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Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
SrAu4In4 and Sr4Au9In13: polar intermetallic structures with cations in augmented hexagonal prismatic environments
Andriy Palasyuk1, Jing-Cao Dai, John D Corbett
1Ames Laboratory-DOE and Department of Chemistry, Iowa State University, Ames, IA 50011, USA.
Abstract:
The title compounds were synthesized via high-temperature reactions of the elements in welded Ta tubes and characterized by single-crystal X-ray diffraction analyses and band structure calculations. SrAu(3.76(2))In(4.24) crystallizes in the YCo5In3 structure type with two of eight network sites occupied by mixtures of Au and In: Pnma, Z = 4, a = 13.946(7), b = 4.458(2), c = 12.921(6) A. Its phase breadth appears to be small. Sr4Au9In 13 exhibits a new structure type, P_6 m2, Z = 1, a = 12.701(2), c = 4.4350(9) A. The Sr atoms in both compounds center hexagonal prisms of nominally alternating In and Au atoms and also have nine augmenting (outer) Au + In atoms around their waists so as to define 21-vertex Sr@Au9M4In8 (M = Au/In) and Sr@Au9In12 polyhedra, respectively. The relatively larger Sr content in the second phase also leads to condensation of some of the ideal building units into trefoil-like cages with edge-shared six-member rings. One overall driving force for the formation of these structures can be viewed as the need for each Sr cation to have as many close neighbors as possible in the more anionic Au-In network. The results also depend on the cation size as well as on the flexibility of the anionic network and an efficient intercluster condensation mode as all clusters are shared. Band structure calculations (LMTO-ASA) emphasize the greater strengths (overlap populations) of the Au-In bonds and confirm expectations that both compounds are metallic.
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