Laurelite, Pb7F12Cl2, from the Grand Reef mine, Graham County, Arizona, is hexagonal, Pbar6, with a = 10.267(1) and c = 3.9844(4) Å and Z = 1. The crystal structure was solved by direct methods and refined to R = 0.035 and R(w2) = 0.089 for 693 measured reflections (Fo > 9 sigma(Fo)). The structure is related to that of alpha-PbF2. Both are based upon ninefold-coordinated Pb as tricapped trigonal prisms (TCTPs), which share edges and faces. The two structures can be described with respect to the face-sharing linkages of their TCTPs. The structure of alpha-PbF2 consists of corrugated sheets of face-sharing TCTPs that interlock by edge-sharing perpendicular to the c axis. In laurelite, the Pb2 TCTPs form three-membered face-sharing clusters about the threefold axis that are propagated into trigonal cylinders by sharing faces in the direction of the c axis. The Pb1 and Pb3 TCTPs are linked by face-sharing into a three-dimensional framework with corresponding cylindrical voids. Asymmetric coordinations about Pb1 and Pb2 are attributed to the stereoactive lone-pair effect. Although the coordinations about the anions appear to disallow substitution of OH for F, stacking defects along the c axis provide a mechanism for accommodating limited OH or H2O for F substitution. A new density determination yielded 7.65(5) g/cm3, in reasonable agreement with the density of 7.77 g/cm3 calculated on the basis of the empirical formula Pb0.97[F1.68Cl0.25(H2O)(0.07)], Z = 7.

Laurelite: Its crystal structure and relationship to alpha-PbF2

MERLINO, STEFANO;PASERO, MARCO;PERCHIAZZI, NATALE;
1996

Abstract

Laurelite, Pb7F12Cl2, from the Grand Reef mine, Graham County, Arizona, is hexagonal, Pbar6, with a = 10.267(1) and c = 3.9844(4) Å and Z = 1. The crystal structure was solved by direct methods and refined to R = 0.035 and R(w2) = 0.089 for 693 measured reflections (Fo > 9 sigma(Fo)). The structure is related to that of alpha-PbF2. Both are based upon ninefold-coordinated Pb as tricapped trigonal prisms (TCTPs), which share edges and faces. The two structures can be described with respect to the face-sharing linkages of their TCTPs. The structure of alpha-PbF2 consists of corrugated sheets of face-sharing TCTPs that interlock by edge-sharing perpendicular to the c axis. In laurelite, the Pb2 TCTPs form three-membered face-sharing clusters about the threefold axis that are propagated into trigonal cylinders by sharing faces in the direction of the c axis. The Pb1 and Pb3 TCTPs are linked by face-sharing into a three-dimensional framework with corresponding cylindrical voids. Asymmetric coordinations about Pb1 and Pb2 are attributed to the stereoactive lone-pair effect. Although the coordinations about the anions appear to disallow substitution of OH for F, stacking defects along the c axis provide a mechanism for accommodating limited OH or H2O for F substitution. A new density determination yielded 7.65(5) g/cm3, in reasonable agreement with the density of 7.77 g/cm3 calculated on the basis of the empirical formula Pb0.97[F1.68Cl0.25(H2O)(0.07)], Z = 7.
Merlino, Stefano; Pasero, Marco; Perchiazzi, Natale; Kampf, Ar
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/205165
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