Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
177701 | Dyes and Pigments | 2007 | 6 Pages |
Abstract
Several titanium phthalocyanines tetra- and octa-substituted with dimethylaminoethylsulfanyl groups on peripheral positions have been synthesized and characterized. These phthalocyanines were converted into water-soluble quaternized products by reaction with methyl iodide. The capping of the titanyl (metaloxo) inner core with catechol and 2,3-dihydroxynaphthalene and complexation of peripheral donor groups of octakis(2-dimethylaminoethylsulfanyl)phthalocyaninatooxotitanium(IV) with Pd(II) ions to obtain multinuclear product were also studied. The new compounds were characterized using elemental analyses, 1H NMR, IR, mass and UV–vis spectral data.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Yasin Arslanoğlu, Esin Hamuryudan,