Bis(homopiperazine-1,4-diium) cyclo­tetra­phosphate–telluric acid (1/2)

Hemissi, H.; Rzaigui, M.; Al-Deyab, S.S.

doi:10.1107/S1600536810038225

organic compounds

CRYSTALLOGRAPHIC
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ISSN: 2056-9890

Volume 66| Part 11| November 2010| Page o2712

https://doi.org/10.1107/S1600536810038225

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Bis(homopiperazine-1,4-diium) cyclotetraphosphate–telluric acid (1/2)

Hanène Hemissi,^a ^* Mohammed Rzaigui ^a and Salem S. Al-Deyab ^b

^aLaboratoire de Chimie des Matériaux, Faculté des Sciences de Bizerte, 7021 Zarzouna Bizerte, Tunisia, and ^bPetrochemical Research Chair, College of Science, King Saud University, Riyadh, Saudi Arabia
^*Correspondence e-mail: hanene.hemissi@fsb.rnu.tn

(Received 13 August 2010; accepted 24 September 2010; online 2 October 2010)

The title compound, 2C₅H₁₄N₂²⁺·P₄O₁₂⁴⁻·2Te(OH)₆, involves doubly protonated homopiperazinium cations, cyclotetraphosphate anions and telluric acid molecules. The framework possesses very large channels wherein the organic cations reside. A network of O—H⋯O, N—H⋯O and C—H⋯O hydrogen bonds consolidates the crystal packing.

Related literature

For the properties of materials containing telluric acid, see: Chabchoub et al. (2006 ); Khemakhem, (1999 ). For related structures containing phosphate rings and telluric acid, see: Averbuch-Pouchot & Durif (1987a ,b ); Durif et al. (1982 ). For hydrogen bonding, see: Blessing (1986 ); Brown (1976 ). For deviations in four-membered phosphate rings having the same $[\overline{1}]$ internal symmetry, see: Durif (1995 ); A similar conformation for the same organic molecule was observed in (C₅H₁₄N₂)(H₂AsO₄)₂, see: Wilkinson & Harrison (2006 ). For the synthesis, see: Ondik (1964 ).

Experimental

Crystal data

C₅H₁₄N₂²⁺·0.5P₄O₁₂⁴⁻·Te(OH)₆
M_r = 489.77
Monoclinic, C 2/c
a = 20.826 (3) Å
b = 8.3600 (13) Å
c = 17.030 (8) Å
β = 101.65 (3)°
V = 2903.9 (14) Å³
Z = 8
Ag Kα radiation
λ = 0.56083 Å
μ = 1.24 mm⁻¹
T = 293 K
0.2 × 0.18 × 0.16 mm

Data collection

Enraf–Nonius CAD-4 diffractometer
8219 measured reflections
6346 independent reflections
4847 reflections with I > 2σ(I)
R_int = 0.027
2 standard reflections every 120 min intensity decay: 5%

Refinement

R[F² > 2σ(F²)] = 0.033
wR(F²) = 0.084
S = 1.01
6346 reflections
223 parameters
12 restraints
H atoms treated by a mixture of independent and constrained refinement
Δρ_max = 1.99 e Å⁻³
Δρ_min = −1.19 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O1—H1⋯O12ⁱ	0.86 (2)	1.85 (2)	2.686 (3)	165 (2)
N1—H1B⋯O4ⁱⁱ	0.90	2.15	2.898 (3)	140
N1—H1B⋯O9ⁱⁱⁱ	0.90	2.42	3.002 (3)	123
N1—H1A⋯O2^iv	0.90	1.89	2.763 (3)	162
O2—H2⋯O9^v	0.86 (2)	1.83 (2)	2.688 (3)	172 (3)
N2—H2A⋯O12	0.90	1.89	2.769 (3)	167
N2—H2B⋯O11^vi	0.90	1.85	2.739 (3)	172
O3—H3⋯O8^v	0.84 (3)	2.05 (3)	2.881 (3)	170 (4)
O4—H4⋯O1^vii	0.85 (3)	1.85 (3)	2.695 (3)	175 (3)
O5—H5⋯O8^viii	0.87 (3)	1.85 (3)	2.719 (3)	172 (3)
O6—H6⋯O9^ix	0.83 (3)	1.90 (2)	2.722 (3)	171 (3)
C2—H2C⋯O1^x	0.97	2.60	3.162 (3)	117
C4—H4B⋯O5ⁱ	0.97	2.43	3.256 (4)	142
C5—H5B⋯O11^xi	0.97	2.31	3.265 (4)	168
Symmetry codes: (i) $[-x+{\script{1\over 2}}, -y+{\script{1\over 2}}, -z+1]$ ; (ii) -x, -y+1, -z+1; (iii) $[-x+{\script{1\over 2}}, y+{\script{1\over 2}}, -z+{\script{3\over 2}}]$ ; (iv) x, y, z+1; (v) $[x-{\script{1\over 2}}, -y+{\script{1\over 2}}, z-{\script{1\over 2}}]$ ; (vi) $[-x+{\script{1\over 2}}, y-{\script{1\over 2}}, -z+{\script{3\over 2}}]$ ; (vii) $[-x, y, -z+{\script{1\over 2}}]$ ; (viii) $[-x+{\script{1\over 2}}, y-{\script{1\over 2}}, -z+{\script{1\over 2}}]$ ; (ix) $[-x+{\script{1\over 2}}, y+{\script{1\over 2}}, -z+{\script{1\over 2}}]$ ; (x) $[x, -y, z+{\script{1\over 2}}]$ ; (xi) $[x, -y+1, z+{\script{1\over 2}}]$ .

Data collection: CAD-4 EXPRESS (Enraf–Nonius, 1994 ); cell refinement: CAD-4 EXPRESS; data reduction: XCAD4 (Harms & Wocadlo, 1996 ); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997 ); software used to prepare material for publication: WinGX (Farrugia, 1999 ).

Supporting information

Crystal structure: contains datablocks I, global. DOI: https://doi.org/10.1107/S1600536810038225/bv2159sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536810038225/bv2159Isup2.hkl

checkCIF report

Comment top

Materials containing telluric acid exhibit many interesting physical properties such as ferroelectricity and protonic conduction (Chabchoub et al.,2006; Khemakhem, 1999). On the chemical plane, telluric acid has the property to form adduct compounds with many kinds of phosphates and was extensively investigated during the past thirty years. With cyclotriphosphate, several adduct compounds of telluric acid have been identified whereas with cyclotetraphosphate only three inorganic telluric acid-adduct compounds are reported: (NH₄)₄P₄O₁₂.Te(OH)₆.2H₂O (Durif et al.,1982), K₄P₄O₁₂.Te(OH)₆.2H₂O and Rb₄P₄O₁₂.Te(OH)₆.2H₂O (Averbuch-Pouchot & Durif, 1987a b). In the present work, we report the first telluric acid-adduct compound of an organic cyclotetraphosphate (C₅H₁₄N₂)₂P₄O₁₂.2Te(OH)₆(I). The configuration of different components of (I) is shown in Figure 1. In the crystal structure of this compound, P₄O₁₂^4-and Te(OH)₆ form an anionic three-dimensional framework. The negative charge of this is compensated by the diprotonated amine (C₅H₁₄N₂)²⁺. Figure 2 shows the total atomic arrangement projected along the [1 0 1] direction. This projection shows that the inorganic entities form very large channels wherein the organic cations are located. The telluric acid molecules Te(OH)₆ are linked pair-wise by two symmetric strong O—H···O hydrogen bonds, with an O···O distance of 2.695 (3) Å, into dimers where the Te···Te distance is 5.102 (5) Å. The tellurium atom is surrounded by six OH groups in a rather regular octahedral arrangement as indicated by the Te-O distances ranging from 1.905 (2) to 1.916 (2) Å, the cis and trans O-Te-O angles which are found in the 87.4 (1)-92.94 (9) ° and 175.03 (9)-178.8 (1)° ranges, respectively, and Te—O—H angles ranging from 107 (3) to 116 (3)°. Each Te(OH)₆ dimer is linked to six P₄O₁₂ rings and two homopiperazinium (C₅H₁₄N₂)²⁺ through a three-dimensional hydrogen bonding network O—H···O and N—H···O (Fig. 3). The P₄O₁₂ ring anions are centrosymmetric and are built by only two crystallographically independent PO₄ tetrahedra with P-O distances ranging from 1.477 (2) to 1.605 (2) Å and O-P-O angles ranging from 103.9 (1) to 120.2 (2)° with a mean value (109.22°) very close to the ideal value (109.28°). In spite of these large ranges in P-O distances and O-P-O angles, which can be explained by different environments of oxygen atoms, the PO₄ tetrahedron is described by regular oxygen atom arrangement with the phosphorus atom shifted by 0.122 and 0.149 Å from the centre of gravity . The cyclic anion is distorted as evidenced by P—P—P angles (81.60 (1) and 98.40 (1)°) which show a pronounced deviation from the ideal value (90°). Such deviation is commonly observed in tetramembered phosphoric rings having the same -1 internal symmetry (Durif, 1995). Only one homopiperazinium cation (C₅H₁₄N₂)²⁺ exists in the asymmetric unit and adopts a chair conformation as evidenced by the mean deviation (±0.0251 Å) from the least square plane defined by the four constituent atoms N1, N2, C1 and C3 and the remaining atoms C2, C4 and C5 displaced from the plane by 0.7495 (3), 0.6175 (3) and -0.2661 (3) Å, respectively. A similar conformation for the same organic molecule was observed in (C₅H₁₄N₂)(H₂AsO₄)₂ (Wilkinson & Harrison, 2006) with important difference that the "seat" chair was defined by one N atom and three C atoms rather than two N atoms and two C atoms as found here. The organic and inorganic components exert between them different interactions (electrostatic, hydrogen bonds and Van der Waals) to form a stable three-dimensional network. The examination of the hydrogen-bond scheme shows the existence of four strong hydrogen bonds with distances O···O ranging from 2.686 (3) to 2.722 (3) Å. The other bonds are weaker, with O(N,C)···O distances falling from 2.739 (3) to 3.265 (4) Å (Blessing, 1986; Brown, 1976).

Related literature top

For the properties of materials containing telluric acid, see: Chabchoub et al. (2006); Khemakhem, (1999). For related structures containing phosphoric rings and telluric acid, see: Averbuch-Pouchot & Durif (1987a,b); Durif et al. (1982). For hydrogen bonding, see: Blessing (1986); Brown (1976). For deviations in four-membered phosphoric rings having the same 1 internal symmetry, see: Durif (1995); A similar conformation for the same organic molecule was observed in (C₅H₁₄N₂)(H₂AsO₄)₂, see: Wilkinson & Harrison (2006). For the synthesis, see: Ondik (1964).

Experimental top

Crystals of the title compound were prepared by adding ethanolic solution (5 ml) of homopiperazine (10 mmol) dropwise to an aqueous solution of cyclotetraphosphoric acid (5 mmol, 20 ml). The obtained solution was added to an aquous solution of telluric acid (10 mmol, 15 ml). Good quality of colourless prisms were obtained after a slow evaporation during few days at ambient temperature. The cyclotetraphosphoric acid H₄P₄O₁₂, was produced from Na₄P₄O₁₂.4H₂O, prepared according to the Ondik process (Ondik, 1964), through an ion-exchange resin in H-state (Amberlite IR 120).

Structure description top

Computing details top

Data collection: CAD-4 EXPRESS (Enraf–Nonius, 1994); cell refinement: CAD-4 EXPRESS (Enraf–Nonius, 1994); data reduction: XCAD4 (Harms & Wocadlo, 1996); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997); software used to prepare material for publication: WinGX (Farrugia, 1999).

Figures top

	Fig. 1. An ORTEP view of (I) with the atom-labelling scheme. Displacement ellipsoids are drawn at the 50% probability level. H atoms are represented as small spheres of arbitrary radii. [Symmetry codes: (i) 1/2 - x, 1/2 - y, 1 - z].
	Fig. 2. Projection of (I) along [1 0 1] direction. Some hydrogen atoms are omitted for clarity.
	Fig. 3. A perspective view of the atomic arrangement of (I).

Bis(piperazine-1,4-diium) cyclotetraphosphate–telluric acid (1/2) top

Crystal data top

C₅H₁₄N₂²⁺·0.5P₄O₁₂⁴⁻·Te(OH)₆	F(000) = 1936
M_r = 489.77	D_x = 2.241 Mg m⁻³
Monoclinic, C2/c	Ag Kα radiation, λ = 0.56083 Å
Hall symbol: -C 2yc	Cell parameters from 25 reflections
a = 20.826 (3) Å	θ = 9.0–10.9°
b = 8.3600 (13) Å	µ = 1.24 mm⁻¹
c = 17.030 (8) Å	T = 293 K
β = 101.65 (3)°	Prism, colourless
V = 2903.9 (14) Å³	0.2 × 0.18 × 0.16 mm
Z = 8

Data collection top

Enraf–Nonius CAD-4 diffractometer	R_int = 0.027
Radiation source: Enraf Nonius FR590	θ_max = 27.0°, θ_min = 2.1°
Graphite monochromator	h = −33→33
Non–profiled ω scans	k = 0→13
8219 measured reflections	l = −5→27
6346 independent reflections	2 standard reflections every 120 min
4847 reflections with I > 2σ(I)	intensity decay: 5%

Refinement top

Refinement on F²	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F² > 2σ(F²)] = 0.033	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.084	H atoms treated by a mixture of independent and constrained refinement
S = 1.01	w = 1/[σ²(F_o²) + (0.0482P)²] where P = (F_o² + 2F_c²)/3
6346 reflections	(Δ/σ)_max = 0.001
223 parameters	Δρ_max = 1.99 e Å⁻³
12 restraints	Δρ_min = −1.19 e Å⁻³

Crystal data top

C₅H₁₄N₂²⁺·0.5P₄O₁₂⁴⁻·Te(OH)₆	V = 2903.9 (14) Å³
M_r = 489.77	Z = 8
Monoclinic, C2/c	Ag Kα radiation, λ = 0.56083 Å
a = 20.826 (3) Å	µ = 1.24 mm⁻¹
b = 8.3600 (13) Å	T = 293 K
c = 17.030 (8) Å	0.2 × 0.18 × 0.16 mm
β = 101.65 (3)°

Data collection top

Enraf–Nonius CAD-4 diffractometer	R_int = 0.027
8219 measured reflections	2 standard reflections every 120 min
6346 independent reflections	intensity decay: 5%
4847 reflections with I > 2σ(I)

Refinement top

R[F² > 2σ(F²)] = 0.033	12 restraints
wR(F²) = 0.084	H atoms treated by a mixture of independent and constrained refinement
S = 1.01	Δρ_max = 1.99 e Å⁻³
6346 reflections	Δρ_min = −1.19 e Å⁻³
223 parameters

Special details top

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 (Å²) top

	x	y	z	U_iso*/U_eq
C5	0.17222 (12)	0.3358 (3)	0.92873 (16)	0.0227 (5)
H5A	0.1782	0.2247	0.9450	0.027*
H5B	0.1909	0.4014	0.9747	0.027*
C4	0.20920 (13)	0.3672 (3)	0.86247 (18)	0.0253 (5)
H4A	0.1880	0.4538	0.8291	0.030*
H4B	0.2535	0.4010	0.8860	0.030*
H3	−0.0202 (13)	0.058 (5)	0.080 (2)	0.060 (14)*
H4	−0.0415 (18)	0.298 (4)	0.1851 (19)	0.039 (11)*
H1	0.1244 (7)	0.217 (4)	0.2504 (13)	0.027 (9)*
H6	0.0994 (18)	0.505 (3)	0.1086 (14)	0.053 (13)*
H2	−0.0171 (9)	0.333 (4)	0.0087 (11)	0.024 (8)*
H5	0.1230 (13)	0.094 (3)	0.068 (2)	0.047 (12)*
Te1	0.053963 (7)	0.257312 (16)	0.128185 (8)	0.01399 (4)
P1	0.35495 (3)	0.28147 (6)	0.49522 (3)	0.01199 (9)
P2	0.26836 (3)	0.30733 (7)	0.61119 (3)	0.01214 (9)
O10	0.32281 (8)	0.22730 (19)	0.56907 (10)	0.0161 (3)
O7	0.29316 (8)	0.3056 (2)	0.42301 (10)	0.0167 (3)
O9	0.39402 (8)	0.1419 (2)	0.47840 (11)	0.0199 (3)
O1	0.08267 (8)	0.2069 (2)	0.23924 (11)	0.0200 (3)
O11	0.25530 (8)	0.4740 (2)	0.58395 (11)	0.0197 (3)
N2	0.21224 (11)	0.2239 (2)	0.81152 (15)	0.0223 (4)
H2A	0.2422	0.2419	0.7812	0.027*
H2B	0.2264	0.1404	0.8438	0.027*
O4	−0.02504 (9)	0.3469 (2)	0.15028 (12)	0.0239 (4)
O6	0.09666 (11)	0.4585 (2)	0.15090 (12)	0.0273 (4)
O8	0.38702 (8)	0.4392 (2)	0.51103 (11)	0.0197 (3)
O12	0.28855 (8)	0.2710 (2)	0.69789 (10)	0.0217 (3)
O2	0.02429 (9)	0.3119 (3)	0.01751 (11)	0.0229 (4)
O5	0.13208 (8)	0.1739 (3)	0.10185 (12)	0.0254 (4)
C3	0.14949 (14)	0.1782 (3)	0.75778 (16)	0.0268 (5)
H3A	0.1564	0.0813	0.7292	0.032*
H3B	0.1368	0.2621	0.7183	0.032*
N1	0.10076 (10)	0.3697 (3)	0.90552 (13)	0.0211 (4)
H1A	0.0817	0.3340	0.9451	0.025*
H1B	0.0955	0.4765	0.9031	0.025*
C2	0.09384 (13)	0.1504 (3)	0.80154 (17)	0.0245 (5)
H2C	0.0595	0.0911	0.7665	0.029*
H2D	0.1099	0.0841	0.8481	0.029*
O3	0.01479 (9)	0.0496 (2)	0.11451 (13)	0.0253 (4)
C1	0.06439 (13)	0.3009 (4)	0.82876 (18)	0.0289 (5)
H1C	0.0619	0.3812	0.7871	0.035*
H1D	0.0199	0.2775	0.8344	0.035*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
C5	0.0248 (11)	0.0218 (10)	0.0203 (11)	0.0009 (9)	0.0014 (9)	−0.0054 (9)
C4	0.0217 (10)	0.0176 (10)	0.0379 (15)	−0.0035 (8)	0.0093 (10)	−0.0031 (10)
Te1	0.01393 (6)	0.01490 (6)	0.01358 (6)	0.00039 (5)	0.00382 (4)	0.00058 (5)
P1	0.0102 (2)	0.0138 (2)	0.0119 (2)	−0.00096 (16)	0.00219 (17)	−0.00043 (17)
P2	0.0121 (2)	0.0149 (2)	0.0091 (2)	−0.00041 (17)	0.00137 (17)	−0.00098 (18)
O10	0.0179 (7)	0.0176 (7)	0.0150 (7)	0.0030 (5)	0.0081 (6)	0.0033 (5)
O7	0.0144 (6)	0.0184 (7)	0.0153 (7)	−0.0029 (5)	−0.0016 (5)	0.0042 (6)
O9	0.0178 (7)	0.0238 (8)	0.0187 (8)	0.0042 (6)	0.0051 (6)	−0.0050 (6)
O1	0.0178 (7)	0.0266 (8)	0.0151 (7)	0.0017 (6)	0.0023 (6)	0.0054 (6)
O11	0.0218 (8)	0.0140 (7)	0.0224 (8)	0.0010 (6)	0.0023 (7)	−0.0022 (6)
N2	0.0252 (9)	0.0183 (8)	0.0275 (11)	0.0030 (7)	0.0152 (9)	0.0046 (7)
O4	0.0236 (8)	0.0291 (9)	0.0213 (8)	0.0106 (7)	0.0101 (7)	0.0080 (7)
O6	0.0435 (11)	0.0192 (8)	0.0191 (9)	−0.0103 (8)	0.0060 (8)	−0.0019 (7)
O8	0.0191 (7)	0.0189 (7)	0.0198 (8)	−0.0068 (6)	0.0010 (6)	−0.0013 (6)
O12	0.0173 (7)	0.0394 (10)	0.0084 (6)	−0.0014 (7)	0.0021 (6)	0.0014 (6)
O2	0.0170 (7)	0.0376 (10)	0.0142 (7)	0.0013 (7)	0.0034 (6)	0.0046 (7)
O5	0.0146 (7)	0.0335 (10)	0.0282 (10)	0.0016 (7)	0.0045 (7)	−0.0091 (8)
C3	0.0350 (13)	0.0285 (12)	0.0182 (11)	0.0024 (10)	0.0083 (10)	−0.0008 (10)
N1	0.0248 (9)	0.0209 (9)	0.0197 (10)	0.0009 (7)	0.0094 (8)	−0.0039 (7)
C2	0.0254 (11)	0.0217 (11)	0.0261 (12)	−0.0026 (9)	0.0042 (10)	−0.0058 (9)
O3	0.0218 (8)	0.0196 (8)	0.0326 (11)	−0.0040 (6)	0.0009 (8)	0.0022 (7)
C1	0.0222 (11)	0.0325 (13)	0.0306 (14)	0.0044 (10)	0.0021 (10)	−0.0068 (11)

Geometric parameters (Å, º) top

C5—N1	1.488 (3)	O7—P2ⁱ	1.6033 (17)
C5—C4	1.512 (4)	O1—H1	0.855 (13)
C5—H5A	0.9700	N2—C3	1.486 (4)
C5—H5B	0.9700	N2—H2A	0.9000
C4—N2	1.488 (3)	N2—H2B	0.9000
C4—H4A	0.9700	O4—H4	0.846 (18)
C4—H4B	0.9700	O6—H6	0.830 (17)
Te1—O5	1.9050 (18)	O2—H2	0.862 (16)
Te1—O6	1.9050 (18)	O5—H5	0.874 (17)
Te1—O1	1.9119 (19)	C3—C2	1.517 (4)
Te1—O3	1.9124 (18)	C3—H3A	0.9700
Te1—O4	1.9130 (18)	C3—H3B	0.9700
Te1—O2	1.916 (2)	N1—C1	1.488 (4)
P1—O8	1.4784 (17)	N1—H1A	0.9000
P1—O9	1.4831 (17)	N1—H1B	0.9000
P1—O7	1.6028 (18)	C2—C1	1.513 (4)
P1—O10	1.6046 (18)	C2—H2C	0.9700
P2—O11	1.4766 (18)	C2—H2D	0.9700
P2—O12	1.4825 (19)	O3—H3	0.840 (19)
P2—O7ⁱ	1.6033 (17)	C1—H1C	0.9700
P2—O10	1.6052 (17)	C1—H1D	0.9700

N1—C5—C4	113.7 (2)	P1—O10—P2	132.59 (11)
N1—C5—H5A	108.8	P1—O7—P2ⁱ	131.58 (11)
C4—C5—H5A	108.8	Te1—O1—H1	107.4 (15)
N1—C5—H5B	108.8	C3—N2—C4	115.5 (2)
C4—C5—H5B	108.8	C3—N2—H2A	108.4
H5A—C5—H5B	107.7	C4—N2—H2A	108.4
N2—C4—C5	112.5 (2)	C3—N2—H2B	108.4
N2—C4—H4A	109.1	C4—N2—H2B	108.4
C5—C4—H4A	109.1	H2A—N2—H2B	107.5
N2—C4—H4B	109.1	Te1—O4—H4	116 (3)
C5—C4—H4B	109.1	Te1—O6—H6	110.3 (17)
H4A—C4—H4B	107.8	Te1—O2—H2	109.4 (13)
O5—Te1—O6	89.15 (9)	Te1—O5—H5	110.6 (16)
O5—Te1—O1	92.34 (9)	N2—C3—C2	113.6 (2)
O6—Te1—O1	87.36 (8)	N2—C3—H3A	108.8
O5—Te1—O3	90.15 (9)	C2—C3—H3A	108.8
O6—Te1—O3	175.03 (9)	N2—C3—H3B	108.8
O1—Te1—O3	87.75 (9)	C2—C3—H3B	108.8
O5—Te1—O4	177.38 (9)	H3A—C3—H3B	107.7
O6—Te1—O4	89.95 (9)	C1—N1—C5	117.7 (2)
O1—Te1—O4	90.08 (8)	C1—N1—H1A	107.9
O3—Te1—O4	90.96 (8)	C5—N1—H1A	107.9
O5—Te1—O2	88.67 (9)	C1—N1—H1B	107.9
O6—Te1—O2	91.96 (9)	C5—N1—H1B	107.9
O1—Te1—O2	178.78 (8)	H1A—N1—H1B	107.2
O3—Te1—O2	92.94 (9)	C1—C2—C3	114.8 (2)
O4—Te1—O2	88.91 (8)	C1—C2—H2C	108.6
O8—P1—O9	119.45 (10)	C3—C2—H2C	108.6
O8—P1—O7	106.91 (10)	C1—C2—H2D	108.6
O9—P1—O7	109.72 (10)	C3—C2—H2D	108.6
O8—P1—O10	110.71 (10)	H2C—C2—H2D	107.5
O9—P1—O10	105.15 (10)	Te1—O3—H3	107 (3)
O7—P1—O10	103.86 (9)	N1—C1—C2	115.1 (2)
O11—P2—O12	120.22 (11)	N1—C1—H1C	108.5
O11—P2—O7ⁱ	111.00 (9)	C2—C1—H1C	108.5
O12—P2—O7ⁱ	106.65 (10)	N1—C1—H1D	108.5
O11—P2—O10	110.78 (10)	C2—C1—H1D	108.5
O12—P2—O10	106.01 (10)	H1C—C1—H1D	107.5
O7ⁱ—P2—O10	100.20 (9)

Symmetry code: (i) −x+1/2, −y+1/2, −z+1.

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O1—H1···O12ⁱ	0.86 (2)	1.85 (2)	2.686 (3)	165 (2)
N1—H1B···O4ⁱⁱ	0.90	2.15	2.898 (3)	140
N1—H1B···O9ⁱⁱⁱ	0.90	2.42	3.002 (3)	123
N1—H1A···O2^iv	0.90	1.89	2.763 (3)	162
O2—H2···O9^v	0.86 (2)	1.83 (2)	2.688 (3)	172 (3)
N2—H2A···O12	0.90	1.89	2.769 (3)	167
N2—H2B···O11^vi	0.90	1.85	2.739 (3)	172
O3—H3···O8^v	0.84 (3)	2.05 (3)	2.881 (3)	170 (4)
O4—H4···O1^vii	0.85 (3)	1.85 (3)	2.695 (3)	175 (3)
O5—H5···O8^viii	0.87 (3)	1.85 (3)	2.719 (3)	172 (3)
O6—H6···O9^ix	0.83 (3)	1.90 (2)	2.722 (3)	171 (3)
C2—H2C···O1^x	0.97	2.60	3.162 (3)	117
C4—H4B···O5ⁱ	0.97	2.43	3.256 (4)	142
C5—H5B···O11^xi	0.97	2.31	3.265 (4)	168

Symmetry codes: (i) −x+1/2, −y+1/2, −z+1; (ii) −x, −y+1, −z+1; (iii) −x+1/2, y+1/2, −z+3/2; (iv) x, y, z+1; (v) x−1/2, −y+1/2, z−1/2; (vi) −x+1/2, y−1/2, −z+3/2; (vii) −x, y, −z+1/2; (viii) −x+1/2, y−1/2, −z+1/2; (ix) −x+1/2, y+1/2, −z+1/2; (x) x, −y, z+1/2; (xi) x, −y+1, z+1/2.

Experimental details

Crystal data
Chemical formula	C₅H₁₄N₂²⁺·0.5P₄O₁₂⁴⁻·Te(OH)₆
M_r	489.77
Crystal system, space group	Monoclinic, C2/c
Temperature (K)	293
a, b, c (Å)	20.826 (3), 8.3600 (13), 17.030 (8)
β (°)	101.65 (3)
V (Å³)	2903.9 (14)
Z	8
Radiation type	Ag Kα, λ = 0.56083 Å
µ (mm⁻¹)	1.24
Crystal size (mm)	0.2 × 0.18 × 0.16

Data collection
Diffractometer	Enraf–Nonius CAD-4
Absorption correction	–
No. of measured, independent and observed [I > 2σ(I)] reflections	8219, 6346, 4847
R_int	0.027
(sin θ/λ)_max (Å⁻¹)	0.809

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.033, 0.084, 1.01
No. of reflections	6346
No. of parameters	223
No. of restraints	12
H-atom treatment	H atoms treated by a mixture of independent and constrained refinement
Δρ_max, Δρ_min (e Å⁻³)	1.99, −1.19

Computer programs: CAD-4 EXPRESS (Enraf–Nonius, 1994), XCAD4 (Harms & Wocadlo, 1996), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 for Windows (Farrugia, 1997), WinGX (Farrugia, 1999).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O1—H1···O12ⁱ	0.856 (16)	1.851 (17)	2.686 (3)	165 (2)
N1—H1B···O4ⁱⁱ	0.90	2.15	2.898 (3)	140
N1—H1B···O9ⁱⁱⁱ	0.90	2.42	3.002 (3)	123
N1—H1A···O2^iv	0.90	1.89	2.763 (3)	162
O2—H2···O9^v	0.86 (2)	1.831 (19)	2.688 (3)	172 (3)
N2—H2A···O12	0.90	1.89	2.769 (3)	167
N2—H2B···O11^vi	0.90	1.85	2.739 (3)	172
O3—H3···O8^v	0.84 (3)	2.05 (3)	2.881 (3)	170 (4)
O4—H4···O1^vii	0.85 (3)	1.85 (3)	2.695 (3)	175 (3)
O5—H5···O8^viii	0.87 (3)	1.85 (3)	2.719 (3)	172 (3)
O6—H6···O9^ix	0.83 (3)	1.90 (2)	2.722 (3)	171 (3)
C2—H2C···O1^x	0.97	2.60	3.162 (3)	117
C4—H4B···O5ⁱ	0.97	2.43	3.256 (4)	142
C5—H5B···O11^xi	0.97	2.31	3.265 (4)	168

References

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