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dc.contributor.authorKovala-Demertzi, D.en
dc.contributor.authorDokorou, V.en
dc.contributor.authorCiunik, M.en
dc.contributor.authorKourkoumelis, N.en
dc.contributor.authorDemertzis, M. A.en
dc.date.accessioned2015-11-24T19:00:42Z-
dc.date.available2015-11-24T19:00:42Z-
dc.identifier.issn0268-2605-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19580-
dc.rightsDefault Licence-
dc.subjectanti-inflammatory drugsen
dc.subjectmefenamic aciden
dc.subjectorganotinen
dc.subjectstructureen
dc.subjectanti-tuberculosis agentsen
dc.subjectpenta-coordinated moleculesen
dc.subjectdiorganotin derivativesen
dc.subjectdrug interactionsen
dc.subjectdiclofenacen
dc.subjectadductsen
dc.subjectmossbaueren
dc.subjectbehavioren
dc.subjecttin(iv)en
dc.subjectnmren
dc.titleOrganotin mefenamic complexes - preparations, spectroscopic studies and crystal structure of a triphenyltin ester of mefenamic acid: novel anti-tuberculosis agentsen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1002/noc.308-
heal.identifier.secondary<Go to ISI>://WOS:000176488200004-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/aoc.308/asset/308_ftp.pdf?v=1&t=hhiqsvkf&s=d4f165c22d23e309cce6f6aa1143a9065a3fe078-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2002-
heal.abstractThe triphenyltin adduct of mefenamic acid, [SnPh3L] (1), the monophenyltin complex [PhSnOL](n) (2), and the dibutyltin complex [SnBu2L2] (3), where HL is 2-[bis(2,3-dimethylphenyl)amino]benzoic acid (mefenamic acid), have been prepared and structurally characterized by means of vibrational, H-1 and C-13 NMR spectroscopies. The crystal structure of I has been determined by X-ray crystallography. X-ray analysis revealed a pseudo-pentacoordinated structure containing Ph3Sn coordinated to the carboxylato group. The structural distortion is a displacement from the tetrahedron toward the trigonal bipyramid. Significant C-H-pi interactions and intramolecular hydrogen bonds stabilize the structure 1. The polar imino hydrogen atom participates in intramolecular hydrogen bonds. Complex I is self-assembled via C - H-pi and stacking interactions. Vibrational and NMR data are discussed in terms of the crystal structure and the proposed structures for 1-3. Compounds 1 and 3 were tested for antimycobacterial activity against Mycobacterium tuberculosis H37Rv. Copyright (C) 2002 John Wiley Sons, Ltd.en
heal.journalNameApplied Organometallic Chemistryen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
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