Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/16936
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dc.contributor.authorTzimopoulos, D.en
dc.contributor.authorCzapik, A.en
dc.contributor.authorGdaniec, M.en
dc.contributor.authorBakas, T.en
dc.contributor.authorIsab, A. A.en
dc.contributor.authorVarvogli, A. C.en
dc.contributor.authorAkrivos, P. D.en
dc.date.accessioned2015-11-24T18:34:26Z-
dc.date.available2015-11-24T18:34:26Z-
dc.identifier.issn0022-2860-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/16936-
dc.rightsDefault Licence-
dc.subjecttinen
dc.subjecttriorganotin carboxylatesen
dc.subjectx-ray diffractionen
dc.subjectmossbauer spectroscopyen
dc.subjectnmr spectroscopyen
dc.subjectmopac computationsen
dc.subjectpyridine hydrogen-bondsen
dc.subjectsn-119 nmr-spectraen
dc.subjectsupramolecular synthonsen
dc.subjectcomplexesen
dc.subjectligandsen
dc.subjectc-13en
dc.subjecttriorganotin(iv)en
dc.subjecttriphenyltinen
dc.subjectderivativesen
dc.subjectbenzoatesen
dc.titleSynthesis and study of triorganostannyl esters of 3-,4-and 3,5-pyridinylimino substituted aminobenzoic acids: Crystal structures of dimorphs of aqua-trimethyltin 3-pyridinyliminobenzoateen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI 10.1016/j.molstruc.2009.11.038-
heal.identifier.secondary<Go to ISI>://000275391900009-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0022286009007388/1-s2.0-S0022286009007388-main.pdf?_tid=f313c790b0b1a87f47a1154cc8edf28a&acdnat=1334136506_36a9fe4dc14704b637c99a3143f8925e-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιώνel
heal.publicationDate2010-
heal.abstractThe synthesis and the structural investigation of triorganostannyl esters of the 3- and 4-[1-pyridin-2-yl-methylidene]- and 3,5-bis-[1-pyridin-2-yl-methylidene]-benzoic acids are reported with methyl, n-butyl, cyclohexyl, phenyl and benzyl substituents on tin. The organic carboxylates may be considered as iminopyridines emerging from the condensation of the corresponding aminobenzoic acid with pyridine-2-carboxaldehyde. In this respect it is interesting to investigate their physicochemical properties since their coordination to metal centers will affect both the photophysical properties of the metal and the conformation and intermolecular interactions of the ligands. Therefore, the structure of the above triorganotin compounds is studied and discussed in relation to those of the unsubstituted benzoates as well as of the free ligands. X-ray crystallography and a coalescence of spectroscopic methods applied both in the solid state and in Solution have been used in this effort. (C) 2009 Elsevier B.V. All rights reserved.en
heal.journalNameJournal of Molecular Structureen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
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