Synthesis, thermal and spectroscopic properties, and crystal structures of [Co(bba)2(H2O)(phen)] and [Ni(bba)2(H 2O)(butOH)(phen)] (bba = 2-benzoylbenzoate, phen = 1,10-phenanthroline, butOH = butanol)

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Aquabis(2-benzoylbenzoato)(1,10-phenanthroline)cobalt(II) and aquabis(2-benzoylbenzoato) (butanol)(1,10-phenanthroline)nickel(II) have been prepared and characterized by elemental analyses, IR and electronic spectroscopy, magnetic measurements, and single-crystal X-ray diffraction. [Co(bba)2(H2O)(phen)] (1) and [Ni(bba)2(H 2O)(butOH)(phen)] (2) consist of neutral monomeric units and crystallize in the monoclinic (P2(1)) and triclinic (P1) crystal systems, respectively. The cobalt(II) and nickel(II) sit on inversion centres and exhibit distorted octahedral coordination. Phen is bidentate chelating. In 1, bba is both monodentate and bidentate, whereas in 2 bba is only monodentate. bba ligands are coordinated to metal(II) with carboxylates and IR spectra of both complexes display characteristic absorptions of carboxylate anions {ν(OCO)asym and ν(OCO)sym} of bba. Thermal analysis shows that mass losses of 1 from 105°C to 456°C correspond to decomposition of phen and bba, while for 2 these occur at 271-529°C. © 2011 Taylor & Francis.

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AlanDeğerDil
dc.contributor.authorCaglar, Sema
dc.contributor.authorHeren, Zerrin
dc.contributor.authorBüyükgüngör, Orhan
dc.date.accessioned2026-10-18T20:30:23.816992820Z
dc.date.available2026-10-18T20:30:23.816992820Z
dc.date.issued2011
dc.description.abstractAquabis(2-benzoylbenzoato)(1,10-phenanthroline)cobalt(II) and aquabis(2-benzoylbenzoato) (butanol)(1,10-phenanthroline)nickel(II) have been prepared and characterized by elemental analyses, IR and electronic spectroscopy, magnetic measurements, and single-crystal X-ray diffraction. [Co(bba)2(H2O)(phen)] (1) and [Ni(bba)2(H 2O)(butOH)(phen)] (2) consist of neutral monomeric units and crystallize in the monoclinic (P2(1)) and triclinic (P1) crystal systems, respectively. The cobalt(II) and nickel(II) sit on inversion centres and exhibit distorted octahedral coordination. Phen is bidentate chelating. In 1, bba is both monodentate and bidentate, whereas in 2 bba is only monodentate. bba ligands are coordinated to metal(II) with carboxylates and IR spectra of both complexes display characteristic absorptions of carboxylate anions {ν(OCO)asym and ν(OCO)sym} of bba. Thermal analysis shows that mass losses of 1 from 105°C to 456°C correspond to decomposition of phen and bba, while for 2 these occur at 271-529°C. © 2011 Taylor & Francis.
dc.identifier.doi10.1080/00958972.2011.566923
dc.identifier.eissn1029-0389
dc.identifier.endpage1298
dc.identifier.issn1029-0389
dc.identifier.issue7
dc.identifier.scopus2-s2.0-84881367960
dc.identifier.startpage1289
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15543
dc.identifier.volume64
dc.identifier.wosWOS:000289573100008
dc.language.isoen
dc.publisherTAYLOR & FRANCIS LTD
dc.relation.ispartofJournal of Coordination Chemistry
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject1,10-Phenanthroline
dc.subject2-Benzoylbenzoic acid
dc.subjectCobalt(II) complex
dc.subjectCrystal structure
dc.subjectNickel(II) complex
dc.titleSynthesis, thermal and spectroscopic properties, and crystal structures of [Co(bba)2(H2O)(phen)] and [Ni(bba)2(H 2O)(butOH)(phen)] (bba = 2-benzoylbenzoate, phen = 1,10-phenanthroline, butOH = butanol)
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus12
rdl.citation.wos12
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)