Synthesis of phthalocyanines crosswise-substituted with two alkylsulfanyl and two crown-ether

Kandaz, Mehmet; Sönmez, Mine

dc.contributor.authors	Agirtas, MS; Sonmez, M; Kandaz, M; Bekaroglu, O;
dc.date.accessioned	2020-02-24T14:15:21Z
dc.date.available	2020-02-24T14:15:21Z
dc.date.issued	2001
dc.identifier.citation	Agirtas, MS; Sonmez, M; Kandaz, M; Bekaroglu, O; (2001). Synthesis of phthalocyanines crosswise-substituted with two alkylsulfanyl and two crown-ether. INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 40, 1238-1236
dc.identifier.issn	0376-4699
dc.identifier.uri	https://hdl.handle.net/20.500.12619/44872
dc.description.abstract	Crosswise-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.
dc.language	English
dc.publisher	NATL INST SCIENCE COMMUNICATION
dc.subject	Chemistry
dc.title	Synthesis of phthalocyanines crosswise-substituted with two alkylsulfanyl and two crown-ether
dc.type	Article
dc.identifier.volume	40
dc.identifier.startpage	1236
dc.identifier.endpage	1238
dc.contributor.department	Sakarya Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü
dc.contributor.saüauthor	Kandaz, Mehmet
dc.contributor.saüauthor	Sönmez, Mine
dc.relation.journal	INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY
dc.identifier.wos	WOS:000172928900020
dc.contributor.author	Kandaz, Mehmet
dc.contributor.author	Sönmez, Mine