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The title compound, Na+·C5H9N2O7P2-·4H2O, is an isomer of zoledronate, a potent bone antiresorptive bis­phospho­nate drug having significant activity against several parasitic protozoa. The crystal structure of isozoledronate consists of bisphosphonate dimers coordinated by two Na+ ions. The dimers are held together through an extensive hydrogen-bonding network. The crystals exhibit non-merohedral twinning that roughly superimposes the a and b axes, and inverts the c axis.

Supporting information

cif

Crystallographic Information File (CIF) https://doi.org/10.1107/S0108270102019522/gg1144sup1.cif
Contains datablocks I, global

hkl

Structure factor file (CIF format) https://doi.org/10.1107/S0108270102019522/gg1144Isup2.hkl
Contains datablock I

CCDC reference: 201261

Comment top

The title compound is an isomer of zoledronate, a potent bone antiresorptive bisphosphonate drug (marketed by Novartis as Zometa). Isozoledronate, as well as a series of other bisphosphonates, have recently been shown to have significant activity against Trypanosoma cruzi, a parasitic protozoan which is the causative agent of Chagas' disease, and Trypanosoma brucei, the causative agent of African sleeping sickness (Martin et al., 2001). It is of importance to understand the key structural features of bisphosphonates that lead to their activity. In order to develop good quantitative structure-activity relationship (QSAR) methods, information is needed on the patterns of protonation and charge distribution, since these influence the predictive power of the QSAR method. Isozoledronate has a wide range of possible protonation states and charge distributions, arising from the phosphonates and the imidazole ring, so to gain a better understanding of these charge distributions, the crystal structure of monosodium [1-hydroxy-2-(1H-imidazol-3-ium-4-yl)ethane-1,1-diyl]bis(phosphonate) tetrahydrate, isozoledronate, (I), is reported herein. \sch

In the crystal structure of (I), both N atoms (N1 and N3) in the imidazole ring are protonated, leading to a +1 charge in the ring, while both phosphonate groups have only one protonated O atom, leading to a -1 charge on each phosphonate group. The isozoledronate anion is also coordinated to one Na+ cation, leading to the zwitterionic character found in many bisphosphonates (Vega et al., 1996, 1998). Inspection of the bond distances in the imidazole ring shows two short [N1—C2 1.327 (3) and N3—C2 1.315 (3) Å] and two long [N1—C5 1.384 (2) and N3—C4 1.370 (3) Å] N—C bonds, implying partial double-bond character between atoms C2 and N1/N3, but essentially single-bond character at N1—C5 and N3—C4, consistent with an approximately equal charge distribution on the two N atoms. The other double bond in the ring is found at C4—C5.

Analysis of the bond distances in the phosphonate groups [P1—O2 1.506 (1), P1—O3 1.498 (1) and P1—O4 1.591 (1) Å, and P2—O5 1.499 (1), P2—O6 1.524 (1) and P2—O7 1.569 (2) Å] reveals one protonated O atom on each phosphonate group, namely O4 and O7, and two nonprotonated O atoms on each, namely O2 and O3, and O5 and O6, resulting in a -1 charge on each phosphonate group. The orientation of the phosphonate groups with respect to the ring is very similar to that recently found in risedronate, both with respect to the backbone C—C—C angles [C5—C6—C7 113.4 (2)° in (I), C3—C2—C1 117.4 (4)° in RHP, C3—C2—C1 117.5 (3)° in RMH and C3—C2—C1 114.8 (2)° in RDH] and to the torsion angles between the phosphonate groups and the ring [P1—C5—C6—C7 62.0 (2)° in (I), P1—C1—C2—C3 52.6 (5)° in RHP, P1—C1—C2—C3 57.7 (3)° in RMH and P1—C1—C2—C3 61.8 (3)° in RDH], where RHP, RMH and RDH are analogues of (I) (Gossman et al., 2002).

Compound (I) consists of anionic dimers coordinated by two Na+ cations, as shown in Fig. 1. These dimers are held together through an extensive hydrogen-bonding network, consisting of at least 13 hydrogen bonds.

Experimental top

Crystals of (I) were grown by vapour diffusion of ethanol into water. All crystals examined exhibited non-merohedral twinning, which roughly superimposed the a and b axes and inverted the c axis. Two distinct triclinic cells were identified using SMART (Bruker, 2001) and integrated using SAINT (Bruker, 2001). Unit-cell parameters were determined from both components using SAINT. The twin law by rows was (0 1 0, 1 0 0, 1/2 1/2 - 1). Non-overlapping reflections from the primary orientation were used for phasing. Four frame series were filtered for statistical outliers and then sorted, merged, scaled and corrected for absorption using TWINABS, an unpublished upgrade of SADABS (Bruker, 2001) written for non-merohedral twins. A unique section of reciprocal space was measured. However, owing to the close proximity of the non-merohedral twins, reflections filtered as statistical outliers left the fraction of data measured at full theta slightly less than ideal (0.88). Combined data with complete or no overlap were used for refinement. Crystal decay was monitored by collecting identical frames at the beginning and end of the experiment. No correction for decay as a function of X-ray exposure time was applied.

Refinement top

Systematic conditions suggested the ambiguous space group. Inversion symmetry was imposed on the dimer. R—H distances were restrained to ideal values, with an effective s.u. of 0.02 Å, and H—O—H angles were also restrained to ideal values (s.u. 0.04°). The remaining H-atom parameters were independently refined without restraints. The relative volume of the secondary orientation converged at 0.2687 (7). The choice of space group was confirmed by successful convergence of the full-matrix least-squares refinement on F2 (SHELXL97; Sheldrick, 2001). The highest peaks in the final difference Fourier map were located along the C—P bonds; the final map had no other significant features. A final analysis of the variance between observed and calculated structure factors showed no dependence on amplitude or resolution.

Computing details top

Data collection: SMART (Bruker, 2001); cell refinement: SAINT (Bruker, 2001); data reduction: SAINT; program(s) used to solve structure: SHELXTL (Bruker, 2001); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: CIFTAB in SHELXL97 (Sheldrick, 2001).

Figures top
[Figure 1] Fig. 1. A view of the molecular structure of (I), showing the atom-numbering scheme. Displacement ellipsoids are drawn at the 35% probability level and H atoms are shown as small spheres of arbitrary radii.
Monosodium [1-hydroxy-2-(1H-imidazol-3-ium-4-yl)ethane-1,1-diyl]bis(phosphonate) tetrahydrate top
Crystal data top
Na(C5H9N2O7P2)·4H2OZ = 2
Mr = 366.14F(000) = 380
Triclinic, P1Dx = 1.781 Mg m3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 6.6664 (19) ÅCell parameters from 864 reflections
b = 6.6765 (19) Åθ = 2.6–28.1°
c = 15.5711 (18) ŵ = 0.41 mm1
α = 84.075 (4)°T = 193 K
β = 82.803 (5)°Prism, colourless
γ = 85.776 (5)°0.22 × 0.22 × 0.10 mm
V = 682.6 (3) Å3
Data collection top
Siemens Platform CCD area-detector
diffractometer
3252 independent reflections
Radiation source: normal-focus sealed tube2769 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.000
profile data from ω scansθmax = 25.4°, θmin = 2.7°
Absorption correction: multi-scan
(SAINT and SADABS; Bruker, 2001)
h = 78
Tmin = 0.915, Tmax = 0.960k = 78
3252 measured reflectionsl = 018
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.029Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.077All H-atom parameters refined
S = 1.04 w = 1/[σ2(Fo2) + (0.046P)2 + 0.0847P]
where P = (Fo2 + 2Fc2)/3
3252 reflections(Δ/σ)max < 0.001
259 parametersΔρmax = 0.28 e Å3
20 restraintsΔρmin = 0.27 e Å3
Crystal data top
Na(C5H9N2O7P2)·4H2Oγ = 85.776 (5)°
Mr = 366.14V = 682.6 (3) Å3
Triclinic, P1Z = 2
a = 6.6664 (19) ÅMo Kα radiation
b = 6.6765 (19) ŵ = 0.41 mm1
c = 15.5711 (18) ÅT = 193 K
α = 84.075 (4)°0.22 × 0.22 × 0.10 mm
β = 82.803 (5)°
Data collection top
Siemens Platform CCD area-detector
diffractometer
3252 independent reflections
Absorption correction: multi-scan
(SAINT and SADABS; Bruker, 2001)
2769 reflections with I > 2σ(I)
Tmin = 0.915, Tmax = 0.960Rint = 0.000
3252 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.02920 restraints
wR(F2) = 0.077All H-atom parameters refined
S = 1.04Δρmax = 0.28 e Å3
3252 reflectionsΔρmin = 0.27 e Å3
259 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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
N11.1410 (2)0.2747 (2)0.10652 (10)0.0164 (4)
H11.194 (3)0.286 (3)0.1536 (12)0.030 (6)*
C21.2389 (3)0.2330 (3)0.03025 (13)0.0186 (4)
H21.382 (2)0.220 (3)0.0173 (13)0.022 (6)*
N31.1050 (3)0.2244 (3)0.02430 (10)0.0174 (4)
H31.130 (4)0.194 (4)0.0769 (11)0.039 (7)*
C40.9146 (3)0.2604 (3)0.01783 (12)0.0164 (4)
H40.796 (3)0.264 (3)0.0086 (12)0.023 (6)*
C50.9349 (3)0.2899 (3)0.10087 (12)0.0140 (4)
C60.7764 (3)0.3262 (3)0.17512 (12)0.0163 (4)
H6A0.833 (3)0.384 (3)0.2223 (12)0.023 (6)*
H6B0.677 (3)0.423 (3)0.1499 (12)0.013 (5)*
C70.6660 (3)0.1333 (3)0.21377 (11)0.0132 (4)
Na10.83701 (12)0.21278 (12)0.44202 (5)0.0207 (2)
O10.5836 (2)0.0608 (2)0.14323 (8)0.0164 (3)
H1A0.513 (4)0.040 (4)0.1605 (18)0.045 (8)*
O20.96870 (19)0.0481 (2)0.31484 (8)0.0189 (3)
O30.9747 (2)0.1488 (2)0.18177 (8)0.0196 (3)
O40.7222 (2)0.2211 (2)0.31403 (9)0.0201 (3)
H4A0.799 (4)0.325 (3)0.3184 (18)0.057 (9)*
O60.31938 (19)0.3641 (2)0.24684 (8)0.0157 (3)
O50.53436 (19)0.2770 (2)0.37243 (8)0.0189 (3)
O70.3417 (2)0.0112 (2)0.32022 (9)0.0186 (3)
H7A0.218 (3)0.025 (4)0.3183 (17)0.046 (8)*
O81.2015 (3)0.1361 (2)0.50374 (10)0.0299 (4)
H8A1.233 (5)0.171 (5)0.5510 (14)0.077 (11)*
H8B1.298 (4)0.183 (5)0.4692 (17)0.080 (12)*
O90.6735 (2)0.3534 (2)0.57010 (9)0.0230 (3)
H9A0.636 (4)0.261 (3)0.6055 (15)0.044 (8)*
H9B0.605 (4)0.457 (3)0.5829 (16)0.045 (8)*
O100.9998 (2)0.4954 (2)0.36354 (9)0.0193 (3)
H10A1.074 (3)0.546 (4)0.3934 (14)0.043 (8)*
H10B1.079 (3)0.451 (4)0.3218 (13)0.044 (8)*
O111.3723 (2)0.2652 (2)0.14860 (10)0.0217 (3)
H11A1.249 (3)0.225 (5)0.153 (2)0.076 (12)*
H11B1.375 (4)0.372 (3)0.1817 (14)0.039 (8)*
P10.85337 (7)0.05516 (8)0.25666 (3)0.01313 (13)
P20.45611 (7)0.20966 (7)0.29463 (3)0.01322 (13)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
N10.0145 (8)0.0214 (9)0.0136 (8)0.0015 (7)0.0030 (7)0.0013 (7)
C20.0152 (11)0.0194 (11)0.0199 (10)0.0006 (8)0.0016 (8)0.0015 (8)
N30.0211 (9)0.0176 (9)0.0127 (8)0.0012 (7)0.0015 (7)0.0019 (7)
C40.0157 (10)0.0160 (10)0.0177 (10)0.0031 (8)0.0034 (8)0.0007 (8)
C50.0148 (10)0.0109 (9)0.0162 (9)0.0031 (7)0.0021 (7)0.0009 (7)
C60.0182 (11)0.0148 (10)0.0154 (10)0.0006 (8)0.0000 (8)0.0017 (8)
C70.0116 (9)0.0161 (10)0.0121 (9)0.0002 (7)0.0018 (7)0.0031 (7)
Na10.0218 (4)0.0215 (5)0.0187 (4)0.0011 (3)0.0017 (3)0.0025 (3)
O10.0170 (7)0.0201 (8)0.0130 (7)0.0034 (6)0.0033 (5)0.0018 (6)
O20.0143 (7)0.0239 (8)0.0196 (7)0.0010 (6)0.0044 (6)0.0061 (6)
O30.0175 (7)0.0236 (8)0.0167 (7)0.0052 (6)0.0000 (6)0.0050 (6)
O40.0171 (7)0.0160 (8)0.0246 (8)0.0006 (6)0.0023 (6)0.0040 (6)
O60.0138 (7)0.0175 (7)0.0152 (7)0.0016 (5)0.0008 (5)0.0015 (5)
O50.0156 (7)0.0252 (8)0.0160 (7)0.0023 (6)0.0024 (5)0.0054 (6)
O70.0107 (7)0.0193 (7)0.0245 (7)0.0005 (6)0.0019 (6)0.0036 (6)
O80.0413 (10)0.0300 (9)0.0174 (8)0.0060 (8)0.0015 (8)0.0010 (7)
O90.0270 (9)0.0183 (9)0.0223 (8)0.0007 (7)0.0013 (6)0.0014 (7)
O100.0172 (8)0.0198 (8)0.0209 (8)0.0018 (6)0.0026 (6)0.0037 (6)
O110.0173 (8)0.0199 (8)0.0269 (8)0.0017 (6)0.0014 (6)0.0015 (7)
P10.0112 (3)0.0151 (3)0.0128 (2)0.00070 (19)0.00098 (19)0.00133 (19)
P20.0113 (2)0.0157 (3)0.0123 (2)0.00069 (19)0.00083 (19)0.00129 (19)
Geometric parameters (Å, º) top
N1—C21.327 (3)Na1—O8i2.4150 (19)
N1—C51.384 (2)Na1—O82.719 (2)
N1—H10.866 (15)O1—H1A0.85 (3)
C2—N31.315 (3)O2—P11.5060 (14)
C2—H20.947 (16)O3—P11.4983 (14)
N3—C41.370 (3)O4—P11.5912 (14)
N3—H30.856 (16)O4—H4A0.833 (17)
C4—C51.353 (3)O6—P21.5235 (13)
C4—H40.931 (15)O5—P21.4991 (13)
C5—C61.492 (3)O7—P21.5687 (15)
C6—C71.559 (3)O7—H7A0.825 (17)
C6—H6A0.990 (15)O8—Na1i2.4150 (19)
C6—H6B0.980 (14)O8—H8A0.847 (17)
C7—O11.429 (2)O8—H8B0.843 (17)
C7—P21.8411 (19)O9—H9A0.815 (16)
C7—P11.8421 (18)O9—H9B0.828 (16)
Na1—O102.3927 (17)O10—H10A0.829 (16)
Na1—O92.3955 (17)O10—H10B0.846 (16)
Na1—O52.3986 (16)O11—H11A0.842 (17)
Na1—O22.4029 (15)O11—H11B0.837 (16)
C2—N1—C5109.08 (16)O2—Na1—O8i79.37 (6)
C2—N1—H1126.7 (15)O10—Na1—O882.90 (6)
C5—N1—H1124.2 (15)O9—Na1—O894.75 (6)
N3—C2—N1108.45 (18)O5—Na1—O8173.89 (6)
N3—C2—H2126.6 (13)O2—Na1—O889.46 (5)
N1—C2—H2124.9 (13)O8i—Na1—O881.92 (7)
C2—N3—C4109.07 (17)C7—O1—H1A111.4 (18)
C2—N3—H3126.3 (17)P1—O2—Na1128.03 (8)
C4—N3—H3124.5 (17)P1—O4—H4A106 (2)
C5—C4—N3107.52 (17)P2—O5—Na1136.23 (8)
C5—C4—H4128.6 (13)P2—O7—H7A114.7 (19)
N3—C4—H4123.9 (13)Na1i—O8—Na198.08 (7)
C4—C5—N1105.86 (17)Na1i—O8—H8A95 (2)
C4—C5—C6129.75 (18)Na1—O8—H8A126 (2)
N1—C5—C6124.37 (17)Na1i—O8—H8B127 (2)
C5—C6—C7113.37 (16)Na1—O8—H8B113 (2)
C5—C6—H6A111.7 (12)H8A—O8—H8B99 (2)
C7—C6—H6A109.0 (12)Na1—O9—H9A108.4 (19)
C5—C6—H6B104.4 (11)Na1—O9—H9B138.1 (18)
C7—C6—H6B108.2 (11)H9A—O9—H9B108 (2)
H6A—C6—H6B110.1 (16)Na1—O10—H10A111.6 (18)
O1—C7—C6106.18 (14)Na1—O10—H10B107.3 (18)
O1—C7—P2108.75 (12)H10A—O10—H10B105 (2)
C6—C7—P2107.82 (13)H11A—O11—H11B105 (2)
O1—C7—P1110.29 (12)O3—P1—O2116.91 (8)
C6—C7—P1108.68 (12)O3—P1—O4109.30 (8)
P2—C7—P1114.75 (9)O2—P1—O4109.17 (8)
O10—Na1—O9102.25 (6)O3—P1—C7108.58 (8)
O10—Na1—O594.05 (5)O2—P1—C7107.32 (8)
O9—Na1—O591.07 (6)O4—P1—C7104.88 (8)
O10—Na1—O283.19 (6)O5—P2—O6115.87 (8)
O9—Na1—O2173.48 (6)O5—P2—O7110.52 (8)
O5—Na1—O284.91 (5)O6—P2—O7108.71 (8)
O10—Na1—O8i156.91 (6)O5—P2—C7111.01 (8)
O9—Na1—O8i96.27 (6)O6—P2—C7106.68 (8)
O5—Na1—O8i99.32 (6)O7—P2—C7103.23 (8)
C5—N1—C2—N31.1 (2)Na1—O2—P1—O3179.17 (8)
N1—C2—N3—C40.4 (2)Na1—O2—P1—O454.50 (11)
C2—N3—C4—C50.5 (2)Na1—O2—P1—C758.65 (11)
N3—C4—C5—N11.2 (2)O1—C7—P1—O339.48 (14)
N3—C4—C5—C6177.26 (19)C6—C7—P1—O376.54 (14)
C2—N1—C5—C41.4 (2)P2—C7—P1—O3162.69 (9)
C2—N1—C5—C6177.13 (18)O1—C7—P1—O2166.70 (12)
C4—C5—C6—C774.3 (3)C6—C7—P1—O250.69 (14)
N1—C5—C6—C7103.8 (2)P2—C7—P1—O270.08 (12)
C5—C6—C7—O156.66 (19)O1—C7—P1—O477.27 (13)
C5—C6—C7—P2173.07 (13)C6—C7—P1—O4166.71 (12)
C5—C6—C7—P161.98 (18)P2—C7—P1—O445.94 (12)
O10—Na1—O2—P1123.31 (10)Na1—O5—P2—O6147.48 (10)
O5—Na1—O2—P128.60 (10)Na1—O5—P2—O788.32 (12)
O8i—Na1—O2—P171.89 (10)Na1—O5—P2—C725.60 (14)
O8—Na1—O2—P1153.77 (10)O1—C7—P2—O5177.03 (11)
Na1i—Na1—O2—P1116.20 (9)C6—C7—P2—O568.25 (13)
O10—Na1—O5—P292.86 (12)P1—C7—P2—O552.99 (12)
O9—Na1—O5—P2164.78 (12)O1—C7—P2—O655.89 (14)
O2—Na1—O5—P210.08 (12)C6—C7—P2—O658.84 (13)
O8i—Na1—O5—P268.25 (13)P1—C7—P2—O6179.92 (9)
Na1i—Na1—O5—P261.30 (15)O1—C7—P2—O758.60 (13)
O10—Na1—O8—Na1i162.55 (7)C6—C7—P2—O7173.32 (11)
O9—Na1—O8—Na1i95.67 (7)P1—C7—P2—O765.44 (11)
O2—Na1—O8—Na1i79.34 (6)
Symmetry code: (i) x+2, y, z+1.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N1—H1···O6ii0.87 (2)1.90 (2)2.751 (2)168 (2)
N3—H3···O3iii0.86 (2)1.92 (2)2.678 (2)148 (2)
N3—H3···O1iii0.86 (2)2.65 (2)3.248 (2)128 (2)
O1—H1A···O11iv0.85 (3)1.86 (3)2.667 (2)156 (3)
O4—H4A···O10v0.83 (2)1.88 (2)2.6722 (19)157 (3)
O7—H7A···O2iv0.83 (2)1.67 (2)2.4914 (19)179 (3)
O8—H8A···O4i0.85 (2)2.22 (2)3.061 (2)170 (3)
O8—H8B···O5ii0.84 (2)2.12 (2)2.960 (2)173 (3)
O9—H9A···O7vi0.82 (2)2.06 (2)2.826 (2)157 (3)
O9—H9A···O4vi0.82 (2)2.57 (2)3.134 (2)127 (2)
O9—H9B···O5vii0.83 (2)2.09 (2)2.907 (2)171 (3)
O10—H10A···O9viii0.83 (2)2.02 (2)2.816 (2)160 (2)
O10—H10B···O6ii0.85 (2)1.95 (2)2.7736 (19)163 (2)
O11—H11A···O30.84 (2)1.87 (2)2.708 (2)170 (3)
O11—H11B···O6ix0.84 (2)1.98 (2)2.793 (2)165 (2)
Symmetry codes: (i) x+2, y, z+1; (ii) x+1, y, z; (iii) x+2, y, z; (iv) x1, y, z; (v) x, y1, z; (vi) x+1, y, z+1; (vii) x+1, y+1, z+1; (viii) x+2, y+1, z+1; (ix) x+1, y1, z.

Experimental details

Crystal data
Chemical formulaNa(C5H9N2O7P2)·4H2O
Mr366.14
Crystal system, space groupTriclinic, P1
Temperature (K)193
a, b, c (Å)6.6664 (19), 6.6765 (19), 15.5711 (18)
α, β, γ (°)84.075 (4), 82.803 (5), 85.776 (5)
V3)682.6 (3)
Z2
Radiation typeMo Kα
µ (mm1)0.41
Crystal size (mm)0.22 × 0.22 × 0.10
Data collection
DiffractometerSiemens Platform CCD area-detector
diffractometer
Absorption correctionMulti-scan
(SAINT and SADABS; Bruker, 2001)
Tmin, Tmax0.915, 0.960
No. of measured, independent and
observed [I > 2σ(I)] reflections
3252, 3252, 2769
Rint0.000
(sin θ/λ)max1)0.603
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.029, 0.077, 1.04
No. of reflections3252
No. of parameters259
No. of restraints20
H-atom treatmentAll H-atom parameters refined
Δρmax, Δρmin (e Å3)0.28, 0.27

Computer programs: SMART (Bruker, 2001), SAINT (Bruker, 2001), SAINT, SHELXTL (Bruker, 2001), SHELXTL, CIFTAB in SHELXL97 (Sheldrick, 2001).

Selected geometric parameters (Å, º) top
N1—C21.327 (3)O3—P11.4983 (14)
N1—C51.384 (2)O4—P11.5912 (14)
C2—N31.315 (3)O6—P21.5235 (13)
N3—C41.370 (3)O5—P21.4991 (13)
C4—C51.353 (3)O7—P21.5687 (15)
O2—P11.5060 (14)
C5—C6—C7113.37 (16)P2—C7—P1114.75 (9)
C5—C6—C7—P161.98 (18)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N1—H1···O6i0.866 (15)1.898 (16)2.751 (2)168 (2)
N3—H3···O3ii0.856 (16)1.915 (19)2.678 (2)148 (2)
N3—H3···O1ii0.856 (16)2.65 (2)3.248 (2)128 (2)
O1—H1A···O11iii0.85 (3)1.86 (3)2.667 (2)156 (3)
O4—H4A···O10iv0.833 (17)1.884 (19)2.6722 (19)157 (3)
O7—H7A···O2iii0.825 (17)1.666 (17)2.4914 (19)179 (3)
O8—H8A···O4v0.847 (17)2.224 (17)3.061 (2)170 (3)
O8—H8B···O5i0.843 (17)2.121 (18)2.960 (2)173 (3)
O9—H9A···O7vi0.815 (16)2.058 (18)2.826 (2)157 (3)
O9—H9A···O4vi0.815 (16)2.57 (2)3.134 (2)127 (2)
O9—H9B···O5vii0.828 (16)2.086 (17)2.907 (2)171 (3)
O10—H10A···O9viii0.829 (16)2.024 (18)2.816 (2)160 (2)
O10—H10B···O6i0.846 (16)1.952 (18)2.7736 (19)163 (2)
O11—H11A···O30.842 (17)1.874 (19)2.708 (2)170 (3)
O11—H11B···O6ix0.837 (16)1.975 (18)2.793 (2)165 (2)
Symmetry codes: (i) x+1, y, z; (ii) x+2, y, z; (iii) x1, y, z; (iv) x, y1, z; (v) x+2, y, z+1; (vi) x+1, y, z+1; (vii) x+1, y+1, z+1; (viii) x+2, y+1, z+1; (ix) x+1, y1, z.
 

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