metal-organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 68| Part 3| March 2012| Pages m249-m250

trans-Tetra­aqua­bis­­(isonicotinamide-κN1)cobalt(II) bis­­(3-hy­dr­oxy­benzoate) tetra­hydrate

aDepartment of Chemistry, Kafkas University, 36100 Kars, Turkey, bDepartment of Physics, Sakarya University, 54187 Esentepe, Sakarya, Turkey, and cDepartment of Physics, Hacettepe University, 06800 Beytepe, Ankara, Turkey
*Correspondence e-mail: merzifon@hacettepe.edu.tr

(Received 24 January 2012; accepted 30 January 2012; online 4 February 2012)

The asymmetric unit of the title compound, [Co(C6H6N2O)2(H2O)4](C7H5O3)2·4H2O, contains one-half of the complex cation with the CoII ion located on an inversion center, a 3-hy­droxy­benzoate counter-anion and two uncoordinated water mol­ecules. Four water O atoms in the equatorial plane around the CoII ion [Co—O = 2.0593 (16) and 2.1118 (16) Å] form a slightly distorted square-planar arrangement, and the distorted octahedral geometry is completed by the two N atoms [Co—N = 2.1306 (18) Å] from two isonicotinamide ligands. In the anion, the carboxyl­ate group is twisted from the attached benzene ring at 8.84 (17)°. In the crystal, a three-dimensional hydrogen-bonding network, formed by classical O—H⋯O and N—H⋯O hydrogen bonds, consolidates the crystal packing, which exhibits ππ inter­actions between the benzene and pyridine rings, with centroid–centroid distances of 3.458 (1) and 3.606 (1) Å, respectively.

Related literature

For related structures, see: Hökelek, Dal, Tercan, Özbek et al. (2009[Hökelek, T., Dal, H., Tercan, B., Özbek, F. E. & Necefoğlu, H. (2009). Acta Cryst. E65, m1330-m1331.]); Hökelek, Dal, Tercan, Aybirdi et al. (2009[Hökelek, T., Dal, H., Tercan, B., Aybirdi, Ö. & Necefoğlu, H. (2009). Acta Cryst. E65, m627-m628.]); Hökelek, Yılmaz, Tercan, Gürgen et al. (2009[Hökelek, T., Yılmaz, F., Tercan, B., Gürgen, F. & Necefoğlu, H. (2009). Acta Cryst. E65, m1101-m1102.]); Hökelek, Yılmaz, Tercan, Özbek et al. (2009[Hökelek, T., Yılmaz, F., Tercan, B., Özbek, F. E. & Necefoğlu, H. (2009). Acta Cryst. E65, m768-m769.]); Hökelek, Yılmaz, Tercan, Sertçelik et al. (2009[Hökelek, T., Yılmaz, F., Tercan, B., Sertçelik, M. & Necefoğlu, H. (2009). Acta Cryst. E65, m1130-m1131.]); Sertçelik et al. (2009a[Sertçelik, M., Tercan, B., Şahin, E., Necefoğlu, H. & Hökelek, T. (2009a). Acta Cryst. E65, m326-m327.],b[Sertçelik, M., Tercan, B., Şahin, E., Necefoğlu, H. & Hökelek, T. (2009b). Acta Cryst. E65, m389-m390.]); Zaman et al. (2012[Zaman, İ. G., Çaylak Delibaş, N., Necefoğlu, H. & Hökelek, T. (2012). Acta Cryst. E68, m200-m201.]).

[Scheme 1]

Experimental

Crystal data
  • [Co(C6H6N2O)2(H2O)4](C7H5O3)2·4H2O

  • Mr = 721.53

  • Monoclinic, P 21 /n

  • a = 6.7032 (2) Å

  • b = 17.0523 (4) Å

  • c = 13.5406 (3) Å

  • β = 100.194 (3)°

  • V = 1523.32 (7) Å3

  • Z = 2

  • Mo Kα radiation

  • μ = 0.65 mm−1

  • T = 100 K

  • 0.29 × 0.28 × 0.14 mm

Data collection
  • Bruker Kappa APEXII CCD area-detector diffractometer

  • Absorption correction: multi-scan (SADABS; Bruker, 2005[Bruker (2005). SADABS. Bruker AXS Inc., Madison, Wisconsin, USA.]) Tmin = 0.840, Tmax = 0.916

  • 14243 measured reflections

  • 3779 independent reflections

  • 3590 reflections with I > 2σ(I)

  • Rint = 0.019

Refinement
  • R[F2 > 2σ(F2)] = 0.034

  • wR(F2) = 0.086

  • S = 1.23

  • 3779 reflections

  • 258 parameters

  • 16 restraints

  • H atoms treated by a mixture of independent and constrained refinement

  • Δρmax = 0.47 e Å−3

  • Δρmin = −0.42 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A DA D—H⋯A
N2—H21⋯O2i 0.86 (3) 2.18 (3) 3.031 (3) 170 (3)
N2—H22⋯O8ii 0.85 (4) 2.20 (4) 3.007 (3) 158 (3)
O3—H31⋯O7 0.91 (4) 1.81 (4) 2.711 (2) 170 (4)
O5—H51⋯O3ii 0.96 (3) 1.76 (3) 2.715 (2) 171 (3)
O5—H52⋯O2iii 0.86 (3) 1.95 (4) 2.782 (2) 163 (4)
O6—H61⋯O4iv 0.95 (3) 1.73 (3) 2.685 (2) 178 (4)
O6—H62⋯O2v 0.82 (3) 1.89 (4) 2.683 (2) 161 (3)
O7—H71⋯O1i 0.98 (3) 1.76 (4) 2.740 (3) 179 (3)
O8—H81⋯O1 0.96 (4) 1.81 (4) 2.760 (3) 174 (3)
O8—H82⋯O7vi 0.83 (5) 2.06 (4) 2.807 (3) 149 (5)
Symmetry codes: (i) [-x+{\script{1\over 2}}, y+{\script{1\over 2}}, -z+{\script{3\over 2}}]; (ii) [x+{\script{1\over 2}}, -y+{\script{1\over 2}}, z-{\script{1\over 2}}]; (iii) -x+1, -y, -z+1; (iv) [x-{\script{1\over 2}}, -y+{\script{1\over 2}}, z-{\script{1\over 2}}]; (v) -x, -y, -z+1; (vi) [-x-{\script{1\over 2}}, y-{\script{1\over 2}}, -z+{\script{3\over 2}}].

Data collection: APEX2 (Bruker, 2007[Bruker (2007). APEX2 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.]); cell refinement: SAINT (Bruker, 2007[Bruker (2007). APEX2 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.]); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); molecular graphics: Mercury (Macrae et al., 2006[Macrae, C. F., Edgington, P. R., McCabe, P., Pidcock, E., Shields, G. P., Taylor, R., Towler, M. & van de Streek, J. (2006). J. Appl. Cryst. 39, 453-457.]); software used to prepare material for publication: WinGX (Farrugia, 1999[Farrugia, L. J. (1999). J. Appl. Cryst. 32, 837-838.]) and PLATON (Spek, 2009[Spek, A. L. (2009). Acta Cryst. D65, 148-155.]).

Supporting information


Comment top

As a part of our ongoing investigation on transition metal complexes of nicotinamide (NA) and/or the nicotinic acid derivative N,N-diethylnicotinamide (DENA) (Hökelek, Dal, Tercan, Özbek et al., 2009; Hökelek, Dal, Tercan, Aybirdi et al., 2009; Hökelek, Yılmaz, Tercan, Gürgen et al., 2009; Hökelek, Yılmaz, Tercan, Özbek et al., 2009; Hökelek, Yılmaz, Tercan, Sertçelik et al., 2009; Sertçelik et al., 2009a,b), the title compound was synthesized and its crystal structure is reported herein.

The title compound (I) is isostructural with the related Ni complex (Zaman et al., 2012). In (I) (Fig. 1), four O atoms (O5, O6, and the symmetry-related atoms, O5', O6') in the equatorial plane around the Co atom form a slightly distorted square-planar arrangement, while the slightly distorted octahedral coordination is completed by the two pyridine N atoms (N1, N1') of the INA ligands at 2.1306 (18) Å from the Co atom in the axial positions (Fig. 1). The average Co—O bond length is 2.0856 (16) Å. The intramolecular O—H···O hydrogen bonds (Table 1) link the uncoordinated water molecules to the HB anion. The dihedral angle between the planar carboxylate group (O1/O2/C1) and the benzene ring A (C2—C7) is 8.84 (17)°, while that between rings A and B (N1/C8—C12) is 1.24 (7)°.

In the crystal structure, intermolecular O—H···O and N—H···O hydrogen bonds (Table 1) link the molecules into a three-dimensional network, in which they may be effective in the stabilization of the structure. ππ Contacts between the benzene and pyridine rings, Cg1—Cg2 and Cg1—Cg2i, [symmetry code: (i) -1 + x, y, z, where Cg1 and Cg2 are centroids of the rings A (C2—C7) and B (N1/C8—C12), respectively] may further stabilize the structure, with centroid-centroid distances of 3.606 (1) and 3.458 (1) Å, respectively.

Related literature top

For related structures, see: Hökelek, Dal, Tercan, Özbek et al. (2009); Hökelek, Dal, Tercan, Aybirdi et al. (2009); Hökelek, Yılmaz, Tercan, Gürgen et al. (2009); Hökelek, Yılmaz, Tercan, Özbek et al. (2009); Hökelek, Yılmaz, Tercan, Sertçelik et al. (2009); Sertçelik et al. (2009a,b); Zaman et al. (2012).

Experimental top

The title compound was prepared by the reaction of CoSO4.7H2O (1.406 g, 5 mmol) in H2O (100 ml) and INA (1.220 g, 10 mmol) in H2O (50 ml) with sodium 3-hydroxybenzoate (1.601 g, 10 mmol) in H2O (100 ml). The mixture was filtered and set aside to crystallize at ambient temperature for three weeks, giving orange single crystals.

Refinement top

Atoms H51, H52, H61, H62, H71, H72, H81 and H82 (for H2O), H21 and H22 (for NH2) and H31 (for OH) were located in difference Fourier map and were refined by applying bond length restraints. The C-bound H-atoms were positioned geometrically (C—H = 0.93 Å) and constrained to ride on their parent atoms, with Uiso(H) = 1.2 × Ueq(C).

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: Mercury (Macrae et al., 2006); software used to prepare material for publication: WinGX (Farrugia, 1999) and PLATON (Spek, 2009).

Figures top
[Figure 1] Fig. 1. The molecular structure of (I) with the atom-numbering scheme [symmetry code: (') -x, -y, -z]. Displacement ellipsoids are drawn at the 50% probability level. Hydrogen bonds are shown as dashed lines.
trans-Tetraaquabis(isonicotinamide-κN1)cobalt(II) bis(3-hydroxybenzoate) tetrahydrate top
Crystal data top
[Co(C6H6N2O)2(H2O)4](C7H5O3)2·4H2OF(000) = 754
Mr = 721.53Dx = 1.573 Mg m3
Monoclinic, P21/nMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ynCell parameters from 9057 reflections
a = 6.7032 (2) Åθ = 2.4–28.4°
b = 17.0523 (4) ŵ = 0.65 mm1
c = 13.5406 (3) ÅT = 100 K
β = 100.194 (3)°Block, orange
V = 1523.32 (7) Å30.29 × 0.28 × 0.14 mm
Z = 2
Data collection top
Bruker Kappa APEXII CCD area-detector
diffractometer
3779 independent reflections
Radiation source: fine-focus sealed tube3590 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.019
ϕ and ω scansθmax = 28.4°, θmin = 2.4°
Absorption correction: multi-scan
(SADABS; Bruker, 2005)
h = 88
Tmin = 0.840, Tmax = 0.916k = 2221
14243 measured reflectionsl = 1518
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)] = 0.034Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.086H atoms treated by a mixture of independent and constrained refinement
S = 1.23 w = 1/[σ2(Fo2) + (0.0269P)2 + 1.4849P]
where P = (Fo2 + 2Fc2)/3
3779 reflections(Δ/σ)max < 0.001
258 parametersΔρmax = 0.47 e Å3
16 restraintsΔρmin = 0.42 e Å3
Crystal data top
[Co(C6H6N2O)2(H2O)4](C7H5O3)2·4H2OV = 1523.32 (7) Å3
Mr = 721.53Z = 2
Monoclinic, P21/nMo Kα radiation
a = 6.7032 (2) ŵ = 0.65 mm1
b = 17.0523 (4) ÅT = 100 K
c = 13.5406 (3) Å0.29 × 0.28 × 0.14 mm
β = 100.194 (3)°
Data collection top
Bruker Kappa APEXII CCD area-detector
diffractometer
3779 independent reflections
Absorption correction: multi-scan
(SADABS; Bruker, 2005)
3590 reflections with I > 2σ(I)
Tmin = 0.840, Tmax = 0.916Rint = 0.019
14243 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.03416 restraints
wR(F2) = 0.086H atoms treated by a mixture of independent and constrained refinement
S = 1.23Δρmax = 0.47 e Å3
3779 reflectionsΔρmin = 0.42 e Å3
258 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
Co10.50000.00000.50000.00895 (12)
O10.1791 (2)0.11648 (9)0.83771 (12)0.0148 (3)
O20.0778 (2)0.04189 (9)0.70323 (12)0.0136 (3)
O30.0160 (3)0.39111 (10)0.72117 (13)0.0160 (3)
H310.005 (6)0.430 (2)0.675 (3)0.045 (11)*
O40.6007 (3)0.33160 (9)0.81945 (12)0.0166 (3)
O50.6814 (2)0.04700 (10)0.40186 (12)0.0141 (3)
H510.627 (6)0.074 (2)0.341 (2)0.057 (12)*
H520.759 (5)0.0138 (18)0.380 (3)0.039 (10)*
O60.2333 (2)0.03327 (10)0.40967 (13)0.0157 (3)
H610.190 (5)0.0815 (12)0.378 (3)0.039 (10)*
H620.151 (5)0.0013 (15)0.381 (3)0.039 (10)*
O70.0014 (3)0.51872 (10)0.60055 (13)0.0168 (3)
H710.113 (5)0.554 (2)0.623 (3)0.056 (12)*
H720.006 (10)0.516 (4)0.541 (2)0.13 (3)*
O80.0938 (3)0.06685 (11)0.95512 (13)0.0195 (4)
H810.006 (5)0.086 (2)0.912 (3)0.049 (11)*
H820.200 (6)0.054 (4)0.917 (4)0.16 (3)*
N10.5124 (3)0.11063 (11)0.57398 (14)0.0107 (3)
N20.4839 (3)0.39703 (12)0.67598 (15)0.0144 (4)
H210.473 (5)0.441 (2)0.705 (2)0.023 (8)*
H220.440 (5)0.396 (2)0.613 (3)0.030 (9)*
C10.1091 (3)0.10798 (13)0.74547 (16)0.0112 (4)
C20.0580 (3)0.18067 (12)0.68279 (16)0.0106 (4)
C30.0646 (3)0.25369 (13)0.72979 (16)0.0118 (4)
H30.10190.25750.79910.014*
C40.0151 (3)0.32060 (13)0.67240 (17)0.0122 (4)
C50.0363 (3)0.31556 (13)0.56836 (17)0.0141 (4)
H50.06780.36070.53020.017*
C60.0403 (3)0.24293 (14)0.52186 (17)0.0141 (4)
H60.07350.23950.45230.017*
C70.0052 (3)0.17518 (13)0.57864 (17)0.0126 (4)
H70.00040.12650.54730.015*
C80.5612 (3)0.11620 (13)0.67453 (16)0.0117 (4)
H80.58800.07030.71170.014*
C90.5732 (3)0.18675 (13)0.72507 (17)0.0124 (4)
H90.60910.18810.79460.015*
C100.5308 (3)0.25590 (12)0.67073 (16)0.0108 (4)
C110.4790 (3)0.25056 (13)0.56688 (17)0.0122 (4)
H110.44910.29550.52810.015*
C120.4724 (3)0.17733 (13)0.52206 (16)0.0119 (4)
H120.43860.17440.45250.014*
C130.5415 (3)0.33216 (13)0.72758 (17)0.0118 (4)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Co10.01097 (19)0.0073 (2)0.00830 (19)0.00020 (14)0.00093 (14)0.00006 (14)
O10.0186 (8)0.0140 (8)0.0116 (7)0.0004 (6)0.0015 (6)0.0008 (6)
O20.0155 (7)0.0089 (7)0.0159 (8)0.0015 (6)0.0015 (6)0.0008 (6)
O30.0239 (8)0.0094 (7)0.0144 (8)0.0002 (6)0.0022 (6)0.0015 (6)
O40.0260 (9)0.0117 (8)0.0113 (8)0.0024 (6)0.0011 (6)0.0020 (6)
O50.0170 (8)0.0133 (8)0.0132 (7)0.0007 (6)0.0060 (6)0.0012 (6)
O60.0159 (8)0.0094 (7)0.0188 (8)0.0001 (6)0.0048 (6)0.0009 (6)
O70.0196 (8)0.0134 (8)0.0164 (8)0.0028 (6)0.0006 (7)0.0005 (6)
O80.0235 (9)0.0188 (9)0.0177 (8)0.0023 (7)0.0076 (7)0.0004 (7)
N10.0102 (8)0.0107 (8)0.0113 (8)0.0007 (6)0.0020 (6)0.0010 (7)
N20.0211 (9)0.0097 (9)0.0117 (9)0.0005 (7)0.0014 (8)0.0025 (7)
C10.0091 (9)0.0118 (10)0.0134 (10)0.0006 (7)0.0035 (7)0.0011 (8)
C20.0094 (9)0.0104 (10)0.0125 (10)0.0010 (7)0.0027 (7)0.0016 (7)
C30.0119 (9)0.0127 (10)0.0108 (9)0.0021 (7)0.0016 (8)0.0003 (8)
C40.0110 (9)0.0098 (10)0.0159 (10)0.0008 (7)0.0023 (8)0.0016 (8)
C50.0145 (10)0.0121 (10)0.0153 (10)0.0012 (8)0.0018 (8)0.0033 (8)
C60.0145 (10)0.0163 (11)0.0110 (10)0.0013 (8)0.0009 (8)0.0001 (8)
C70.0125 (9)0.0116 (10)0.0139 (10)0.0021 (7)0.0028 (8)0.0017 (8)
C80.0132 (9)0.0095 (9)0.0122 (10)0.0000 (7)0.0023 (8)0.0012 (8)
C90.0127 (9)0.0128 (10)0.0116 (10)0.0006 (8)0.0014 (8)0.0003 (8)
C100.0094 (9)0.0092 (9)0.0138 (10)0.0011 (7)0.0025 (7)0.0013 (8)
C110.0136 (9)0.0094 (10)0.0132 (10)0.0008 (7)0.0019 (8)0.0008 (8)
C120.0129 (9)0.0115 (10)0.0114 (10)0.0012 (7)0.0022 (8)0.0007 (8)
C130.0120 (9)0.0108 (10)0.0132 (10)0.0026 (7)0.0039 (8)0.0019 (8)
Geometric parameters (Å, º) top
Co1—O52.1118 (16)N2—H210.85 (3)
Co1—O5i2.1118 (16)N2—H220.85 (4)
Co1—O62.0593 (16)C2—C11.507 (3)
Co1—O6i2.0593 (16)C2—C31.396 (3)
Co1—N12.1306 (18)C2—C71.395 (3)
Co1—N1i2.1306 (18)C3—H30.9300
O1—C11.262 (3)C4—C31.387 (3)
O2—C11.264 (3)C5—C41.392 (3)
O3—C41.371 (3)C5—C61.388 (3)
O3—H310.91 (4)C5—H50.9300
O4—C131.237 (3)C6—H60.9300
O5—H510.963 (18)C7—C61.391 (3)
O5—H520.85 (2)C7—H70.9300
O6—H610.948 (17)C8—C91.379 (3)
O6—H620.82 (2)C8—H80.9300
O7—H710.978 (18)C9—C101.392 (3)
O7—H720.81 (2)C9—H90.9300
O8—H810.960 (18)C11—C101.390 (3)
O8—H820.83 (3)C11—C121.386 (3)
N1—C81.346 (3)C11—H110.9300
N1—C121.339 (3)C12—H120.9300
N2—C131.328 (3)C13—C101.506 (3)
O5i—Co1—O5180.0C7—C2—C3120.2 (2)
O5—Co1—N188.91 (7)C2—C3—H3120.2
O5—Co1—N1i91.09 (7)C4—C3—C2119.6 (2)
O5i—Co1—N191.09 (7)C4—C3—H3120.2
O5i—Co1—N1i88.91 (7)O3—C4—C3118.1 (2)
O6—Co1—O593.32 (7)O3—C4—C5121.4 (2)
O6—Co1—O5i86.68 (7)C3—C4—C5120.5 (2)
O6i—Co1—O5i93.32 (7)C4—C5—H5120.1
O6i—Co1—O586.68 (7)C6—C5—C4119.7 (2)
O6—Co1—O6i180.0C6—C5—H5120.1
O6—Co1—N189.59 (7)C5—C6—C7120.4 (2)
O6i—Co1—N190.41 (7)C5—C6—H6119.8
O6—Co1—N1i90.41 (7)C7—C6—H6119.8
O6i—Co1—N1i89.59 (7)C2—C7—H7120.2
N1i—Co1—N1180.0C6—C7—C2119.6 (2)
C4—O3—H31108 (2)C6—C7—H7120.2
Co1—O5—H51123 (2)N1—C8—C9123.1 (2)
Co1—O5—H52115 (2)N1—C8—H8118.5
H52—O5—H51101 (3)C9—C8—H8118.5
Co1—O6—H61132 (2)C8—C9—C10119.2 (2)
Co1—O6—H62123 (2)C8—C9—H9120.4
H62—O6—H61104 (2)C10—C9—H9120.4
H71—O7—H72104 (3)C9—C10—C13118.31 (19)
H81—O8—H82105 (3)C11—C10—C9118.0 (2)
C8—N1—Co1121.36 (14)C11—C10—C13123.65 (19)
C12—N1—Co1121.18 (14)C10—C11—H11120.5
C12—N1—C8117.46 (19)C12—C11—C10119.0 (2)
C13—N2—H21122 (2)C12—C11—H11120.5
C13—N2—H22121 (2)N1—C12—C11123.2 (2)
H21—N2—H22116 (3)N1—C12—H12118.4
O1—C1—O2123.5 (2)C11—C12—H12118.4
O1—C1—C2118.07 (19)O4—C13—N2123.2 (2)
O2—C1—C2118.38 (19)O4—C13—C10119.00 (19)
C3—C2—C1119.43 (19)N2—C13—C10117.83 (19)
C7—C2—C1120.39 (19)
O5—Co1—N1—C8130.62 (16)C1—C2—C7—C6179.56 (19)
O5i—Co1—N1—C849.38 (16)C3—C2—C7—C60.2 (3)
O5—Co1—N1—C1249.21 (16)O3—C4—C3—C2177.66 (19)
O5i—Co1—N1—C12130.79 (16)C5—C4—C3—C21.5 (3)
O6—Co1—N1—C8136.06 (16)C6—C5—C4—O3178.4 (2)
O6i—Co1—N1—C843.94 (16)C6—C5—C4—C30.7 (3)
O6—Co1—N1—C1244.12 (16)C4—C5—C6—C70.5 (3)
O6i—Co1—N1—C12135.88 (16)C2—C7—C6—C51.0 (3)
Co1—N1—C8—C9179.20 (16)N1—C8—C9—C100.8 (3)
C12—N1—C8—C90.6 (3)C8—C9—C10—C110.4 (3)
Co1—N1—C12—C11179.88 (16)C8—C9—C10—C13178.98 (19)
C8—N1—C12—C110.0 (3)C12—C11—C10—C90.3 (3)
C3—C2—C1—O18.0 (3)C12—C11—C10—C13179.57 (19)
C3—C2—C1—O2171.26 (19)C10—C11—C12—N10.5 (3)
C7—C2—C1—O1171.73 (19)O4—C13—C10—C95.0 (3)
C7—C2—C1—O29.0 (3)O4—C13—C10—C11175.7 (2)
C1—C2—C3—C4179.20 (19)N2—C13—C10—C9174.3 (2)
C7—C2—C3—C41.1 (3)N2—C13—C10—C115.0 (3)
Symmetry code: (i) x+1, y, z+1.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N2—H21···O2ii0.86 (3)2.18 (3)3.031 (3)170 (3)
N2—H22···O8iii0.85 (4)2.20 (4)3.007 (3)158 (3)
O3—H31···O70.91 (4)1.81 (4)2.711 (2)170 (4)
O5—H51···O3iii0.96 (3)1.76 (3)2.715 (2)171 (3)
O5—H52···O2i0.86 (3)1.95 (4)2.782 (2)163 (4)
O6—H61···O4iv0.95 (3)1.73 (3)2.685 (2)178 (4)
O6—H62···O2v0.82 (3)1.89 (4)2.683 (2)161 (3)
O7—H71···O1ii0.98 (3)1.76 (4)2.740 (3)179 (3)
O8—H81···O10.96 (4)1.81 (4)2.760 (3)174 (3)
O8—H82···O7vi0.83 (5)2.06 (4)2.807 (3)149 (5)
Symmetry codes: (i) x+1, y, z+1; (ii) x+1/2, y+1/2, z+3/2; (iii) x+1/2, y+1/2, z1/2; (iv) x1/2, y+1/2, z1/2; (v) x, y, z+1; (vi) x1/2, y1/2, z+3/2.

Experimental details

Crystal data
Chemical formula[Co(C6H6N2O)2(H2O)4](C7H5O3)2·4H2O
Mr721.53
Crystal system, space groupMonoclinic, P21/n
Temperature (K)100
a, b, c (Å)6.7032 (2), 17.0523 (4), 13.5406 (3)
β (°) 100.194 (3)
V3)1523.32 (7)
Z2
Radiation typeMo Kα
µ (mm1)0.65
Crystal size (mm)0.29 × 0.28 × 0.14
Data collection
DiffractometerBruker Kappa APEXII CCD area-detector
diffractometer
Absorption correctionMulti-scan
(SADABS; Bruker, 2005)
Tmin, Tmax0.840, 0.916
No. of measured, independent and
observed [I > 2σ(I)] reflections
14243, 3779, 3590
Rint0.019
(sin θ/λ)max1)0.670
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.034, 0.086, 1.23
No. of reflections3779
No. of parameters258
No. of restraints16
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å3)0.47, 0.42

Computer programs: APEX2 (Bruker, 2007), SAINT (Bruker, 2007), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), Mercury (Macrae et al., 2006), WinGX (Farrugia, 1999) and PLATON (Spek, 2009).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N2—H21···O2i0.86 (3)2.18 (3)3.031 (3)170 (3)
N2—H22···O8ii0.85 (4)2.20 (4)3.007 (3)158 (3)
O3—H31···O70.91 (4)1.81 (4)2.711 (2)170 (4)
O5—H51···O3ii0.96 (3)1.76 (3)2.715 (2)171 (3)
O5—H52···O2iii0.86 (3)1.95 (4)2.782 (2)163 (4)
O6—H61···O4iv0.95 (3)1.73 (3)2.685 (2)178 (4)
O6—H62···O2v0.82 (3)1.89 (4)2.683 (2)161 (3)
O7—H71···O1i0.98 (3)1.76 (4)2.740 (3)179 (3)
O8—H81···O10.96 (4)1.81 (4)2.760 (3)174 (3)
O8—H82···O7vi0.83 (5)2.06 (4)2.807 (3)149 (5)
Symmetry codes: (i) x+1/2, y+1/2, z+3/2; (ii) x+1/2, y+1/2, z1/2; (iii) x+1, y, z+1; (iv) x1/2, y+1/2, z1/2; (v) x, y, z+1; (vi) x1/2, y1/2, z+3/2.
 

Acknowledgements

The authors are indebted to Anadolu University and to the Medicinal Plants and Medicine Research Centre of Anadolu University, Eskişehir, Turkey, for the use of the X-ray diffractometer.

References

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Volume 68| Part 3| March 2012| Pages m249-m250
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