Issue 2, 2002

Abstract

Layered mixed divalent metal phosphonates Mg1 − xZnx(O3PR)·H2O [with R = CH3, C2H3, C6H5] and Ni1 − xZnx(O3PR)·H2O [with R = CH3, C2H3, C6H5, (CH2)2COOH] have been prepared by heating, respectively, mixed divalent magnesium–zinc hydroxides and nickel–zinc hydroxides above the melting point of the phosphonic acid being used. A range of pre-formed mixed divalent metal hydroxides Mg1 − xZnx(OH)2 and Ni1 − xZnx(OH)2 with different ratios of Zn content (x = 0, 0.1, 0.25, 0.5) are obtained by isomorphous substitution of zinc into the, respective, Mg(OH)2 and Ni(OH)2 brucite-type structure: space group P[3 with combining macron]m1; a = 3.13–3.15 Å, c = 4.63–4.77 Å). The phosphonate materials have been characterized by X-ray powder diffraction, IR, TGA, and 31P MAS NMR. Mg1 − xZnx(O3PR)·H2O and Ni1 − xZnx(O3PR)·H2O crystallize in an orthorhombic system with space group Pmn21 with b = 5.55–5.69 Å, c = 4.71–4.86 Å and a varying according to the size of the organic group R.

Graphical abstract: Synthesis and characterization of new layered mixed metal phosphonate materials magnesium–zinc phosphonates Mg1 − xZnx(O3PR)·H2O and nickel–zinc phosphonates Ni1 − xZnx(O3PR)·H2O using mixed divalent magnesium–zinc and nickel–zinc hydroxides

Article information

Article type
Paper
Submitted
26 Jun 2001
Accepted
25 Oct 2001
First published
18 Dec 2001

J. Mater. Chem., 2002,12, 350-355

Synthesis and characterization of new layered mixed metal phosphonate materials magnesium–zinc phosphonates Mg1 − xZnx(O3PR)·H2O and nickel–zinc phosphonates Ni1 − xZnx(O3PR)·H2O using mixed divalent magnesium–zinc and nickel–zinc hydroxides

B. Menaa and I. J. Shannon, J. Mater. Chem., 2002, 12, 350 DOI: 10.1039/B105559N

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