Synthesis of imine bond containing insoluble polymeric ligand and its transition metal complexes, structural characterization and catalytic activity on esterification reaction

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Özet

In this study, synthesis of insoluble polymeric ligand (L) and its transition metal complexes [Cu(L) Cl2]·2H2O (1), [Co(L)Cl2(H2O)2] (2) and [Ni(L)Cl2(H2O)2] (3), having the azomethine groups, were synthesized by the condensation reactions of the diamines and dialdehydes. The structural properties were characterized by the analytical and spectroscopic methods using by elemental analysis, Fourier Transform Infrared, Thermo Gravimetric Analysis, Powder X-ray Diffraction, magnetic susceptibility and Inductively Coupled Plasma. The solubilities of the synthesized polymeric materials were also investigated and found as insoluble some organic and inorganic solvents. Additionally, their catalytic performance was carried out for the esterification reaction of acetic acid and butyl acetate. The highest conversion rate is 75.75% by using catalyst 1. The esterification of butanol gave butyl acetate with 100% selectivity.

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Tam Kayıt
AlanDeğerDil
dc.contributor.authorGönül, İlyas
dc.contributor.authorAy, Burak
dc.contributor.authorKaraca, Serkan
dc.contributor.authorSaribiyik, Oguz Yunus
dc.contributor.authorYildiz, Emel
dc.contributor.authorSerin, Selahattin
dc.date.accessioned2026-10-22T10:23:40.717767662Z
dc.date.available2026-10-22T10:23:40.717767662Z
dc.date.issued2017
dc.description.abstractIn this study, synthesis of insoluble polymeric ligand (L) and its transition metal complexes [Cu(L) Cl2]·2H2O (1), [Co(L)Cl2(H2O)2] (2) and [Ni(L)Cl2(H2O)2] (3), having the azomethine groups, were synthesized by the condensation reactions of the diamines and dialdehydes. The structural properties were characterized by the analytical and spectroscopic methods using by elemental analysis, Fourier Transform Infrared, Thermo Gravimetric Analysis, Powder X-ray Diffraction, magnetic susceptibility and Inductively Coupled Plasma. The solubilities of the synthesized polymeric materials were also investigated and found as insoluble some organic and inorganic solvents. Additionally, their catalytic performance was carried out for the esterification reaction of acetic acid and butyl acetate. The highest conversion rate is 75.75% by using catalyst 1. The esterification of butanol gave butyl acetate with 100% selectivity.
dc.identifier.doi10.1080/15685551.2017.1332139
dc.identifier.eissn1568-5551
dc.identifier.endpage448
dc.identifier.issn1385-772X
dc.identifier.issue1
dc.identifier.pmid29491815
dc.identifier.scopus2-s2.0-85054827190
dc.identifier.startpage441
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/15171
dc.identifier.volume20
dc.identifier.wosWOS:000402070600006
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofDesigned Monomers and Polymers
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectEsterification reaction
dc.subjectHeterogeneous catalyst
dc.subjectInsoluble polymer
dc.subjectSchiff base
dc.subject.classificationPolymer Science
dc.subject.otherChelation
dc.subject.otherCondensation reactions
dc.subject.otherEsterification
dc.subject.otherEsters
dc.subject.otherGravimetric analysis
dc.subject.otherInductively coupled plasma
dc.subject.otherLigands
dc.subject.otherMagnetic susceptibility
dc.subject.otherMetal complexes
dc.subject.otherPolymers
dc.subject.otherSpectroscopic analysis
dc.subject.otherSynthesis (chemical)
dc.subject.otherThermogravimetric analysis
dc.subject.otherTransition metal compounds
dc.subject.otherTransition metals
dc.subject.otherCatalytic performance
dc.subject.otherEsterification reactions
dc.subject.otherFourier transform infra reds
dc.subject.otherHeterogeneous catalyst
dc.subject.otherInsoluble polymers
dc.subject.otherPowder X ray diffraction
dc.subject.otherSchiff-base
dc.subject.otherStructural characterization
dc.subject.otherCatalyst activity
dc.titleSynthesis of imine bond containing insoluble polymeric ligand and its transition metal complexes, structural characterization and catalytic activity on esterification reaction
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex7
rdl.citation.scopus4
rdl.citation.wos4
rdl.departmentFaculty of Engineering and Natural Science, Department of Genetic and Bioengineering, Gumushane University, Gumushane, Turkey
rdl.oa.statusgold
rdl.oa.urlhttps://www.tandfonline.com/doi/pdf/10.1080/15685551.2017.1332139?needAccess=true
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)