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dc.contributor.authorPapatriantafyllopoulou, C.en
dc.contributor.authorKostakis, G. E.en
dc.contributor.authorRaptopoulou, C. P.en
dc.contributor.authorTerzis, A.en
dc.contributor.authorPerlepes, S. P.en
dc.contributor.authorPlakatouras, J. C.en
dc.date.accessioned2015-11-24T16:40:33Z-
dc.date.available2015-11-24T16:40:33Z-
dc.identifier.issn0020-1693-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8290-
dc.rightsDefault Licence-
dc.subjectcadmium(ii) sulfate complexesen
dc.subjectcoordination polymersen
dc.subjectmethyl 2-pyridyl ketone oxime complexesen
dc.subjectvibrational spectraen
dc.subjectzinc(ii) sulfate complexesen
dc.subject3d-metal cluster chemistryen
dc.subjectx-ray structuresen
dc.subjectliganden
dc.subjectcopper(ii)en
dc.subjectzinc(ii)en
dc.subjectcrystalen
dc.subjectni(ii)en
dc.subjectchainen
dc.subjectbonden
dc.titleInvestigation of the MSO(4) center dot xH(2)O (M = Zn, x=7; M = Cd, x=8/3)/methyl 2-pyridyl ketone oxime reaction system: A novel Cd(II) coordination polymer versus mononuclear and dinuclear Zn(II) complexesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI 10.1016/j.ica.2008.10.033-
heal.identifier.secondary<Go to ISI>://000265467300038-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0020169308006464/1-s2.0-S0020169308006464-main.pdf?_tid=fdc96efb06f6b5c14e24896dea5e1e6c&acdnat=1333035941_91f7e484da485c946ffa71fad41a9e3a-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2009-
heal.abstractThe reactions of methyl 2-pyridyl ketone oxime, (py)C(Me)NOH, with MSO4 center dot xH(2)O (M = Zn, x = 7; M = Cd, x = 8/3), in the absence of an external base, have been investigated. The synthetic study has led to the two new complexes [Zn(SO(4)){(py)C(Me)NOH}(H(2)O)(3)] center dot H(2)O (1 center dot H(2)O) and [Zn(2)(SO(4))(2){(py)C(Me)NOH} (4)] center dot (py)C(Me)NOH [2 center dot (py)C(Me)NOH], and the coordination polymer [Cd(SO(4)){(py)C(Me)NOH} (H(2)O)](n) center dot [Cd(SO(4)){(py)C(Me)NOH}(H(2)O)(2)] n (3). In the three complexes the organic ligand chelates through its nitrogen atoms. The sulfate anion in 1 center dot H(2)O is monodentate; the complex molecule is the mer isomer considering the positions of the aqua ligands. The Zn(II) centers in 2 center dot (py)C(Me)NOH are bridged by two syn, anti eta(1): eta(1): mu(2) SO(4)(2-) ligands; each metal ion has the cis- cis-trans disposition of the coordinated sulfate oxygen, pyridyl nitrogen and oxime nitrogens, respectively. The molecular structure of 3 is unique consisting of two different linear and ladder - type chains. pi-pi stacking interactions and/or hydrogen bonds lead to the formation of interesting supramolecular architectures in the three complexes. The thermal decomposition of complex 3 has been studied. Characteristic vibrational (IR, Raman) bands are discussed in terms of the nature of bonding and the structures of the three complexes. (C) 2008 Elsevier B. V. All rights reserved.en
heal.publisherElsevieren
heal.journalNameInorganica Chimica Actaen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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