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Solid-state P-31 NMR study of octacalcium phosphate incorporated with succinate
Author(s) -
Tim W. T. Tsai,
FangChieh Chou,
YaoHung Tseng,
Jerry C. C. Chan
Publication year - 2010
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/b923338e
Subject(s) - octacalcium phosphate , chemistry , magic angle spinning , homonuclear molecule , crystallography , phosphate , crystal structure , nuclear magnetic resonance spectroscopy , solid state nuclear magnetic resonance , hydrolysis , inorganic chemistry , stereochemistry , molecule , organic chemistry , nuclear magnetic resonance , physics
Octacalcium phosphate (OCP) is an important model compound in the study of biomineralization. The octacalcium phosphate-succinate (OCPS) compound is prepared and characterized by (31)P solid-state NMR spectroscopy. Taking advantage of the fact that the crystal structures of OCP and OCPS are very similar, an NMR strategy based on the (31)P homonuclear double-quantum spectroscopy is developed to assign all the peaks observed in the (31)P magic-angle spinning spectrum of OCPS. On the basis of our experimental data, the molecular formula of OCPS is determined to be Ca(7.81)(HPO(4))(1.82)(PO(4))(3.61)(succinate)(0.56).zH(2)O, where z<or= 0.5. We find that mainly the phosphorus species at the P5 site will be displaced when succinate ions are incorporated to form the OCPS lattice. The stability of OCPS is significantly higher than OCP with respect to the hydrolysis reaction at high pH conditions. We conclude that the hydration layer of OCP is playing the key role in the structural transformation of OCP.

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