The synthesis and characterization of metal-free and metallophthalocyanine polymers by microwave irradiation containing diazadithia macrocyclic moieties

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A tetranitrile monomer was synthesized by nucleophilic aromatic substitution of N,N'-(2,2'-(propane-1,3-diylbis(sulfanediyl))bis(ethane-2,1-diyl))bis(4-methylbenzenesulfonamide) onto 4-nitrophthalonitrile. A metal-free phthalocyanine polymer was prepared by the reaction of the tetranitrile monomer under N-2 in the presence of 2-(dimethylamino)ethanol at 145 degrees C for 24 h. Zinc(II), copper(II), cobalt(II), nickel(II), lead (II), phthalocyanine polymers were prepared by reaction of the tetranitrile with the chlorides of zinc (II), copper (II), cobalt (II), nickel (II), lead (II), employing microwave irradiation in the presence 2-(dimethylamino)ethanol at 175 degrees C, 350 W for 10 min. The thermal stabilities of the phthalocyanine compounds were determined by thermogravimetric analysis. The new compounds were characterized by a combination of IR, H-1 NMR, C-13 NMR, UV-vis, elemental analysis and MS spectral data. (C) 2009 Elsevier Ltd. All rights reserved.

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AlanDeğerDil
dc.contributor.authorKaya, Elif Celenk
dc.contributor.authorKaradeniz, Huelya
dc.contributor.authorKantekin, Halit
dc.date.accessioned2026-10-22T10:26:08.877022966Z
dc.date.available2026-10-22T10:26:08.877022966Z
dc.date.issued2010-05
dc.description.abstractA tetranitrile monomer was synthesized by nucleophilic aromatic substitution of N,N'-(2,2'-(propane-1,3-diylbis(sulfanediyl))bis(ethane-2,1-diyl))bis(4-methylbenzenesulfonamide) onto 4-nitrophthalonitrile. A metal-free phthalocyanine polymer was prepared by the reaction of the tetranitrile monomer under N-2 in the presence of 2-(dimethylamino)ethanol at 145 degrees C for 24 h. Zinc(II), copper(II), cobalt(II), nickel(II), lead (II), phthalocyanine polymers were prepared by reaction of the tetranitrile with the chlorides of zinc (II), copper (II), cobalt (II), nickel (II), lead (II), employing microwave irradiation in the presence 2-(dimethylamino)ethanol at 175 degrees C, 350 W for 10 min. The thermal stabilities of the phthalocyanine compounds were determined by thermogravimetric analysis. The new compounds were characterized by a combination of IR, H-1 NMR, C-13 NMR, UV-vis, elemental analysis and MS spectral data. (C) 2009 Elsevier Ltd. All rights reserved.
dc.description.sponsorshipThe Scientific Technological Research Council of Turkey [107T429]
dc.identifier.doi10.1016/j.dyepig.2009.10.021
dc.identifier.eissn1873-3743
dc.identifier.endpage182
dc.identifier.issn0143-7208
dc.identifier.issue3
dc.identifier.startpage177
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/15854
dc.identifier.volume85
dc.identifier.wosWOS:000274276900014
dc.language.isoen
dc.publisherELSEVIER SCI LTD
dc.relation.ispartofDYES AND PIGMENTS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectPhthalonitrile
dc.subjectPolymeric phthalocyanines
dc.subjectMetallophthalocyanine
dc.subjectMicrowave-assisted
dc.subjectMacrocyclic compound
dc.subjectMixed-donor macrocyclic
dc.subject.classificationChemistry, Applied
dc.subject.classificationEngineering, Chemical
dc.subject.classificationMaterials Science, Textiles
dc.subject.classificationChemistry
dc.subject.classificationEngineering
dc.subject.classificationMaterials Science
dc.subject.otherPHTHALOCYANINE THIN-FILMS
dc.subject.otherSOLAR-CELLS
dc.subject.otherPHOTODYNAMIC THERAPY
dc.subject.otherINCLUSION COMPLEXES
dc.subject.otherPHOTODETECTORS
dc.subject.otherDERIVATIVES
dc.subject.otherSENSITIZERS
dc.subject.otherBRIDGES
dc.subject.otherDESIGN
dc.subject.otherROUTE
dc.titleThe synthesis and characterization of metal-free and metallophthalocyanine polymers by microwave irradiation containing diazadithia macrocyclic moieties
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex10
rdl.citation.wos9
rdl.oa.statusclosed
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)