Issue 30, 2019

SrPt3In2 – an orthorhombically distorted coloring variant of SrIn5

Abstract

The new intermetallic phase SrPt3In2 was synthesized by induction-melting of the elements in a sealed tantalum ampoule followed by long-term annealing for crystal growth. The SrPt3In2 structure was refined from single crystal X-ray diffraction data: Imma, a = 1674.7(6), b = 921.2(4), c = 971.2(4) pm, wR2 = 0.0551, 1192 F2 values and 55 variables. Electronic structure calculations indicate strong covalent Pt–In bonding and a substantial charge transfer from the strontium atoms to the three-dimensional [Pt3In2]δ polyanionic network. The strontium atoms fill larger cavities within the network and the bonding of strontium to the polyanion is of the electrostatic type. The Bader charge calculations classify SrPt3In2 as a ternary platinide. The close relationship between the SrPt3In2 structure and the aristotype CaCu5 is discussed on the basis of a group–subgroup scheme in the Bärnighausen formalism along with other CaCu5 coloring variants and superstructures.

Graphical abstract: SrPt3In2 – an orthorhombically distorted coloring variant of SrIn5

Supplementary files

Article information

Article type
Paper
Submitted
30 Apr 2019
Accepted
30 Jun 2019
First published
01 Jul 2019

Dalton Trans., 2019,48, 11411-11420

SrPt3In2 – an orthorhombically distorted coloring variant of SrIn5

I. R. Muts, V. Hlukhyy, Y. V. Galadzhun, P. Solokha, S. Seidel, R. Hoffmann, R. Pöttgen and V. I. Zaremba, Dalton Trans., 2019, 48, 11411 DOI: 10.1039/C9DT01808E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements