Published August 2006 | Version v1
Journal article

A series of borate-rich metalloborophosphates Na2[M IIB3P2O11(OH)].0.67H2O (M II=Mg, Mn, Fe, Co, Ni, Cu, Zn): Synthesis, structure and magnetic susceptibility

  • 1. Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)
  • 2. Physics Department, Graduate School of Science, Tohoku University, Sendai 980-8578 (Japan)
  • 3. China University of Geoscience, X-ray Laboratory, Beijing 100083 (China)

Description

A series of metalloborophosphates Na2[M IIB3P2O11(OH)].0.67H2O (M II=Mg, Mn, Fe, Co, Ni, Cu, Zn) have been prepared hydrothermally and their structures have been solved by single-crystal diffraction techniques. They all crystallize in a hexagonal space group P63 and form a 3D microporous structure with 12-membered ring channels consisted of octahedral (M IIO6), tetrahedral (BO4, PO4) and triangular (BO2(OH)) units, in which the counter Na+ cations and water molecules are located. The Na+ cations are mobile and can be exchanged by Li+ in a melt of LiNO3. Their open frameworks are thermal stable up to about 500 deg. C. Completed solid solutions between two different transition metals can also be obtained. Magnetic properties of Na2[M IIB3P2O11(OH)].0.67H2O (M II=Mn, Co, Ni, Cu) have been investigated. - Graphical abstract: A series of metalloborophosphates Na2[M IIB3P2O11(OH)].0.67H2O (M II=Mg, Mn, Fe, Co, Ni, Cu, Zn) were synthesized under hydrothermal conditions (473 K). The structure consists of microporous 3D open framework with 12-membered ring channels composed of octahedral (M IIO6), tetrahedral (BO4, PO4) and triangular (BO2(OH)) units

Additional details

Identifiers

DOI
10.1016/j.jssc.2006.04.052;
PII
S0022-4596(06)00240-4;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
179
Journal Issue
8
Journal Page Range
p. 2534-2540
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.