Synthesis and characterization of functionalized unsymmetrically substituted tetrachalcogenofulvalenes
β Scribed by Fabre, J.M.; Chakroune, S.; Giral, L.; Gorgues, A.; Salle, M.
- Book ID
- 121974998
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 154 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0379-6779
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Unsymmetric push-pull phthalocyanines with a high degree of conjugation achieved by introducing Ο-delocalized electron substituents were synthesized by statistical condensation of two different diiminoisoindolines. The characterization and spectroscopic properties of these push-pull phthalocyanines
A series of new unsymmetrically substituted subphthalocyanines containing iodo or octylthioether substituents on the outer aromatic rings have been synthesized. The statistical reaction of one equivalent of 1,2-dicyano-3-iodobenzene whether with two equivalents of 1,2-dicyano-4-octylthiobenzene or w