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Amino-substitutedgem-diphosphonic acids: Dissociation mechanism and the structure of species in aqueous solutions
Authors:A G Matveeva  M P Pasechnik  P V Petrovskii  S V Matveev  S A Pisareva
Institution:(1) A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813 Moscow, Russian Federation
Abstract:The mechanism of dissociation of amino-substitutedgem-diphosphonic acids R2N(CH2) n CR'(PO3H2)2 with different lengths of the alkylidene chain and different substituents at the N atom was studied by vibrational (IR, Raman) and NMR (1H,14N,31P) spectroscopy using data of conformational analysis (molecular mechanical) data. The important role of intramolecular H-bonds and cyclic solvates for the stabilization of various conformations and tautomeric forms of ions was demonstrated. The spectral data that allow one to consider thegem-diphosphonate group as a single acidic center were found. Translated fromIzvestiya Akademii Nauk Seriya Khimicheskaya, No. 6, pp. 1051–1064, June, 2000.
Keywords:ω  -aminoalkylidenediphosphonic acids            gem-diphosphonates  dissociation mechanism  IR  Raman  and1H            14N  and31P NMR spectra  conformational analysis  hydrogen bonds
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