Crystal structures of the hydrothermally synthesized chromates KSc<sub>3</sub>(CrO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>, KIn<sub>3</sub>(CrO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>, RbIn<sub>3</sub>(CrO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>, and AgIn<sub>3</sub>(CrO<sub>4</sub>)<sub>2</sub>(OH)<sub>6</sub>

Author(s)
Uwe Kolitsch
Abstract

Four new alunite-type chromates, KSc

3(CrO

4)

2(OH)

6, KIn

3(CrO

4)

2(OH)

6, RbIn

3(CrO

4)

2(OH)

6, and AgIn

3(CrO

4)

2(OH)

6, have been prepared by mild hydrothermal synthesis at T = 220 °C as well-developed, thick tabular to pseudo-octahedral crystals with maximum dimensions between approximately 0.5 and 1 mm. The crystal structures were refined from single-crystal intensity data (MoKα X-radiation, CCD area detector, 293 K, 2θ

max = 70°). The new members adopt the alunite parent structure-type (space group R3m, no. 166), with a = 7.763(1)/7.813(1)/7.817(1)/7.845(1), c = 17.575(3)/17.682(3)/18.075(3)/16.997(3) Å, V = 917.2(2)/934.8 (2)/956.5(2)/905.9(2) Å

3 (Z = 3), and R(F) = 1.36 / 1.21 / 1.23 / 1.33%, respectively. The H atoms could be located in each compound. Hydrogen bonds are all within a very close range (O3⋯O1 = 2.959-3.020 Å). All alkali and Sc/In sites are fully occupied, and the alkali atoms do not show any positional disorder, unlike Ag which is distinctly off-origin in AgIn

3(CrO

4)

2(OH)2

6. Average bond-lengths are as follows:

[12]K-O = 3.003,

[6]Sc-O = 2.106,

[4]Cr-O = 1.653 Å (KSc member);

[12]K-O = 3.000,

[6]In- O = 2.145,

[4]Cr-O = 1.653 Å (KIn);

[12]Rb-O = 3.051,

[6]In-O = 2.147, Cr-O = 1.653 Å (RbIn); and

[9]Ag-O = 2.826,

[6]In-O = 2.142,

[4]Cr-O = 1.648 Å (AgIn). The origin and possible meaning of a small, but conspicuous residual-density peak at (0, 0, 0.5) in the In members is discussed. These chromates represent the first structurally characterized Sc and In members of the large alunite supergroup, and may serve as analogues in future studies of naturally occurring Fe or sulfate members. Alunite-type Cs analogues could not be synthesized hydrothermally, in agreement with the fact that no natural or synthetic Cs compounds with the alunite topology have been reported so far. Instead, the syntheses yielded orthorhombic CsSc(CrO

4)

2 [CsCr

3+(Cr

6+O

4)

2-type] and monoclinic CsIn(CrO

4)

2 [(NH

4)Fe(CrO

4)

2-type].

Organisation(s)
Department of Mineralogy and Crystallography
External organisation(s)
Naturhistorisches Museum Wien (NHM)
Journal
The Canadian Mineralogist
Volume
53
Pages
833-844
No. of pages
12
ISSN
0008-4476
DOI
https://doi.org/10.3749/canmin.1400103
Publication date
09-2016
Peer reviewed
Yes
Austrian Fields of Science 2012
105116 Mineralogy, 105113 Crystallography
Keywords
ASJC Scopus subject areas
Geochemistry and Petrology
Portal url
https://ucrisportal.univie.ac.at/en/publications/1c2bba99-5871-4216-b46c-9a80cea06cf8