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Acta Cryst. (2008). E64, m1284-m1285    [ doi:10.1107/S1600536808029061 ]

Diaqua(2,2'-bipyridine-5,5'-dicarboxylato-[kappa]2N,N')(ethylenediamine-[kappa]2N,N')copper(II) 2.5-hydrate

M. Yousefi, A. Khalighi, N. Tadayon Pour, V. Amani and H. R. Khavasi

Abstract top

In the molecule of the title compound, [Cu(C12H6N2O4)(C2H8N2)(H2O)2]·2.5H2O, the CuII atom is six-coordinated in a distorted octahedral configuration by two N atoms from a 2,2'-bipyridine-5,5'-dicarboxylate anion, two N atoms from ethylenediamine and two O atoms from two water molecules. There are also two and a half water molecules in the asymmetric unit. The planar five-membered ring is nearly coplanar with the adjacent pyridine rings, while the other five-membered ring adopts a twisted conformation, probably due to hydrogen bonding. In the crystal structure, intra- and intermolecular N-H...O and O-H...O hydrogen bonds link the molecules.

Comment top

2,2'-Bipyridine-5,5'-dicarboxylic acid (BPDCH2) is a good bridging ligand, and numerous complexes with BPDCH2 anions have been prepared, such as that of cobalt (Min et al., 2002), platinum (Geary et al., 2003; Hafizovic et al., 2006), neodyminum (Schoknechta & Kempe, 2004), ruthenium and rhodium (Matthews et al., 2004) complexes. For further investigation of 2,2'-bipyridine-5,5'-dicarboxylic acid, we synthesized the title compound and report herein its crystal structure.

In the title compound, (Fig. 1), the CuII atom is six-coordinated in a distorted octahedral configuration by two N atoms from 2,2'-bipyridine-5,5'-dicarboxylate anion, two N atoms from ethylenediamine and two O atoms from two water molecules (Table 1). There are also two and a half water molecules in the asymmetric unit. Rings A (N1/C1/C2/C4–C6), B (N2/C7–C10/C12) and C (Cu1/N1/N2/C6/C7) are, of course, planar, and the dihedral angles between them are A/B = 1.43 (3)°, A/C = 2.09 (3)° and B/C = 2.45 (3)°. So, they are nearly coplanar, while ring D (Cu1/N3/N4/C13/C14) adopts twisted conformation, probably due to the hydrogen bondings.

In the crystal structure, intra- and intermolecular N—H···O and O—H···O hydrogen bonds (Table 2) link the molecules (Fig. 2), in which they may be effective in the stabilization of the structure.

Related literature top

For complexes involving 2,2'-bipyridine-5,5'-dicarboxylate anions, see: Min et al. (2002); Geary et al. (2003); Hafizovic et al. (2006); Schoknechta & Kempe (2004); Matthews et al. (2004).

Experimental top

For the preparation of the title compound, ethylenediamine (0.15 g, 2.50 mmol) was added to a suspension of 2,2'-bipyridine-5,5'-dicarboxylic acid (0.21 g, 0.83 mmol) in water (10 ml) and the resulting colorless solution was added to CuCl2.2H2O (0.14 g, 0.83 mmol) in water (10 ml). The resulting blue solution was stirred at 323 K for 15 min, and then was left to evaporate slowly at room temperature. After one week, blue plate crystals of the title compound were isolated (yield; 0.26 g, 70.01%, m.p. 488 K).

Refinement top

H3A, H3B, H4B, H4C (for NH2) and H5B, H5C, H6A, H6B, H7A, H7B, H8B, H9B, H9C (for H2O) atoms were located in difference syntheses and refined isotropically [N—H = 0.85 (4)–0.89 (4) Å and Uiso(H) = 0.035 (8)–0.043 (9) Å2; O—H = 0.72 (5)–0.97 (6) Å and Uiso(H) = 0.041 (10)–0.11 (2) Å2]. The remaining H atoms were positioned geometrically, with C—H = 0.93 and 0.97 Å for aromatic and methylene H, respectively, and constrained to ride on their parent atoms with Uiso(H) = 1.2Ueq(C).

Computing details top

Data collection: SMART (Bruker, 1998); cell refinement: SAINT (Bruker, 1998); data reduction: SAINT (Bruker, 1998); program(s) used to solve structure: SHELXTL (Sheldrick, 2008); program(s) used to refine structure: SHELXTL (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997); software used to prepare material for publication: WinGX (Farrugia, 1999).

Figures top
[Figure 1] Fig. 1. The molecular structure of the title molecule, with the atom-numbering scheme. Displacement ellipsoids are drawn at the 40% probability level.
[Figure 2] Fig. 2. A packing diagram of the title compound. Hydrogen bonds are shown as dashed lines.
Diaqua(2,2'-bipyridine-5,5'-dicarboxylato-k2N,N')(ethylenediamine-k2N,N')copper(II) 2.5-hydrate top
Crystal data top
[Cu(C12H6N2O4)(C2H8N2)(H2O)2]·2.5H2OF(000) = 1856
Mr = 446.92Dx = 1.619 Mg m−3
Monoclinic, C2/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -C 2ycCell parameters from 1976 reflections
a = 31.730 (6) Åθ = 2.2–29.3°
b = 7.2481 (14) ŵ = 1.25 mm−1
c = 18.421 (4) ÅT = 298 K
β = 120.05 (3)°Plate, blue
V = 3667.1 (17) Å30.50 × 0.18 × 0.07 mm
Z = 8
Data collection top
Bruker SMART CCD area-detector
diffractometer		4887 independent reflections
Radiation source: fine-focus sealed tube4221 reflections with I > 2σ(I)
graphiteRint = 0.043
φ and ω scansθmax = 29.3°, θmin = 2.2°
Absorption correction: multi-scan
(SADABS; Sheldrick, 1998)		h = −43→43
Tmin = 0.770, Tmax = 0.923k = −9→9
13747 measured reflectionsl = −25→25
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)] = 0.045Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.120H atoms treated by a mixture of independent and constrained refinement
S = 1.10 w = 1/[σ2(Fo2) + (0.0582P)2 + 5.7488P]
where P = (Fo2 + 2Fc2)/3
4887 reflections(Δ/σ)max = 0.015
301 parametersΔρmax = 1.71 e Å−3
0 restraintsΔρmin = −0.64 e Å−3
Crystal data top
[Cu(C12H6N2O4)(C2H8N2)(H2O)2]·2.5H2OV = 3667.1 (17) Å3
Mr = 446.92Z = 8
Monoclinic, C2/cMo Kα radiation
a = 31.730 (6) ŵ = 1.25 mm−1
b = 7.2481 (14) ÅT = 298 K
c = 18.421 (4) Å0.50 × 0.18 × 0.07 mm
β = 120.05 (3)°
Data collection top
Bruker SMART CCD area-detector
diffractometer		4887 independent reflections
Absorption correction: multi-scan
(SADABS; Sheldrick, 1998)		4221 reflections with I > 2σ(I)
Tmin = 0.770, Tmax = 0.923Rint = 0.043
13747 measured reflectionsθmax = 29.3°
Refinement top
R[F2 > 2σ(F2)] = 0.045H atoms treated by a mixture of independent and constrained refinement
wR(F2) = 0.120Δρmax = 1.71 e Å−3
S = 1.10Δρmin = −0.64 e Å−3
4887 reflectionsAbsolute structure: ?
301 parametersFlack parameter: ?
0 restraintsRogers parameter: ?
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
Cu10.129145 (10)0.87872 (5)0.482858 (17)0.02876 (10)
O10.28103 (9)1.1389 (6)0.78353 (15)0.0769 (10)
O20.33829 (8)1.2562 (4)0.76199 (13)0.0501 (5)
O30.09405 (8)0.6749 (3)0.10781 (12)0.0447 (5)
O40.05397 (7)0.5529 (3)0.16672 (12)0.0410 (4)
O50.10527 (11)1.2087 (4)0.42720 (19)0.0570 (6)
H5B0.0955 (18)1.190 (7)0.375 (4)0.078 (15)*
H5C0.0838 (19)1.250 (8)0.424 (3)0.081 (18)*
O60.15861 (10)0.5703 (4)0.55005 (19)0.0513 (6)
H6A0.1748 (14)0.577 (5)0.596 (3)0.041 (10)*
H6B0.133 (2)0.484 (9)0.535 (4)0.101 (19)*
O70.41911 (13)1.2811 (5)0.74176 (19)0.0621 (7)
H7A0.3946 (18)1.303 (7)0.744 (3)0.062 (13)*
H7B0.434 (2)1.192 (10)0.764 (4)0.11 (2)*
O80.00000.9968 (6)0.25000.0568 (9)
H8B0.0210 (17)1.050 (7)0.252 (4)0.066 (15)*
O90.03530 (9)0.5945 (4)−0.05647 (15)0.0511 (6)
H9B0.0049 (17)0.569 (6)−0.080 (3)0.063 (12)*
H9C0.056 (2)0.608 (7)0.004 (4)0.097 (17)*
N10.19871 (7)0.9679 (3)0.53881 (12)0.0270 (4)
N20.14333 (7)0.8272 (3)0.38928 (12)0.0252 (4)
N30.11694 (8)0.9366 (3)0.57706 (13)0.0274 (4)
H3A0.1385 (13)0.896 (5)0.624 (2)0.043 (9)*
H3B0.1155 (12)1.055 (5)0.581 (2)0.035 (8)*
N40.05847 (7)0.8043 (3)0.41939 (14)0.0300 (4)
H4B0.0422 (13)0.848 (5)0.369 (2)0.037 (8)*
H4C0.0557 (12)0.682 (5)0.418 (2)0.037 (8)*
C10.22492 (9)1.0341 (4)0.61691 (15)0.0331 (5)
H10.21111.03360.65110.040*
C20.27180 (8)1.1035 (3)0.64927 (15)0.0298 (5)
C30.29927 (10)1.1729 (4)0.73932 (16)0.0384 (6)
C40.29229 (8)1.0998 (3)0.59865 (15)0.0290 (5)
H4A0.32351.14570.61830.035*
C50.26621 (8)1.0276 (3)0.51827 (14)0.0271 (4)
H5A0.28001.02200.48410.033*
C60.21916 (8)0.9637 (3)0.48967 (13)0.0226 (4)
C70.18787 (8)0.8846 (3)0.40512 (13)0.0223 (4)
C80.20220 (8)0.8669 (3)0.34572 (14)0.0279 (4)
H8A0.23280.90740.35730.033*
C90.17036 (9)0.7882 (3)0.26864 (14)0.0284 (5)
H9A0.17950.77590.22810.034*
C100.12496 (8)0.7278 (3)0.25224 (14)0.0257 (4)
C110.08798 (9)0.6439 (3)0.16880 (14)0.0293 (5)
C120.11346 (8)0.7489 (4)0.31536 (14)0.0287 (5)
H120.08340.70630.30560.034*
C130.06969 (9)0.8537 (4)0.55719 (16)0.0340 (5)
H13A0.05710.91360.58950.041*
H13B0.07380.72340.57110.041*
C140.03498 (9)0.8794 (4)0.46480 (16)0.0332 (5)
H14A0.00470.81480.44820.040*
H14B0.02781.00930.45200.040*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Cu10.02016 (14)0.04566 (19)0.01986 (14)−0.00232 (11)0.00958 (11)−0.00645 (12)
O10.0448 (13)0.154 (3)0.0339 (11)−0.0239 (16)0.0215 (10)−0.0362 (16)
O20.0412 (11)0.0628 (14)0.0320 (10)−0.0159 (10)0.0077 (9)−0.0168 (10)
O30.0551 (12)0.0527 (12)0.0221 (8)−0.0170 (10)0.0163 (8)−0.0079 (8)
O40.0333 (9)0.0507 (11)0.0298 (9)−0.0135 (8)0.0090 (8)−0.0066 (8)
O50.0548 (15)0.0671 (17)0.0513 (15)0.0147 (13)0.0281 (13)0.0149 (13)
O60.0509 (14)0.0504 (13)0.0545 (15)0.0021 (11)0.0278 (13)0.0043 (12)
O70.0718 (19)0.0669 (18)0.0573 (16)0.0017 (15)0.0396 (15)0.0151 (14)
O80.054 (2)0.057 (2)0.0453 (19)0.0000.0144 (18)0.000
O90.0465 (12)0.0693 (16)0.0318 (10)−0.0222 (11)0.0153 (9)−0.0088 (10)
N10.0205 (8)0.0369 (10)0.0204 (8)−0.0018 (7)0.0079 (7)−0.0056 (8)
N20.0213 (8)0.0325 (10)0.0206 (8)−0.0014 (7)0.0096 (7)−0.0041 (7)
N30.0262 (9)0.0355 (11)0.0206 (9)0.0039 (8)0.0118 (8)0.0020 (8)
N40.0237 (9)0.0398 (12)0.0253 (9)−0.0018 (8)0.0115 (8)−0.0014 (9)
C10.0244 (10)0.0483 (14)0.0233 (10)−0.0004 (10)0.0095 (9)−0.0095 (10)
C20.0249 (10)0.0344 (12)0.0219 (10)0.0017 (9)0.0056 (8)−0.0048 (9)
C30.0298 (12)0.0499 (15)0.0248 (11)0.0014 (11)0.0058 (9)−0.0130 (11)
C40.0240 (10)0.0298 (11)0.0262 (10)−0.0037 (8)0.0073 (8)−0.0034 (9)
C50.0253 (10)0.0309 (11)0.0228 (10)−0.0025 (8)0.0103 (8)−0.0013 (9)
C60.0226 (9)0.0227 (10)0.0197 (9)0.0010 (8)0.0085 (8)−0.0014 (8)
C70.0218 (9)0.0238 (9)0.0194 (9)0.0003 (8)0.0088 (8)0.0002 (8)
C80.0268 (10)0.0336 (11)0.0241 (10)−0.0054 (9)0.0133 (9)−0.0024 (9)
C90.0325 (11)0.0333 (12)0.0211 (10)−0.0023 (9)0.0147 (9)−0.0014 (9)
C100.0285 (10)0.0266 (10)0.0184 (9)0.0006 (8)0.0090 (8)−0.0009 (8)
C110.0330 (11)0.0280 (11)0.0199 (9)−0.0015 (9)0.0079 (9)−0.0029 (8)
C120.0236 (10)0.0375 (12)0.0230 (10)−0.0036 (9)0.0102 (8)−0.0057 (9)
C130.0332 (12)0.0447 (14)0.0304 (12)0.0028 (10)0.0207 (10)0.0034 (10)
C140.0238 (10)0.0434 (13)0.0333 (12)0.0025 (10)0.0150 (9)0.0015 (11)
Geometric parameters (Å, °) top
O5—Cu12.563 (3)C4—C51.387 (3)
O5—H5B0.86 (6)C4—H4A0.9300
O5—H5C0.72 (5)C5—C61.390 (3)
O6—Cu12.499 (3)C5—H5A0.9300
O6—H6A0.74 (4)C6—N11.353 (3)
O6—H6B0.96 (6)C6—C71.481 (3)
O7—H7A0.81 (5)C7—N21.357 (3)
O7—H7B0.78 (7)C7—C81.385 (3)
O8—H8B0.76 (6)C8—C91.388 (3)
O9—H9B0.86 (5)C8—H8A0.9300
O9—H9C0.97 (6)C9—C101.386 (3)
N1—Cu12.018 (2)C9—H9A0.9300
N2—Cu12.0225 (19)C10—C121.390 (3)
N3—Cu12.003 (2)C10—C111.518 (3)
N3—H3A0.85 (4)C11—O41.249 (3)
N3—H3B0.86 (4)C11—O31.252 (3)
N4—Cu12.015 (2)C12—N21.335 (3)
N4—H4B0.87 (4)C12—H120.9300
N4—H4C0.89 (4)C13—N31.481 (3)
C1—N11.339 (3)C13—C141.506 (4)
C1—C21.390 (3)C13—H13A0.9700
C1—H10.9300C13—H13B0.9700
C2—C41.378 (3)C14—N41.475 (3)
C2—C31.522 (3)C14—H14A0.9700
C3—O11.237 (4)C14—H14B0.9700
C3—O21.247 (4)
O5—Cu1—O6174.49 (10)C4—C2—C1118.0 (2)
O5—Cu1—N186.22 (11)C4—C2—C3122.5 (2)
O5—Cu1—N288.78 (10)C1—C2—C3119.5 (2)
O5—Cu1—N390.26 (10)O1—C3—O2126.1 (3)
O5—Cu1—N489.86 (11)O1—C3—C2116.8 (3)
O6—Cu1—N189.50 (10)O2—C3—C2117.1 (3)
O6—Cu1—N293.97 (10)C2—C4—C5119.9 (2)
O6—Cu1—N386.84 (10)C2—C4—H4A120.1
O6—Cu1—N494.56 (11)C5—C4—H4A120.1
N3—Cu1—N485.24 (9)C4—C5—C6118.9 (2)
N3—Cu1—N197.29 (9)C4—C5—H5A120.5
N4—Cu1—N1175.34 (9)C6—C5—H5A120.5
N3—Cu1—N2177.97 (9)N1—C6—C5121.5 (2)
N4—Cu1—N296.54 (8)N1—C6—C7114.76 (18)
N1—Cu1—N280.87 (8)C5—C6—C7123.7 (2)
H5B—O5—H5C101 (5)N2—C7—C8121.3 (2)
H6A—O6—H6B112 (5)N2—C7—C6115.00 (18)
H7A—O7—H7B118 (6)C8—C7—C6123.65 (19)
H9B—O9—H9C123 (4)C7—C8—C9119.2 (2)
Cu1—O5—H5B100 (3)C7—C8—H8A120.4
Cu1—O5—H5C120 (5)C9—C8—H8A120.4
H5B—O5—H5C100 (6)C10—C9—C8119.8 (2)
Cu1—O6—H6B113 (4)C10—C9—H9A120.1
H6A—O6—H6B112 (5)C8—C9—H9A120.1
Cu1—O6—H6A112 (3)C9—C10—C12117.5 (2)
C1—N1—C6118.6 (2)C9—C10—C11122.6 (2)
C1—N1—Cu1126.54 (17)C12—C10—C11119.8 (2)
C6—N1—Cu1114.80 (14)O4—C11—O3125.9 (2)
C12—N2—C7118.72 (19)O4—C11—C10117.5 (2)
C12—N2—Cu1126.92 (16)O3—C11—C10116.7 (2)
C7—N2—Cu1114.34 (15)N2—C12—C10123.4 (2)
C13—N3—Cu1108.16 (16)N2—C12—H12118.3
C13—N3—H3A108 (2)C10—C12—H12118.3
Cu1—N3—H3A114 (2)N3—C13—C14107.8 (2)
C13—N3—H3B110 (2)N3—C13—H13A110.1
Cu1—N3—H3B108 (2)C14—C13—H13A110.1
H3A—N3—H3B109 (3)N3—C13—H13B110.1
C14—N4—Cu1107.68 (16)C14—C13—H13B110.1
C14—N4—H4B106 (2)H13A—C13—H13B108.5
Cu1—N4—H4B114 (2)N4—C14—C13107.7 (2)
C14—N4—H4C108 (2)N4—C14—H14A110.2
Cu1—N4—H4C110 (2)C13—C14—H14A110.2
H4B—N4—H4C110 (3)N4—C14—H14B110.2
N1—C1—C2123.1 (2)C13—C14—H14B110.2
N1—C1—H1118.5H14A—C14—H14B108.5
C2—C1—H1118.5
C1—N1—Cu1—N32.7 (2)N2—C7—C8—C9−0.3 (4)
C6—N1—Cu1—N3−175.05 (17)C6—C7—C8—C9179.0 (2)
C1—N1—Cu1—N2−178.1 (2)C7—C8—C9—C10−0.2 (4)
C6—N1—Cu1—N24.10 (17)C8—C9—C10—C12−0.3 (4)
C12—N2—Cu1—N4−6.3 (2)C8—C9—C10—C11178.8 (2)
C7—N2—Cu1—N4171.90 (17)C9—C10—C11—O4162.4 (2)
C12—N2—Cu1—N1177.6 (2)C12—C10—C11—O4−18.6 (3)
C7—N2—Cu1—N1−4.19 (16)C9—C10—C11—O3−18.6 (4)
C13—N3—Cu1—N413.46 (17)C12—C10—C11—O3160.4 (2)
C13—N3—Cu1—N1−170.47 (17)C9—C10—C12—N21.5 (4)
C14—N4—Cu1—N315.41 (18)C11—C10—C12—N2−177.6 (2)
C14—N4—Cu1—N2−163.62 (17)N3—C13—C14—N453.5 (3)
N1—C1—C2—C4−1.4 (4)C2—C1—N1—C61.8 (4)
N1—C1—C2—C3−178.9 (3)C2—C1—N1—Cu1−175.9 (2)
C4—C2—C3—O1−167.1 (3)C5—C6—N1—C1−0.5 (4)
C1—C2—C3—O110.4 (4)C7—C6—N1—C1178.7 (2)
C4—C2—C3—O211.9 (4)C5—C6—N1—Cu1177.44 (18)
C1—C2—C3—O2−170.6 (3)C7—C6—N1—Cu1−3.3 (3)
C1—C2—C4—C5−0.3 (4)C10—C12—N2—C7−2.0 (4)
C3—C2—C4—C5177.2 (2)C10—C12—N2—Cu1176.16 (18)
C2—C4—C5—C61.4 (4)C8—C7—N2—C121.4 (3)
C4—C5—C6—N1−1.1 (4)C6—C7—N2—C12−178.0 (2)
C4—C5—C6—C7179.8 (2)C8—C7—N2—Cu1−177.01 (18)
N1—C6—C7—N2−0.2 (3)C6—C7—N2—Cu13.6 (2)
C5—C6—C7—N2179.0 (2)C14—C13—N3—Cu1−39.3 (2)
N1—C6—C7—C8−179.6 (2)C13—C14—N4—Cu1−40.8 (3)
C5—C6—C7—C8−0.4 (4)
Hydrogen-bond geometry (Å, °) top
D—H···AD—HH···AD···AD—H···A
N3—H3A···O2i0.84 (3)2.11 (3)2.881 (3)153 (4)
N3—H3B···O3ii0.86 (4)2.21 (4)3.031 (3)159 (4)
N4—H4B···O80.87 (3)2.20 (3)3.054 (3)171 (4)
N4—H4C···O9iii0.89 (4)2.23 (4)3.069 (4)158 (4)
O5—H5B···O7iv0.86 (6)1.97 (6)2.807 (4)164 (5)
O5—H5C···O9ii0.72 (7)2.08 (6)2.779 (5)165 (5)
O6—H6A···O1i0.74 (5)1.99 (5)2.726 (4)171 (4)
O6—H6B···O3iii0.95 (7)2.51 (7)3.267 (4)136 (5)
O7—H7A···O20.82 (6)2.00 (6)2.776 (5)158 (5)
O7—H7B···O4v0.78 (7)2.11 (7)2.827 (4)153 (7)
O8—H8B···O7iv0.76 (6)2.22 (6)2.969 (5)178 (8)
O9—H9B···O4vi0.86 (6)1.96 (5)2.744 (4)152 (5)
O9—H9C···O30.97 (6)1.74 (6)2.706 (3)169 (4)
Symmetry codes: (i) −x+1/2, y−1/2, −z+3/2; (ii) x, −y+2, z+1/2; (iii) x, −y+1, z+1/2; (iv) −x+1/2, −y+5/2, −z+1; (v) −x+1/2, −y+3/2, −z+1; (vi) −x, −y+1, −z.
Table 1
Selected geometric parameters (Å, °) top
O5—Cu12.563 (3)N2—Cu12.0225 (19)
O6—Cu12.499 (3)N3—Cu12.003 (2)
N1—Cu12.018 (2)N4—Cu12.015 (2)
O5—Cu1—O6174.49 (10)O6—Cu1—N494.56 (11)
O5—Cu1—N186.22 (11)N3—Cu1—N485.24 (9)
O5—Cu1—N288.78 (10)N3—Cu1—N197.29 (9)
O5—Cu1—N390.26 (10)N4—Cu1—N1175.34 (9)
O5—Cu1—N489.86 (11)N3—Cu1—N2177.97 (9)
O6—Cu1—N189.50 (10)N4—Cu1—N296.54 (8)
O6—Cu1—N293.97 (10)N1—Cu1—N280.87 (8)
O6—Cu1—N386.84 (10)
Table 2
Hydrogen-bond geometry (Å, °) top
D—H···AD—HH···AD···AD—H···A
N3—H3A···O2i0.84 (3)2.11 (3)2.881 (3)153 (4)
N3—H3B···O3ii0.86 (4)2.21 (4)3.031 (3)159 (4)
N4—H4B···O80.87 (3)2.20 (3)3.054 (3)171 (4)
N4—H4C···O9iii0.89 (4)2.23 (4)3.069 (4)158 (4)
O5—H5B···O7iv0.86 (6)1.97 (6)2.807 (4)164 (5)
O5—H5C···O9ii0.72 (7)2.08 (6)2.779 (5)165 (5)
O6—H6A···O1i0.74 (5)1.99 (5)2.726 (4)171 (4)
O6—H6B···O3iii0.95 (7)2.51 (7)3.267 (4)136 (5)
O7—H7A···O20.82 (6)2.00 (6)2.776 (5)158 (5)
O7—H7B···O4v0.78 (7)2.11 (7)2.827 (4)153 (7)
O8—H8B···O7iv0.76 (6)2.22 (6)2.969 (5)178 (8)
O9—H9B···O4vi0.86 (6)1.96 (5)2.744 (4)152 (5)
O9—H9C···O30.97 (6)1.74 (6)2.706 (3)169 (4)
Symmetry codes: (i) −x+1/2, y−1/2, −z+3/2; (ii) x, −y+2, z+1/2; (iii) x, −y+1, z+1/2; (iv) −x+1/2, −y+5/2, −z+1; (v) −x+1/2, −y+3/2, −z+1; (vi) −x, −y+1, −z.
Acknowledgements top

We are grateful to the Islamic Azad University, Shahr-e-Rey Branch, for financial support.

references
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