4.5 Article

Organoantimony(V) Phosphinates, Phosphonates, and Seleninates

Journal

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume 2013, Issue 24, Pages 4345-4352

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201300348

Keywords

Antimony; Phosphorus; Selenium; Sb-C bond cleavage; Polyoxometalates

Funding

  1. Department of Science and Technology under the Science & Engineering Research Board (SERB)
  2. Council of Scientific and Industrial Research (CSIR)

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The reaction of polymeric triphenylantimony oxide with various protic ligands like phenylphosphinic acid, diphenylphosphinic acid, tert-butylphosphonic acid, and phenylseleninic acid has been investigated. Single-crystal X-ray structural elucidation revealed the formation of [Ph3Sb(HPhPO2)(2)](2) (1), [Ph3Sb(Ph2PO2)(2)] (2), [Ph3Sb(tert-BuPO3H)(2)] (3), [Ph3Sb(PhSeO2)(2)](2) (4), and [(Ph3Sb)(2)(-O)(-PhSeO2)(2)] (5), respectively. Hydrolysis and dearylation of 3 yielded [(Ph2Sb)(2)(PhSb)((3)-O)((2)-O)(2)(OH)(2)(-tBuPO(3))(2){(C2H5)(4)N}(2)] (6) possessing in situ generated Ph2Sb(O)(OH) and PhSbO3H2 moieties. The P-31 NMR spectrum of 1 shows P-H three-bond coupling seen for the first time in organophosphorus-based compounds. Further P-31 NMR spectroscopy at lower temperatures revealed 1 to be a fluxional molecule. Se-77 NMR spectroscopy indicates the formation of different molecular clusters from crystallization processes carried out under varying solvent conditions.

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