Agirtas, MSSönmez, MKandaz, MBekaroglu, O2025-05-102025-05-1020010376-46992-s2.0-0035679650https://hdl.handle.net/20.500.14720/4507Kandaz, Mehmet/0000-0001-7904-5735Crosswise-substutited phthalocyanines with two nitro and two dodecylsulfanyl groups are synthesized by a 1:1 condensation of 1,3-dihydro-1,3-diimino-6-(n-dodecylsulfanyl) isoimino indolenine with 6-nitro-1,3,3-trichloroisoindolenine in the presence of sodium methoxide, hydroquinone and triethylamine. Nitro substituents are reduced to amines by sodium sulfide and condensation of the amino groups with benzo-15-crown-5-aldehyde results in a new Pe with two benzo-15-crown-5-imino substituents. The compounds have been characterized by elemental analyses, UV/Vis and IR spectroscopy.eninfo:eu-repo/semantics/closedAccessArticle4012Q4N/A12361238WOS:000172928900020