Publication:
Synthesis, characterisation and electrochemistry of derivatisable novel -tetra 7-oxycoumarin-3-carboxylate-substituted metallophthalocyanines

dc.contributor.authorÖZKAYA, ALİ RIZA
dc.contributor.authorsDur, Eyup; Ozkaya, Ali Riza; Bulut, Mustafa
dc.date.accessioned2022-03-12T17:50:20Z
dc.date.accessioned2026-01-10T21:42:01Z
dc.date.available2022-03-12T17:50:20Z
dc.date.issued2011
dc.description.abstractNovel -tetra-substituted metallophthalocyanines (ZnPc (3), CoPc (4), CuPc (5) and NiPc (6)) have been synthesised by cyclotetramerisation of a novel ligand, ethyl 7-(2,3-dicyanophenoxy)coumarin-3-carboxylate, with the relevant metal acetates. In addition, two derivatives of 3, slightly water-soluble tetrakis[7-oxycoumarin-3-carboxylic acid] phthalocyaninatozinc(II) and tetrakis[7-oxo-3-(ethyl piperidine-3-carboxlate)-coumarin]phthalocyaninatozinc(II), were prepared by its reaction with HCl (37%) and heating with ethyl 3-piperidinecarboxylate, respectively. The newly prepared compounds have been characterised by FT-IR, UV-vis, MALDI-TOF mass and 1H NMR spectroscopies. The redox behaviour of 3-6 was also investigated by voltammetry and in situ spectroelectrochemistry.
dc.identifier.doi10.1080/10610278.2010.521829
dc.identifier.eissn1029-0478
dc.identifier.issn1061-0278
dc.identifier.urihttps://hdl.handle.net/11424/230157
dc.identifier.wosWOS:000290674800006
dc.language.isoeng
dc.publisherTAYLOR & FRANCIS LTD
dc.relation.ispartofSUPRAMOLECULAR CHEMISTRY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectmetallophthalocyanine
dc.subjectcoumarin
dc.subjectalpha substitution
dc.subjectethyl nipecotate
dc.subjectelectrochemistry
dc.subjectMETAL-FREE
dc.subjectPHTHALOCYANINES
dc.subjectACID
dc.subjectSPECTROELECTROCHEMISTRY
dc.subjectANTIFUNGAL
dc.subjectCOMPLEXES
dc.subjectCOUMARIN
dc.titleSynthesis, characterisation and electrochemistry of derivatisable novel -tetra 7-oxycoumarin-3-carboxylate-substituted metallophthalocyanines
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage388
oaire.citation.issue5
oaire.citation.startPage379
oaire.citation.titleSUPRAMOLECULAR CHEMISTRY
oaire.citation.volume23

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