6533b7dbfe1ef96bd12708e3
RESEARCH PRODUCT
Diphenyltin(IV) complexes of the 5-[(E)-2-(aryl)-1-diazenyl]quinolin-8-olates: Synthesis and multinuclear NMR, 119Sn Mössbauer, electrospray ionization MS, X-ray characterization and assessment of in vitro cytotoxicity
Ulli EnglertRobert JiráskoAntonín LyčkaTushar S. Basu BaulEleonora RivarolaMichal HolčapekArchana MizarDick De Vossubject
StereochemistryLigandArylElectrospray ionizationOrganic Chemistrychemistry.chemical_elementCrystal structureBiochemistryMedicinal chemistryInorganic ChemistrySolventchemistry.chemical_compoundchemistryMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryTinSingle crystaldescription
Abstract A series of cis-bis{5-[(E)-2-(aryl)-1-diazenyl]quinolinolato}diphenyltin(IV) complexes have been synthesized and characterized by 1H, 13C, 119Sn NMR, ESI-MS, IR and 119mSn Mossbauer spectroscopic techniques in combination with elemental analysis. The structures of a ligand L6H (i.e., 5-[(E)-2-(4-ethoxyphenyl)-1-diazenyl]quinolin-8-ol) and three diphenyltin(IV) complexes, viz., Ph2Sn(L1)2 · (CH3)2CO (1), Ph2Sn(L4)2 (4) and Ph2Sn(L5)2 (5) (L = 5-[(E)-2-(aryl)-1-diazenyl]quinolin-8-ol: aryl = phenyl – (L1H); 4′-methylphenyl – (L4H) and 4′-bromophenyl – (L5H)) were determined by single crystal X-ray diffraction. In general, the complexes were found to adopt a distorted cis-octahedral arrangement around the tin atom. These complexes retain their solid-state structure in non-coordinating solvent as evidenced by 119Sn NMR spectroscopic results. The in vitro cytotoxicity of 1 is reported and compared with Ph2Sn(Ox)2 (Ox = deprotonated quinolin-8-ol) against seven well characterized human tumor cell lines.
year | journal | country | edition | language |
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2006-08-01 | Journal of Organometallic Chemistry |