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Synthesis of phthalocyanines crosswise-substituted with two alkylsulfanyl and two amino groups

Dabak, S; Bekaroglu, O


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  "@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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