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Synthesis and crystal structure of Li_0.52Mg_0.96Sc_0.52Si₂O₆ orthopyroxene

Department of Geosciences, University of Arizona, Tucson, Arizona 85721-0077, U.S.A.

Correspondence: ^* E-mail: hyang{at}geo.arizona.edu

Li_0.52Mg_0.96Sc_0.52Si₂O₆ orthopyroxene was synthesized by the flux method and its structure studied with single-crystal X-ray diffraction. The crystal is orthorhombic with space group Pbca and unit-cell parameters a = 18.259(5), b = 8.883(2), c = 5.271(1) Å, and V = 854.9(3) ų. The structure refinement shows that the M1 and M2 sites are occupied by (0.48 Mg + 0.52 Sc) and (0.48 Mg + 0.52 Li), respectively. While the O3-O3-O3 kinking angle (165.40°) of the silicate tetrahedral A chain appears to be normal when compared with reported data, the kinking angle (151.92°) of the B chain is the largest of all orthopyroxenes examined at ambient conditions. This is the first orthopyroxene structure that contains more than 50% trivalent and monovalent cations in the M1 and M2 sites, respectively, and displays a kinking angle of the tetrahedral B chain that is greater than 150°. Our study demonstrates the stability of the new pyroxene structure type predicted by Pannhorst (1979) at room temperature.

Key Words: Li_0.52Mg_0.96Sc_0.52Si₂O₆ • orthopyroxene • crystal structure • X-ray diffraction