication status | Published - Feb 1 2012 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry