{N′-[(E)-1-(5-Bromo-2-oxidophen­yl)ethyl­idene-κO]-4-methyl­benzohydrazidato-κ2N′,O}(pyridine-κN)nickel(II)

Zheng, C.-Z.; Wang, L.; Liu, J.; Wang, Y.-J.

doi:10.1107/S1600536811029114

metal-organic compounds

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ISSN: 2056-9890

Volume 67| Part 8| August 2011| Page m1132

doi:10.1107/S1600536811029114

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{N′-[(E)-1-(5-Bromo-2-oxidophenyl)ethylidene-κO]-4-methylbenzohydrazidato-κ²N′,O}(pyridine-κN)nickel(II)

Chang-Zheng Zheng,^a Liang Wang,^a ^* Juan Liu ^a and Yu-Jie Wang ^a

^aCollege of Environment and Chemical Engineering, Xi'an Polytechnic University, 710048 Xi'an, Shaanxi, People's Republic of China
^*Correspondence e-mail: wllily315668256@yahoo.com.cn

(Received 14 July 2011; accepted 19 July 2011; online 23 July 2011)

The central Ni^II atom in the title complex, [Ni(C₁₆H₁₃BrN₂O₂)(C₅H₅N)], is in a square-planar trans-N₂O₂ environment defined by the NO₂ donor atoms of the tridentate hydrazone ligand and the monodentate pyridine ligand. The pyridine molecule forms a dihedral angle of 9.99 (11)° with the least-squares plane through the NiN₂O₂ atoms.

Related literature

For the biological and coordination properties of aroylhydrazones, see: Ali et al. (2004 ); Carcelli et al. (1995 ); Cheng et al. (1996 ); Desai et al. (2001 ); El-Masry et al. (2000 ); Singh & Dash (1988 ); Zheng et al. (2008 ).

Experimental

Crystal data

[Ni(C₁₆H₁₃BrN₂O₂)(C₅H₅N)]
M_r = 483.00
Monoclinic, C 2/c
a = 32.376 (18) Å
b = 6.145 (4) Å
c = 22.752 (13) Å
β = 122.063 (8)°
V = 3836 (4) Å³
Z = 8
Mo Kα radiation
μ = 3.12 mm⁻¹
T = 298 K
0.21 × 0.16 × 0.12 mm

Data collection

Bruker SMART CCD area-detector diffractometer
Absorption correction: multi-scan (SADABS; Sheldrick, 1996 ) T_min = 0.561, T_max = 0.706
9451 measured reflections
3403 independent reflections
2415 reflections with I > 2σ(I)
R_int = 0.044

Refinement

R[F² > 2σ(F²)] = 0.038
wR(F²) = 0.093
S = 1.03
3403 reflections
253 parameters
H-atom parameters constrained
Δρ_max = 0.40 e Å⁻³
Δρ_min = −0.38 e Å⁻³

Table 1
Selected bond lengths (Å)

Ni1—O1	1.794 (3)
Ni1—O2	1.826 (3)
Ni1—N2	1.835 (3)
Ni1—N3	1.941 (3)

Data collection: SMART (Bruker, 1996 ); cell refinement: SAINT (Bruker, 1996); 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/S1600536811029114/tk2766sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536811029114/tk2766Isup2.hkl

Supporting information file. DOI: 10.1107/S1600536811029114/tk2766Isup3.cdx

checkCIF report

Comment top

Hydrazones are an important class of Schiff bases compounds which has attracted much attention because of their biological activities (Carcelli et al., 1995) such as antimicrobial, antifungal, antitumor and as herbicides (El-Masry et al., 2000; Singh & Dash, 1988; Desai et al., 2001), and strong tendency to chelate to transition metals (Ali et al., 2004; Cheng et al., 1996). As an extension of our work on the structural characterization of aroylhydrazone derivatives (Zheng et al., 2008), the title compound was synthesized and its crystal structure is reported here.

The coordination polyhedron about the nickel ion in the title complex is essentially planar, Fig. 1. The coordination environment of nickel is comprised of one pyridine ligand and one hydrazone ligand (two O atoms, one N atom) so that the central nickel atom is four-coordinated, Table 1.

Related literature top

For the biological and coordination properties of aroylhydrazones, see: Ali et al. (2004); Carcelli et al. (1995); Cheng et al. (1996); Desai et al. (2001); El-Masry et al. (2000); Singh & Dash (1988); Zheng et al. (2008).

Experimental top

p-Methyl ethylbenzoate (8.21 g, 0.05 mol) was dissolved in ethanol (50 ml) at room temperature and heated at 363 K, followed by the addition of hydrazine hydrate (3.00 g, 0.060 mol). Subsequently, the mixture was refluxed for 10 h, and then cooled to room temperature. The crystals were precipitated and collected by filtration. The product was recrystallized from ethanol and dried under reduced pressure to give 4-methylbenzohydrazide.

4-methylbenzohydrazide (3.75 g, 0.025 mol) was dissolved in ethanol (50 ml) at room temperature and heated at 363 K, followed by the addition of 5-bromo-2-hydroxyphenyl ethyl ketone (5.38 g, 0.025 mol). Subsequently, the mixture was refluxed for 9 h, and then cooled to room temperature. The crystals were precipitated and collected by filtration. The product was recrystallized from ethanol and dried under reduced pressure to give compound N'- [(E)-(5-Bromo-2-hydroxyphenyl)-(methyl)methylene]-4-methylbenzohydrazide.

A mixture of N'-[(E)-(5-Bromo-2-hydroxyphenyl)-(methyl)methylene] -4-methylbenzohydrazide (0.035 g, 0.10 mmol), NiCl₂.6H₂O (0.024 g, 0.10 mmol), pyridine (0.0079 g, 0.10 mmol), and H₂O (5.00 ml), several drops of acetone was placed in a Parr Teflon-lined stainless steel vessel (25 ml). The vessel was sealed and heated at 393 K for 3 d. After the mixture was slowly cooled to room temperature, red crystals were obtained (yield 41%).

Computing details top

Data collection: SMART (Bruker 1996); cell refinement: SAINT (Bruker 1996); data reduction: SAINT (Bruker 1996); 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. The molecular structure of the title compound, showing displacement ellipsoids drawn at the 30% probability level. H atoms are presented as a small spheres of arbitrary radius.

{N'-[(E)-1-(5-Bromo-2-oxidophenyl)ethylidene-κO]-4- methylbenzohydrazidato-κ²N',O}(pyridine-κN)nickel(II) top

Crystal data top

[Ni(C₁₆H₁₃BrN₂O₂)(C₅H₅N)]	F(000) = 1952
M_r = 483.00	D_x = 1.673 Mg m⁻³
Monoclinic, C2/c	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -C 2yc	Cell parameters from 2511 reflections
a = 32.376 (18) Å	θ = 3.2–23.3°
b = 6.145 (4) Å	µ = 3.12 mm⁻¹
c = 22.752 (13) Å	T = 298 K
β = 122.063 (8)°	Block, red
V = 3836 (4) Å³	0.21 × 0.16 × 0.12 mm
Z = 8

Data collection top

Bruker SMART CCD area-detector diffractometer	3403 independent reflections
Radiation source: fine-focus sealed tube	2415 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.044
ϕ and ω scans	θ_max = 25.1°, θ_min = 1.5°
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)	h = −31→38
T_min = 0.561, T_max = 0.706	k = −6→7
9451 measured reflections	l = −27→26

Refinement top

Refinement on F²	Secondary atom site location: difference Fourier map
Least-squares matrix: full	Hydrogen site location: inferred from neighbouring sites
R[F² > 2σ(F²)] = 0.038	H-atom parameters constrained
wR(F²) = 0.093	w = 1/[σ²(F_o²) + (0.0398P)² + 0.067P] where P = (F_o² + 2F_c²)/3
S = 1.03	(Δ/σ)_max < 0.001
3403 reflections	Δρ_max = 0.40 e Å⁻³
253 parameters	Δρ_min = −0.38 e Å⁻³
0 restraints	Extinction correction: SHELXL97 (Sheldrick, 2008)
Primary atom site location: structure-invariant direct methods	Extinction coefficient: 0.0113 (15)

Crystal data top

[Ni(C₁₆H₁₃BrN₂O₂)(C₅H₅N)]	V = 3836 (4) Å³
M_r = 483.00	Z = 8
Monoclinic, C2/c	Mo Kα radiation
a = 32.376 (18) Å	µ = 3.12 mm⁻¹
b = 6.145 (4) Å	T = 298 K
c = 22.752 (13) Å	0.21 × 0.16 × 0.12 mm
β = 122.063 (8)°

Data collection top

Bruker SMART CCD area-detector diffractometer	3403 independent reflections
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)	2415 reflections with I > 2σ(I)
T_min = 0.561, T_max = 0.706	R_int = 0.044
9451 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.038	0 restraints
wR(F²) = 0.093	H-atom parameters constrained
S = 1.03	Δρ_max = 0.40 e Å⁻³
3403 reflections	Δρ_min = −0.38 e Å⁻³
253 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

	x	y	z	U_iso*/U_eq
Ni1	0.039679 (16)	0.25481 (7)	0.15523 (2)	0.04140 (15)
Br1	−0.214719 (15)	0.57208 (8)	−0.01235 (2)	0.07427 (19)
O1	−0.01744 (9)	0.1671 (4)	0.14220 (12)	0.0521 (6)
O2	0.09732 (8)	0.3432 (4)	0.16657 (11)	0.0461 (6)
N1	0.04942 (11)	0.6167 (5)	0.09492 (13)	0.0453 (7)
N2	0.01454 (11)	0.4946 (4)	0.09898 (13)	0.0418 (7)
N3	0.07198 (11)	0.0131 (5)	0.21834 (14)	0.0447 (7)
C1	0.25839 (16)	0.9041 (8)	0.1443 (2)	0.0827 (14)
H1A	0.2839	0.7978	0.1605	0.124*
H1B	0.2700	1.0277	0.1748	0.124*
H1C	0.2486	0.9493	0.0983	0.124*
C2	0.21573 (15)	0.8065 (7)	0.14342 (18)	0.0559 (10)
C3	0.21831 (14)	0.6056 (7)	0.17226 (19)	0.0601 (11)
H3	0.2477	0.5306	0.1947	0.072*
C4	0.17830 (14)	0.5144 (6)	0.16844 (18)	0.0534 (10)
H4	0.1810	0.3774	0.1875	0.064*
C5	0.13426 (13)	0.6209 (6)	0.13698 (17)	0.0439 (9)
C6	0.13174 (15)	0.8249 (7)	0.1090 (2)	0.0594 (10)
H6	0.1026	0.9018	0.0876	0.071*
C7	0.17177 (16)	0.9138 (7)	0.1127 (2)	0.0647 (11)
H7	0.1692	1.0510	0.0938	0.078*
C8	0.09144 (13)	0.5231 (6)	0.13248 (17)	0.0424 (9)
C9	−0.03004 (13)	0.5689 (5)	0.06399 (16)	0.0425 (8)
C10	−0.04099 (14)	0.7722 (6)	0.02212 (18)	0.0537 (10)
H10A	−0.0467	0.8895	0.0448	0.081*
H10B	−0.0695	0.7501	−0.0232	0.081*
H10C	−0.0138	0.8075	0.0179	0.081*
C11	−0.06813 (12)	0.4555 (6)	0.06651 (16)	0.0405 (8)
C12	−0.06026 (13)	0.2605 (6)	0.10355 (17)	0.0440 (9)
C13	−0.09983 (14)	0.1556 (7)	0.09951 (19)	0.0545 (10)
H13	−0.0948	0.0229	0.1220	0.065*
C14	−0.14580 (15)	0.2406 (7)	0.0637 (2)	0.0570 (10)
H14	−0.1718	0.1676	0.0614	0.068*
C15	−0.15255 (14)	0.4378 (7)	0.03092 (17)	0.0517 (10)
C16	−0.11546 (14)	0.5416 (6)	0.03128 (17)	0.0479 (9)
H16	−0.1215	0.6728	0.0077	0.058*
C17	0.04736 (15)	−0.1465 (6)	0.22590 (18)	0.0509 (9)
H17	0.0135	−0.1401	0.2007	0.061*
C18	0.07017 (17)	−0.3209 (7)	0.26964 (19)	0.0587 (11)
H18	0.0518	−0.4301	0.2733	0.070*
C19	0.11926 (17)	−0.3323 (7)	0.30699 (19)	0.0645 (12)
H19	0.1351	−0.4494	0.3364	0.077*
C20	0.14525 (17)	−0.1681 (8)	0.3008 (2)	0.0700 (12)
H20	0.1791	−0.1707	0.3264	0.084*
C21	0.12057 (15)	−0.0002 (7)	0.2563 (2)	0.0626 (11)
H21	0.1385	0.1105	0.2523	0.075*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Ni1	0.0472 (3)	0.0340 (3)	0.0408 (3)	0.0066 (2)	0.0218 (2)	0.0065 (2)
Br1	0.0558 (3)	0.0908 (4)	0.0771 (3)	0.0253 (2)	0.0359 (2)	0.0117 (3)
O1	0.0495 (15)	0.0417 (15)	0.0595 (15)	0.0057 (13)	0.0252 (13)	0.0160 (12)
O2	0.0519 (15)	0.0379 (14)	0.0463 (13)	0.0045 (12)	0.0246 (12)	0.0109 (12)
N1	0.0529 (19)	0.0368 (19)	0.0454 (16)	0.0034 (15)	0.0256 (15)	0.0046 (14)
N2	0.0534 (19)	0.0298 (16)	0.0438 (16)	0.0051 (14)	0.0269 (14)	0.0033 (13)
N3	0.0533 (19)	0.0390 (19)	0.0411 (16)	0.0073 (15)	0.0246 (15)	0.0047 (13)
C1	0.069 (3)	0.094 (4)	0.083 (3)	−0.022 (3)	0.040 (3)	0.006 (3)
C2	0.058 (3)	0.059 (3)	0.046 (2)	−0.012 (2)	0.025 (2)	−0.0014 (19)
C3	0.050 (2)	0.066 (3)	0.062 (2)	0.003 (2)	0.028 (2)	0.010 (2)
C4	0.060 (3)	0.045 (2)	0.059 (2)	0.005 (2)	0.034 (2)	0.0097 (19)
C5	0.054 (2)	0.037 (2)	0.0426 (19)	0.0020 (18)	0.0266 (18)	−0.0007 (16)
C6	0.060 (3)	0.049 (2)	0.067 (3)	0.006 (2)	0.032 (2)	0.013 (2)
C7	0.075 (3)	0.046 (3)	0.075 (3)	−0.006 (2)	0.041 (2)	0.013 (2)
C8	0.054 (2)	0.034 (2)	0.0400 (19)	0.0012 (18)	0.0247 (17)	0.0000 (16)
C9	0.055 (2)	0.032 (2)	0.0396 (18)	0.0096 (18)	0.0239 (17)	0.0006 (16)
C10	0.062 (3)	0.041 (2)	0.053 (2)	0.0079 (19)	0.028 (2)	0.0117 (18)
C11	0.045 (2)	0.038 (2)	0.0388 (18)	0.0073 (17)	0.0231 (16)	−0.0006 (16)
C12	0.046 (2)	0.043 (2)	0.0408 (19)	0.0072 (18)	0.0215 (17)	0.0007 (17)
C13	0.056 (2)	0.049 (2)	0.065 (2)	0.006 (2)	0.036 (2)	0.010 (2)
C14	0.058 (3)	0.059 (3)	0.064 (2)	0.002 (2)	0.040 (2)	−0.001 (2)
C15	0.053 (2)	0.061 (3)	0.045 (2)	0.012 (2)	0.0281 (18)	−0.0001 (19)
C16	0.055 (2)	0.044 (2)	0.045 (2)	0.0145 (19)	0.0264 (18)	0.0059 (17)
C17	0.061 (2)	0.039 (2)	0.050 (2)	0.005 (2)	0.0271 (19)	0.0058 (18)
C18	0.085 (3)	0.042 (2)	0.054 (2)	0.006 (2)	0.041 (2)	0.0081 (19)
C19	0.090 (3)	0.054 (3)	0.053 (2)	0.029 (3)	0.040 (3)	0.016 (2)
C20	0.067 (3)	0.069 (3)	0.073 (3)	0.029 (3)	0.036 (2)	0.030 (2)
C21	0.059 (3)	0.063 (3)	0.069 (3)	0.016 (2)	0.036 (2)	0.024 (2)

Geometric parameters (Å, º) top

Ni1—O1	1.794 (3)	C6—H6	0.9300
Ni1—O2	1.826 (3)	C7—H7	0.9300
Ni1—N2	1.835 (3)	C9—C11	1.444 (5)
Ni1—N3	1.941 (3)	C9—C10	1.495 (5)
Br1—C15	1.897 (4)	C10—H10A	0.9600
O1—C12	1.315 (4)	C10—H10B	0.9600
O2—C8	1.305 (4)	C10—H10C	0.9600
N1—C8	1.295 (4)	C11—C16	1.402 (5)
N1—N2	1.399 (4)	C11—C12	1.408 (5)
N2—C9	1.306 (4)	C12—C13	1.393 (5)
N3—C17	1.331 (5)	C13—C14	1.365 (5)
N3—C21	1.336 (5)	C13—H13	0.9300
C1—C2	1.496 (5)	C14—C15	1.378 (5)
C1—H1A	0.9600	C14—H14	0.9300
C1—H1B	0.9600	C15—C16	1.356 (5)
C1—H1C	0.9600	C16—H16	0.9300
C2—C7	1.376 (6)	C17—C18	1.380 (5)
C2—C3	1.380 (5)	C17—H17	0.9300
C3—C4	1.371 (5)	C18—C19	1.349 (6)
C3—H3	0.9300	C18—H18	0.9300
C4—C5	1.375 (5)	C19—C20	1.368 (6)
C4—H4	0.9300	C19—H19	0.9300
C5—C6	1.388 (5)	C20—C21	1.367 (5)
C5—C8	1.464 (5)	C20—H20	0.9300
C6—C7	1.368 (5)	C21—H21	0.9300

O1—Ni1—O2	178.81 (10)	N2—C9—C11	119.9 (3)
O1—Ni1—N2	95.14 (12)	N2—C9—C10	119.5 (3)
O2—Ni1—N2	84.33 (12)	C11—C9—C10	120.7 (3)
O1—Ni1—N3	89.75 (12)	C9—C10—H10A	109.5
O2—Ni1—N3	90.82 (12)	C9—C10—H10B	109.5
N2—Ni1—N3	174.87 (13)	H10A—C10—H10B	109.5
C12—O1—Ni1	127.4 (2)	C9—C10—H10C	109.5
C8—O2—Ni1	110.6 (2)	H10A—C10—H10C	109.5
C8—N1—N2	108.7 (3)	H10B—C10—H10C	109.5
C9—N2—N1	116.2 (3)	C16—C11—C12	117.3 (3)
C9—N2—Ni1	130.1 (3)	C16—C11—C9	119.5 (3)
N1—N2—Ni1	113.7 (2)	C12—C11—C9	123.2 (3)
C17—N3—C21	116.8 (3)	O1—C12—C13	116.6 (3)
C17—N3—Ni1	122.3 (3)	O1—C12—C11	124.3 (3)
C21—N3—Ni1	120.8 (3)	C13—C12—C11	119.1 (3)
C2—C1—H1A	109.5	C14—C13—C12	122.3 (4)
C2—C1—H1B	109.5	C14—C13—H13	118.8
H1A—C1—H1B	109.5	C12—C13—H13	118.8
C2—C1—H1C	109.5	C13—C14—C15	118.0 (4)
H1A—C1—H1C	109.5	C13—C14—H14	121.0
H1B—C1—H1C	109.5	C15—C14—H14	121.0
C7—C2—C3	117.1 (4)	C16—C15—C14	121.6 (4)
C7—C2—C1	120.9 (4)	C16—C15—Br1	119.4 (3)
C3—C2—C1	122.0 (4)	C14—C15—Br1	118.9 (3)
C4—C3—C2	121.3 (4)	C15—C16—C11	121.4 (4)
C4—C3—H3	119.4	C15—C16—H16	119.3
C2—C3—H3	119.4	C11—C16—H16	119.3
C3—C4—C5	121.5 (4)	N3—C17—C18	122.5 (4)
C3—C4—H4	119.3	N3—C17—H17	118.7
C5—C4—H4	119.3	C18—C17—H17	118.7
C4—C5—C6	117.4 (3)	C19—C18—C17	119.6 (4)
C4—C5—C8	121.5 (3)	C19—C18—H18	120.2
C6—C5—C8	121.0 (3)	C17—C18—H18	120.2
C7—C6—C5	120.6 (4)	C18—C19—C20	118.7 (4)
C7—C6—H6	119.7	C18—C19—H19	120.6
C5—C6—H6	119.7	C20—C19—H19	120.6
C6—C7—C2	122.1 (4)	C21—C20—C19	118.9 (4)
C6—C7—H7	119.0	C21—C20—H20	120.6
C2—C7—H7	119.0	C19—C20—H20	120.6
N1—C8—O2	122.6 (3)	N3—C21—C20	123.4 (4)
N1—C8—C5	119.2 (3)	N3—C21—H21	118.3
O2—C8—C5	118.2 (3)	C20—C21—H21	118.3

N2—Ni1—O1—C12	0.0 (3)	N1—N2—C9—C11	−178.7 (3)
N3—Ni1—O1—C12	178.4 (3)	Ni1—N2—C9—C11	−0.2 (5)
N2—Ni1—O2—C8	1.6 (2)	N1—N2—C9—C10	0.8 (4)
N3—Ni1—O2—C8	−176.7 (2)	Ni1—N2—C9—C10	179.3 (2)
C8—N1—N2—C9	179.6 (3)	N2—C9—C11—C16	177.2 (3)
C8—N1—N2—Ni1	0.9 (3)	C10—C9—C11—C16	−2.3 (5)
O1—Ni1—N2—C9	1.2 (3)	N2—C9—C11—C12	−2.2 (5)
O2—Ni1—N2—C9	−179.9 (3)	C10—C9—C11—C12	178.3 (3)
O1—Ni1—N2—N1	179.6 (2)	Ni1—O1—C12—C13	177.4 (2)
O2—Ni1—N2—N1	−1.4 (2)	Ni1—O1—C12—C11	−2.2 (5)
O1—Ni1—N3—C17	9.5 (3)	C16—C11—C12—O1	−175.9 (3)
O2—Ni1—N3—C17	−169.5 (3)	C9—C11—C12—O1	3.5 (5)
O1—Ni1—N3—C21	−170.7 (3)	C16—C11—C12—C13	4.5 (5)
O2—Ni1—N3—C21	10.3 (3)	C9—C11—C12—C13	−176.1 (3)
C7—C2—C3—C4	2.0 (6)	O1—C12—C13—C14	177.0 (3)
C1—C2—C3—C4	−177.2 (4)	C11—C12—C13—C14	−3.4 (5)
C2—C3—C4—C5	−1.3 (6)	C12—C13—C14—C15	−0.3 (6)
C3—C4—C5—C6	0.1 (5)	C13—C14—C15—C16	2.9 (5)
C3—C4—C5—C8	179.6 (3)	C13—C14—C15—Br1	−174.5 (3)
C4—C5—C6—C7	0.4 (5)	C14—C15—C16—C11	−1.6 (5)
C8—C5—C6—C7	−179.2 (3)	Br1—C15—C16—C11	175.8 (2)
C5—C6—C7—C2	0.4 (6)	C12—C11—C16—C15	−2.1 (5)
C3—C2—C7—C6	−1.5 (6)	C9—C11—C16—C15	178.4 (3)
C1—C2—C7—C6	177.7 (4)	C21—N3—C17—C18	−1.2 (5)
N2—N1—C8—O2	0.6 (4)	Ni1—N3—C17—C18	178.6 (3)
N2—N1—C8—C5	−179.8 (3)	N3—C17—C18—C19	0.5 (6)
Ni1—O2—C8—N1	−1.7 (4)	C17—C18—C19—C20	0.6 (6)
Ni1—O2—C8—C5	178.6 (2)	C18—C19—C20—C21	−0.9 (6)
C4—C5—C8—N1	−171.3 (3)	C17—N3—C21—C20	0.8 (6)
C6—C5—C8—N1	8.2 (5)	Ni1—N3—C21—C20	−179.0 (3)
C4—C5—C8—O2	8.3 (5)	C19—C20—C21—N3	0.2 (7)
C6—C5—C8—O2	−172.2 (3)

Experimental details

Crystal data
Chemical formula	[Ni(C₁₆H₁₃BrN₂O₂)(C₅H₅N)]
M_r	483.00
Crystal system, space group	Monoclinic, C2/c
Temperature (K)	298
a, b, c (Å)	32.376 (18), 6.145 (4), 22.752 (13)
β (°)	122.063 (8)
V (Å³)	3836 (4)
Z	8
Radiation type	Mo Kα
µ (mm⁻¹)	3.12
Crystal size (mm)	0.21 × 0.16 × 0.12

Data collection
Diffractometer	Bruker SMART CCD area-detector diffractometer
Absorption correction	Multi-scan (SADABS; Sheldrick, 1996)
T_min, T_max	0.561, 0.706
No. of measured, independent and observed [I > 2σ(I)] reflections	9451, 3403, 2415
R_int	0.044
(sin θ/λ)_max (Å⁻¹)	0.596

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.038, 0.093, 1.03
No. of reflections	3403
No. of parameters	253
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.40, −0.38

Computer programs: SMART (Bruker 1996), SAINT (Bruker 1996), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008).

Selected bond lengths (Å) top

Ni1—O1	1.794 (3)	Ni1—N2	1.835 (3)
Ni1—O2	1.826 (3)	Ni1—N3	1.941 (3)

Acknowledgements

The authors thank the National Natural Science Foundation of Shaanxi Province, China, for financial support (2009JM2012).

References

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