کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1308053 | 975162 | 2006 | 12 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Stability constants and multinuclear NMR measurements of phosphonic acid derivatives with aluminum in aqueous solutions Stability constants and multinuclear NMR measurements of phosphonic acid derivatives with aluminum in aqueous solutions](/preview/png/1308053.png)
We are reporting the stability constants of the different complexes between phosphonoacetic acid (PAA), phosphonoformic acid (PFA), aminomethylphosphonic acid (AMPA), aminoethylphosphonic acid (AEPA) and methylenediphosphonic acid (MDP) with the aluminum metal ion in aqueous solutions. (In this study the term aluminum is reserved for the 3+ ion.) The affinity of the phosphonic acid derivatives to chelate aluminum has been tested by potentiometric titrations with I = 0.10 M KNO3 at 25 ± 0.1 °C. The proposed aluminum–ligand complex structures have been confirmed by 31P NMR, 13C NMR, and 27Al NMR experiments. Both PAA and PFA formed simple one to one complexes. The respective values for PAA are log β111 = 13.57, log β110 = 10.58, and log β11−1 = 5.84. The respective values for PFA are log β112 = 15.24, log β111 = 13.11, and log β110 = 6.88. In contrast to PAA and PFA, the major species formed with AMPA and AEPA consist of a series of dimeric complexes. The 31P NMR spectra of these complexes indicate that the amine groups do not co-ordinate to aluminum and remain protonated. In addition to these dimeric complexes, a monoprotonated monomer of Al–AMPA also has been detected. The 27Al NMR experiments indicated that the aluminum is hexacoordinated in all the complexes in this study and the hydroxide ion did not remove aluminium from its complexes. Among the ligands studied, PAA and PFA were able to solubilize aluminum at physiological pH. A comparison between the acidities and the chelating properties of the ligands used is presented.
A series of dimers of aluminum with aminoalkylphosphonates have been detected. 31P NMR spectra indicated that the amine groups do not coordinate to aluminum. In contrast to these dimers, the carboxyphosphonates showed a series of monomers. 27Al NMR experiments indicated that the aluminum is hexacoordinated and the hydroxide ion did not remove aluminium from its complexes.Figure optionsDownload as PowerPoint slide
Journal: Inorganica Chimica Acta - Volume 359, Issue 4, 1 March 2006, Pages 1135–1146