Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807047770/cv2309sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807047770/cv2309Isup2.hkl |
CCDC reference: 658541
Key indicators
- Single-crystal X-ray study
- T = 293 K
- Mean (C-C) = 0.007 Å
- R factor = 0.047
- wR factor = 0.148
- Data-to-parameter ratio = 12.8
checkCIF/PLATON results
No syntax errors found
Alert level C PLAT063_ALERT_3_C Crystal Probably too Large for Beam Size ....... 0.69 mm PLAT125_ALERT_4_C No _symmetry_space_group_name_Hall Given ....... ? PLAT153_ALERT_1_C The su's on the Cell Axes are Equal (x 100000) 300 Ang. PLAT341_ALERT_3_C Low Bond Precision on C-C Bonds (x 1000) Ang ... 7 PLAT710_ALERT_4_C Delete 1-2-3 or 2-3-4 Linear Torsion Angle ... # 3 N5 -NI1 -N2 -C12 142.00 2.00 1.555 1.555 1.555 1.555 PLAT710_ALERT_4_C Delete 1-2-3 or 2-3-4 Linear Torsion Angle ... # 8 N5 -NI1 -N2 -N1 -35.00 2.00 1.555 1.555 1.555 1.555 PLAT710_ALERT_4_C Delete 1-2-3 or 2-3-4 Linear Torsion Angle ... # 25 N2 -NI1 -N5 -C29 139.00 2.00 1.555 1.555 1.555 1.555 PLAT710_ALERT_4_C Delete 1-2-3 or 2-3-4 Linear Torsion Angle ... # 30 N2 -NI1 -N5 -N4 -40.00 2.00 1.555 1.555 1.555 1.555
Alert level G PLAT199_ALERT_1_G Check the Reported _cell_measurement_temperature 293 K PLAT200_ALERT_1_G Check the Reported _diffrn_ambient_temperature . 293 K PLAT794_ALERT_5_G Check Predicted Bond Valency for Ni1 (2) 2.23
0 ALERT level A = In general: serious problem 0 ALERT level B = Potentially serious problem 8 ALERT level C = Check and explain 3 ALERT level G = General alerts; check 3 ALERT type 1 CIF construction/syntax error, inconsistent or missing data 0 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 5 ALERT type 4 Improvement, methodology, query or suggestion 1 ALERT type 5 Informative message, check
A dimethylformamide solution (10 ml) of H2L (0.073 g, 0.25 mmol) and KOH (0.014 g, 0.25 mmol) was mixed with a pyridine solution (10 ml) of Ni(OAC)24H2O (0.062 g, 0.25 mmol). The mixture was stirred for 4 h, filtered, and was left to stand. Two weeks later, red crystals were isolated from the solution (m.p. >573 K). Analysis, calculated for C34H24N6NiO4: C 63.88, H 3.78, N 13.15%; found: C 63.76, H 3.80, N 13.01%.
All H atoms were placed in geometrically idealized positions (O—H 0.82 and C—H 0.93 Å) and treated as riding on their parent atoms, with Uiso(H) = 1.2Ueq(C) and Uiso(H) = 1.5Ueq(O).
The chemistry of aroylhydrazones is widely studied due to their coordination abilities to metal ions (Beghidja et al., 2006) and their biological activities (Mostafa & Haifaa, 2007). Our group have reported the crystal structures of two aroylhydrazone complexes - [Cu(C12H12N2O3)(C5H5N)] (Liu et al., 2005a) and [Ni(C18H12N2O3)(C5H5N)] (Liu et al., 2005b). As an extension of our work on the structural characterization of aroylhydrazone derivatives, the title complex, (I), was synthesized and characterized.
In (I) (Fig. 1), the Ni ion is six-coordinated by four N atoms and two O atoms in a distorted octahedron geometry. Each ligand coordinate the Ni ion in a tridentate mode via N atom of the azomethine group, O atom of the the hydroxyl group and N atom of the pyridine ring. Each ligand forms two five-membered chelate rings Ni—N—N—C—O and Ni—N—C—C—N with the nickel atom. The atoms N3, N6, O3 and O1 constitute the equatorial plane, with the mean deviation from plane of 0.43 (6) Å. The angles O1—Ni1—N3 and O3—Ni1—N6 are 155.95 (12) and 155.93 (13)°, respectively. The axial positions are occupied by the atoms N5 and N2. The angle of N5—Ni1—N2 is 176.33 (14)°. There are two intramolecular O2—H2···N1 and O4—H4···N4 hydrogen bonds (Table 1 and Fig. 1).
In the crystal, the weak intermolecular C—H···O hydrogen bonds (Table 1) contribute to the crystal packing stabilization.
For related crystal structures of Cu and Ni complexes with aroylhydrazone derivatives, see Liu et al. (2005a,b). For general background, see Beghidja et al. (2006), and for the specific biological activities of aroylhydrazones, see Mostafa & Haifaa (2007).
Data collection: SMART (Siemens, 1996); cell refinement: SAINT (Siemens, 1996); data reduction: SAINT (Siemens, 1996); program(s) used to solve structure: SHELXS97 (Sheldrick, 1997a); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997a); molecular graphics: SHELXTL (Sheldrick, 1997b); software used to prepare material for publication: SHELXTL (Sheldrick, 1997b).
[Ni(C17H12N3O2)2] | F(000) = 1320 |
Mr = 639.30 | Dx = 1.437 Mg m−3 |
Monoclinic, P21/c | Mo Kα radiation, λ = 0.71073 Å |
a = 21.257 (3) Å | Cell parameters from 3186 reflections |
b = 11.653 (3) Å | θ = 2.4–22.9° |
c = 11.938 (3) Å | µ = 0.71 mm−1 |
β = 91.686 (3)° | T = 293 K |
V = 2955.6 (10) Å3 | Plate, red |
Z = 4 | 0.69 × 0.66 × 0.13 mm |
Siemens SMART CCD area-detector diffractometer | 5202 independent reflections |
Radiation source: fine-focus sealed tube | 3068 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.089 |
φ and ω scans | θmax = 25.0°, θmin = 1.9° |
Absorption correction: multi-scan (SADABS; Sheldrick, 1996) | h = −25→23 |
Tmin = 0.641, Tmax = 0.914 | k = −13→9 |
14859 measured reflections | l = −14→13 |
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)] = 0.047 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.149 | H-atom parameters constrained |
S = 1.01 | w = 1/[σ2(Fo2) + (0.0602P)2 + 0.6517P] where P = (Fo2 + 2Fc2)/3 |
5202 reflections | (Δ/σ)max = 0.001 |
408 parameters | Δρmax = 0.34 e Å−3 |
0 restraints | Δρmin = −0.45 e Å−3 |
[Ni(C17H12N3O2)2] | V = 2955.6 (10) Å3 |
Mr = 639.30 | Z = 4 |
Monoclinic, P21/c | Mo Kα radiation |
a = 21.257 (3) Å | µ = 0.71 mm−1 |
b = 11.653 (3) Å | T = 293 K |
c = 11.938 (3) Å | 0.69 × 0.66 × 0.13 mm |
β = 91.686 (3)° |
Siemens SMART CCD area-detector diffractometer | 5202 independent reflections |
Absorption correction: multi-scan (SADABS; Sheldrick, 1996) | 3068 reflections with I > 2σ(I) |
Tmin = 0.641, Tmax = 0.914 | Rint = 0.089 |
14859 measured reflections |
R[F2 > 2σ(F2)] = 0.047 | 0 restraints |
wR(F2) = 0.149 | H-atom parameters constrained |
S = 1.01 | Δρmax = 0.34 e Å−3 |
5202 reflections | Δρmin = −0.45 e Å−3 |
408 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 | ||
Ni1 | 0.24926 (2) | 0.45673 (5) | 1.00715 (4) | 0.03962 (19) | |
N1 | 0.31082 (16) | 0.5566 (3) | 0.8193 (3) | 0.0468 (9) | |
N2 | 0.26876 (15) | 0.5813 (3) | 0.9004 (3) | 0.0433 (8) | |
N3 | 0.18729 (15) | 0.5883 (3) | 1.0576 (3) | 0.0405 (8) | |
N4 | 0.19264 (15) | 0.2411 (3) | 1.0620 (3) | 0.0444 (9) | |
N5 | 0.23030 (15) | 0.3252 (3) | 1.1058 (3) | 0.0428 (8) | |
N6 | 0.30319 (16) | 0.4982 (3) | 1.1532 (3) | 0.0480 (9) | |
O1 | 0.31986 (13) | 0.3844 (3) | 0.9151 (2) | 0.0511 (8) | |
O2 | 0.37269 (18) | 0.5822 (3) | 0.6396 (3) | 0.0745 (10) | |
H2 | 0.3465 | 0.5973 | 0.6865 | 0.112* | |
O3 | 0.18427 (12) | 0.3650 (2) | 0.9110 (2) | 0.0435 (7) | |
O4 | 0.12798 (17) | 0.0556 (2) | 1.0564 (3) | 0.0663 (9) | |
H4 | 0.1537 | 0.1029 | 1.0800 | 0.099* | |
C1 | 0.33299 (18) | 0.4505 (4) | 0.8363 (3) | 0.0413 (10) | |
C2 | 0.4035 (2) | 0.3014 (4) | 0.7651 (3) | 0.0512 (12) | |
H2A | 0.3924 | 0.2582 | 0.8271 | 0.061* | |
C3 | 0.37842 (18) | 0.4088 (4) | 0.7523 (3) | 0.0436 (10) | |
C4 | 0.3953 (2) | 0.4740 (4) | 0.6578 (3) | 0.0541 (12) | |
C5 | 0.4366 (2) | 0.4292 (5) | 0.5824 (4) | 0.0639 (14) | |
H5 | 0.4480 | 0.4735 | 0.5215 | 0.077* | |
C6 | 0.4619 (2) | 0.3181 (5) | 0.5953 (4) | 0.0575 (13) | |
C7 | 0.44529 (19) | 0.2531 (4) | 0.6885 (4) | 0.0533 (12) | |
C8 | 0.4700 (2) | 0.1419 (5) | 0.7015 (4) | 0.0710 (15) | |
H8 | 0.4593 | 0.0984 | 0.7634 | 0.085* | |
C9 | 0.5087 (3) | 0.0976 (6) | 0.6261 (5) | 0.0848 (18) | |
H9 | 0.5241 | 0.0235 | 0.6353 | 0.102* | |
C10 | 0.5258 (2) | 0.1631 (6) | 0.5335 (5) | 0.0867 (19) | |
H10 | 0.5533 | 0.1324 | 0.4821 | 0.104* | |
C11 | 0.5032 (2) | 0.2693 (6) | 0.5180 (4) | 0.0785 (17) | |
H11 | 0.5148 | 0.3114 | 0.4557 | 0.094* | |
C12 | 0.2399 (2) | 0.6765 (4) | 0.9079 (4) | 0.0521 (12) | |
H12 | 0.2462 | 0.7362 | 0.8577 | 0.063* | |
C13 | 0.19617 (19) | 0.6866 (4) | 1.0007 (3) | 0.0469 (11) | |
C14 | 0.1689 (2) | 0.7886 (4) | 1.0314 (4) | 0.0656 (14) | |
H14 | 0.1760 | 0.8553 | 0.9909 | 0.079* | |
C15 | 0.1311 (2) | 0.7901 (4) | 1.1229 (4) | 0.0689 (14) | |
H15 | 0.1126 | 0.8581 | 1.1457 | 0.083* | |
C16 | 0.1211 (2) | 0.6909 (4) | 1.1798 (4) | 0.0604 (13) | |
H16 | 0.0954 | 0.6903 | 1.2416 | 0.072* | |
C17 | 0.14953 (19) | 0.5914 (4) | 1.1450 (3) | 0.0508 (11) | |
H17 | 0.1421 | 0.5238 | 1.1839 | 0.061* | |
C18 | 0.17036 (18) | 0.2725 (4) | 0.9597 (3) | 0.0388 (10) | |
C19 | 0.10074 (18) | 0.2221 (3) | 0.8001 (3) | 0.0417 (10) | |
H19 | 0.1155 | 0.2878 | 0.7654 | 0.050* | |
C20 | 0.12551 (18) | 0.1931 (3) | 0.9040 (3) | 0.0381 (10) | |
C21 | 0.1047 (2) | 0.0897 (4) | 0.9549 (4) | 0.0485 (11) | |
C22 | 0.0590 (2) | 0.0251 (4) | 0.9018 (4) | 0.0555 (12) | |
H22 | 0.0456 | −0.0422 | 0.9354 | 0.067* | |
C23 | 0.0318 (2) | 0.0575 (4) | 0.7981 (4) | 0.0479 (11) | |
C24 | 0.05415 (19) | 0.1566 (3) | 0.7443 (3) | 0.0434 (10) | |
C25 | 0.0279 (2) | 0.1874 (4) | 0.6383 (4) | 0.0554 (12) | |
H25 | 0.0428 | 0.2519 | 0.6017 | 0.066* | |
C26 | −0.0189 (2) | 0.1237 (5) | 0.5895 (4) | 0.0650 (14) | |
H26 | −0.0357 | 0.1442 | 0.5195 | 0.078* | |
C27 | −0.0418 (2) | 0.0276 (5) | 0.6446 (5) | 0.0732 (15) | |
H27 | −0.0746 | −0.0142 | 0.6116 | 0.088* | |
C28 | −0.0173 (2) | −0.0059 (4) | 0.7443 (5) | 0.0649 (14) | |
H28 | −0.0327 | −0.0715 | 0.7784 | 0.078* | |
C29 | 0.25446 (19) | 0.3233 (4) | 1.2053 (3) | 0.0503 (12) | |
H29 | 0.2491 | 0.2617 | 1.2536 | 0.060* | |
C30 | 0.2909 (2) | 0.4242 (4) | 1.2374 (3) | 0.0514 (12) | |
C31 | 0.3103 (2) | 0.4486 (5) | 1.3469 (4) | 0.0744 (16) | |
H31 | 0.3017 | 0.3979 | 1.4046 | 0.089* | |
C32 | 0.3428 (3) | 0.5496 (6) | 1.3691 (5) | 0.090 (2) | |
H32 | 0.3554 | 0.5680 | 1.4422 | 0.108* | |
C33 | 0.3562 (3) | 0.6220 (5) | 1.2828 (5) | 0.0805 (17) | |
H33 | 0.3788 | 0.6893 | 1.2959 | 0.097* | |
C34 | 0.3356 (2) | 0.5933 (5) | 1.1769 (4) | 0.0618 (13) | |
H34 | 0.3448 | 0.6427 | 1.1184 | 0.074* |
U11 | U22 | U33 | U12 | U13 | U23 | |
Ni1 | 0.0449 (3) | 0.0372 (3) | 0.0370 (3) | 0.0009 (3) | 0.0062 (2) | 0.0018 (2) |
N1 | 0.052 (2) | 0.046 (2) | 0.043 (2) | −0.0032 (19) | 0.0177 (17) | 0.0012 (17) |
N2 | 0.047 (2) | 0.042 (2) | 0.0417 (19) | −0.0034 (19) | 0.0059 (16) | −0.0001 (17) |
N3 | 0.0388 (18) | 0.039 (2) | 0.0438 (19) | 0.0003 (18) | 0.0075 (15) | 0.0060 (17) |
N4 | 0.049 (2) | 0.038 (2) | 0.047 (2) | 0.0005 (19) | 0.0070 (16) | 0.0088 (17) |
N5 | 0.045 (2) | 0.045 (2) | 0.039 (2) | 0.0068 (19) | 0.0072 (16) | 0.0055 (17) |
N6 | 0.046 (2) | 0.056 (2) | 0.042 (2) | 0.004 (2) | 0.0039 (16) | −0.0093 (19) |
O1 | 0.0570 (18) | 0.0515 (19) | 0.0453 (16) | 0.0092 (16) | 0.0111 (14) | 0.0083 (15) |
O2 | 0.101 (3) | 0.071 (2) | 0.054 (2) | 0.018 (2) | 0.0344 (18) | 0.0169 (18) |
O3 | 0.0544 (17) | 0.0339 (16) | 0.0422 (16) | −0.0044 (15) | 0.0016 (13) | 0.0072 (13) |
O4 | 0.102 (3) | 0.0379 (19) | 0.059 (2) | −0.0121 (19) | 0.0050 (18) | 0.0136 (16) |
C1 | 0.041 (2) | 0.045 (3) | 0.039 (2) | −0.001 (2) | 0.0021 (18) | −0.002 (2) |
C2 | 0.051 (3) | 0.055 (3) | 0.047 (3) | −0.001 (3) | 0.005 (2) | −0.003 (2) |
C3 | 0.041 (2) | 0.054 (3) | 0.036 (2) | −0.002 (2) | 0.0038 (18) | −0.004 (2) |
C4 | 0.061 (3) | 0.061 (3) | 0.041 (2) | 0.007 (3) | 0.011 (2) | 0.003 (2) |
C5 | 0.071 (3) | 0.081 (4) | 0.041 (3) | 0.002 (3) | 0.018 (2) | 0.002 (3) |
C6 | 0.046 (3) | 0.081 (4) | 0.046 (3) | 0.006 (3) | 0.006 (2) | −0.011 (3) |
C7 | 0.041 (3) | 0.068 (3) | 0.051 (3) | 0.007 (3) | 0.002 (2) | −0.010 (3) |
C8 | 0.072 (3) | 0.074 (4) | 0.068 (3) | 0.023 (3) | 0.003 (3) | −0.009 (3) |
C9 | 0.074 (4) | 0.090 (5) | 0.090 (4) | 0.031 (4) | −0.001 (3) | −0.022 (4) |
C10 | 0.063 (3) | 0.119 (6) | 0.079 (4) | 0.028 (4) | 0.010 (3) | −0.035 (4) |
C11 | 0.066 (3) | 0.111 (5) | 0.060 (3) | 0.015 (4) | 0.019 (3) | −0.014 (3) |
C12 | 0.061 (3) | 0.039 (3) | 0.058 (3) | 0.002 (3) | 0.019 (2) | 0.011 (2) |
C13 | 0.047 (3) | 0.042 (3) | 0.052 (3) | 0.006 (2) | 0.009 (2) | 0.002 (2) |
C14 | 0.082 (4) | 0.037 (3) | 0.079 (3) | 0.008 (3) | 0.028 (3) | 0.008 (3) |
C15 | 0.079 (3) | 0.048 (3) | 0.081 (4) | 0.018 (3) | 0.028 (3) | −0.005 (3) |
C16 | 0.063 (3) | 0.060 (3) | 0.060 (3) | 0.009 (3) | 0.022 (2) | −0.002 (3) |
C17 | 0.054 (3) | 0.044 (3) | 0.055 (3) | −0.004 (2) | 0.015 (2) | 0.002 (2) |
C18 | 0.044 (2) | 0.033 (2) | 0.040 (2) | 0.009 (2) | 0.0140 (19) | 0.004 (2) |
C19 | 0.044 (2) | 0.030 (2) | 0.052 (3) | −0.002 (2) | 0.015 (2) | 0.002 (2) |
C20 | 0.043 (2) | 0.026 (2) | 0.046 (2) | 0.000 (2) | 0.0141 (19) | −0.0025 (19) |
C21 | 0.065 (3) | 0.028 (2) | 0.052 (3) | 0.000 (2) | 0.019 (2) | 0.004 (2) |
C22 | 0.067 (3) | 0.029 (3) | 0.072 (3) | −0.015 (2) | 0.025 (3) | −0.001 (2) |
C23 | 0.049 (3) | 0.034 (3) | 0.061 (3) | −0.003 (2) | 0.020 (2) | −0.012 (2) |
C24 | 0.043 (2) | 0.033 (2) | 0.055 (3) | 0.000 (2) | 0.012 (2) | −0.010 (2) |
C25 | 0.054 (3) | 0.048 (3) | 0.065 (3) | −0.006 (3) | 0.004 (2) | −0.005 (2) |
C26 | 0.063 (3) | 0.064 (4) | 0.067 (3) | 0.002 (3) | −0.007 (3) | −0.012 (3) |
C27 | 0.060 (3) | 0.068 (4) | 0.092 (4) | −0.015 (3) | 0.007 (3) | −0.026 (3) |
C28 | 0.065 (3) | 0.046 (3) | 0.085 (4) | −0.016 (3) | 0.020 (3) | −0.012 (3) |
C29 | 0.054 (3) | 0.054 (3) | 0.043 (3) | 0.010 (3) | 0.008 (2) | 0.012 (2) |
C30 | 0.050 (3) | 0.065 (3) | 0.039 (2) | 0.014 (3) | 0.003 (2) | 0.003 (2) |
C31 | 0.085 (4) | 0.095 (5) | 0.042 (3) | 0.018 (4) | −0.010 (2) | 0.000 (3) |
C32 | 0.096 (4) | 0.108 (5) | 0.064 (4) | 0.028 (4) | −0.033 (3) | −0.029 (4) |
C33 | 0.085 (4) | 0.077 (4) | 0.078 (4) | 0.009 (3) | −0.022 (3) | −0.026 (3) |
C34 | 0.058 (3) | 0.063 (3) | 0.064 (3) | −0.001 (3) | −0.003 (2) | −0.012 (3) |
Ni1—N5 | 1.982 (3) | C11—H11 | 0.9300 |
Ni1—N2 | 1.983 (3) | C12—C13 | 1.472 (5) |
Ni1—O1 | 2.066 (3) | C12—H12 | 0.9300 |
Ni1—O3 | 2.068 (3) | C13—C14 | 1.376 (6) |
Ni1—N6 | 2.114 (3) | C14—C15 | 1.376 (6) |
Ni1—N3 | 2.120 (3) | C14—H14 | 0.9300 |
N1—C1 | 1.336 (5) | C15—C16 | 1.360 (6) |
N1—N2 | 1.368 (4) | C15—H15 | 0.9300 |
N2—C12 | 1.272 (5) | C16—C17 | 1.377 (6) |
N3—C17 | 1.336 (5) | C16—H16 | 0.9300 |
N3—C13 | 1.347 (5) | C17—H17 | 0.9300 |
N4—C18 | 1.349 (5) | C18—C20 | 1.473 (5) |
N4—N5 | 1.360 (4) | C19—C20 | 1.375 (5) |
N5—C29 | 1.280 (5) | C19—C24 | 1.403 (5) |
N6—C34 | 1.331 (6) | C19—H19 | 0.9300 |
N6—C30 | 1.355 (5) | C20—C21 | 1.426 (5) |
O1—C1 | 1.254 (5) | C21—C22 | 1.370 (6) |
O2—C4 | 1.364 (5) | C22—C23 | 1.401 (6) |
O2—H2 | 0.8200 | C22—H22 | 0.9300 |
O3—C18 | 1.263 (4) | C23—C24 | 1.410 (6) |
O4—C21 | 1.354 (5) | C23—C28 | 1.417 (6) |
O4—H4 | 0.8200 | C24—C25 | 1.413 (6) |
C1—C3 | 1.494 (5) | C25—C26 | 1.360 (6) |
C2—C3 | 1.367 (6) | C25—H25 | 0.9300 |
C2—C7 | 1.411 (6) | C26—C27 | 1.392 (7) |
C2—H2A | 0.9300 | C26—H26 | 0.9300 |
C3—C4 | 1.415 (6) | C27—C28 | 1.343 (7) |
C4—C5 | 1.378 (6) | C27—H27 | 0.9300 |
C5—C6 | 1.409 (6) | C28—H28 | 0.9300 |
C5—H5 | 0.9300 | C29—C30 | 1.454 (6) |
C6—C7 | 1.399 (6) | C29—H29 | 0.9300 |
C6—C11 | 1.412 (6) | C30—C31 | 1.389 (6) |
C7—C8 | 1.405 (6) | C31—C32 | 1.385 (7) |
C8—C9 | 1.340 (7) | C31—H31 | 0.9300 |
C8—H8 | 0.9300 | C32—C33 | 1.368 (8) |
C9—C10 | 1.401 (8) | C32—H32 | 0.9300 |
C9—H9 | 0.9300 | C33—C34 | 1.367 (6) |
C10—C11 | 1.339 (7) | C33—H33 | 0.9300 |
C10—H10 | 0.9300 | C34—H34 | 0.9300 |
N5—Ni1—N2 | 176.33 (14) | C13—C12—H12 | 122.0 |
N5—Ni1—O1 | 99.45 (12) | N3—C13—C14 | 122.3 (4) |
N2—Ni1—O1 | 77.76 (13) | N3—C13—C12 | 114.3 (4) |
N5—Ni1—O3 | 77.62 (13) | C14—C13—C12 | 123.3 (4) |
N2—Ni1—O3 | 99.83 (12) | C13—C14—C15 | 118.8 (4) |
O1—Ni1—O3 | 88.73 (11) | C13—C14—H14 | 120.6 |
N5—Ni1—N6 | 78.55 (15) | C15—C14—H14 | 120.6 |
N2—Ni1—N6 | 104.12 (14) | C16—C15—C14 | 119.3 (5) |
O1—Ni1—N6 | 98.46 (12) | C16—C15—H15 | 120.4 |
O3—Ni1—N6 | 155.94 (13) | C14—C15—H15 | 120.4 |
N5—Ni1—N3 | 104.59 (13) | C15—C16—C17 | 119.2 (4) |
N2—Ni1—N3 | 78.25 (13) | C15—C16—H16 | 120.4 |
O1—Ni1—N3 | 155.95 (12) | C17—C16—H16 | 120.4 |
O3—Ni1—N3 | 96.94 (12) | N3—C17—C16 | 122.5 (4) |
N6—Ni1—N3 | 85.81 (13) | N3—C17—H17 | 118.7 |
C1—N1—N2 | 108.8 (3) | C16—C17—H17 | 118.7 |
C12—N2—N1 | 124.0 (4) | O3—C18—N4 | 124.6 (4) |
C12—N2—Ni1 | 118.9 (3) | O3—C18—C20 | 119.1 (4) |
N1—N2—Ni1 | 117.0 (3) | N4—C18—C20 | 116.3 (4) |
C17—N3—C13 | 117.8 (4) | C20—C19—C24 | 122.8 (4) |
C17—N3—Ni1 | 129.3 (3) | C20—C19—H19 | 118.6 |
C13—N3—Ni1 | 112.0 (2) | C24—C19—H19 | 118.6 |
C18—N4—N5 | 109.8 (3) | C19—C20—C21 | 118.4 (4) |
C29—N5—N4 | 124.0 (4) | C19—C20—C18 | 118.6 (4) |
C29—N5—Ni1 | 118.8 (3) | C21—C20—C18 | 122.9 (4) |
N4—N5—Ni1 | 117.2 (2) | O4—C21—C22 | 119.3 (4) |
C34—N6—C30 | 118.8 (4) | O4—C21—C20 | 121.3 (4) |
C34—N6—Ni1 | 129.1 (3) | C22—C21—C20 | 119.4 (4) |
C30—N6—Ni1 | 110.8 (3) | C21—C22—C23 | 121.9 (4) |
C1—O1—Ni1 | 109.2 (3) | C21—C22—H22 | 119.0 |
C4—O2—H2 | 109.5 | C23—C22—H22 | 119.0 |
C18—O3—Ni1 | 110.3 (2) | C22—C23—C24 | 119.2 (4) |
C21—O4—H4 | 109.5 | C22—C23—C28 | 122.6 (4) |
O1—C1—N1 | 126.7 (4) | C24—C23—C28 | 118.2 (4) |
O1—C1—C3 | 117.8 (4) | C19—C24—C23 | 118.1 (4) |
N1—C1—C3 | 115.6 (4) | C19—C24—C25 | 122.8 (4) |
C3—C2—C7 | 122.8 (4) | C23—C24—C25 | 119.1 (4) |
C3—C2—H2A | 118.6 | C26—C25—C24 | 120.6 (5) |
C7—C2—H2A | 118.6 | C26—C25—H25 | 119.7 |
C2—C3—C4 | 118.3 (4) | C24—C25—H25 | 119.7 |
C2—C3—C1 | 118.7 (4) | C25—C26—C27 | 119.9 (5) |
C4—C3—C1 | 123.0 (4) | C25—C26—H26 | 120.1 |
O2—C4—C5 | 118.3 (4) | C27—C26—H26 | 120.1 |
O2—C4—C3 | 121.8 (4) | C28—C27—C26 | 121.4 (5) |
C5—C4—C3 | 120.0 (5) | C28—C27—H27 | 119.3 |
C4—C5—C6 | 121.7 (4) | C26—C27—H27 | 119.3 |
C4—C5—H5 | 119.2 | C27—C28—C23 | 120.8 (5) |
C6—C5—H5 | 119.2 | C27—C28—H28 | 119.6 |
C7—C6—C5 | 118.7 (4) | C23—C28—H28 | 119.6 |
C7—C6—C11 | 118.6 (5) | N5—C29—C30 | 115.3 (4) |
C5—C6—C11 | 122.8 (5) | N5—C29—H29 | 122.3 |
C6—C7—C8 | 119.0 (4) | C30—C29—H29 | 122.3 |
C6—C7—C2 | 118.6 (4) | N6—C30—C31 | 120.7 (5) |
C8—C7—C2 | 122.4 (5) | N6—C30—C29 | 115.6 (4) |
C9—C8—C7 | 121.0 (5) | C31—C30—C29 | 123.7 (5) |
C9—C8—H8 | 119.5 | C32—C31—C30 | 119.1 (5) |
C7—C8—H8 | 119.5 | C32—C31—H31 | 120.5 |
C8—C9—C10 | 120.0 (6) | C30—C31—H31 | 120.5 |
C8—C9—H9 | 120.0 | C33—C32—C31 | 119.6 (5) |
C10—C9—H9 | 120.0 | C33—C32—H32 | 120.2 |
C11—C10—C9 | 120.7 (5) | C31—C32—H32 | 120.2 |
C11—C10—H10 | 119.6 | C34—C33—C32 | 118.5 (6) |
C9—C10—H10 | 119.6 | C34—C33—H33 | 120.8 |
C10—C11—C6 | 120.7 (5) | C32—C33—H33 | 120.8 |
C10—C11—H11 | 119.7 | N6—C34—C33 | 123.4 (5) |
C6—C11—H11 | 119.7 | N6—C34—H34 | 118.3 |
N2—C12—C13 | 116.1 (4) | C33—C34—H34 | 118.3 |
N2—C12—H12 | 122.0 | ||
C1—N1—N2—C12 | 179.2 (4) | C11—C6—C7—C8 | −0.3 (7) |
C1—N1—N2—Ni1 | −4.0 (4) | C5—C6—C7—C2 | 0.6 (6) |
N5—Ni1—N2—C12 | 142 (2) | C11—C6—C7—C2 | −179.3 (4) |
O1—Ni1—N2—C12 | −177.3 (4) | C3—C2—C7—C6 | 0.0 (6) |
O3—Ni1—N2—C12 | 96.1 (3) | C3—C2—C7—C8 | −179.0 (4) |
N6—Ni1—N2—C12 | −81.6 (3) | C6—C7—C8—C9 | −0.3 (7) |
N3—Ni1—N2—C12 | 1.0 (3) | C2—C7—C8—C9 | 178.7 (5) |
N5—Ni1—N2—N1 | −35 (2) | C7—C8—C9—C10 | 1.0 (8) |
O1—Ni1—N2—N1 | 5.7 (3) | C8—C9—C10—C11 | −1.1 (9) |
O3—Ni1—N2—N1 | −80.9 (3) | C9—C10—C11—C6 | 0.5 (8) |
N6—Ni1—N2—N1 | 101.4 (3) | C7—C6—C11—C10 | 0.2 (7) |
N3—Ni1—N2—N1 | −176.0 (3) | C5—C6—C11—C10 | −179.7 (5) |
N5—Ni1—N3—C17 | 8.4 (4) | N1—N2—C12—C13 | 179.6 (3) |
N2—Ni1—N3—C17 | −174.0 (4) | Ni1—N2—C12—C13 | 2.9 (5) |
O1—Ni1—N3—C17 | −170.1 (3) | C17—N3—C13—C14 | 1.4 (6) |
O3—Ni1—N3—C17 | 87.3 (4) | Ni1—N3—C13—C14 | −169.1 (4) |
N6—Ni1—N3—C17 | −68.7 (4) | C17—N3—C13—C12 | 178.2 (4) |
N5—Ni1—N3—C13 | 177.5 (3) | Ni1—N3—C13—C12 | 7.7 (4) |
N2—Ni1—N3—C13 | −4.9 (3) | N2—C12—C13—N3 | −7.3 (6) |
O1—Ni1—N3—C13 | −1.0 (5) | N2—C12—C13—C14 | 169.5 (4) |
O3—Ni1—N3—C13 | −103.6 (3) | N3—C13—C14—C15 | −0.3 (7) |
N6—Ni1—N3—C13 | 100.4 (3) | C12—C13—C14—C15 | −176.8 (4) |
C18—N4—N5—C29 | 174.7 (4) | C13—C14—C15—C16 | −0.7 (8) |
C18—N4—N5—Ni1 | −6.3 (4) | C14—C15—C16—C17 | 0.5 (8) |
N2—Ni1—N5—C29 | 139 (2) | C13—N3—C17—C16 | −1.6 (6) |
O1—Ni1—N5—C29 | 98.6 (3) | Ni1—N3—C17—C16 | 167.0 (3) |
O3—Ni1—N5—C29 | −174.8 (3) | C15—C16—C17—N3 | 0.7 (7) |
N6—Ni1—N5—C29 | 1.8 (3) | Ni1—O3—C18—N4 | 2.8 (5) |
N3—Ni1—N5—C29 | −80.7 (3) | Ni1—O3—C18—C20 | −178.8 (2) |
N2—Ni1—N5—N4 | −40 (2) | N5—N4—C18—O3 | 2.0 (5) |
O1—Ni1—N5—N4 | −80.5 (3) | N5—N4—C18—C20 | −176.4 (3) |
O3—Ni1—N5—N4 | 6.1 (2) | C24—C19—C20—C21 | 2.6 (6) |
N6—Ni1—N5—N4 | −177.3 (3) | C24—C19—C20—C18 | −175.0 (3) |
N3—Ni1—N5—N4 | 100.1 (3) | O3—C18—C20—C19 | 0.7 (5) |
N5—Ni1—N6—C34 | −173.5 (4) | N4—C18—C20—C19 | 179.1 (3) |
N2—Ni1—N6—C34 | 9.1 (4) | O3—C18—C20—C21 | −176.8 (4) |
O1—Ni1—N6—C34 | 88.5 (4) | N4—C18—C20—C21 | 1.7 (5) |
O3—Ni1—N6—C34 | −165.3 (3) | C19—C20—C21—O4 | 179.0 (4) |
N3—Ni1—N6—C34 | −67.7 (4) | C18—C20—C21—O4 | −3.6 (6) |
N5—Ni1—N6—C30 | −7.1 (3) | C19—C20—C21—C22 | −2.8 (6) |
N2—Ni1—N6—C30 | 175.4 (3) | C18—C20—C21—C22 | 174.6 (4) |
O1—Ni1—N6—C30 | −105.1 (3) | O4—C21—C22—C23 | 178.2 (4) |
O3—Ni1—N6—C30 | 1.0 (5) | C20—C21—C22—C23 | 0.0 (6) |
N3—Ni1—N6—C30 | 98.7 (3) | C21—C22—C23—C24 | 3.1 (6) |
N5—Ni1—O1—C1 | 171.4 (3) | C21—C22—C23—C28 | −177.4 (4) |
N2—Ni1—O1—C1 | −6.2 (3) | C20—C19—C24—C23 | 0.5 (6) |
O3—Ni1—O1—C1 | 94.2 (3) | C20—C19—C24—C25 | 178.9 (4) |
N6—Ni1—O1—C1 | −108.9 (3) | C22—C23—C24—C19 | −3.3 (6) |
N3—Ni1—O1—C1 | −10.1 (5) | C28—C23—C24—C19 | 177.2 (4) |
N5—Ni1—O3—C18 | −4.6 (2) | C22—C23—C24—C25 | 178.3 (4) |
N2—Ni1—O3—C18 | 172.7 (2) | C28—C23—C24—C25 | −1.3 (6) |
O1—Ni1—O3—C18 | 95.4 (2) | C19—C24—C25—C26 | −177.4 (4) |
N6—Ni1—O3—C18 | −12.8 (4) | C23—C24—C25—C26 | 1.0 (6) |
N3—Ni1—O3—C18 | −108.1 (2) | C24—C25—C26—C27 | 0.5 (7) |
Ni1—O1—C1—N1 | 6.8 (5) | C25—C26—C27—C28 | −1.9 (8) |
Ni1—O1—C1—C3 | −173.8 (3) | C26—C27—C28—C23 | 1.6 (8) |
N2—N1—C1—O1 | −2.3 (6) | C22—C23—C28—C27 | −179.5 (5) |
N2—N1—C1—C3 | 178.3 (3) | C24—C23—C28—C27 | 0.0 (6) |
C7—C2—C3—C4 | 0.1 (6) | N4—N5—C29—C30 | −177.3 (3) |
C7—C2—C3—C1 | 178.1 (4) | Ni1—N5—C29—C30 | 3.7 (5) |
O1—C1—C3—C2 | 0.0 (6) | C34—N6—C30—C31 | 1.8 (6) |
N1—C1—C3—C2 | 179.4 (4) | Ni1—N6—C30—C31 | −166.2 (3) |
O1—C1—C3—C4 | 177.9 (4) | C34—N6—C30—C29 | 179.1 (4) |
N1—C1—C3—C4 | −2.7 (6) | Ni1—N6—C30—C29 | 11.1 (4) |
C2—C3—C4—O2 | −179.5 (4) | N5—C29—C30—N6 | −10.3 (5) |
C1—C3—C4—O2 | 2.6 (7) | N5—C29—C30—C31 | 167.0 (4) |
C2—C3—C4—C5 | −0.7 (7) | N6—C30—C31—C32 | −0.3 (7) |
C1—C3—C4—C5 | −178.7 (4) | C29—C30—C31—C32 | −177.4 (4) |
O2—C4—C5—C6 | −179.8 (4) | C30—C31—C32—C33 | −1.3 (8) |
C3—C4—C5—C6 | 1.3 (7) | C31—C32—C33—C34 | 1.5 (8) |
C4—C5—C6—C7 | −1.2 (7) | C30—N6—C34—C33 | −1.6 (7) |
C4—C5—C6—C11 | 178.7 (4) | Ni1—N6—C34—C33 | 163.8 (4) |
C5—C6—C7—C8 | 179.6 (4) | C32—C33—C34—N6 | 0.0 (8) |
D—H···A | D—H | H···A | D···A | D—H···A |
O4—H4···N4 | 0.82 | 1.83 | 2.561 (4) | 148 |
O2—H2···N1 | 0.82 | 1.84 | 2.567 (4) | 147 |
C15—H15···O4i | 0.93 | 2.56 | 3.195 (6) | 126 |
C32—H32···O2ii | 0.93 | 2.38 | 3.295 (6) | 168 |
Symmetry codes: (i) x, y+1, z; (ii) x, y, z+1. |
Experimental details
Crystal data | |
Chemical formula | [Ni(C17H12N3O2)2] |
Mr | 639.30 |
Crystal system, space group | Monoclinic, P21/c |
Temperature (K) | 293 |
a, b, c (Å) | 21.257 (3), 11.653 (3), 11.938 (3) |
β (°) | 91.686 (3) |
V (Å3) | 2955.6 (10) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 0.71 |
Crystal size (mm) | 0.69 × 0.66 × 0.13 |
Data collection | |
Diffractometer | Siemens SMART CCD area-detector |
Absorption correction | Multi-scan (SADABS; Sheldrick, 1996) |
Tmin, Tmax | 0.641, 0.914 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 14859, 5202, 3068 |
Rint | 0.089 |
(sin θ/λ)max (Å−1) | 0.595 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.047, 0.149, 1.01 |
No. of reflections | 5202 |
No. of parameters | 408 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.34, −0.45 |
Computer programs: SMART (Siemens, 1996), SAINT (Siemens, 1996), SHELXS97 (Sheldrick, 1997a), SHELXL97 (Sheldrick, 1997a), SHELXTL (Sheldrick, 1997b).
D—H···A | D—H | H···A | D···A | D—H···A |
O4—H4···N4 | 0.82 | 1.83 | 2.561 (4) | 148.4 |
O2—H2···N1 | 0.82 | 1.84 | 2.567 (4) | 146.9 |
C15—H15···O4i | 0.93 | 2.56 | 3.195 (6) | 125.8 |
C32—H32···O2ii | 0.93 | 2.38 | 3.295 (6) | 167.6 |
Symmetry codes: (i) x, y+1, z; (ii) x, y, z+1. |
The chemistry of aroylhydrazones is widely studied due to their coordination abilities to metal ions (Beghidja et al., 2006) and their biological activities (Mostafa & Haifaa, 2007). Our group have reported the crystal structures of two aroylhydrazone complexes - [Cu(C12H12N2O3)(C5H5N)] (Liu et al., 2005a) and [Ni(C18H12N2O3)(C5H5N)] (Liu et al., 2005b). As an extension of our work on the structural characterization of aroylhydrazone derivatives, the title complex, (I), was synthesized and characterized.
In (I) (Fig. 1), the Ni ion is six-coordinated by four N atoms and two O atoms in a distorted octahedron geometry. Each ligand coordinate the Ni ion in a tridentate mode via N atom of the azomethine group, O atom of the the hydroxyl group and N atom of the pyridine ring. Each ligand forms two five-membered chelate rings Ni—N—N—C—O and Ni—N—C—C—N with the nickel atom. The atoms N3, N6, O3 and O1 constitute the equatorial plane, with the mean deviation from plane of 0.43 (6) Å. The angles O1—Ni1—N3 and O3—Ni1—N6 are 155.95 (12) and 155.93 (13)°, respectively. The axial positions are occupied by the atoms N5 and N2. The angle of N5—Ni1—N2 is 176.33 (14)°. There are two intramolecular O2—H2···N1 and O4—H4···N4 hydrogen bonds (Table 1 and Fig. 1).
In the crystal, the weak intermolecular C—H···O hydrogen bonds (Table 1) contribute to the crystal packing stabilization.