Synthesis and Structures of A Series of Novel Rare Earth Transition Metal Sulfates
Seven new rare earth transition metal sulfates were synthesized by hydrothermal reactions under conditions slightly above the critical point of water. Their crystal structures were determined from single crystal X-ray data. The compositions of the new compounds can be represented by two general form...
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| Published in | Journal of rare earths Vol. 24; no. 6; pp. 659 - 662 |
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| Main Author | |
| Format | Journal Article |
| Language | English |
| Published |
Elsevier B.V
01.12.2006
Department of Chemistry and Texas Center for Superconductivity, University of Houston, Houston, TX 77204-5003, USA |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1002-0721 2509-4963 |
| DOI | 10.1016/S1002-0721(07)60004-0 |
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| Summary: | Seven new rare earth transition metal sulfates were synthesized by hydrothermal reactions under conditions slightly above the critical point of water. Their crystal structures were determined from single crystal X-ray data. The compositions of the new compounds can be represented by two general formulae : REM (OH) 3 (SO4) and RE2M (OH) 3 (SO4) 2F (H2O) with RE = Gd, Tb, Dy ; M = Ni, Cu. Three different crystal structure types were found for the formula REM (OH) 3 (SO4). The structures of the new compounds all feature infinite chains of REOn coordination polyhedra, which are connected to chains of CuO6 or NiO6 octabedra. The limited size range of the rare earth cations observed in these compounds is most likely because of interactions between the octabedral chains and the chains of REOn polyhedra. The new compounds are closely related to the known yttrium transition metal sulfates. |
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| Bibliography: | 11-2788/TF O614.3 hydrothermal synthesis O782.1 rare earth sulfate transition metal sulfate crystal structure rare earth sulfate; transition metal sulfate; hydrothermal synthesis ; crystal structure ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
| ISSN: | 1002-0721 2509-4963 |
| DOI: | 10.1016/S1002-0721(07)60004-0 |