E. Quarez, F. Abraham and O. Mentré, “Synthesis, Crystal Structure and Characterization of New 12H Hexagonal Perovskite-Related Oxides Ba₆M₂Na₂X₂O₁₇ (M=Ru, Nb, Ta, Sb; X=V, Cr, Mn, P, As)” Journal of Solid State Chemistry, Vol. 176, No. 1, 2003, pp. 137-150. doi:10.1016/S0022-4596(03)00379-7

has been cited by the following article:

• TITLE: EXAFS Studies of Ruthenium Based Double Perovskite ALaMnRuO6 (A = Ca, Sr, Ba)

  AUTHORS: Rubina Shaheen, Javaid Bashir, Muhammad Nasir Khan

  KEYWORDS: A. Oxides; A. Ceramics; C. EXAFS; D. Crystal Structure

  JOURNAL NAME: Materials Sciences and Applications, Vol.3 No.1, January 12, 2012

  ABSTRACT: Room and liquid nitrogen temperatures Mn K-edge extended X-ray fine structure (EXAFS) studies were carried out on powder samples of ALaMnRuO6 (A = Ca, Sr, Ba) perovskites. The EXAFS analysis of Mn K-edge spectra showed MnO6 octahedra are distorted. Among the three perovskites, the polyhedral distortion is highest for SrLaMnRuO6 (Δ = 1.4 × 10–3). For CaLaMnRuO6 (Δ = 0.5 × 10–3) and BaLaMnRuO6, (Δ = 0.7 × 10–3), the smaller values of distortion parameters indicate that the MnO6 octahedra are relatively regular and undistorted in the latter two systems. In SrLaMnRuO6, MnO6 distortion appears to be of orthorhombic (Q2) type whereas for CaLaMnRuO6 and BaLaMnRuO6, the distortion is of tetragonal or Q3 type. The Mn-O distances as determined from the EXAFS measurements, increases with the increase in the size of the divalent cation. No structural changes occurred in the local environment around Mn atom when the temperature was lowered from room to liquid nitrogen temperature.