Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
175885 | Dyes and Pigments | 2015 | 8 Pages |
•Axially ligated by pyridine derivatives of ZnPc complexes are obtained.•Two polymorphic forms of ZnPc(3,4-Dimepy) and one form of ZnPc(4-Etpy) are reported.•UV–Vis spectra of ZnPcL dyes show that Pc π-system is not perturbed by the axial L.•The ZnPcL dyes are about 3–4 times more soluble than the parent ZnPc pigment.•3D MESP maps are helpful for understand the interaction of ZnPc with pyridine derivatives.
Two complexes of zinc phthalocyanine monoaxially ligated by 3,4-dimethylpyridine (1) and 4-ethylpyridine (2) were obtained in crystalline forms. Compound 1 depending on the crystallisation condition crystallises in two crystalline modifications, i.e. monoclinic (P21/c, 1m) and orthorhombic (Pccn, 1o), whereas compound 2 crystallises only in one orthorhombic form (Pccn space system). Structures 1o and 2 are isotypic; an explanation of that behaviour was proposed. Each structure contains the zinc phthalocyanine and the ligand molecules in molar ratio 1:1, which was confirmed by X-ray single diffraction and thermogravimetric analysis. Ligation of the ZnPc by N-ring aromatic ligands with formation of complexes 1 and 2 does not change the colouring properties, but increases their solubility in the organic solvents comparing to the parent ZnPc pigment.
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