The chromatographic behavior of tetra-4-tert-butylphthalocynine; its 1 : 1
complexes of Zn(II), Cu(II), Mg(II), Ni(II), Pd(TI), Co(II), Rh(III), and S
n(IV); 1 : 2 complexes of LU(III), Dy(III), and Tb(III); and a linear dimer
of copper hexa-4-tert-butyldiphthalocyanine were studied on hydrophobized,
aminated, and unmodified silica gels. The retention of the above complexes
was studied as a function on the composition of the mobile phase, the natu
re of the metal atom, the number of macrocycles in the ligand, and the leng
th of the chromatographic column. It was shown that hydrophobized silica ge
ls with acetone, acetonitrile-acetate (1 : 1), methanol-ethyl acetate (1 :
1), and dimethylformamide mobile phases are the most selective systems for
determining the purity of the phthalocyanines. For each compound, an indivi
dual, usually symmetrical peak was observed. The parameters of these peaks
can be used for the rapid identification and sensitive determination of the
compounds studied. The detection limits were at a level of n x 10(-8) M.