Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/9806
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dc.contributor.authorStamatatos, T. C.en
dc.contributor.authorPerlepes, S. P.en
dc.contributor.authorManos, M. J.en
dc.contributor.authorTasiopoulos, A. J.en
dc.contributor.authorKlouras, N.en
dc.date.accessioned2015-11-24T16:51:56Z-
dc.date.available2015-11-24T16:51:56Z-
dc.identifier.issn0095-8972-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9806-
dc.rightsDefault Licence-
dc.subjecttris(cyclopentadienyl)hexamethoxido-oxidotrititanium(iv) triiodideen
dc.subjectbis(eta(5)-cyclopentadienyl)diiodotitanium(iv)en
dc.subjecttriangular titanium(iv) complexesen
dc.subjectmethanolysis routeen
dc.subjectcrystal structuresen
dc.subjectreactivity studiesen
dc.subjectcrystal-structureen
dc.subjecttitanocene dichlorideen
dc.subjecttitanium(iv) complexesen
dc.subjectsolid-stateen
dc.subjecttrinuclearen
dc.subjectchemistryen
dc.subjectspectraen
dc.subjecthalidesen
dc.subjectpolymerizationen
dc.subjectzirconoceneen
dc.titleUnexpected formation, X-ray structure, and characterization of the triangular [Ti3O(OMe)(6)(eta(5)-C5H5)(3)](I-3) complex from hydrolysis and methanolysis of [Ti(eta(5)-C5H5)(2)I-2]en
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1080/00958972.2011.597850-
heal.identifier.secondary<Go to ISI>://000299441700017-
heal.identifier.secondaryhttp://www.tandfonline.com/doi/pdf/10.1080/00958972.2011.597850-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2011-
heal.abstractA convenient route has been developed for the formation of [(Ti3O)-O-IV(OMe)(6)(eta(5)-C5H5)(3)](I-3) (2) involving methanolysis (and possibly hydrolysis) of species derived from titanocene diiodide, [Ti-IV(eta(5)-C5H5)(2)I-2] (1), under aerobic conditions. Single-crystal X-ray crystallography reveals that the cation of 2 consists of three Ti-IV's in a triangular arrangement bridged by a central mu(3)-oxide; the latter lies 0.686 angstrom out of the Ti-3 plane. Each edge of the triangle is bridged by oxygen of eta(1) : mu-MeO-. Terminal ligation is provided by three methoxide and three cyclopentadienyl groups. All Ti-IV centers are five-coordinate in an extremely distorted geometry. IR and electronic data are discussed in terms of the known structure and coordination modes of O2-, MeO-, and eta(5)-C5H5-. A proposal for the mechanism of the unexpected formation of the triiodide (I-3(-)) counteranion that is present in the crystal structure of 2 is also provided.en
heal.publisherElsevieren
heal.journalNameJournal of Coordination Chemistryen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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