An original method based on metal-free ligand and lanthanide acetate direct interaction in the presence of a strong organic base (DBU) is used to prepare sandwich-type gadolinium and ytterbium crown-ether substituted phthalocyanines bis[4,5,4′,5′,4″,5″,4‴,5‴-tetrakis(1,4,7,10,13-pentaoxatridecamethy
Synthesis and aggregation behaviour of phthalocyanines substituted with flexible crown ether
✍ Scribed by I. Gürol; V. Ahsen
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 78 KB
- Volume
- 04
- Category
- Article
- ISSN
- 1088-4246
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✦ Synopsis
The synthesis of metal-free and metallo derivatives ( Ni , Zn ) of tetrasubstituted phthalocyanines (Pcs) obtained from 4-[methyleneoxy(15-crown-5)]phthalonitrile is described. The new compounds have been characterized by elemental analyses, IR, ^1^ H and ^13^ C NMR , MS and UV-vis. The thermal stabilities of the compounds were determined by thermogravimetric analysis. The alkali metal ions bound to crown ether groups force dimerization of the phthalocyanine units in solution, as observed in the electronic spectra by the broadening of the Q band transition at 675 nm. The highest affinity for potassium ion was observed in the case of the NiPc derivative in solvent extraction experiments.
📜 SIMILAR VOLUMES
Soluble and less soluble phthalocyaninatocopper(II) derivatives (4a and 4b) were prepared from the corresponding 7-[(4'-benzo-15-crown-5)oyl]-15, 16-dibromo-2,3,6,7,8,9,11,12-octahydro-5H-benzo[e]- ] tetraoxaazacyclopentadecine (3a) and 7-(2'-tosylaminoethyl)-15, 16-dibromo-2,3,6,7,8,9,11, 12-octahy