Dihydro­nium tetra­chromate(VI), (H₃O)₂Cr₄O₁₃

Abstract

The crystal structure of (H₃O)₂Cr₄O₁₃ is isotypic with K₂Cr₄O₁₃. The finite tetra­chromate anion in the title structure consists of four vertex-sharing CrO₄ tetra­hedra and exhibits a typical zigzag arrangement. The crystal packing is stabilized by hydrogen bonds between these anions and hydro­nium cations. The two different hydro­nium cations are surrounded by nine O atoms of tetra­chromate anions, with O⋯O distances ranging between 2.866 (8) and 3.282 (7) Å.

Related literature  

The title chromate is isotypic with its potassium analogue (Casari & Langer, 2005 ▶). Löfgren (1973 ▶) and Kolitsch (2004 ▶) determined the structures of the corresponding Rb and Cs salts, respectively. For industrial applications of tetra­chromates, see: Cainelli & Cardillo (1984 ▶); Çengeloğlu et al. (2003 ▶). For related bond-length data, see: Casari et al. (2007 ▶). For cell parameters of further isolated compounds stated in the experimental procedure, see: Durif & Averbuch-Pouchot (1978 ▶) and Rahman et al. (2003 ▶).

Experimental  

Crystal data  

• (H₃O)₂Cr₄O₁₃

• M _r = 454.05

• Monoclinic,

• a = 8.9765 (13) Å

• b = 7.6431 (8) Å

• c = 9.3451 (14) Å

• β = 91.888 (18)°

• V = 640.80 (15) ų

• Z = 2

• Mo Kα radiation

• μ = 3.37 mm⁻¹

• T = 293 K

• 1.0 × 0.4 × 0.2 mm

Data collection  

• Stoe IPDS I diffractometer

• Absorption correction: numerical [X-RED (Stoe & Cie, 2001 ▶) and X-SHAPE (Stoe & Cie, 1999 ▶)] T _min = 0.121, T _max = 0.314

• 5900 measured reflections

• 2696 independent reflections

• 2497 reflections with I > 2σ(I)

• R _int = 0.040

Refinement  

• R[F ² > 2σ(F ²)] = 0.040

• wR(F ²) = 0.110

• S = 1.06

• 2696 reflections

• 174 parameters

• 2 restraints

• Δρ_max = 0.69 e Å⁻³

• Δρ_min = −0.58 e Å⁻³

• Absolute structure: Flack (1983 ▶), 1212 Friedel pairs

• Flack parameter: 0.53 (4)

Data collection: IPDS (Stoe & Cie, 1997 ▶); cell refinement: IPDS; data reduction: IPDS; program(s) used to solve structure: SIR92 (Altomare et al., 1993 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: DIAMOND (Crystal Impact, 2012 ▶); software used to prepare material for publication: SHELXL97.

Supplementary Material

Additional supplementary materials: crystallographic information; 3D view; checkCIF report

supplementary crystallographic information

Comment

One of the characteristic properties of the elements of group 6 of the periodic table is their ability to build anionic polyoxo compounds with the corresponding elements in high oxidation states - the so called polyoxometalates. This property is profoundly exhibited by the oxoanions of the heavier elements Mo(VI) and W(VI), whereas the respective compounds of Cr(VI), i.e. polyoxochromates, are not built readily. Despite of this fact, polyoxochromates are of chemical and industrial importance due to their high oxidation potential. Accordingly, they are used as oxidants of organic compounds (Cainelli & Cardillo, 1984) and in hexavalent chromium plating (Çengeloǧlu et al., 2003).

The title compound, (H₃O)₂Cr₄O₁₃, is only the fourth tetrachromate(VI) described and characterized by single-crystal X-ray diffraction so far. The first three are salts of alkali metals, viz. the potassium (Casari & Langer, 2005), the rubidium (Löfgren, 1973), and the caesium salt (Kolitsch, 2004). (H₃O)₂Cr₄O₁₃ was isolated from a reaction mixture containing Na₂Cr₂O₇, nitric acid and a large excess of CrO₃ along with several possibly unrelated species.

The crystal structure of (H₃O)₂Cr₄O₁₃ is isotypic with that of K₂Cr₄O₁₃ (Casari & Langer, 2005) and accordingly exhibits the space group Pc. The cell volume of (H₃O)₂(Cr₄O₁₃) is 640.80 (15) ų at room temperature. It exceeds the cell volume of the potassium analogue measured at 173 K by roughly 44 ų. The finite tetrachromate anion is composed of four condensed CrO₄ tetrahedra and exhibits the typical zigzag arrangement (Figs. 1,2) described by Casari & Langer (2005). The two hydronium ions have two crystallographically different positions. They interact with nine oxygen atoms of the tetrachromate anions through hydrogen bonds. Although the H atoms of the hydronium cations could not be located, the distances between the hydronium O atoms and the surrounding tetrachromate O atoms between 2.866 (8) and 3.282 (7) Å point to moderate to weak O—H···O hydrogen bonds. These distances are quite similar to the distances between O atoms of water molecules and dichromate ions in Na₂Cr₂O₇^.H₂O (Casari et al., 2007) which indicates hydrogen bonds of typical strength for this class of compounds.

Experimental

Na₂Cr₂O₇ (26 mg, 0.1 mmol) and CrO₃ (1.600 g, 16 mmol) were dissolved in 0.5 ml H₂O. This solution was added to a solution of AgClO₄ (22.5 mg, 0.1 mmol) and theobromine (18 mg, 0.1 mmol) in 16.5 ml of nitric acid. After 2.5 months crystals of (H₃O)(ClO₄) (Rahman et al., 2003) and Ag₂(Cr₂O₇) (Durif & Averbuch-Pouchot, 1978) were isolated and characterized by X-ray difractometric unit-cell determinations. Orange-red crystals of the title compound were obtained from the mother liquor after another half year.

Refinement

The investigated crystal was racemically twinned, similarly to the potassium compound (Casari & Langer, 2005). The refined Flack paramter indicates a twin component ratio of 53 (4):47 (4). It was not possible to unambiguously locate the H atoms of the hydronium cations. They were therefore omitted from the refinement.

Figures

Fig. 1.

Hydrogen bonds between the hydronium ion (O1W) and the surrounding tetrachromate anions. The oxygen atom of the hydronium ion is shown with anisotropic displacement parameters at the 50% probability level. Chromate anions are shown as green-blue tetrahedra. Dashed lines denote O···O contacts between the cation and the anions.

Fig. 2.

Hydrogen bonding framework within the unit cell of the compound. See Fig. 1 for legend.

Crystal data

(H3O)2Cr4O13	F(000) = 444
Mr = 454.05	Dx = 2.353 Mg m−3
Monoclinic, Pc	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P -2yc	Cell parameters from 1754 reflections
a = 8.9765 (13) Å	θ = 1.9–28.2°
b = 7.6431 (8) Å	µ = 3.37 mm−1
c = 9.3451 (14) Å	T = 293 K
β = 91.888 (18)°	Block, orange-red
V = 640.80 (15) Å3	1.0 × 0.4 × 0.2 mm
Z = 2

Data collection

Stoe IPDS I diffractometer	2696 independent reflections
Radiation source: fine-focus sealed tube	2497 reflections with I > 2σ(I)
Graphite monochromator	Rint = 0.040
φ scans	θmax = 28.1°, θmin = 2.3°
Absorption correction: numerical [X-RED (Stoe & Cie, 2001) and X-SHAPE (Stoe & Cie, 1999)]	h = −11→11
Tmin = 0.121, Tmax = 0.314	k = −9→9
5900 measured reflections	l = −12→12

Refinement

Refinement on F2	Secondary atom site location: difference Fourier map
Least-squares matrix: full	w = 1/[σ2(Fo2) + (0.0842P)2] where P = (Fo2 + 2Fc2)/3
R[F2 > 2σ(F2)] = 0.040	(Δ/σ)max < 0.001
wR(F2) = 0.110	Δρmax = 0.69 e Å−3
S = 1.06	Δρmin = −0.58 e Å−3
2696 reflections	Extinction correction: SHELXL97 (Sheldrick, 2008), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4
174 parameters	Extinction coefficient: 0.083 (5)
2 restraints	Absolute structure: Flack (1983), 1212 Friedel pairs
Primary atom site location: structure-invariant direct methods	Flack parameter: 0.53 (4)

Special details

Experimental. A suitable single-crystal was carefully selected under a microscope and mounted in a glass capillary. The scattering intensities were collected on an imaging plate diffractometer (IPDS I, Stoe & Cie) equipped with a fine focus sealed tube X-ray source (Mo Kα, λ = 0.71073 Å) operating at 50 kV and 40 mA. Intensity data for the title compound were collected at room temperature by φ-scans in 100 frames (0 < φ < 200°, Δφ = 2°, exposure time of 7 min) in the 2 Θ range 3.8 to 56.3°. Structure solution and refinement were carried out using the programs SIR92 (Altomare et al., 1993) and SHELXL97 (Sheldrick, 1997) embedded into WinGX program package (Farrugia, 1999). A numerical absorption correction (X-RED (Stoe & Cie, 2001) was applied after optimization of the crystal shape (X-SHAPE (Stoe & Cie, 1999)). The last cycles of refinement included atomic positions and anisotropic parameters for all non-hydrogen atoms. Positions of hydrogen atoms were not determined. The final difference maps were free of any chemically significant features. The refinement was based on F2 for ALL reflections.

Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.

Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Ų)

	x	y	z	Uiso*/Ueq
Cr2	0.44108 (9)	1.10692 (11)	1.05710 (8)	0.0219 (2)
Cr1	0.12169 (8)	0.92974 (12)	1.17627 (8)	0.0242 (2)
Cr3	0.44219 (9)	1.44260 (12)	0.83187 (8)	0.0263 (2)
Cr4	0.78483 (9)	1.42919 (12)	0.79827 (9)	0.0283 (2)
O21	0.4560 (6)	0.9751 (8)	0.9295 (4)	0.0437 (12)
O31	0.4312 (7)	1.3165 (9)	0.7003 (5)	0.0542 (13)
O14	0.2882 (5)	1.0642 (5)	1.1542 (4)	0.0324 (9)
O33	0.6117 (5)	1.5476 (5)	0.8324 (4)	0.0296 (8)
O12	0.1024 (6)	0.7916 (8)	1.0473 (6)	0.0497 (12)
O22	0.5891 (5)	1.0957 (7)	1.1545 (4)	0.0401 (11)
O23	0.4224 (5)	1.3239 (6)	0.9907 (4)	0.0334 (9)
O43	0.9211 (5)	1.5638 (6)	0.8196 (5)	0.0360 (10)
O11	−0.0193 (5)	1.0612 (6)	1.1705 (5)	0.0395 (11)
O13	0.1342 (5)	0.8307 (8)	1.3278 (6)	0.0522 (14)
O42	0.7792 (7)	1.3587 (12)	0.6374 (7)	0.074 (2)
O32	0.3119 (5)	1.5822 (7)	0.8197 (6)	0.0477 (13)
O41	0.8015 (6)	1.2744 (8)	0.9121 (7)	0.0595 (16)
O1W	0.0967 (6)	0.4158 (8)	1.0652 (6)	0.0469 (12)
O2W	0.7959 (6)	0.9005 (7)	0.9169 (5)	0.0456 (12)

Atomic displacement parameters (Ų)

	U11	U22	U33	U12	U13	U23
Cr2	0.0205 (3)	0.0256 (4)	0.0197 (3)	−0.0006 (3)	0.0010 (2)	0.0020 (3)
Cr1	0.0221 (4)	0.0208 (5)	0.0296 (4)	−0.0019 (3)	0.0017 (3)	0.0052 (3)
Cr3	0.0235 (4)	0.0274 (5)	0.0278 (4)	−0.0021 (3)	0.0004 (3)	0.0068 (3)
Cr4	0.0255 (4)	0.0222 (5)	0.0374 (4)	−0.0005 (3)	0.0057 (3)	−0.0052 (3)
O21	0.047 (3)	0.060 (4)	0.0242 (18)	0.010 (2)	0.0025 (17)	−0.0114 (18)
O31	0.063 (3)	0.062 (4)	0.038 (2)	−0.024 (3)	0.0033 (19)	−0.008 (2)
O14	0.034 (2)	0.029 (3)	0.0349 (19)	−0.0062 (15)	0.0083 (16)	0.0006 (13)
O33	0.0289 (19)	0.024 (2)	0.036 (2)	−0.0003 (16)	0.0045 (15)	0.0024 (14)
O12	0.048 (3)	0.035 (3)	0.065 (3)	−0.003 (2)	−0.004 (2)	−0.017 (2)
O22	0.027 (2)	0.058 (3)	0.035 (2)	−0.0030 (18)	−0.0041 (16)	0.0082 (17)
O23	0.038 (2)	0.028 (2)	0.0344 (19)	−0.0032 (18)	0.0057 (15)	0.0107 (14)
O43	0.026 (2)	0.036 (3)	0.046 (2)	−0.0044 (15)	0.0092 (17)	0.0016 (16)
O11	0.030 (2)	0.040 (3)	0.049 (2)	0.0044 (16)	0.0039 (18)	0.0018 (17)
O13	0.038 (2)	0.061 (4)	0.057 (3)	−0.010 (2)	0.002 (2)	0.034 (3)
O42	0.059 (4)	0.092 (5)	0.071 (4)	0.006 (3)	0.007 (3)	−0.047 (4)
O32	0.029 (3)	0.057 (4)	0.057 (3)	0.006 (2)	−0.0039 (19)	0.022 (2)
O41	0.048 (3)	0.034 (3)	0.097 (4)	0.002 (2)	0.010 (3)	0.026 (3)
O1W	0.044 (3)	0.051 (3)	0.046 (2)	0.007 (2)	0.0014 (19)	−0.0030 (19)
O2W	0.043 (3)	0.049 (4)	0.044 (2)	0.009 (2)	−0.0039 (19)	0.0003 (19)

Geometric parameters (Å, º)

Cr2—O21	1.570 (4)	Cr3—O31	1.563 (6)
Cr2—O22	1.588 (4)	Cr3—O32	1.584 (5)
Cr2—O14	1.701 (4)	Cr3—O33	1.720 (5)
Cr2—O23	1.776 (4)	Cr3—O23	1.754 (4)
Cr1—O13	1.606 (4)	Cr4—O41	1.595 (5)
Cr1—O12	1.607 (5)	Cr4—O42	1.596 (6)
Cr1—O11	1.615 (5)	Cr4—O43	1.606 (5)
Cr1—O14	1.831 (4)	Cr4—O33	1.836 (5)
O21—Cr2—O22	108.1 (3)	O32—Cr3—O33	109.7 (3)
O21—Cr2—O14	111.9 (2)	O31—Cr3—O23	110.0 (3)
O22—Cr2—O14	111.0 (2)	O32—Cr3—O23	108.3 (2)
O21—Cr2—O23	110.1 (3)	O33—Cr3—O23	110.7 (2)
O22—Cr2—O23	108.5 (2)	O41—Cr4—O42	112.2 (4)
O14—Cr2—O23	107.3 (2)	O41—Cr4—O43	109.7 (3)
O13—Cr1—O12	110.7 (3)	O42—Cr4—O43	109.5 (4)
O13—Cr1—O11	110.8 (3)	O41—Cr4—O33	108.1 (2)
O12—Cr1—O11	108.6 (3)	O42—Cr4—O33	109.3 (3)
O13—Cr1—O14	109.3 (2)	O43—Cr4—O33	108.0 (2)
O12—Cr1—O14	110.6 (2)	Cr2—O14—Cr1	147.5 (3)
O11—Cr1—O14	106.8 (2)	Cr3—O33—Cr4	121.6 (2)
O31—Cr3—O32	109.3 (3)	Cr3—O23—Cr2	140.1 (3)
O31—Cr3—O33	108.9 (3)