Dergi makalesi Açık Erişim
Dabak, S; Bekaroglu, O
{ "@context": "https://schema.org/", "@id": 102459, "@type": "ScholarlyArticle", "creator": [ { "@type": "Person", "name": "Dabak, S" }, { "@type": "Person", "name": "Bekaroglu, O" } ], "datePublished": "1997-01-01", "description": "Crosswise-substituted phthalocyanines (4, 4a-c) with two nitro and two dodecylsulfanyl groups are synthesized by a 2:2 condensation of 1,3-dihydro-1,3-diimino-6-(n-dodecylsulfanyl)isoiminoindolenine (2) with 6-nitro-1,3,3-trichloroisoindolenine (3) in the presence of sodium methoxide, hydroquinone and triethylamine. Nitro substituents are reduced to amines by sodium sulfide and condensation of the amine groups with ferrocenylaldehyde results in a new pc with two ferrocenylimino substituents, The novel compounds are characterized by UV/vis, mass and H-1-NMR spectroscopy.", "headline": "Synthesis of phthalocyanines crosswise-substituted with two alkylsulfanyl and two amino groups", "identifier": 102459, "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", "license": "http://www.opendefinition.org/licenses/cc-by", "name": "Synthesis of phthalocyanines crosswise-substituted with two alkylsulfanyl and two amino groups", "url": "https://aperta.ulakbim.gov.tr/record/102459" }
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Dabak, S. ve Bekaroglu, O. (1997). Synthesis of phthalocyanines crosswise-substituted with two alkylsulfanyl and two amino groups. NEW JOURNAL OF CHEMISTRY, 21(2), 267–271. https://aperta.ulakbim.gov.tr/record/102459 adresinden erişildi.