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In the crystal structure of the title complex, C8H5NO7·H2O, intra- and inter­molecular O—H...O hydrogen bonds result in the formation of a supra­molecular network structure.

Supporting information

cif

Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807045199/hk2323sup1.cif
Contains datablocks I, global

hkl

Structure factor file (CIF format) https://doi.org/10.1107/S1600536807045199/hk2323Isup2.hkl
Contains datablock I

CCDC reference: 1296708

Key indicators

  • Single-crystal X-ray study
  • T = 273 K
  • Mean [sigma](C-C) = 0.004 Å
  • R factor = 0.052
  • wR factor = 0.148
  • Data-to-parameter ratio = 11.4

checkCIF/PLATON results

No syntax errors found



Alert level B PLAT230_ALERT_2_B Hirshfeld Test Diff for O3 - C8 .. 18.21 su PLAT230_ALERT_2_B Hirshfeld Test Diff for O4 - C8 .. 12.42 su PLAT430_ALERT_2_B Short Inter D...A Contact O2 .. O2 .. 2.60 Ang. PLAT482_ALERT_4_B Small D-H..A Angle Rep for O1 .. O6 .. 88.00 Deg.
Alert level C PLAT029_ALERT_3_C _diffrn_measured_fraction_theta_full Low ....... 0.98 PLAT042_ALERT_1_C Calc. and Rep. MoietyFormula Strings Differ .... ? PLAT066_ALERT_1_C Predicted and Reported Transmissions Identical . ? PLAT230_ALERT_2_C Hirshfeld Test Diff for C3 - C8 .. 6.43 su PLAT242_ALERT_2_C Check Low Ueq as Compared to Neighbors for C8 PLAT250_ALERT_2_C Large U3/U1 Ratio for Average U(i,j) Tensor .... 2.20 PLAT432_ALERT_2_C Short Inter X...Y Contact O5 .. C8 .. 3.00 Ang. PLAT480_ALERT_4_C Long H...A H-Bond Reported H1 .. O6 .. 2.73 Ang.
Alert level G PLAT860_ALERT_3_G Note: Number of Least-Squares Restraints ....... 4
0 ALERT level A = In general: serious problem 4 ALERT level B = Potentially serious problem 8 ALERT level C = Check and explain 1 ALERT level G = General alerts; check 2 ALERT type 1 CIF construction/syntax error, inconsistent or missing data 7 ALERT type 2 Indicator that the structure model may be wrong or deficient 2 ALERT type 3 Indicator that the structure quality may be low 2 ALERT type 4 Improvement, methodology, query or suggestion 0 ALERT type 5 Informative message, check

Comment top

In the synthesis of crystal structures by design, the assembly of molecular units in predefined arrangements is a key goal (Desiraju, 1995, 1997; Braga et al., 1998). Due to carboxyl groups are one of the most important classes of biological ligands, the coordination of metal-carboxyl groups complexes are of critical importance in biological systems, organic materials and coordination chemistry. Recently, carboxyl groups with variable coordination modes have been used to construct metal-organic supramolecular structures (Mccann et al., 1996; Mccann et al., 1995; Wai et al., 1990; Yaghi et al., 1996; Min & Lee 2002; Maira et al., 2001). We originally attempted to synthesize complexes featuring La metal chains by reaction of the lanthanum(III) ion with 2-hydroxy-5-nitro-1,3-benzenedicarboxylic acid ligand. Unfortunately, we obtained only the title compound, (I), and we report herein its crystal structure.

In the molecule of (I) (Fig. 1), the ligand bond lengths and angles are within normal ranges (Allen et al., 1987). It contains one (C8H5NO7) molecule and one water molecule.

In the crystal structure, intramolecular and intermolecular O—H···O hydrogen bonds (Table 1, Fig. 2) result in the formation of a supramolecular network structure.

Related literature top

For general background, see: Desiraju (1995, 1997); Braga et al. (1998); Mccann et al. (1995, 1996); Wai et al. (1990); Yaghi et al. (1996); Min & Lee (2002); Maira et al. (2001). For bond-length data, see: Allen et al. (1987).

Experimental top

Crystals of the title compound were synthesized using hydrothermal method in a 23 ml Teflon-lined Parr bomb, which was then sealed. Lanthanum (III) nitrate hexahydrate (216.4 mg, 0.5 mmol), 2-hydroxy-5-nitro-1,3-benzenedicarboxylic acid (226.2 mg, 1 mmol), ammonia (0.5 mol/l, 4 ml) and distilled water (2 g) were placed into the bomb and sealed. The bomb was then heated under autogenous pressure up to 443 K over the course of 7 d and allowed to cool at room temperature for 24 h. Upon opening the bomb, a clear colorless solution was decanted from small colorless crystals. These crystals were washed with distilled water followed by ethanol, and allowed to air-dry at room temperature. Found: C 39.08, H 2.84, N 5.67%; analysis calculated for C8H7NO8: C 39.20, H 2.88, N 5.71%.

Refinement top

H8A and H8B (for H2O) were located in difference syntheses and refined isotropically [O—H = 0.84 (4) and 0.841 (19) Å, Uiso(H) = 0.11 (5) and 0.114 (18) Å2]. The remaining H atoms were positioned geometrically, with O—H = 0.82 Å (for OH) and C—H = 0.93 Å for aromatic H, and constrained to ride on their parent atoms, with Uiso(H) = xUeq(C,O), where x = 1.2 for aromatic H atoms and x = 1.5 for all other H atoms.

Structure description top

In the synthesis of crystal structures by design, the assembly of molecular units in predefined arrangements is a key goal (Desiraju, 1995, 1997; Braga et al., 1998). Due to carboxyl groups are one of the most important classes of biological ligands, the coordination of metal-carboxyl groups complexes are of critical importance in biological systems, organic materials and coordination chemistry. Recently, carboxyl groups with variable coordination modes have been used to construct metal-organic supramolecular structures (Mccann et al., 1996; Mccann et al., 1995; Wai et al., 1990; Yaghi et al., 1996; Min & Lee 2002; Maira et al., 2001). We originally attempted to synthesize complexes featuring La metal chains by reaction of the lanthanum(III) ion with 2-hydroxy-5-nitro-1,3-benzenedicarboxylic acid ligand. Unfortunately, we obtained only the title compound, (I), and we report herein its crystal structure.

In the molecule of (I) (Fig. 1), the ligand bond lengths and angles are within normal ranges (Allen et al., 1987). It contains one (C8H5NO7) molecule and one water molecule.

In the crystal structure, intramolecular and intermolecular O—H···O hydrogen bonds (Table 1, Fig. 2) result in the formation of a supramolecular network structure.

For general background, see: Desiraju (1995, 1997); Braga et al. (1998); Mccann et al. (1995, 1996); Wai et al. (1990); Yaghi et al. (1996); Min & Lee (2002); Maira et al. (2001). For bond-length data, see: Allen et al. (1987).

Computing details top

Data collection: SMART (Siemens, 1996); cell refinement: SAINT (Siemens, 1996); data reduction: SAINT (Siemens, 1996); program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: SHELXTL (Siemens, 1996); software used to prepare material for publication: SHELXTL (Siemens, 1996).

Figures top
[Figure 1] Fig. 1. The molecular structure of the title molecule, with the atom-numbering scheme. Displacement ellipsoids are drawn at the 30% probability level.
[Figure 2] Fig. 2. A packing diagram of (I). Hydrogen bonds are shown as dashed lines.
2-Hydroxy-5-nitrobenzene-1,3-dicarboxylic acid monohydrate top
Crystal data top
C8H5NO7·H2OF(000) = 1008
Mr = 245.15Dx = 1.737 Mg m3
Monoclinic, C2/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -C 2ycCell parameters from 1481 reflections
a = 25.21 (2) Åθ = 2.8–26.6°
b = 6.5072 (16) ŵ = 0.16 mm1
c = 12.331 (2) ÅT = 273 K
β = 112.019 (4)°Prism, colourless
V = 1875.3 (17) Å30.24 × 0.15 × 0.15 mm
Z = 8
Data collection top
Bruker APEXII area-detector
diffractometer
1885 independent reflections
Radiation source: fine-focus sealed tube972 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.032
φ and ω scansθmax = 26.5°, θmin = 3.3°
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)
h = 3131
Tmin = 0.963, Tmax = 0.977k = 78
6094 measured reflectionsl = 1515
Refinement top
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.052H atoms treated by a mixture of independent and constrained refinement
wR(F2) = 0.148 w = 1/[σ2(Fo2) + (0.078P)2 + 0.002P]
where P = (Fo2 + 2Fc2)/3
S = 1.02(Δ/σ)max < 0.001
1885 reflectionsΔρmax = 0.35 e Å3
166 parametersΔρmin = 0.21 e Å3
4 restraintsExtinction correction: SHELXL97 (Sheldrick, 1997), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4
Primary atom site location: structure-invariant direct methodsExtinction coefficient: 0.0090 (18)
Crystal data top
C8H5NO7·H2OV = 1875.3 (17) Å3
Mr = 245.15Z = 8
Monoclinic, C2/cMo Kα radiation
a = 25.21 (2) ŵ = 0.16 mm1
b = 6.5072 (16) ÅT = 273 K
c = 12.331 (2) Å0.24 × 0.15 × 0.15 mm
β = 112.019 (4)°
Data collection top
Bruker APEXII area-detector
diffractometer
1885 independent reflections
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)
972 reflections with I > 2σ(I)
Tmin = 0.963, Tmax = 0.977Rint = 0.032
6094 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0524 restraints
wR(F2) = 0.148H atoms treated by a mixture of independent and constrained refinement
S = 1.02Δρmax = 0.35 e Å3
1885 reflectionsΔρmin = 0.21 e Å3
166 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
xyzUiso*/Ueq
O10.53249 (7)0.2530 (3)1.04704 (15)0.0707 (6)
H10.56450.24421.04500.106*
O20.50754 (9)0.2174 (4)0.86014 (17)0.0995 (8)
O30.29255 (7)0.1309 (3)0.63171 (16)0.0799 (7)
O40.24253 (8)0.3055 (3)0.70484 (16)0.0794 (6)
H40.21760.28040.64090.119*
O50.30610 (8)0.3717 (3)1.11233 (16)0.0838 (7)
O60.39253 (10)0.3002 (4)1.21843 (18)0.0951 (8)
O70.40213 (7)0.2101 (3)0.72900 (15)0.0714 (6)
H70.43690.21120.74610.107*
O80.63201 (8)0.2289 (3)1.02771 (18)0.0718 (6)
N10.35410 (10)0.3194 (4)1.1251 (2)0.0646 (6)
C10.43547 (9)0.2452 (4)0.9353 (2)0.0525 (6)
C20.39111 (11)0.2307 (4)0.8239 (2)0.0548 (6)
C30.33520 (10)0.2446 (4)0.8197 (2)0.0515 (6)
C40.32271 (10)0.2745 (3)0.9165 (2)0.0542 (6)
H4A0.28500.28820.91080.105*
C50.36655 (10)0.2839 (4)1.0212 (2)0.0523 (6)
C60.42274 (10)0.2691 (4)1.0321 (2)0.0544 (6)
H60.45190.27541.10570.105*
C70.49519 (10)0.2385 (4)0.9441 (2)0.0605 (7)
C80.28731 (9)0.2262 (3)0.71083 (18)0.0424 (6)
H8B0.630 (2)0.215 (7)0.959 (2)0.114 (18)*
H8A0.5964 (12)0.22 (3)1.010 (6)0.11 (5)*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
O10.0384 (11)0.1043 (15)0.0618 (12)0.0009 (10)0.0099 (9)0.0009 (9)
O20.0435 (11)0.198 (3)0.0589 (13)0.0025 (12)0.0217 (10)0.0002 (12)
O30.0514 (11)0.1153 (17)0.0653 (12)0.0086 (11)0.0131 (9)0.0093 (11)
O40.0411 (11)0.1231 (17)0.0646 (12)0.0067 (11)0.0092 (9)0.0062 (11)
O50.0599 (13)0.1226 (17)0.0794 (13)0.0043 (11)0.0382 (11)0.0094 (12)
O60.0739 (15)0.157 (2)0.0506 (12)0.0154 (13)0.0186 (11)0.0037 (12)
O70.0377 (10)0.1242 (16)0.0524 (11)0.0002 (10)0.0171 (8)0.0026 (9)
O80.0440 (11)0.0945 (15)0.0713 (14)0.0003 (9)0.0152 (9)0.0031 (10)
N10.0570 (15)0.0803 (16)0.0606 (14)0.0003 (11)0.0269 (13)0.0038 (11)
C10.0351 (13)0.0693 (16)0.0517 (15)0.0004 (11)0.0146 (12)0.0017 (11)
C20.0440 (14)0.0723 (16)0.0478 (14)0.0008 (12)0.0170 (12)0.0006 (11)
C30.0385 (13)0.0645 (16)0.0490 (13)0.0005 (10)0.0136 (11)0.0046 (11)
C40.0423 (14)0.0608 (16)0.0605 (16)0.0002 (10)0.0205 (13)0.0033 (11)
C50.0480 (15)0.0633 (15)0.0471 (13)0.0036 (11)0.0197 (11)0.0008 (11)
C60.0397 (13)0.0674 (16)0.0517 (14)0.0008 (11)0.0119 (11)0.0003 (11)
C70.0388 (14)0.0849 (19)0.0535 (15)0.0001 (12)0.0123 (13)0.0042 (12)
C80.0260 (12)0.0659 (15)0.0347 (12)0.0002 (10)0.0106 (9)0.0025 (10)
Geometric parameters (Å, º) top
O1—C71.268 (3)N1—C51.448 (3)
O1—H10.8200C1—C61.356 (3)
O2—C71.196 (3)C1—C21.412 (3)
O3—C81.204 (3)C1—C71.469 (4)
O4—C81.218 (3)C2—C31.393 (4)
O4—H40.8200C3—C41.358 (3)
O5—N11.209 (3)C3—C81.435 (3)
O6—N11.201 (3)C4—C51.350 (3)
O7—C21.308 (3)C4—H4A0.9300
O7—H70.8200C5—C61.375 (4)
O8—H8B0.841 (19)C6—H60.9300
O8—H8A0.84 (4)
C7—O1—H1109.5C5—C4—C3118.1 (2)
C8—O4—H4109.5C5—C4—H4A121.0
C2—O7—H7109.5C3—C4—H4A121.0
H8B—O8—H8A95 (3)C4—C5—C6122.3 (2)
O6—N1—O5124.2 (2)C4—C5—N1118.8 (2)
O6—N1—C5117.8 (2)C6—C5—N1118.8 (2)
O5—N1—C5117.9 (2)C1—C6—C5119.8 (2)
C6—C1—C2120.1 (2)C1—C6—H6120.1
C6—C1—C7120.8 (2)C5—C6—H6120.1
C2—C1—C7119.1 (2)O2—C7—O1122.6 (2)
O7—C2—C3121.6 (2)O2—C7—C1122.1 (2)
O7—C2—C1121.4 (2)O1—C7—C1115.3 (2)
C3—C2—C1117.0 (2)O3—C8—O4123.3 (2)
C4—C3—C2122.7 (2)O3—C8—C3119.4 (2)
C4—C3—C8116.3 (2)O4—C8—C3117.2 (2)
C2—C3—C8121.0 (2)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O7—H7···O2i0.822.252.876 (3)134
O1—H1···O6ii0.822.732.816 (3)88
O8—H8A···O20.84 (4)2.31 (5)3.043 (3)145 (7)
O7—H7···O20.821.812.541 (3)148
Symmetry codes: (i) x+1, y, z+3/2; (ii) x+1, y, z+5/2.

Experimental details

Crystal data
Chemical formulaC8H5NO7·H2O
Mr245.15
Crystal system, space groupMonoclinic, C2/c
Temperature (K)273
a, b, c (Å)25.21 (2), 6.5072 (16), 12.331 (2)
β (°) 112.019 (4)
V3)1875.3 (17)
Z8
Radiation typeMo Kα
µ (mm1)0.16
Crystal size (mm)0.24 × 0.15 × 0.15
Data collection
DiffractometerBruker APEXII area-detector
Absorption correctionMulti-scan
(SADABS; Sheldrick, 1996)
Tmin, Tmax0.963, 0.977
No. of measured, independent and
observed [I > 2σ(I)] reflections
6094, 1885, 972
Rint0.032
(sin θ/λ)max1)0.627
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.052, 0.148, 1.02
No. of reflections1885
No. of parameters166
No. of restraints4
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å3)0.35, 0.21

Computer programs: SMART (Siemens, 1996), SAINT (Siemens, 1996), SHELXS97 (Sheldrick, 1997), SHELXL97 (Sheldrick, 1997), SHELXTL (Siemens, 1996).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O7—H7···O2i0.822.252.876 (3)134
O1—H1···O6ii0.822.732.816 (3)88
O8—H8A···O20.84 (4)2.31 (5)3.043 (3)145 (7)
O7—H7···O20.821.812.541 (3)148
Symmetry codes: (i) x+1, y, z+3/2; (ii) x+1, y, z+5/2.
 

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