Journal
JOURNAL OF SOLID STATE CHEMISTRY
Volume 179, Issue 11, Pages 3456-3460Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jssc.2006.07.010
Keywords
binary lanthanide polytelluride; synthesis; crystal structure; hypostoichiometry
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Single crystals of the new binaries CeTe1.90 and SmTe1.80 have been obtained. CeTe1.90 was synthesized at 1023 K from the reaction of Ce, TeO2, and Te with the use of a CsCl flux. It crystallizes in the tetragonal space group P4(2)/n with 20 formula units in a cell of dimensions at 153 K of a = 10.0261(5), c = 18.1336(12) angstrom, V = 1822.84(18)angstrom(3). It is isostructural with the LnSe(1.9) polyselenides (Ln = La, Ce, Pr) and with SmS1.90. SmTe1.80 was synthesized at 1223 K from the reaction of Sm and Te in a KBr flux. SmTe1.80 crystallizes in a new structural type in the tetragonal space group P4/n with 20 formula units in a cell of dimensions at 153 K of a = 9.7026(4), c = 18-0072(14) angstrom, V = 1695.21(14)angstrom(3). Both of these layered structures, which may be derived from the ZrSiS structure type, consist of double layers of [LnTe] polyhedra separated by planar Te nets that contain vacancies. In these nets the shortest Te-Te distances are 2.9194(5), 3.1204(5), and 3.3324(6) angstrom in CeTe1.90 and 2.878(1), 2.9932(3), and 3.2114(7) angstrom in SmTe1.80. Neither a simple delineation of the Te-Te bonding nor an assignment of individual formal oxidation states is possible in either of these compounds if one takes strict account of the Te-Te distances. (c) 2006 Elsevier Inc. All rights reserved.
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