Synthesis and crystal structure of cerium(IV) bis-(phosphite).

The structure of cerium(IV) bis-(phosphite), Ce(HPO3)2, has been solved by single-crystal X-ray diffraction and has trigonal (P-3m1) symmetry. The cerium(IV) cation exhibits site symmetry -3m. and is octa-hedrally coordinated by O atoms of the phosphite ligands (point group symmetry 3m.). The highly symmetrical compound has a layered structure parallel to the ab plane, and is closely related to zirconium(IV) bis-(phosphite) solved via powder X-ray diffraction with trigonal (P-3 symmetry. Structural details of the two compounds are comparatively discussed.

Chemical context

Phospho­nates are commonly employed within the petroleum industry as anti­oxidants. Inter­actions between these anti­oxidants and possible metal impurities could potentially have unintended consequences in the processing of petroleum products. We are currently studying these inter­actions by exploring the crystalline materials formed via solvothermal syntheses of lanthanides with phospho­rous acid.

Phospho­rous acid (H3PO3) is a powerful reducing agent and is exceedingly water soluble. The anion HPO3 2− has many different names in the literature, including (but not limited to) phosphite, phospho­nate, phospho­rus(III) oxoanion, oxophosphate(III) and hydridotrioxidophosphate(2-). According to IUPAC, when the hydrogen atom is directly bonded to the phospho­rus atom, it is to be named phospho­nate; whereas when the anion tautomerizes to the PO2(OH)2− anion, it is named as phosphite. However, the latter ion is rarely identified in the solid state. While IUPAC prefers HPO3 2− to be named phospho­nate, this name is also used for organo­phospho­rus compounds with the general formula R-PO(OH)2 or R-PO(OR)2, where R = alkyl or aryl groups. To eliminate any confusion with organo­phospho­rus compounds and to be consistent with the recent literature, we will herein refer to the HPO3 2− anion as phosphite.

The phosphite anion has many structural similarities to both phosphates and organo­phospho­nates. In the phosphite anion, a hydrogen atom has replaced one of the oxygen atoms, which would be found in phosphate; also, the phosphite anion contains no P—C bonds that are found in phospho­nates. Phosphite itself can be used as a precursor for making a vast array of phospho­nates. In phosphite, the central phospho­rus atom is PIII instead of the more air-stable PV, which provides the opportunity for redox chemistry. This ability to act as a reducing agent has led to several mixed-valent uranium compounds (Villa et al., 2012 ▸; Villa, Marr et al., 2013 ▸; Villa, Alekseev et al., 2013 ▸). Moving towards the lanthanides, lanthanide phosphite compounds have been synthesized in one of two main ways: hydro­thermally (Cross et al., 2012 ▸; Ewald et al., 2003 ▸, 2005 ▸; Foulon et al., 1993a ▸,b ▸,1995 ▸; Loukili et al., 1988 ▸, 1991 ▸; Tijani et al., 1988 ▸; Xiong et al., 2006 ▸, 2009 ▸; Zhang et al., 1992 ▸) and phosphite flux reactions (Zakharova et al., 2003 ▸). We have expanded this chemistry by exploring solvothermal syntheses of lanthanide phosphites. Herein we will discuss the crystal structure of the title compound, a new cerium(IV) bis­(phosphite).

Structural commentary

The title compound Ce(HPO3)2 crystallizes in the space group P m1. The smallest repeating unit contains one cerium(IV), one oxygen, one phospho­rus(III) and one hydrogen atom. This simple structure contains slightly distorted octa­hedrally coordinated cerium(IV) cations (site symmetry m.; Fig. 1 ▸), which are linked together by corner-sharing phosphite ligands. These phosphite ligands have a slightly distorted tetra­hedral configuration (point group symmetry 3m.). Each phospho­rus(III) atom in the phosphite ligand is bonded to three oxygen atoms, comprising the bottom of the tetra­hedron, and one hydrogen atom. The sheets of Ce(HPO3)2, which are located in the ab plane, contain alternating up–down phosphite ligands around the cerium(IV) metal cation, as indicated by the different directions of the hydrogen atoms (Figs. 2 ▸, 3 ▸). These sheets are layered down the c axis, where each cerium(IV) atom resides directly below the cerium above it at a distance of 5.6099 (3) Å, which corresponds to the length of the c axis; between the layers, the Ce—Ce—Ce angle is 180.0° (Fig. 3 ▸).

Figure 1

The coordination sphere of the cerium(IV) atom with atoms of the asymmetric unit labelled. Displacement ellipsoids are drawn at the 50% probability level. Bond lengths and angles can be found in Table 1 ▸.

Figure 2

The sheet-like arrangement of the polyhedra parallel to the ab plane in the crystal structure of Ce(HPO3)2. The unit cell is shown with blue dashed lines. This polyhedral representation contains the same color scheme as Fig. 1 ▸.

Figure 3

The stacking of the cerium(IV) phosphite sheets are shown in a projection along the a axis. Again, the unit cell is shown with blue dashed lines and the color scheme is the same as the above images.

This structure is closely related to a known zirconium(IV) bis­(phosphite), Zr(HPO3)2, which was isolated via a very different synthesis route involving refluxing in concentrated phospho­rous acid and using HF to precipitate the desired compound (Millini et al., 1993 ▸). The structure was elucidated from powder X-ray diffraction data and has many similarities to the title structure shown above (Table 1 ▸). The main difference between the two is the metal–oxygen bond length, where the Ce—O bond length is unsurprisingly slightly longer. The zirconium coordination appears to be a bit closer to being octa­hedral than the cerium, but they are nearly the same after comparing the error of refinement.

Table 1

Comparison of bond lengths and angles (Å, °) in Ce(HPO3)2 (P m1) and Zr(HPO3)2 (P )

Bond lengths	Ce(HPO3)2	Zr(HPO3)2	bond angles	Ce(HPO3)2	Zr(HPO3)2
Metal—O	2.2193 (19)	2.05 (2)	O—metal—O	88.85 (8), 91.15 (8)	89.2 (4), 90.8 (4)
P—O	1.5168 (19)	1.52 (1)	metal—O—P	162.28 (14)	162.1 (3)
P—H	1.44 (6)	1.43 (fixed)	O—P—O	112.07 (8)	111.2 (5)
			O—P—H	106.73 (9)	107.6 (6)

Zr(HPO3)2 data from Millini et al. (1993 ▸).

Synthesis and crystallization

Cerium(IV) bis­(phosphite) was synthesized solvothermally in aceto­nitrile (CH3CN). A stock solution of 1.00 M H3PO3 was prepared in aceto­nitrile. 0.0572 grams of ceric ammonium nitrate, (NH4)2Ce(NO3)6, was placed into a PTFE liner along with 2 ml of the 1.00 M phospho­rous acid solution, yielding a solution 0.0522 M ceric ammonium nitrate. This gives an approximate molar ratio of cerium(IV) to phosphite of 1:20. After the cerium was completely dissolved, the PTFE liner was capped and sealed inside of a stainless steel autoclave. This was then placed into a programmable box furnace and heated to 363 K over a period of 30 minutes, held at 363 K for four h and then cooled for 975 minutes down to 298 K (or a rate of 4 K per hour).

The resulting mixture was washed with cold water and then placed into a plastic petri dish. The excess water was removed and the crystals were dispersed with aceto­nitrile. The large, hexa­gonal prisms of the title compound were light yellow in color. Many suitable crystals were present. A large crystal was isolated in immersion oil and broken perpendicular to the hexa­gonal face to yield a clean crystal for single-crystal X-ray diffraction.

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 2 ▸. The hydrogen-atom position was placed as a riding atom on the phospho­rus position. The maximum electron density peaks are 0.330 e− Å−3 (located between P1 and O1 at 0.686 and 0.838 Å, respectively), 0.320 e− Å−3 (located adjacent to O1 at 0.608 Å) and 0.250 e Å−3 (located adjacent to Ce1 at 0.692 Å), which lead to nothing reasonable. All other maximum density peaks are under 0.2 e− Å−3. The minimum electron density is a very minimal at −0.609 e− Å−3. Two electron density holes of about the same magnitude reside around the phospho­rus atom.

Table 2

Experimental details

Crystal data
Chemical formula	Ce(HPO3)2
M r	300.08
Crystal system, space group	Trigonal, P m1
Temperature (K)	293
a, c (Å)	5.6859 (3), 5.6099 (3)
V (Å3)	157.07 (2)
Z	1
Radiation type	Mo Kα
μ (mm−1)	7.71
Crystal size (mm)	0.21 × 0.09 × 0.08
Data collection
Diffractometer	Rigaku SCX-Mini
Absorption correction	Multi-scan (CrysAlis PRO; Rigaku OD, 2015 ▸)
T min, T max	0.799, 1.000
No. of measured, independent and observed [I > 2σ(I)] reflections	1852, 197, 197
R int	0.018
(sin θ/λ)max (Å−1)	0.713
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S	0.010, 0.029, 1.26
No. of reflections	197
No. of parameters	13
H-atom treatment	Only H-atom coordinates refined
Δρmax, Δρmin (e Å−3)	0.51, −0.35

Computer programs: CrysAlis PRO (Rigaku OD, 2015 ▸), SHELXT (Sheldrick, 2015a ▸), SHELXL2014 (Sheldrick, 2015b ▸), OLEX2 (Dolomanov et al., 2009 ▸) and CrystalMaker (Palmer, 2014 ▸),.

Crystal structure: contains datablock(s) I. DOI: 10.1107/S205698901701115X/wm5407sup1.cif

CCDC reference: 1565300

Additional supporting information: crystallographic information; 3D view; checkCIF report

Ce(HPO3)2	Dx = 3.172 Mg m−3
Mr = 300.08	Mo Kα radiation, λ = 0.71073 Å
Trigonal, P3m1	Cell parameters from 1912 reflections
a = 5.6859 (3) Å	θ = 4.0–32.7°
c = 5.6099 (3) Å	µ = 7.71 mm−1
V = 157.07 (2) Å3	T = 293 K
Z = 1	Hexagonal, clear light yellow
F(000) = 138	0.21 × 0.09 × 0.08 mm

Rigaku SCX-Mini diffractometer	197 independent reflections
Radiation source: fine-focus sealed X-ray tube, Enhance (Mo) X-ray Source	197 reflections with I > 2σ(I)
Graphite monochromator	Rint = 0.018
ω scans	θmax = 30.5°, θmin = 5.5°
Absorption correction: multi-scan (CrysAlis PRO; Rigaku OD, 2015)	h = −8→8
Tmin = 0.799, Tmax = 1.000	k = −8→8
1852 measured reflections	l = −7→8

Refinement on F2	Primary atom site location: dual
Least-squares matrix: full	Hydrogen site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.010	Only H-atom coordinates refined
wR(F2) = 0.029	w = 1/[σ2(Fo2) + (0.0148P)2 + 0.0962P] where P = (Fo2 + 2Fc2)/3
S = 1.26	(Δ/σ)max < 0.001
197 reflections	Δρmax = 0.51 e Å−3
13 parameters	Δρmin = −0.35 e Å−3
0 restraints

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

Refinement. The structure was refined using SHELXT (Sheldrick, 2015) Intrinsic Phasing and SHELXL (Sheldrick, 2015). Olex2 (Dolomanov et al., 2009) was used as a graphical interface. Images of the above compound were made using CrystalMaker for Windows, version 9.2.8 (CrystalMaker, 2017). The refinement proceeded without any incidents and without any need for modelling disorder or twinning or restraints. The crystal was then mounted on MiTeGen Microloop with non-drying immersion oil. The crystal was then optically aligned on the Rigaku SCX-Mini diffractometer using a digital camera. Initial matrix images were collected to determine the unit cell, validity and proper exposure time. Three hemispheres (where φ= 0.0, 120.0 and 240.0) of data were collected with each consisting 180 images each with 1.00° widths and a 1.00° step. Refinement of the structure was based on F2 against all reflections. The R-factor R is based on F2>2σ(F2), but is not relevant to the choice of reflections for refinement; whereas the weighted R-factor wR and goodness of fit S are based on F2. Due to the presence of exclusively intense diffraction peaks, there is no observable difference between the R factors for all versus gt.

	x	y	z	Uiso*/Ueq
Ce1	1.0000	1.0000	0.5000	0.01612 (11)
P1	0.6667	0.3333	0.19839 (17)	0.01440 (18)
O1	0.81417 (19)	0.6283 (4)	0.2762 (4)	0.0330 (4)
H1	0.6667	0.3333	−0.059 (11)	0.040*

	U11	U22	U33	U12	U13	U23
Ce1	0.00810 (11)	0.00810 (11)	0.03215 (17)	0.00405 (6)	0.000	0.000
P1	0.0114 (3)	0.0114 (3)	0.0204 (4)	0.00569 (13)	0.000	0.000
O1	0.0330 (8)	0.0141 (8)	0.0456 (9)	0.0071 (4)	−0.0037 (4)	−0.0074 (7)

Ce1—O1	2.2193 (19)	P1—H1	1.44 (6)
P1—O1	1.5168 (19)
O1i—Ce1—O1ii	180.0	O1ii—Ce1—O1	91.15 (8)
O1iii—Ce1—O1iv	88.85 (8)	O1i—Ce1—O1v	91.15 (8)
O1i—Ce1—O1iv	88.85 (8)	O1ii—Ce1—O1iv	91.15 (8)
O1—Ce1—O1iv	91.15 (8)	O1—Ce1—O1v	88.85 (8)
O1—Ce1—O1iii	180.00 (9)	O1vi—P1—O1vii	112.07 (8)
O1iii—Ce1—O1v	91.15 (8)	O1vi—P1—O1	112.07 (8)
O1i—Ce1—O1iii	91.15 (8)	O1vii—P1—O1	112.07 (8)
O1i—Ce1—O1	88.85 (8)	O1—P1—H1	106.73 (9)
O1ii—Ce1—O1iii	88.85 (8)	O1vi—P1—H1	106.73 (9)
O1ii—Ce1—O1v	88.85 (8)	O1vii—P1—H1	106.73 (9)
O1iv—Ce1—O1v	180.0	P1—O1—Ce1	162.28 (14)