{2,6-Bis[1-(phenyl­imino)eth­yl]pyridine-κ3N,N′,N′′}dichloridocobalt(II)

Li, X.-G.; Zhong, D.-C.; He, R.; Guo, H.-R.

doi:10.1107/S1600536808013007

metal-organic compounds

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ISSN: 2056-9890

Volume 64| Part 6| June 2008| Page m786

doi:10.1107/S1600536808013007

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{2,6-Bis[1-(phenylimino)ethyl]pyridine-κ³N,N′,N′′}dichloridocobalt(II)

Xiao-Gang Li,^a Di-Chang Zhong,^b Ren He ^a ^* and Hui-Rui Guo ^b

^aDalian University of Technology, State Key Laboratory of Fine Chemicals, Dalian 116012, People's Republic of China, and ^bInstitute of Coordination Catalysis, Yichun University, Yichun, Jiangxi 336000, People's Republic of China
^*Correspondence e-mail: zhong_dichang@yahoo.com.cn

(Received 6 April 2008; accepted 2 May 2008; online 7 May 2008)

In the title complex, [CoCl₂(C₂₁H₁₉N₃)], the Co^II atom is coordinated by one pyridine and two imine N atoms and by two chloride anions in a distorted trigonal bipyramidal geometry. The structure exhibits a pseudo-mirror plane through the metal atom, two chloride anions and the pyridine ring. In the crystal structure, the complexes are connected via intermolecular C—H⋯Cl hydrogen bonding.

Related literature

For related literature on crystal structures of metal complexes of Schiff bases, see: Reardon et al. (2002 ); Pradhan et al. (2003 ); Gibson et al. (2001 ); Trivedi et al. (2007 ); Mentes et al. (2001 ); Esteruelas et al. (2003 ).

Experimental

Crystal data

[CoCl₂(C₂₁H₁₉N₃)]
M_r = 443.22
Monoclinic, P 2₁ /n
a = 10.4580 (3) Å
b = 15.2575 (4) Å
c = 13.1339 (3) Å
β = 95.825 (10)°
V = 2084.86 (9) Å³
Z = 4
Mo Kα radiation
μ = 1.09 mm⁻¹
T = 273 (2) K
0.36 × 0.30 × 0.28 mm

Data collection

Bruker SMART CCD area-detector diffractometer
Absorption correction: none
11050 measured reflections
3665 independent reflections
2594 reflections with I > 2σ(I)
R_int = 0.046

Refinement

R[F² > 2σ(F²)] = 0.036
wR(F²) = 0.075
S = 1.01
3665 reflections
246 parameters
H-atom parameters constrained
Δρ_max = 0.28 e Å⁻³
Δρ_min = −0.26 e Å⁻³

Table 1
Selected geometric parameters (Å, °)

Co1—N23	2.027 (2)
Co1—N24	2.208 (2)
Co1—N22	2.223 (2)
Co1—Cl2	2.2572 (8)
Co1—Cl1	2.2638 (8)

N23—Co1—N24	75.36 (8)
N23—Co1—N22	75.38 (8)
N24—Co1—N22	150.74 (9)
N23—Co1—Cl2	119.07 (6)
N24—Co1—Cl2	96.11 (6)
N22—Co1—Cl2	98.36 (6)
N23—Co1—Cl1	123.81 (6)
N24—Co1—Cl1	96.23 (6)
N22—Co1—Cl1	99.58 (6)
Cl2—Co1—Cl1	117.03 (3)

Table 2
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C2—H2⋯Cl2ⁱ	0.93	2.67	3.545 (3)	156
C7—H7A⋯Cl1ⁱⁱ	0.96	2.76	3.663 (3)	158
C18—H18⋯Cl2ⁱⁱⁱ	0.93	2.83	3.714 (3)	160
Symmetry codes: (i) $[-x+{\script{1\over 2}}, y-{\script{1\over 2}}, -z+{\script{3\over 2}}]$ ; (ii) -x, -y, -z+1; (iii) -x+1, -y, -z+2.

Data collection: SMART (Bruker, 2004 ); cell refinement: SAINT (Bruker, 2004); 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 global, I. DOI: 10.1107/S1600536808013007/nc2100sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536808013007/nc2100Isup2.hkl

checkCIF report

Comment top

Recently, numerous crystal structures of metal-organic complexes with Schiff base ligands derived from 2,6-diacetylpyridine have been reported (Reardon et al., 2002; Esteruelas et al., 2003; Pradhan et al., 2003; Gibson et al., 2002; Trivedi et al., 2007) in last several years. In our ongoing investigations on this topic we report here the crystal structure of the title compound.

In the crystal stucture of the title compound the Co^II atom is coordinated by three N atoms from the Schiff base ligand and two Cl atoms within a distorted trigonal-bipyramid geometry (Table 1 and Fig. 1). The pyridyl N atom and the two Cl atoms are located in the equatorial plane and the apical position are occupied by the two imino N atoms.

The molecules are connected by intermolecular nonclassical C—H···Cl hydrogen bonding between the aromatic and methyl H atoms and the Cl atoms (Table 2 and Fig 2).

Related literature top

For related literature on crystal structures of metal complexes of Schiff bases, see: Reardon et al. (2002); Esteruelad et al. (2003); Pradhan et al. (2003); Gibson et al. (2001 or 2002?); Trivedi et al. (2007); Mentes et al. (2001); Esteruelas et al. (2003).

Experimental top

The ligand Plep (2,6-bis[(1-phenylimino)ethyl]pyridine) was prepared in high yield from condensation of two equivalents of aniline with one equivalent of 2,6-diacetylpyridine in methanol according to the literature (Mentes et al., 2001). The title compound was synthesized as follows: To a solution of Plep (1 mmol) in 10 mL methanol, a solution of CoCl₂.6H₂O (1 mmol) in 10 mL methanol was added dropwise at 333 K. After stirring for half an hour, the mixture was allowed to cool to room temperature and filtered off. On slow evaporation of the solvent from the filtrate at room temperature, red well shaped single crystals of the title compound were obtained in one week.

Computing details top

Data collection: SMART (Bruker, 2004); cell refinement: SMART (Bruker, 2004); data reduction: SAINT (Bruker, 2004); 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. Crystal structure of the title compound with 30% probability displacement ellipsoids and the atom-labeling scheme.
	Fig. 2. Crystal structure of the title compound with C—H···Cl hydrogen bonding shown as dashed lines.

{2,6-Bis[1-(phenylimino)ethyl]pyridine- κ³N,N',N''}dichloridocobalt(II) top

Crystal data top

[CoCl₂(C₂₁H₁₉N₃)]	F(000) = 908
M_r = 443.22	D_x = 1.412 Mg m⁻³
Monoclinic, P2₁/n	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2yn	Cell parameters from 1843 reflections
a = 10.4580 (3) Å	θ = 2.1–25.0°
b = 15.2575 (4) Å	µ = 1.09 mm⁻¹
c = 13.1339 (3) Å	T = 273 K
β = 95.825 (1)°	Block, red
V = 2084.86 (9) Å³	0.36 × 0.30 × 0.28 mm
Z = 4

Data collection top

Bruker SMART CCD area-detector diffractometer	2594 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tube	R_int = 0.046
Graphite monochromator	θ_max = 25.0°, θ_min = 2.1°
ϕ and ω scans	h = −10→12
11050 measured reflections	k = −15→18
3665 independent reflections	l = −15→15

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)] = 0.036	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.075	H-atom parameters constrained
S = 1.01	w = 1/[σ²(F_o²) + (0.0286P)² + 0.0512P] where P = (F_o² + 2F_c²)/3
3665 reflections	(Δ/σ)_max = 0.003
246 parameters	Δρ_max = 0.28 e Å⁻³
0 restraints	Δρ_min = −0.26 e Å⁻³

Crystal data top

[CoCl₂(C₂₁H₁₉N₃)]	V = 2084.86 (9) Å³
M_r = 443.22	Z = 4
Monoclinic, P2₁/n	Mo Kα radiation
a = 10.4580 (3) Å	µ = 1.09 mm⁻¹
b = 15.2575 (4) Å	T = 273 K
c = 13.1339 (3) Å	0.36 × 0.30 × 0.28 mm
β = 95.825 (1)°

Data collection top

Bruker SMART CCD area-detector diffractometer	2594 reflections with I > 2σ(I)
11050 measured reflections	R_int = 0.046
3665 independent reflections

Refinement top

R[F² > 2σ(F²)] = 0.036	0 restraints
wR(F²) = 0.075	H-atom parameters constrained
S = 1.01	Δρ_max = 0.28 e Å⁻³
3665 reflections	Δρ_min = −0.26 e Å⁻³
246 parameters

Special details top

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds 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 > 2sigma(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
Co1	0.24632 (4)	0.03924 (2)	0.67087 (3)	0.03166 (12)
Cl1	0.09612 (7)	0.14576 (5)	0.67423 (5)	0.0441 (2)
Cl2	0.45297 (7)	0.07827 (5)	0.71366 (6)	0.0448 (2)
N24	0.2555 (2)	0.04147 (15)	0.50369 (15)	0.0316 (5)
N22	0.2133 (2)	−0.03183 (16)	0.81359 (15)	0.0343 (6)
C6	0.2297 (2)	−0.03113 (19)	0.45798 (19)	0.0301 (6)
N23	0.20616 (19)	−0.08547 (15)	0.62497 (16)	0.0316 (5)
C14	0.1919 (3)	−0.1139 (2)	0.8020 (2)	0.0353 (7)
C3	0.1514 (3)	−0.2543 (2)	0.5634 (2)	0.0436 (8)
H3	0.1323	−0.3115	0.5425	0.052*
C5	0.2025 (2)	−0.10652 (18)	0.5251 (2)	0.0308 (6)
C1	0.1845 (2)	−0.14705 (19)	0.6945 (2)	0.0331 (7)
C2	0.1571 (3)	−0.23215 (19)	0.6658 (2)	0.0412 (7)
H2	0.1426	−0.2742	0.7146	0.049*
C4	0.1742 (3)	−0.19112 (19)	0.4923 (2)	0.0387 (7)
H4	0.1705	−0.2052	0.4231	0.046*
C7	0.2247 (3)	−0.0470 (2)	0.34516 (19)	0.0423 (8)
H7A	0.1407	−0.0677	0.3200	0.063*
H7B	0.2878	−0.0901	0.3320	0.063*
H7C	0.2424	0.0067	0.3112	0.063*
C16	0.2226 (3)	0.0074 (2)	0.9132 (2)	0.0370 (7)
C21	0.1319 (3)	0.0674 (2)	0.9352 (2)	0.0496 (9)
H21	0.0644	0.0812	0.8862	0.059*
C8	0.2866 (3)	0.11637 (18)	0.44589 (18)	0.0310 (7)
C9	0.4113 (3)	0.1313 (2)	0.4257 (2)	0.0484 (8)
H9	0.4758	0.0919	0.4487	0.058*
C12	0.2231 (3)	0.2498 (2)	0.3586 (2)	0.0487 (8)
H12	0.1595	0.2900	0.3362	0.058*
C13	0.1924 (3)	0.1760 (2)	0.41291 (19)	0.0406 (8)
H13	0.1081	0.1668	0.4271	0.049*
C15	0.1728 (3)	−0.1794 (2)	0.8837 (2)	0.0557 (9)
H15A	0.2453	−0.2183	0.8919	0.084*
H15B	0.0961	−0.2126	0.8645	0.084*
H15C	0.1648	−0.1495	0.9470	0.084*
C10	0.4405 (3)	0.2045 (2)	0.3714 (2)	0.0552 (9)
H10	0.5248	0.2140	0.3572	0.066*
C20	0.1406 (3)	0.1075 (2)	1.0304 (2)	0.0615 (10)
H20	0.0791	0.1485	1.0448	0.074*
C18	0.3299 (4)	0.0281 (2)	1.0814 (2)	0.0651 (11)
H18	0.3971	0.0145	1.1307	0.078*
C11	0.3473 (3)	0.2633 (2)	0.3383 (2)	0.0505 (9)
H11	0.3681	0.3126	0.3018	0.061*
C17	0.3232 (3)	−0.0119 (2)	0.9863 (2)	0.0546 (9)
H17	0.3862	−0.0516	0.9716	0.065*
C19	0.2392 (4)	0.0873 (3)	1.1032 (2)	0.0630 (10)
H19	0.2442	0.1138	1.1672	0.076*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Co1	0.0368 (2)	0.0268 (2)	0.0312 (2)	−0.00071 (18)	0.00279 (16)	0.00155 (18)
Cl1	0.0371 (4)	0.0479 (5)	0.0480 (4)	0.0097 (4)	0.0080 (3)	0.0079 (4)
Cl2	0.0348 (4)	0.0449 (5)	0.0538 (5)	0.0047 (4)	0.0005 (3)	−0.0052 (4)
N24	0.0375 (14)	0.0279 (14)	0.0297 (12)	−0.0017 (11)	0.0045 (10)	0.0018 (11)
N22	0.0395 (14)	0.0349 (16)	0.0289 (13)	0.0041 (12)	0.0053 (10)	0.0033 (11)
C6	0.0260 (15)	0.0336 (18)	0.0310 (15)	0.0001 (13)	0.0042 (12)	0.0003 (14)
N23	0.0330 (13)	0.0288 (14)	0.0331 (13)	0.0000 (11)	0.0040 (10)	0.0038 (11)
C14	0.0356 (17)	0.0346 (19)	0.0364 (16)	0.0044 (14)	0.0070 (13)	0.0094 (14)
C3	0.0452 (19)	0.0274 (18)	0.057 (2)	−0.0019 (14)	0.0012 (16)	−0.0011 (16)
C5	0.0261 (15)	0.0296 (17)	0.0365 (16)	−0.0010 (13)	0.0017 (12)	−0.0026 (13)
C1	0.0316 (16)	0.0270 (18)	0.0409 (17)	0.0028 (13)	0.0054 (13)	0.0065 (14)
C2	0.0419 (19)	0.0287 (19)	0.0535 (19)	0.0042 (14)	0.0065 (15)	0.0129 (15)
C4	0.0373 (17)	0.037 (2)	0.0413 (17)	0.0034 (14)	0.0000 (14)	−0.0058 (15)
C7	0.052 (2)	0.042 (2)	0.0339 (16)	−0.0104 (15)	0.0106 (14)	−0.0066 (14)
C16	0.0446 (18)	0.0403 (19)	0.0274 (15)	−0.0006 (15)	0.0099 (14)	0.0070 (14)
C21	0.047 (2)	0.059 (2)	0.0435 (18)	0.0041 (17)	0.0103 (15)	−0.0010 (17)
C8	0.0398 (17)	0.0307 (17)	0.0223 (14)	−0.0041 (14)	0.0025 (12)	0.0012 (13)
C9	0.0406 (19)	0.048 (2)	0.057 (2)	0.0016 (16)	0.0094 (16)	0.0159 (17)
C12	0.062 (2)	0.042 (2)	0.0404 (18)	0.0053 (17)	−0.0005 (16)	0.0130 (16)
C13	0.0392 (18)	0.044 (2)	0.0393 (17)	0.0009 (15)	0.0049 (14)	0.0096 (15)
C15	0.071 (2)	0.051 (2)	0.0494 (19)	0.0050 (18)	0.0240 (17)	0.0184 (17)
C10	0.049 (2)	0.058 (3)	0.060 (2)	−0.0134 (18)	0.0118 (17)	0.0200 (19)
C20	0.068 (2)	0.067 (3)	0.054 (2)	0.003 (2)	0.0279 (19)	−0.008 (2)
C18	0.087 (3)	0.069 (3)	0.0357 (19)	0.008 (2)	−0.0104 (19)	0.0108 (18)
C11	0.071 (2)	0.045 (2)	0.0363 (17)	−0.0114 (19)	0.0070 (17)	0.0135 (16)
C17	0.069 (2)	0.053 (2)	0.0396 (19)	0.0147 (18)	−0.0019 (17)	0.0086 (17)
C19	0.095 (3)	0.066 (3)	0.0295 (18)	−0.008 (2)	0.0150 (19)	0.0039 (18)

Geometric parameters (Å, º) top

Co1—N23	2.027 (2)	C16—C21	1.369 (4)
Co1—N24	2.208 (2)	C16—C17	1.382 (4)
Co1—N22	2.223 (2)	C21—C20	1.387 (4)
Co1—Cl2	2.2572 (8)	C21—H21	0.9300
Co1—Cl1	2.2638 (8)	C8—C9	1.376 (4)
N24—C6	1.276 (3)	C8—C13	1.378 (4)
N24—C8	1.428 (3)	C9—C10	1.377 (4)
N22—C14	1.278 (3)	C9—H9	0.9300
N22—C16	1.434 (3)	C12—C11	1.368 (4)
C6—C5	1.495 (4)	C12—C13	1.388 (4)
C6—C7	1.497 (3)	C12—H12	0.9300
N23—C1	1.345 (3)	C13—H13	0.9300
N23—C5	1.347 (3)	C15—H15A	0.9600
C14—C1	1.495 (4)	C15—H15B	0.9600
C14—C15	1.495 (4)	C15—H15C	0.9600
C3—C4	1.380 (4)	C10—C11	1.363 (4)
C3—C2	1.382 (4)	C10—H10	0.9300
C3—H3	0.9300	C20—C19	1.368 (4)
C5—C4	1.384 (4)	C20—H20	0.9300
C1—C2	1.374 (4)	C18—C19	1.361 (5)
C2—H2	0.9300	C18—C17	1.386 (4)
C4—H4	0.9300	C18—H18	0.9300
C7—H7A	0.9600	C11—H11	0.9300
C7—H7B	0.9600	C17—H17	0.9300
C7—H7C	0.9600	C19—H19	0.9300

N23—Co1—N24	75.36 (8)	H7A—C7—H7C	109.5
N23—Co1—N22	75.38 (8)	H7B—C7—H7C	109.5
N24—Co1—N22	150.74 (9)	C21—C16—C17	119.4 (3)
N23—Co1—Cl2	119.07 (6)	C21—C16—N22	119.2 (3)
N24—Co1—Cl2	96.11 (6)	C17—C16—N22	121.4 (3)
N22—Co1—Cl2	98.36 (6)	C16—C21—C20	120.1 (3)
N23—Co1—Cl1	123.81 (6)	C16—C21—H21	120.0
N24—Co1—Cl1	96.23 (6)	C20—C21—H21	120.0
N22—Co1—Cl1	99.58 (6)	C9—C8—C13	119.4 (3)
Cl2—Co1—Cl1	117.03 (3)	C9—C8—N24	120.4 (3)
C6—N24—C8	119.6 (2)	C13—C8—N24	120.1 (2)
C6—N24—Co1	115.23 (18)	C10—C9—C8	119.9 (3)
C8—N24—Co1	125.20 (17)	C10—C9—H9	120.0
C14—N22—C16	120.8 (2)	C8—C9—H9	120.0
C14—N22—Co1	114.70 (18)	C11—C12—C13	119.7 (3)
C16—N22—Co1	124.34 (18)	C11—C12—H12	120.1
N24—C6—C5	115.7 (2)	C13—C12—H12	120.1
N24—C6—C7	126.2 (3)	C8—C13—C12	120.2 (3)
C5—C6—C7	118.1 (2)	C8—C13—H13	119.9
C1—N23—C5	120.3 (2)	C12—C13—H13	119.9
C1—N23—Co1	119.86 (18)	C14—C15—H15A	109.5
C5—N23—Co1	119.87 (18)	C14—C15—H15B	109.5
N22—C14—C1	115.8 (2)	H15A—C15—H15B	109.5
N22—C14—C15	127.2 (3)	C14—C15—H15C	109.5
C1—C14—C15	117.0 (3)	H15A—C15—H15C	109.5
C4—C3—C2	119.6 (3)	H15B—C15—H15C	109.5
C4—C3—H3	120.2	C11—C10—C9	120.7 (3)
C2—C3—H3	120.2	C11—C10—H10	119.7
N23—C5—C4	120.7 (3)	C9—C10—H10	119.7
N23—C5—C6	113.7 (2)	C19—C20—C21	120.4 (3)
C4—C5—C6	125.5 (3)	C19—C20—H20	119.8
N23—C1—C2	121.2 (3)	C21—C20—H20	119.8
N23—C1—C14	114.1 (3)	C19—C18—C17	120.6 (3)
C2—C1—C14	124.6 (3)	C19—C18—H18	119.7
C1—C2—C3	119.0 (3)	C17—C18—H18	119.7
C1—C2—H2	120.5	C10—C11—C12	120.1 (3)
C3—C2—H2	120.5	C10—C11—H11	120.0
C3—C4—C5	119.1 (3)	C12—C11—H11	120.0
C3—C4—H4	120.4	C16—C17—C18	119.8 (3)
C5—C4—H4	120.4	C16—C17—H17	120.1
C6—C7—H7A	109.5	C18—C17—H17	120.1
C6—C7—H7B	109.5	C18—C19—C20	119.7 (3)
H7A—C7—H7B	109.5	C18—C19—H19	120.2
C6—C7—H7C	109.5	C20—C19—H19	120.2

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C2—H2···Cl2ⁱ	0.93	2.67	3.545 (3)	156
C7—H7A···Cl1ⁱⁱ	0.96	2.76	3.663 (3)	158
C18—H18···Cl2ⁱⁱⁱ	0.93	2.83	3.714 (3)	160

Symmetry codes: (i) −x+1/2, y−1/2, −z+3/2; (ii) −x, −y, −z+1; (iii) −x+1, −y, −z+2.

Experimental details

Crystal data
Chemical formula	[CoCl₂(C₂₁H₁₉N₃)]
M_r	443.22
Crystal system, space group	Monoclinic, P2₁/n
Temperature (K)	273
a, b, c (Å)	10.4580 (3), 15.2575 (4), 13.1339 (3)
β (°)	95.825 (1)
V (Å³)	2084.86 (9)
Z	4
Radiation type	Mo Kα
µ (mm⁻¹)	1.09
Crystal size (mm)	0.36 × 0.30 × 0.28

Data collection
Diffractometer	Bruker SMART CCD area-detector diffractometer
Absorption correction	–
No. of measured, independent and observed [I > 2σ(I)] reflections	11050, 3665, 2594
R_int	0.046
(sin θ/λ)_max (Å⁻¹)	0.595

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.036, 0.075, 1.01
No. of reflections	3665
No. of parameters	246
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.28, −0.26

Computer programs: SMART (Bruker, 2004), SAINT (Bruker, 2004), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008).

Selected geometric parameters (Å, º) top

Co1—N23	2.027 (2)	Co1—Cl2	2.2572 (8)
Co1—N24	2.208 (2)	Co1—Cl1	2.2638 (8)
Co1—N22	2.223 (2)

N23—Co1—N24	75.36 (8)	N22—Co1—Cl2	98.36 (6)
N23—Co1—N22	75.38 (8)	N23—Co1—Cl1	123.81 (6)
N24—Co1—N22	150.74 (9)	N24—Co1—Cl1	96.23 (6)
N23—Co1—Cl2	119.07 (6)	N22—Co1—Cl1	99.58 (6)
N24—Co1—Cl2	96.11 (6)	Cl2—Co1—Cl1	117.03 (3)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C2—H2···Cl2ⁱ	0.93	2.67	3.545 (3)	156
C7—H7A···Cl1ⁱⁱ	0.96	2.76	3.663 (3)	158
C18—H18···Cl2ⁱⁱⁱ	0.93	2.83	3.714 (3)	160

Symmetry codes: (i) −x+1/2, y−1/2, −z+3/2; (ii) −x, −y, −z+1; (iii) −x+1, −y, −z+2.

References

Bruker (2004). SMART and SAINT Bruker AXS Inc., Madison, Wisconsin, USA. Google Scholar
Esteruelas, M. A., López, A. M., Méndez, L., Olivá, M. & Ońate, E. (2003). Organometallics, 22, 395–406. Web of Science CSD CrossRef CAS Google Scholar
Gibson, V. C., Humphries, M. J., Tellmann, K. P., Wass, D. F., White, A. J. P. & Williams, D. J. (2001). Chem. Commun. 21, 2252–2253. Web of Science CSD CrossRef Google Scholar
Mentes, A., Fawcett, J. & Kemmitt, R. D. W. (2001). Acta Cryst. E57, o424–o425. Web of Science CSD CrossRef IUCr Journals Google Scholar
Pradhan, R., Desplanches, C., Guionneau, P. & Sutter, J.-P. (2003). Inorg. Chem. 42, 6607–6609. Web of Science CSD CrossRef PubMed CAS Google Scholar
Reardon, D., Aharonian, G., Gambarotta, S. & Yap, G. P. A. (2002). Organometallics, 21, 786–788. Web of Science CSD CrossRef CAS Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Trivedi, M., Pandey, D. S. & Xu, Q. (2007). Inorg. Chim. Acta, 360, 2492–2498. Web of Science CSD CrossRef CAS Google Scholar

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Volume 64| Part 6| June 2008| Page m786

doi:10.1107/S1600536808013007

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