Synthesis and separation of structural isomers of 2(3),9 (10),16(17),23(24)-tetrasubstituted phthalocyanines

Citation
B. Gorlach et al., Synthesis and separation of structural isomers of 2(3),9 (10),16(17),23(24)-tetrasubstituted phthalocyanines, CHEM-EUR J, 7(11), 2001, pp. 2459-2465
Citations number
15
Categorie Soggetti
Chemistry
Journal title
CHEMISTRY-A EUROPEAN JOURNAL
ISSN journal
09476539 → ACNP
Volume
7
Issue
11
Year of publication
2001
Pages
2459 - 2465
Database
ISI
SICI code
0947-6539(20010601)7:11<2459:SASOSI>2.0.ZU;2-K
Abstract
The 2(3),9(10),16(17),23(24)-tetrasubstituted metalphthalocyanines 1-7 (M = In, Ni, Zn) were synthesized, as mixtures of four different structural iso mers, from the corresponding 4-alkoxy-1,2-dicyanobenzenes and the appropria te metal salts. Separation of the four structural isomers was successfully achieved on a C-30 alkyl phase by high-performance liquid chromatography (H PLC). The determination of the point groups of the structural isomers was c arried out for 1 and 3, the composition of the structural isomers of 4-7 wa s accomplished by comparing their retention times and UV/Vis spectra with t he data of 1 and 3. For the phthalocyanines 8-10 and the naphthalocyanines 11 and 12 only the C-4h and D-2h isomers could be separated.