Aqua­[4-(hydroxy­imino­meth­yl)pyridine-κN1](pyridine-2,6-dicarboxyl­ato-κ3O2,N,O6)copper(II)

Mutambi, E.M.

doi:10.1107/S1600536808019673

metal-organic compounds

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ISSN: 2056-9890

Volume 64| Part 8| August 2008| Pages m979-m980

doi:10.1107/S1600536808019673

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Aqua[4-(hydroxyiminomethyl)pyridine-κN¹](pyridine-2,6-dicarboxylato-κ³O²,N,O⁶)copper(II)

E. M. Mutambi ^a ^*

^aUniversity of Bristol, Bristol, England BS8 1TS, England
^*Correspondence e-mail: emutambi@yahoo.com

(Received 18 June 2008; accepted 27 June 2008; online 5 July 2008)

In the title compound, [Cu(C₇H₃NO₄)(C₆H₆N₂O)(H₂O)], the coordination geometry of the Cu^II atom can be described as distorted square pyramidal. The basal plane is defined by one N atom and two O atoms from the deprotonated pyridine-2,6-dicarboxylate ligand, and a pyridyl N atom from the 4-pyridyl aldoxime ligand. The apical position is occupied by a water molecule. O—H⋯O hydrogen bonds lead to the formation of a two-dimensional network.

Related literature

For related literature, see: Blake et al. (2002 ); Germán-Acacio et al. (2007 ); Ucar et al. (2007 ); Xie et al. (2004 ).

Experimental

Crystal data

[Cu(C₇H₃NO₄)(C₆H₆N₂O)(H₂O)]
M_r = 368.79
Triclinic, $[P \overline 1]$
a = 6.7826 (2) Å
b = 7.1858 (3) Å
c = 14.8746 (6) Å
α = 76.154 (2)°
β = 87.152 (1)°
γ = 69.739 (1)°
V = 659.91 (4) Å³
Z = 2
Mo Kα radiation
μ = 1.69 mm⁻¹
T = 120 (2) K
0.16 × 0.14 × 0.04 mm

Data collection

Bruker–Nonius APEXII CCD diffractometer
Absorption correction: multi-scan (SADABS; Sheldrick, 1996 ) T_min = 0.763, T_max = 0.925
12553 measured reflections
2951 independent reflections
2814 reflections with I > 2σ(I)
R_int = 0.055

Refinement

R[F² > 2σ(F²)] = 0.039
wR(F²) = 0.103
S = 1.10
2951 reflections
209 parameters
H-atom parameters constrained
Δρ_max = 0.49 e Å⁻³
Δρ_min = −0.47 e Å⁻³

Table 1
Selected geometric parameters (Å, °)

Cu1—N1	1.903 (2)
Cu1—N2	1.957 (2)
Cu1—O2	2.0018 (18)
Cu1—O3	2.0574 (18)
Cu1—O5	2.2273 (18)

N1—Cu1—N2	168.18 (9)
N1—Cu1—O2	81.66 (8)
N2—Cu1—O2	97.18 (8)
N1—Cu1—O3	79.84 (8)
N2—Cu1—O3	99.02 (8)
O2—Cu1—O3	159.29 (8)
N1—Cu1—O5	91.57 (8)
N2—Cu1—O5	100.24 (8)
O2—Cu1—O5	96.71 (7)
O3—Cu1—O5	93.03 (7)

Table 2
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O5—H5C⋯O1ⁱ	0.84	1.93	2.769 (3)	180
O5—H5B⋯O4ⁱⁱ	0.83	2.07	2.836 (3)	155
O5—H5B⋯O6ⁱⁱⁱ	0.83	2.51	2.939 (3)	113
O6—H6⋯O3^iv	0.84	1.89	2.725 (3)	173
Symmetry codes: (i) x, y+1, z; (ii) x-1, y, z; (iii) -x+1, -y+2, -z+1; (iv) -x+2, -y+2, -z+1.

Data collection: APEX2 (Bruker, 2007 ); cell refinement: SAINT (Bruker, 2007); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL.

Supporting information

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536808019673/hy2141sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536808019673/hy2141Isup2.hkl

checkCIF report

Comment top

In the design and synthesis of polymeric complexes, various bridging and chelating ligands have been used extensively. Coordination bonds and hydrogen bonds are the major interactions in these assemblies (Xie et al., 2004). Pyridine-2,6-dicarboxylic acid (H₂pydc) is an efficient ligand with three coordinating sites. H₂pydc coordinates with transition metals in different ways to form various coordination geometries. The relative positions of the coordinating atoms (O and N) determine the type of coordination that will be seen in the molecular structure. The interest in this ligand centers on the versatile yet unpredictable manner in which it coordinates to a wide variety of metals due to its rigid and planar nature (Ucar et al., 2007). This paper aims to report one of the rare coordination modes that can be exhibited by copper(II) when coordinated by H₂pydc, 4-pyridyl aldoxime and H₂O.

The structure of the title compound is shown in Fig. 1. The molecule is approximately planar and the increased co-planarity is due to the resonance between the pyridine rings, which leads to the formation of square-pyramidal geometry (Fig. 1). The elongated square-pyramidal geometry of the structure (Table 1) is typical of Jahn-Teller-distorted copper(II) (Blake et al., 2002). The structure shows hydrogen-bonding interactions, which enhance the formation of two-dimensional network of the structure (Germán-Acacio et al., 2007). Bond lengths and angles are in the range expected for heteroaromatic-oximes and pryridne dicarboxylates. The hydrogen-bonding interactions are presented in Fig. 2. A l l the hydrogen-bonding donors and acceptors are involved in O—H···O hydrogen bonds (Table 2), which organize the molecules into a two-dimensional network (Fig. 3).

Related literature top

For related literature, see: Blake et al. (2002); Germán-Acacio et al. (2007); Ucar et al. (2007); Xie et al. (2004)

Experimental top

An aqueous solution of Cu(CH₃COO)₂.6H₂O (0.290 g, 1 mmol), KOH (0.220 g, 2 mmol) and H₂pydc (0.360 g, 2 mmol) in a 1:2:2 molar ratio was refluxed for 2 h and the resultant reaction mixture was reduced to less than 50 ml. After one day, the grown crystals of K₂[Cu(C₇H₃NO₄)₂] were filtered out and dried in air. Equimolar amounts of K₂[Cu(C₇H₃NO₄)₂] and 4-pyridyl aldoxime were dissolved in water in small vials, respectively, and then mixed together. The solution was left at room temperature in a vapour diffusion setup with ethanol. Blue crystals of the title compound were obtained after 3 weeks.

Computing details top

Data collection: APEX2 (Bruker, 2007); cell refinement: SAINT (Bruker, 2007); data reduction: SAINT (Bruker, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures top

	Fig. 1. Molecular structure of the title compound, showing the coordination geometry. Displacement ellipsoids are drawn at the 50% probability level.
	Fig. 2. Packing diagram viewed down the c-axis, showing hydrogen bonds (dashed lines).
	Fig. 3. View of a two-dimensional hydrogen-bonded layer along the c-axis. Hydrogen bonds are shown as dashed lines.

Aqua[4-(hydroxyiminomethyl)pyridine-κN¹](pyridine-2,6-dicarboxylato- κ³O²,N,O⁶)copper(II) top

Crystal data top

[Cu(C₇H₃NO₄)(C₆H₆N₂O)(H₂O)]	Z = 2
M_r = 368.79	F(000) = 374
Triclinic, P1	D_x = 1.848 Mg m⁻³
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71073 Å
a = 6.7826 (2) Å	Cell parameters from 18028 reflections
b = 7.1858 (3) Å	θ = 2.9–27.5°
c = 14.8746 (6) Å	µ = 1.69 mm⁻¹
α = 76.154 (2)°	T = 120 K
β = 87.152 (1)°	Plate, blue
γ = 69.739 (1)°	0.16 × 0.14 × 0.04 mm
V = 659.91 (4) Å³

Data collection top

Bruker–Nonius APEXII CCD diffractometer	2951 independent reflections
Radiation source: Bruker-Nonius FR591 rotating anode	2814 reflections with I > 2σ(I)
10cm confocal mirrors monochromator	R_int = 0.055
Detector resolution: 4096x4096 pixels / 62x62mm pixels mm^-1	θ_max = 27.4°, θ_min = 3.1°
ϕ and ω scans	h = 0→8
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)	k = −8→9
T_min = 0.763, T_max = 0.925	l = −18→19
12553 measured reflections

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)] = 0.039	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.103	H-atom parameters constrained
S = 1.10	w = 1/[σ²(F_o²) + (0.0515P)² + 1.382P] where P = (F_o² + 2F_c²)/3
2951 reflections	(Δ/σ)_max = 0.001
209 parameters	Δρ_max = 0.49 e Å⁻³
0 restraints	Δρ_min = −0.47 e Å⁻³

Crystal data top

[Cu(C₇H₃NO₄)(C₆H₆N₂O)(H₂O)]	γ = 69.739 (1)°
M_r = 368.79	V = 659.91 (4) Å³
Triclinic, P1	Z = 2
a = 6.7826 (2) Å	Mo Kα radiation
b = 7.1858 (3) Å	µ = 1.69 mm⁻¹
c = 14.8746 (6) Å	T = 120 K
α = 76.154 (2)°	0.16 × 0.14 × 0.04 mm
β = 87.152 (1)°

Data collection top

Bruker–Nonius APEXII CCD diffractometer	2951 independent reflections
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)	2814 reflections with I > 2σ(I)
T_min = 0.763, T_max = 0.925	R_int = 0.055
12553 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.039	0 restraints
wR(F²) = 0.103	H-atom parameters constrained
S = 1.10	Δρ_max = 0.49 e Å⁻³
2951 reflections	Δρ_min = −0.47 e Å⁻³
209 parameters

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²) top

	x	y	z	U_iso*/U_eq
Cu1	0.89909 (5)	0.56560 (4)	0.26849 (2)	0.01368 (12)
C1	0.7448 (4)	0.2868 (4)	0.22309 (17)	0.0146 (5)
C2	0.9262 (4)	0.2935 (4)	0.15912 (17)	0.0140 (5)
C3	1.0017 (4)	0.1862 (4)	0.09243 (18)	0.0165 (5)
H3	0.9379	0.0962	0.0797	0.020*
C4	1.1751 (4)	0.2134 (4)	0.04381 (18)	0.0176 (5)
H4	1.2321	0.1389	−0.0019	0.021*
C5	1.2656 (4)	0.3486 (4)	0.06166 (18)	0.0170 (5)
H5	1.3821	0.3693	0.0281	0.020*
C6	1.1803 (4)	0.4515 (4)	0.12958 (17)	0.0147 (5)
C7	1.2478 (4)	0.6059 (4)	0.16230 (17)	0.0145 (5)
N2	0.8203 (3)	0.6662 (3)	0.38093 (15)	0.0140 (4)
C9	0.8504 (4)	0.8386 (4)	0.38654 (18)	0.0149 (5)
H9	0.9058	0.9087	0.3349	0.018*
C10	0.8047 (4)	0.9181 (4)	0.46359 (18)	0.0152 (5)
H10	0.8249	1.0422	0.4642	0.018*
C11	0.7280 (4)	0.8137 (4)	0.54125 (17)	0.0145 (5)
C12	0.6947 (4)	0.6355 (4)	0.53510 (18)	0.0164 (5)
H12	0.6404	0.5619	0.5859	0.020*
C13	0.7416 (4)	0.5671 (4)	0.45432 (18)	0.0161 (5)
H13	0.7174	0.4465	0.4506	0.019*
C14	0.6845 (4)	0.8833 (4)	0.62729 (18)	0.0169 (5)
H14	0.6167	0.8189	0.6759	0.020*
N1	1.0162 (3)	0.4206 (3)	0.17580 (15)	0.0138 (4)
N3	0.7389 (3)	1.0317 (4)	0.63636 (15)	0.0172 (4)
O1	0.6349 (3)	0.1882 (3)	0.21279 (13)	0.0174 (4)
O2	0.7219 (3)	0.3883 (3)	0.28564 (13)	0.0167 (4)
O3	1.1531 (3)	0.6594 (3)	0.23461 (13)	0.0175 (4)
O4	1.3813 (3)	0.6698 (3)	0.12037 (13)	0.0187 (4)
O5	0.6858 (3)	0.8261 (3)	0.16420 (12)	0.0159 (4)
H5C	0.6703	0.9360	0.1789	0.024*
H5B	0.5729	0.8094	0.1586	0.024*
O6	0.6877 (3)	1.0704 (3)	0.72334 (13)	0.0215 (4)
H6	0.7376	1.1574	0.7314	0.032*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cu1	0.01538 (18)	0.01586 (18)	0.01443 (18)	−0.00932 (13)	0.00346 (12)	−0.00687 (12)
C1	0.0162 (12)	0.0134 (11)	0.0143 (11)	−0.0060 (9)	0.0011 (9)	−0.0022 (9)
C2	0.0149 (11)	0.0129 (11)	0.0144 (11)	−0.0061 (9)	0.0004 (9)	−0.0016 (9)
C3	0.0206 (12)	0.0160 (12)	0.0177 (12)	−0.0105 (10)	0.0004 (10)	−0.0063 (10)
C4	0.0225 (13)	0.0182 (12)	0.0156 (12)	−0.0084 (10)	0.0035 (10)	−0.0086 (10)
C5	0.0179 (12)	0.0186 (12)	0.0160 (12)	−0.0079 (10)	0.0005 (9)	−0.0043 (10)
C6	0.0147 (11)	0.0154 (11)	0.0151 (11)	−0.0071 (9)	0.0008 (9)	−0.0028 (9)
C7	0.0166 (12)	0.0152 (11)	0.0139 (11)	−0.0079 (9)	−0.0011 (9)	−0.0039 (9)
N2	0.0138 (10)	0.0160 (10)	0.0149 (10)	−0.0075 (8)	0.0024 (8)	−0.0056 (8)
C9	0.0136 (11)	0.0145 (11)	0.0161 (12)	−0.0045 (9)	0.0008 (9)	−0.0031 (9)
C10	0.0145 (11)	0.0145 (11)	0.0184 (12)	−0.0073 (9)	−0.0003 (9)	−0.0037 (9)
C11	0.0115 (11)	0.0181 (12)	0.0158 (12)	−0.0071 (9)	0.0009 (9)	−0.0050 (9)
C12	0.0168 (12)	0.0194 (12)	0.0167 (12)	−0.0110 (10)	0.0010 (9)	−0.0038 (10)
C13	0.0144 (11)	0.0181 (12)	0.0182 (12)	−0.0087 (10)	0.0004 (9)	−0.0037 (10)
C14	0.0156 (12)	0.0215 (12)	0.0159 (12)	−0.0091 (10)	0.0018 (9)	−0.0048 (10)
N1	0.0157 (10)	0.0154 (10)	0.0142 (10)	−0.0090 (8)	0.0017 (8)	−0.0054 (8)
N3	0.0170 (10)	0.0240 (11)	0.0152 (10)	−0.0099 (9)	0.0035 (8)	−0.0092 (9)
O1	0.0198 (9)	0.0155 (8)	0.0211 (9)	−0.0109 (7)	0.0014 (7)	−0.0051 (7)
O2	0.0199 (9)	0.0189 (9)	0.0168 (9)	−0.0124 (7)	0.0041 (7)	−0.0066 (7)
O3	0.0184 (9)	0.0222 (9)	0.0178 (9)	−0.0119 (7)	0.0030 (7)	−0.0088 (7)
O4	0.0192 (9)	0.0222 (9)	0.0201 (9)	−0.0129 (8)	0.0035 (7)	−0.0069 (7)
O5	0.0147 (8)	0.0166 (8)	0.0188 (9)	−0.0069 (7)	0.0031 (7)	−0.0072 (7)
O6	0.0280 (10)	0.0280 (10)	0.0190 (9)	−0.0173 (9)	0.0085 (8)	−0.0150 (8)

Geometric parameters (Å, º) top

Cu1—N1	1.903 (2)	C7—O3	1.295 (3)
Cu1—N2	1.957 (2)	N2—C9	1.345 (3)
Cu1—O2	2.0018 (18)	N2—C13	1.348 (3)
Cu1—O3	2.0574 (18)	C9—C10	1.375 (4)
Cu1—O5	2.2273 (18)	C9—H9	0.9500
C1—O1	1.229 (3)	C10—C11	1.401 (3)
C1—O2	1.286 (3)	C10—H10	0.9500
C1—C2	1.524 (3)	C11—C12	1.399 (3)
C2—N1	1.334 (3)	C11—C14	1.463 (4)
C2—C3	1.372 (4)	C12—C13	1.387 (4)
C3—C4	1.397 (4)	C12—H12	0.9500
C3—H3	0.9500	C13—H13	0.9500
C4—C5	1.394 (4)	C14—N3	1.280 (3)
C4—H4	0.9500	C14—H14	0.9500
C5—C6	1.380 (4)	N3—O6	1.390 (3)
C5—H5	0.9500	O5—H5C	0.8400
C6—N1	1.335 (3)	O5—H5B	0.8263
C6—C7	1.520 (3)	O6—H6	0.8400
C7—O4	1.231 (3)

N1—Cu1—N2	168.18 (9)	C9—N2—C13	118.4 (2)
N1—Cu1—O2	81.66 (8)	C9—N2—Cu1	118.92 (17)
N2—Cu1—O2	97.18 (8)	C13—N2—Cu1	122.68 (18)
N1—Cu1—O3	79.84 (8)	N2—C9—C10	123.0 (2)
N2—Cu1—O3	99.02 (8)	N2—C9—H9	118.5
O2—Cu1—O3	159.29 (8)	C10—C9—H9	118.5
N1—Cu1—O5	91.57 (8)	C9—C10—C11	119.2 (2)
N2—Cu1—O5	100.24 (8)	C9—C10—H10	120.4
O2—Cu1—O5	96.71 (7)	C11—C10—H10	120.4
O3—Cu1—O5	93.03 (7)	C12—C11—C10	117.8 (2)
O1—C1—O2	125.2 (2)	C12—C11—C14	119.7 (2)
O1—C1—C2	119.9 (2)	C10—C11—C14	122.5 (2)
O2—C1—C2	114.9 (2)	C13—C12—C11	119.5 (2)
N1—C2—C3	120.4 (2)	C13—C12—H12	120.2
N1—C2—C1	111.3 (2)	C11—C12—H12	120.2
C3—C2—C1	128.3 (2)	N2—C13—C12	122.1 (2)
C2—C3—C4	118.0 (2)	N2—C13—H13	119.0
C2—C3—H3	121.0	C12—C13—H13	119.0
C4—C3—H3	121.0	N3—C14—C11	119.3 (2)
C5—C4—C3	120.7 (2)	N3—C14—H14	120.4
C5—C4—H4	119.7	C11—C14—H14	120.4
C3—C4—H4	119.7	C2—N1—C6	122.9 (2)
C6—C5—C4	117.9 (2)	C2—N1—Cu1	117.51 (17)
C6—C5—H5	121.1	C6—N1—Cu1	119.60 (17)
C4—C5—H5	121.1	C14—N3—O6	110.1 (2)
N1—C6—C5	120.2 (2)	C1—O2—Cu1	113.75 (16)
N1—C6—C7	111.4 (2)	C7—O3—Cu1	113.79 (16)
C5—C6—C7	128.5 (2)	Cu1—O5—H5C	109.5
O4—C7—O3	125.6 (2)	Cu1—O5—H5B	110.7
O4—C7—C6	120.1 (2)	H5C—O5—H5B	112.6
O3—C7—C6	114.3 (2)	N3—O6—H6	109.5

O1—C1—C2—N1	174.9 (2)	C12—C11—C14—N3	171.6 (2)
O2—C1—C2—N1	−5.5 (3)	C10—C11—C14—N3	−7.7 (4)
O1—C1—C2—C3	−6.4 (4)	C3—C2—N1—C6	0.4 (4)
O2—C1—C2—C3	173.2 (2)	C1—C2—N1—C6	179.2 (2)
N1—C2—C3—C4	0.5 (4)	C3—C2—N1—Cu1	179.26 (19)
C1—C2—C3—C4	−178.1 (2)	C1—C2—N1—Cu1	−1.9 (3)
C2—C3—C4—C5	−1.2 (4)	C5—C6—N1—C2	−0.6 (4)
C3—C4—C5—C6	1.0 (4)	C7—C6—N1—C2	179.3 (2)
C4—C5—C6—N1	−0.1 (4)	C5—C6—N1—Cu1	−179.45 (19)
C4—C5—C6—C7	−179.9 (2)	C7—C6—N1—Cu1	0.4 (3)
N1—C6—C7—O4	−171.9 (2)	N2—Cu1—N1—C2	90.7 (4)
C5—C6—C7—O4	7.9 (4)	O2—Cu1—N1—C2	5.49 (18)
N1—C6—C7—O3	7.7 (3)	O3—Cu1—N1—C2	176.1 (2)
C5—C6—C7—O3	−172.5 (2)	O5—Cu1—N1—C2	−91.07 (19)
N1—Cu1—N2—C9	116.4 (4)	N2—Cu1—N1—C6	−90.4 (4)
O2—Cu1—N2—C9	−160.01 (19)	O2—Cu1—N1—C6	−175.6 (2)
O3—Cu1—N2—C9	32.9 (2)	O3—Cu1—N1—C6	−4.92 (19)
O5—Cu1—N2—C9	−61.82 (19)	O5—Cu1—N1—C6	87.88 (19)
N1—Cu1—N2—C13	−61.9 (5)	C11—C14—N3—O6	−178.7 (2)
O2—Cu1—N2—C13	21.7 (2)	O1—C1—O2—Cu1	−170.6 (2)
O3—Cu1—N2—C13	−145.3 (2)	C2—C1—O2—Cu1	9.9 (3)
O5—Cu1—N2—C13	119.9 (2)	N1—Cu1—O2—C1	−8.63 (17)
C13—N2—C9—C10	0.0 (4)	N2—Cu1—O2—C1	−176.76 (17)
Cu1—N2—C9—C10	−178.33 (19)	O3—Cu1—O2—C1	−35.5 (3)
N2—C9—C10—C11	1.6 (4)	O5—Cu1—O2—C1	81.98 (17)
C9—C10—C11—C12	−2.2 (4)	O4—C7—O3—Cu1	168.1 (2)
C9—C10—C11—C14	177.2 (2)	C6—C7—O3—Cu1	−11.5 (3)
C10—C11—C12—C13	1.1 (4)	N1—Cu1—O3—C7	9.31 (17)
C14—C11—C12—C13	−178.3 (2)	N2—Cu1—O3—C7	177.38 (17)
C9—N2—C13—C12	−1.1 (4)	O2—Cu1—O3—C7	36.3 (3)
Cu1—N2—C13—C12	177.19 (19)	O5—Cu1—O3—C7	−81.74 (18)
C11—C12—C13—N2	0.5 (4)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O5—H5C···O1ⁱ	0.84	1.93	2.769 (3)	180
O5—H5B···O4ⁱⁱ	0.83	2.07	2.836 (3)	155
O5—H5B···O6ⁱⁱⁱ	0.83	2.51	2.939 (3)	113
O6—H6···O3^iv	0.84	1.89	2.725 (3)	173

Symmetry codes: (i) x, y+1, z; (ii) x−1, y, z; (iii) −x+1, −y+2, −z+1; (iv) −x+2, −y+2, −z+1.

Experimental details

Crystal data
Chemical formula	[Cu(C₇H₃NO₄)(C₆H₆N₂O)(H₂O)]
M_r	368.79
Crystal system, space group	Triclinic, P1
Temperature (K)	120
a, b, c (Å)	6.7826 (2), 7.1858 (3), 14.8746 (6)
α, β, γ (°)	76.154 (2), 87.152 (1), 69.739 (1)
V (Å³)	659.91 (4)
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	1.69
Crystal size (mm)	0.16 × 0.14 × 0.04

Data collection
Diffractometer	Bruker–Nonius APEXII CCD diffractometer
Absorption correction	Multi-scan (SADABS; Sheldrick, 1996)
T_min, T_max	0.763, 0.925
No. of measured, independent and observed [I > 2σ(I)] reflections	12553, 2951, 2814
R_int	0.055
(sin θ/λ)_max (Å⁻¹)	0.646

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.039, 0.103, 1.10
No. of reflections	2951
No. of parameters	209
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.49, −0.47

Computer programs: APEX2 (Bruker, 2007), SAINT (Bruker, 2007), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008).

Selected geometric parameters (Å, º) top

Cu1—N1	1.903 (2)	Cu1—O3	2.0574 (18)
Cu1—N2	1.957 (2)	Cu1—O5	2.2273 (18)
Cu1—O2	2.0018 (18)

N1—Cu1—N2	168.18 (9)	O2—Cu1—O3	159.29 (8)
N1—Cu1—O2	81.66 (8)	N1—Cu1—O5	91.57 (8)
N2—Cu1—O2	97.18 (8)	N2—Cu1—O5	100.24 (8)
N1—Cu1—O3	79.84 (8)	O2—Cu1—O5	96.71 (7)
N2—Cu1—O3	99.02 (8)	O3—Cu1—O5	93.03 (7)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O5—H5C···O1ⁱ	0.84	1.93	2.769 (3)	180
O5—H5B···O4ⁱⁱ	0.83	2.07	2.836 (3)	155
O5—H5B···O6ⁱⁱⁱ	0.83	2.51	2.939 (3)	113
O6—H6···O3^iv	0.84	1.89	2.725 (3)	173

Symmetry codes: (i) x, y+1, z; (ii) x−1, y, z; (iii) −x+1, −y+2, −z+1; (iv) −x+2, −y+2, −z+1.

Acknowledgements

The author acknowledges the Overseas Research Scholarship Award Scheme and a Postgraduate Scholarship from the University of Bristol for funding, thanks Professor A. G. Orpen, University of Bristol, for his advice and support, and thanks the Structural Chemistry group, University of Bristol.

References

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