Abstract
An adjacently dinaphtho-substituted phthalocyanine with C2v symmetry, which is a structural isomer of naphthalocyanines in the sense that eight benzene units are fused to the tetraazaporphyrin skeleton, has been synthesized and characterized by electronic absorption and magnetic circular dichroism spectroscopy, and molecular orbital calculations within the framework of the ZINDO approximation.
Original language | English |
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Pages (from-to) | 1303-1304 |
Number of pages | 2 |
Journal | Chemistry Letters |
Issue number | 12 |
DOIs | |
Publication status | Published - 1999 |
Externally published | Yes |
ASJC Scopus subject areas
- Chemistry(all)