Abstract

Siidraite, Pb 2 Cu(OH) 2 I 3 , is a new mineral from the Broken Hill deposit in New South Wales, Australia. It occurs as an extremely rare secondary phase alongside marshite, other lead and copper secondaries and supergene cuprite on a single specimen, BM 84642 preserved in the collection of the Natural History Museum, London. Siidraite is yellow and occurs in crystalline grainy aggregates up to 0.3 mm around relict galena. The mineral is translucent with a vitreous lustre and yellow streak, no cleavages or forms have yet been observed. It is non-fluorescent in mixed-wavelength UV light. The calculated density is 6.505 g cm −3 . Siidraite is orthorhombic, space group Fddd , a = 16.7082(9) A, b = 20.846(1) A, c = 21.016(1) A, V = 7320.0(8) A 3 and Z = 32. The empirical formula derived from a combination of electron-microprobe analysis and structure determination is Pb 2.06 Cu 0.89 (OH) 2 I 2.97 , the ideal formula has (in wt%) 8.01 Cu 2 O, 50.01 PbO, 42.65 I and 2.02 H 2 O. The five strongest lines in the calculated X-ray powder diffraction pattern are [( h k l ), d obs (A), I/I max (%)]: [(2 4 6), 2.746, 100], [(4 0 4), 3.270, 81], [(2 6 4), 2.738, 77], [(3 1 5), 3.312, 76], [(3 5 1), 3.296, 69]. The crystal used for structure determination had minor pseudomerohedral twinning on [ 0 1 ¯ 1 ] and the structure was refined taking this into account to R 1 = 0.037, wR 2 = 0.052, GooF = 1.016, based upon 1368 unique reflections having I > 2σ( I ). The structure of siidraite is a framework comprising an alternation of two structural elements, a cubane-like [Pb 4 (OH) 4 ] 4+ group and a [Cu 2 I 6 ] 4− dimer of edge-sharing CuI 4 tetrahedra with non-equivalent Cu. Six halocuprate groups surround each [Pb 4 (OH) 4 ] 4+ nucleus, and each halocuprate group is shared between six adjacent [Pb 4 (OH) 4 ] 4+ groups, five long Pb–I bonds are required to complete the co-ordination of each Pb atom. The resulting Pb(OH) 3 I 5 polyhedra are centred on a tetrahedron of O atoms to form a Pb 4 (OH) 4 I 16 cluster. Siidraite has a unique composition and structure. It is the third naturally occurring halocuprate(I) after marshite and nantokite. A compositionally similar synthetic compound Pb 2 Cu 2 (OH) 2 I 2 Br has been described that has cubane and CuI 4 groups, but a very different structural topology from that of siidraite. Bideauxite, Pb 2 Ag(OH)FCl 3 , which has the [Pb 4 (OH) 4 ] 4+ group, shares some topological features with siidraite.

Highlights

  • Halocuprate(I) compounds characteristically contain monovalent copper and have been studied extensively in the form of organometallic structures, which have technologically significant properties including photoluminescence, magnetism and semiconductivity

  • Siidraite was found during investigation of iodinebearing minerals in the collection of the Natural History Museum, London ( NHM)

  • The structure topology of siidraite is unique and consists of two structural elements that alternate in a checkerboard motif: (1) a Pb4(OH)4 “cubane” group and (2) a Cu2I6 dimer in which a pair of CuI4 tetrahedra share an edge

Read more

Summary

Introduction

Halocuprate(I) compounds characteristically contain monovalent copper and have been studied extensively in the form of organometallic structures, which have technologically significant properties including photoluminescence, magnetism and semiconductivity. As far as we are aware, there is only one inorganic lead-bearing halocuprate(I), Pb2Cu(OH)2BrI2, which occurs only as a synthetic compound (Hu et al, 2011). We report the discovery and characterisation of a related new inorganic halocuprate(I) mineral, siidraite, Pb2Cu(OH)2I3, having a very different crystal structure from Pb2Cu(OH)2BrI2. It is only the third halocuprate(I) mineral after marshite CuI and nantokite CuCl, both of which are rare minerals. Siidraite was found during investigation of iodinebearing minerals in the collection of the Natural History Museum, London ( NHM). Holotype material constitutes the original specimen, BM 84642, and the polished probe block and single-crystal mount removed from it, both registered under the new number BM 2016,1 at the NHM

Occurrence
Physical properties
Chemical composition
Crystal structure
Raman spectroscopy
Powder X-ray diffraction
Discussion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.