Preparation and structural characterization of Ph3Sn(IV)+ complexes with pyridinecarboxylic acids or hydroxypyridene, -pyrimidine and –quinoline.

Lorenzo Pellerito, Michelangelo Scopelliti, Mónika Hered, Gábor Galbács, Attila Szorcsik, Andrea Deák, László Nagy

Risultato della ricerca: Articlepeer review

23 Citazioni (Scopus)

Abstract

A number of [Ph3Sn(IV)](+) complexes formed with ligands containing -OH (-C=O), or -COOH group(s) and aromatic IN) donor atom have been prepared. The binding sites of the ligands were identified by FT-IR spectroscopic measurements. In the complexes containing hydroxy and carboxylate functions, the carboxylato group is coordinated to the organotin(IV) centres in monodentate or bridging bidentate manner. It was also found that in the hydroxypyridine and -pyrimidine complexes the [Ph3Sn(IV)]+ moiety in most cases reacts with the phenolic form of the ligands. The rationalisation of the experimental Sn-119 Mossbauer nuclear quadrupole splittings, vertical bar Delta(exp)vertical bar - according to the point charge model formalism - together with the FT-IR data support the formation of trigonal bipyramidal (Tbp) or octahedral (O-h) molecular structures. Furthermore, X-ray diffraction analysis has been performed on the triphenyltin(IV)-3-phenolato-2(1H )-pyriditione-O,O' single crystals. The penta-coordinated tin center exhibits a Tbp geometry. In case of 2-picolinic acid, a trans-phenylation was observed during the complexation, resulting [Ph2Sn(IV)](2+) complex and Ph4Sn(IV). (c) 2005 Elsevier B.V. All rights reserved.
Lingua originaleEnglish
pagine (da-a)1622-1630
RivistaJournal of Organometallic Chemistry
Volume691(8)
Stato di pubblicazionePublished - 2006

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

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