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Kahlenberg, V., Piotrowski, A., Giester, G. (2000) Crystal structure of Na4[Cu4O2(SO4)4]·MeCl (Me: Na, Cu, ☐) – the synthetic Na-analogue of piypite (caratiite) Mineralogical Magazine, 64 (6) 1099-1108 doi:10.1180/002646100549913

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Reference TypeJournal (article/letter/editorial)
TitleCrystal structure of Na4[Cu4O2(SO4)4]·MeCl (Me: Na, Cu, ☐) – the synthetic Na-analogue of piypite (caratiite)
JournalMineralogical Magazine
AuthorsKahlenberg, V.Author
Piotrowski, A.Author
Giester, G.Author
Year2000 (December)Volume64
Issue6
PublisherMineralogical Society
DOIdoi:10.1180/002646100549913Search in ResearchGate
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Mindat Ref. ID243227Long-form Identifiermindat:1:5:243227:8
GUID0
Full ReferenceKahlenberg, V., Piotrowski, A., Giester, G. (2000) Crystal structure of Na4[Cu4O2(SO4)4]·MeCl (Me: Na, Cu, ☐) – the synthetic Na-analogue of piypite (caratiite) Mineralogical Magazine, 64 (6) 1099-1108 doi:10.1180/002646100549913
Plain TextKahlenberg, V., Piotrowski, A., Giester, G. (2000) Crystal structure of Na4[Cu4O2(SO4)4]·MeCl (Me: Na, Cu, ☐) – the synthetic Na-analogue of piypite (caratiite) Mineralogical Magazine, 64 (6) 1099-1108 doi:10.1180/002646100549913
Abstract/NotesAbstractThe crystal structure of Na4[Cu4O2(SO4)4] MeCl (Me: Na,Cu,☐) has been solved by direct methods and refined to R1 = 0.028 using 2466 independent reflections. The compound is tetragonal with space group P4/n, a = 18.451(1)Å, c = 4.9520(2)Å, Z = 4. The two main building units running parallel to the c-axis comprise: (1) slabs containing SO4 and OCu4 tetrahedra; and (2) chains of corner sharing Me(Cl,O)6 octahedra. The displacement ellipsoids of the atoms occupying the Me sites and of the Cl ions indicate a short-range static disorder. Copper in the slabs exhibits a (4+1) coordination. Both elements form a tunnel structure in which additional Na atoms are incorporated for charge compensation. The structure is closely related to the mineral piypite (K4Cu4O2(SO4)4 MeCl (Me: Na,Cu,☐)): . Furthermore, the structure has a pronounced pseudo-translational symmetry: apart from some of the oxygen sites, all of the nineteen crystallographically distinct positions are related by a pseudo F centring.

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