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Synthesis and Characterization of Soluble Phthalocyanines: Structure-Property Relationship

dc.contributor.authorHanack, Michael
dc.contributor.authorGül, Ahmet
dc.contributor.authorHirsch, Andreas
dc.contributor.authorMandal, Braja K.
dc.contributor.authorSubramanian, L. R.
dc.contributor.authorWitke, Elisabeth
dc.date.accessioned2026-01-26T02:16:59Z
dc.date.issued1990-08-01
dc.description.abstractAbstract (μ-Oxo)bis[octakis(alkoxy)phthalocyaninatoiron (III)] 6a-c are obtained by treatment of the cyclotetramerisation product of 4,5-bis(alkoxy)-phthalonitriles in lithium pentanolate with iron(II) acetate. Compounds 6a-c are reduced to bisaxially coordinated octaalkoxyphthalocyaninatoiron(II) in the presence of ligands such as pyridine and t-butylisocyanide. Reaction of 6a with bidentate bridging ligands (e.g. pyrazine, 1,4-diisocyanobenzene) yields the bridged complexes 8a and 9a. The Mosbauer spectroscopic data are described and compared with the analogous unsubstituted phthalocyaninatoiron derivatives.
dc.description.urihttps://doi.org/10.1080/00268949008036063
dc.description.urihttps://dx.doi.org/10.1080/00268949008036063
dc.identifier.doi10.1080/00268949008036063
dc.identifier.endpage382
dc.identifier.issn1044-1859
dc.identifier.openairedoi_dedup___::c40a49fa331372e73e3c77032b79ba2f
dc.identifier.orcid0000-0003-1458-8872
dc.identifier.startpage365
dc.identifier.urihttps://hdl.handle.net/11527/57210
dc.identifier.volume187
dc.language.isoeng
dc.publisherInforma UK Limited
dc.relation.ispartofMolecular Crystals and Liquid Crystals Incorporating Nonlinear Optics
dc.sdg.typeGoal 3: Good Health and Well-being
dc.titleSynthesis and Characterization of Soluble Phthalocyanines: Structure-Property Relationship
dc.typeArticle
dspace.entity.typePublication

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