Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807062198/cv2358sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807062198/cv2358Isup2.hkl |
CCDC reference: 674072
Benzenetetracarboxylic acid (0.023 g, 0.015 mmol), CuCl2 (0.018 g, 0.013 mmol) and NaOH(0.048 mmol,0.12 mmol), were added in a mixed solvent of ethanol, the mixture was heated for ten hours under reflux, applying stirring and influx. The resultant was then filtered to give a pure solution which was infiltrated by diethyl ether freely in a closed vessel. Two weeks later several single crystals of the size suitable for X-Ray diffraction analysis were obtained.
C-bound H atoms were placed in calculated positions [Csp2—H = 0.93 Å] and refined using a riding model, with Uiso(H) = 1.2Ueq(C). The water' H atoms were found in a difference map and isotropically refined using bond restraint O—H = 0.86 (3) Å.
Data collection: APEX2 (Bruker, 2007); cell refinement: SAINT (Bruker, 2004); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: SHELXTL (Bruker, 2004); software used to prepare material for publication: SHELXTL.
[Cu2(C10H2O8)(H2O)4] | F(000) = 448 |
Mr = 224.63 | Dx = 2.153 Mg m−3 |
Monoclinic, P21/n | Mo Kα radiation, λ = 0.71073 Å |
Hall symbol: -P 2yn | Cell parameters from 1261 reflections |
a = 5.2594 (10) Å | θ = 2.5–25.3° |
b = 16.342 (3) Å | µ = 3.14 mm−1 |
c = 8.1426 (15) Å | T = 298 K |
β = 97.939 (2)° | Block, blue |
V = 693.1 (2) Å3 | 0.28 × 0.19 × 0.15 mm |
Z = 4 |
Bruker APEXII area-detector diffractometer | 1261 independent reflections |
Radiation source: fine-focus sealed tube | 1181 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.107 |
ϕ and ω scan | θmax = 25.3°, θmin = 2.5° |
Absorption correction: multi-scan (SADABS; Sheldrick, 2004) | h = −6→5 |
Tmin = 0.474, Tmax = 0.651 | k = −19→16 |
3586 measured reflections | l = −9→9 |
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)] = 0.046 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.112 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.05 | w = 1/[σ2(Fo2) + (0.0794P)2 + 0.002P] where P = (Fo2 + 2Fc2)/3 |
1261 reflections | (Δ/σ)max = 0.001 |
127 parameters | Δρmax = 0.77 e Å−3 |
6 restraints | Δρmin = −1.63 e Å−3 |
[Cu2(C10H2O8)(H2O)4] | V = 693.1 (2) Å3 |
Mr = 224.63 | Z = 4 |
Monoclinic, P21/n | Mo Kα radiation |
a = 5.2594 (10) Å | µ = 3.14 mm−1 |
b = 16.342 (3) Å | T = 298 K |
c = 8.1426 (15) Å | 0.28 × 0.19 × 0.15 mm |
β = 97.939 (2)° |
Bruker APEXII area-detector diffractometer | 1261 independent reflections |
Absorption correction: multi-scan (SADABS; Sheldrick, 2004) | 1181 reflections with I > 2σ(I) |
Tmin = 0.474, Tmax = 0.651 | Rint = 0.107 |
3586 measured reflections |
R[F2 > 2σ(F2)] = 0.046 | 6 restraints |
wR(F2) = 0.112 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.05 | Δρmax = 0.77 e Å−3 |
1261 reflections | Δρmin = −1.63 e Å−3 |
127 parameters |
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. |
x | y | z | Uiso*/Ueq | ||
O1 | 0.6295 (4) | 0.78499 (13) | 1.0770 (3) | 0.0251 (5) | |
O5 | 0.9211 (4) | 0.87035 (13) | 0.7881 (3) | 0.0234 (5) | |
C4 | 0.8535 (5) | 0.94425 (18) | 0.7784 (4) | 0.0185 (7) | |
Cu1 | 0.14625 (6) | 0.83280 (2) | 0.62933 (4) | 0.0155 (3) | |
O2 | 0.4254 (4) | 0.79262 (13) | 0.8192 (2) | 0.0224 (5) | |
O6 | 0.9316 (4) | 0.99467 (13) | 0.6821 (3) | 0.0263 (6) | |
O3 | −0.1623 (5) | 0.86478 (15) | 0.4160 (3) | 0.0262 (6) | |
C1 | 0.5292 (6) | 0.82451 (18) | 0.9505 (4) | 0.0181 (7) | |
O4 | 0.3800 (4) | 0.90417 (15) | 0.5221 (3) | 0.0307 (6) | |
C5 | 0.6389 (6) | 1.05457 (18) | 0.9193 (4) | 0.0192 (7) | |
H13 | 0.7321 | 1.0916 | 0.8645 | 0.023* | |
C2 | 0.5243 (6) | 0.91568 (18) | 0.9736 (3) | 0.0164 (6) | |
C3 | 0.6668 (5) | 0.97141 (18) | 0.8918 (3) | 0.0174 (6) | |
H3WA | −0.120 (9) | 0.9099 (15) | 0.372 (5) | 0.061 (16)* | |
H4WA | 0.293 (6) | 0.938 (2) | 0.455 (4) | 0.041 (12)* | |
H4WB | 0.515 (6) | 0.888 (3) | 0.482 (5) | 0.062 (15)* | |
H3WB | −0.175 (12) | 0.825 (2) | 0.346 (5) | 0.09 (3)* |
U11 | U22 | U33 | U12 | U13 | U23 | |
O1 | 0.0368 (14) | 0.0178 (11) | 0.0196 (11) | −0.0001 (9) | 0.0002 (9) | 0.0012 (9) |
O5 | 0.0260 (12) | 0.0217 (12) | 0.0254 (11) | 0.0056 (9) | 0.0136 (9) | 0.0008 (9) |
C4 | 0.0162 (15) | 0.0232 (17) | 0.0174 (15) | −0.0011 (12) | 0.0071 (12) | −0.0013 (12) |
Cu1 | 0.0164 (3) | 0.0160 (4) | 0.0162 (4) | 0.00117 (12) | 0.0090 (2) | −0.00035 (12) |
O2 | 0.0250 (12) | 0.0207 (12) | 0.0210 (11) | 0.0012 (9) | 0.0017 (9) | −0.0021 (9) |
O6 | 0.0290 (12) | 0.0264 (11) | 0.0275 (13) | 0.0011 (9) | 0.0182 (10) | 0.0047 (10) |
O3 | 0.0278 (13) | 0.0260 (13) | 0.0268 (12) | −0.0019 (11) | 0.0111 (9) | −0.0018 (11) |
C1 | 0.0154 (16) | 0.0213 (16) | 0.0193 (18) | 0.0006 (11) | 0.0088 (13) | 0.0004 (12) |
O4 | 0.0217 (13) | 0.0379 (14) | 0.0352 (14) | 0.0044 (10) | 0.0134 (11) | 0.0143 (11) |
C5 | 0.0200 (15) | 0.0222 (16) | 0.0168 (15) | −0.0022 (12) | 0.0078 (11) | 0.0018 (12) |
C2 | 0.0164 (15) | 0.0190 (14) | 0.0142 (14) | 0.0018 (11) | 0.0032 (11) | −0.0003 (12) |
C3 | 0.0192 (15) | 0.0206 (15) | 0.0136 (15) | 0.0020 (12) | 0.0060 (11) | −0.0002 (12) |
O1—C1 | 1.267 (4) | O2—C1 | 1.246 (4) |
O1—Cu1i | 1.971 (2) | O3—H3WA | 0.86 (3) |
O5—C4 | 1.258 (4) | O3—H3WB | 0.86 (4) |
O5—Cu1ii | 1.968 (2) | C1—C2 | 1.502 (4) |
C4—O6 | 1.245 (3) | O4—H4WA | 0.86 (3) |
C4—C3 | 1.504 (4) | O4—H4WB | 0.86 (3) |
Cu1—O5iii | 1.968 (2) | C5—C3 | 1.388 (4) |
Cu1—O1iv | 1.971 (2) | C5—C2v | 1.393 (4) |
Cu1—O4 | 1.983 (2) | C5—H13 | 0.9300 |
Cu1—O2 | 2.086 (2) | C2—C5v | 1.393 (4) |
Cu1—O3 | 2.268 (3) | C2—C3 | 1.405 (4) |
C1—O1—Cu1i | 132.4 (2) | Cu1—O3—H3WB | 108 (4) |
C4—O5—Cu1ii | 116.65 (19) | H3WA—O3—H3WB | 112 (3) |
O6—C4—O5 | 124.0 (3) | O2—C1—O1 | 124.6 (3) |
O6—C4—C3 | 119.4 (3) | O2—C1—C2 | 120.6 (3) |
O5—C4—C3 | 116.6 (3) | O1—C1—C2 | 114.6 (3) |
O5iii—Cu1—O1iv | 115.69 (9) | Cu1—O4—H4WA | 110 (3) |
O5iii—Cu1—O4 | 124.88 (9) | Cu1—O4—H4WB | 125 (3) |
O1iv—Cu1—O4 | 119.42 (10) | H4WA—O4—H4WB | 111 (2) |
O5iii—Cu1—O2 | 92.13 (9) | C3—C5—C2v | 122.0 (3) |
O1iv—Cu1—O2 | 81.88 (9) | C3—C5—H13 | 119.0 |
O4—Cu1—O2 | 95.50 (10) | C2v—C5—H13 | 119.0 |
O5iii—Cu1—O3 | 89.96 (9) | C5v—C2—C3 | 119.1 (3) |
O1iv—Cu1—O3 | 93.08 (9) | C5v—C2—C1 | 116.5 (3) |
O4—Cu1—O3 | 87.06 (10) | C3—C2—C1 | 124.4 (3) |
O2—Cu1—O3 | 174.95 (8) | C5—C3—C2 | 118.9 (3) |
C1—O2—Cu1 | 133.2 (2) | C5—C3—C4 | 118.7 (3) |
Cu1—O3—H3WA | 108 (3) | C2—C3—C4 | 122.4 (3) |
Symmetry codes: (i) x+1/2, −y+3/2, z+1/2; (ii) x+1, y, z; (iii) x−1, y, z; (iv) x−1/2, −y+3/2, z−1/2; (v) −x+1, −y+2, −z+2. |
D—H···A | D—H | H···A | D···A | D—H···A |
O3—H3WA···O6vi | 0.86 (3) | 1.93 (2) | 2.767 (3) | 163 (5) |
O3—H3WB···O1vii | 0.86 (4) | 2.38 (4) | 3.112 (3) | 143 (5) |
O3—H3WB···O2iv | 0.86 (4) | 2.01 (4) | 2.748 (3) | 143 (5) |
O4—H4WA···O6vi | 0.86 (3) | 1.87 (3) | 2.726 (3) | 173 (4) |
O4—H4WB···O3ii | 0.86 (3) | 1.89 (3) | 2.744 (3) | 171 (5) |
Symmetry codes: (ii) x+1, y, z; (iv) x−1/2, −y+3/2, z−1/2; (vi) −x+1, −y+2, −z+1; (vii) x−1, y, z−1. |
Experimental details
Crystal data | |
Chemical formula | [Cu2(C10H2O8)(H2O)4] |
Mr | 224.63 |
Crystal system, space group | Monoclinic, P21/n |
Temperature (K) | 298 |
a, b, c (Å) | 5.2594 (10), 16.342 (3), 8.1426 (15) |
β (°) | 97.939 (2) |
V (Å3) | 693.1 (2) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 3.14 |
Crystal size (mm) | 0.28 × 0.19 × 0.15 |
Data collection | |
Diffractometer | Bruker APEXII area-detector diffractometer |
Absorption correction | Multi-scan (SADABS; Sheldrick, 2004) |
Tmin, Tmax | 0.474, 0.651 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 3586, 1261, 1181 |
Rint | 0.107 |
(sin θ/λ)max (Å−1) | 0.601 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.046, 0.112, 1.05 |
No. of reflections | 1261 |
No. of parameters | 127 |
No. of restraints | 6 |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å−3) | 0.77, −1.63 |
Computer programs: APEX2 (Bruker, 2007), SAINT (Bruker, 2004), SAINT, SHELXS97 (Sheldrick, 1997), SHELXL97 (Sheldrick, 1997), SHELXTL (Bruker, 2004), SHELXTL.
D—H···A | D—H | H···A | D···A | D—H···A |
O3—H3WA···O6i | 0.86 (3) | 1.933 (17) | 2.767 (3) | 163 (5) |
O3—H3WB···O1ii | 0.86 (4) | 2.38 (4) | 3.112 (3) | 143 (5) |
O3—H3WB···O2iii | 0.86 (4) | 2.01 (4) | 2.748 (3) | 143 (5) |
O4—H4WA···O6i | 0.86 (3) | 1.87 (3) | 2.726 (3) | 173 (4) |
O4—H4WB···O3iv | 0.86 (3) | 1.89 (3) | 2.744 (3) | 171 (5) |
Symmetry codes: (i) −x+1, −y+2, −z+1; (ii) x−1, y, z−1; (iii) x−1/2, −y+3/2, z−1/2; (iv) x+1, y, z. |
A zinc compound with 1,2,4,5-benzenetetracarboxylate was reported recently (Wang et al., 2007). A slight variation of the synthesis has yielded the title compound, which features trigonal-bipyramidal copper coordination environment.