Synthesis and crystal structure of catena-poly[cobalt(II)-di-μ-chlorido-μ-pyridazine-κ2N1:N2]

Näther, C.; Jess, I.

doi:10.1107/S2056989023007065

research communications

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ISSN: 2056-9890

Volume 79| Part 10| October 2023| Pages 872-876

https://doi.org/10.1107/S2056989023007065

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Synthesis and crystal structure of catena-poly[cobalt(II)-di-μ-chlorido-μ-pyridazine-κ²N¹:N²]

Christian Näther ^a ^* and Inke Jess ^a

^aInstitut für Anorganische Chemie, Universität Kiel, Max-Eyth.-Str. 2, 24118 Kiel, Germany
^*Correspondence e-mail: cnaether@ac.uni-kiel.de

Edited by W. T. A. Harrison, University of Aberdeen, United Kingdom (Received 7 August 2023; accepted 9 August 2023; online 8 September 2023)

The reaction of cobalt dichloride hexahydrate with pyridazine leads to the formation of crystals of the title compound, [CoCl₂(C₄H₄N₂)]_n. This compound is isotypic to a number of compounds with other divalent metal ions. Its asymmetric unit consists of a Co²⁺ atom (site symmetry 2/m), a chloride ion (site symmetry m) and a pyridazine molecule (all atoms with site symmetry m). The Co²⁺ cations are coordinated by four chloride anions and two pyridazine ligands, generating trans-CoN₄Cl₂ octahedra, and are linked into [010] chains by pairs of μ-1,1-bridging chloride anions and bridging pyridazine ligands. In the crystal structure, the pyridazine ligands of neighboring chains are stacked onto each other, indicating π–π interactions. Powder X-ray diffraction proves that a pure crystalline phase was obtained. Differential thermonalysis coupled to thermogravimetry (DTA–TG) reveal that decomposition is observed at about 710 K. Magnetic measurements indicate low-temperature metamagnetic behavior as already observed in a related compound.

Keywords: synthesis; crystal structure; one-dimensional coordination compound.

CCDC reference: 2287781

1. Chemical context

Mono-periodic coordination polymers have always attracted much interest because of their versatile physical properties (Leong & Vittal, 2011 ; Mas-Ballesté et al., 2010 ; Cernák et al., 2002 ; Chen & Suslick, 1993 ; Khlobystov et al., 2001 ). This includes mono-periodic coordination polymers, which can show a variety of different magnetic properties including single-chain magnetic behavior (Lescouëzec et al., 2005 ; Rams et al., 2020 ; Werner et al., 2015 ; Sun et al., 2010 ; Dhers et al., 2015 ). In this context, of interest are coordination polymers based on transition-metal halides in which the metal cations are linked by pairs of μ-1,1-bridging halide anions into chains. The most prominent cations such as Mn^II, Fe^II, Co^II or Ni^II are mostly octahedrally coordinated, which means that for the synthesis of compounds with chain structures, mono-coordinating ligands must be used and several such compounds have already been reported in the literature (Foner et al., 1975 , 1978 ; Qin et al., 2015 ; Zheng et al., 2010 ). Compounds with a chain structure may also be observed if ligands such as tetrazole or pyridazine derivatives are used, in which the nitrogen donor atoms are adjacent. In this case, the chain structure remains unchanged and the co-ligand bridges two neighboring metal cations within the chain (Ivashkevich et al., 2009 ; Masciocchi et al., 1994 ; Thomas & Ramanan, 2016 ). In this context, Masciocchi and coworkers have reported on compounds with the composition NiX₂(C₄H₄N₂) where C₄H₄N₂ = pyridazine (1,2-diazine) with X = Cl, Br that were structurally characterized by X-ray powder diffraction (Masciocchi et al., 1994). In these structures, the Ni^II cations are linked by pairs of halide anions into chains and within the chains, neighboring Ni^II cations are additionally bridged by the pyridazine ligands.

We are also interested in coordination polymers in which the metal cations are linked by small-sized anionic ligands into one- or two-dimensional networks. In the beginning, we investigated compounds based on Cu^I cations and halide anions with additional N-donor coligands because we have found that, upon heating, they lose their coligands in a stepwise manner and transform into new coligand-deficient compounds that show condensed copper–halide networks (Näther & Jess, 2004 ; Näther et al., 2001 , 2007 ). Later we found that this synthetic procedure can also be used for compounds with divalent cations such as Cd^II (Näther et al., 2017 ). In the course of this project, we also became interested in metal-halide compounds with paramagnetic metal cations and as part of these investigations, we reacted CoCl₂ with pyridazine and obtained a compound with the composition CoCl₂(C₄H₄N₂). No entry was found in the Cambridge Structural Database (CSD, version 5.43, last update March 2023; Groom et al., 2016 ) and therefore this compound was characterized by single-crystal X-ray diffraction. Later we found that this compound had already been characterized by X-ray powder diffraction and it was concluded that it is isotypic to its Ni^II counterpart (Masciocchi et al., 1994), which we found is the case.

2. Structural commentary

The reaction of CoCl₂·6H₂O with pyridazine in water in a sealed vessel at 388 K leads to the formation of single crystals of the title compound CoCl₂(C₄H₄N₂). This compound is isotypic to its Mn^II, Fe^II and Ni^II analogs with chloride and bromide as counter-anions, already reported in the literature (Masciocchi et al., 1994). The asymmetric unit consists of one cobalt(II) cation located at (1/4, 1/4, 1/4) on the intersection point of a twofold screw axis and a mirror plane (Wyckoff site 4c, site symmetry 2/m), as well as one chloride anion at (1/2, y, z) that is situated on a mirror plane on Wyckoff site 8h. The asymmetric unit also contains half a pyridazine ligand with all atoms located at (x, 1/4, z) on Wyckoff position 8i (m site symmetry): the complete C₄H₄N₂ ligand is generated by a second mirror plane at x = 1/2 (Fig. 1). The Co^II cations are octahedrally coordinated by four chloride anions and two pyridazine ligands and from the bond lengths and angles, it is obvious that the octahedra are slightly distorted (Table 1). The Co^II cations are linked by pairs of μ-1,1-bridging chloride anions into chains that propagate in the b-axis direction (Fig. 2). The pyridazine ligands also act as bridging ligands, each connecting two neighboring Co^II cations. Within the chains, all of the pyridazine ligands are coplanar. The intrachain Co⋯Co distance is 3.3443 (3) Å.

Table 1
Selected geometric parameters (Å, °)

Co1—N1	2.1282 (19)	Co1—Cl1	2.4626 (4)

N1—Co1—N1ⁱ	180.0	Cl1—Co1—Cl1ⁱ	180.0
N1—Co1—Cl1	87.21 (4)	Cl1—Co1—Cl1ⁱⁱ	83.66 (2)
N1ⁱ—Co1—Cl1	92.79 (4)	Cl1ⁱ—Co1—Cl1ⁱⁱ	96.34 (2)
Symmetry codes: (i) $[-x+{\script{1\over 2}}, -y+{\script{1\over 2}}, -z+{\script{1\over 2}}]$ ; (ii) $[-x+1, -y+{\script{1\over 2}}, z]$ .

Figure 1
Crystal structure of the title compound with labeling and displacement ellipsoids drawn at the 50% probability level. Symmetry codes for the generation of equivalent atoms: (i) −x + 1, $[{3\over 2}]$ − y, z; (ii) −x + 1, −y + 1, −z + 1; (iii) x, − $[{1\over 2}]$ + y, −z + 1.

Figure 2
Fragment of a [010] polymeric chain in the title compound.

3. Supramolecular features

In the crystal structure of the title compound, the chains propagate in the b-axis direction and are arranged in such a way that neighboring pyridazine ligands are perfectly stacked onto each other, forming columns along the crystallographic a axis (Fig. 3). The angle between two neighboring pyridazine ligands is 180° and the distance between their centroids is 3.6109 (1) Å (slippage = 0.264 Å), indicating π–π stacking interactions. One very weak C—H⋯Cl hydrogen bond (Table 2) is observed.

Table 2
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C2—H2⋯Cl1ⁱⁱⁱ	0.95	2.97	3.574 (2)	123
Symmetry code: (iii) $[x-{\script{1\over 2}}, y-{\script{1\over 2}}, z+{\script{1\over 2}}]$ .

Figure 3
Arrangement of the chains in the crystal structure of the title compound with view along the crystallographic a-axis direction.

4. Database survey

Many compounds of the general formula MX₂(C₄H₄N₂) (M = transition metal and X = halide anion have already been reported in the Cambridge Structural Database but there are no hits for cobalt. The compounds with NiCl₂ (CSD refcode POPCIG) and NiBr₂ (POPCOM) were structurally characterized by Rietveld refinements using laboratory X-ray powder diffraction data (Masciocchi et al., 1994). In this contribution, the compounds with Mn, Fe, Co, Cu and Zn with chloride and bromide as anions were also synthesized and from their powder patterns, the lattice parameters were determined, which indicate that the compounds with Mn, Fe and Co are isotypic to the Ni compounds; this is not the case for the compounds with Cu and Zn (Masciocchi et al., 1994). Our determination definitively proves that the title compound is isotypic to its Ni analog. The compounds MCl₂(C₄H₄N₂) with Mn (LANJEQ), Fe (LANJAM) were later determined by single-crystal X-ray diffraction, and their magnetic properties were also investigated (Yi et al., 2002 ).

With copper, additional compounds were investigated by single-crystal X-ray diffraction, including CuCl₂(C₄H₄N₂) (JEFFOS; Thomas & Ramanan, 2016) and CuBr₂(pyridiazine) (JEFFUY; Thomas & Ramanan, 2016). However, most compounds are reported with Cu^I, including CuI(C₄H₄N₂) (CAQXAT; Kromp & Sheldrick, 1999 , and CAQXAT01; Thomas & Ramanan, 2016), CuBr(C₄H₄N₂) (CAQXEX; Kromp & Sheldrick, 1999, and CAQXEX01 and 02; Thomas & Ramanan, 2016), Cu₂I₂(C₄H₄N₂) (CAQXIB; Kromp & Sheldrick, 1999), Cu₂Cl₂(C₄H₄N₂) (CAQXOH; Kromp & Sheldrick, 1999, and CAQXOH01 and 02; Thomas & Ramanan, 2016), two modifications of CuCl(C₄H₄N₂) (EKINOB and EKINUH; Näther & Jess, 2003 , and EKINUH01; Thomas & Ramanan, 2016), Cu₂Br₂(C₄H₄N₂) (EKIPAP; Näther & Jess, 2003, and EKIPAP01; Thomas & Ramanan, 2016).

With diamagnetic Zn^II, three compounds are reported, namely ZnI₂(C₄H₄N₂)₂ (MENSUU; Bhosekar et al., 2006a ), ZnBr₂(C₄H₄N₂)₂ (VEMBEV; Bhosekar et al., 2006b ) and three modifications of ZnCl₂(C₄H₄N₂)₂ (YAFYOU, YAFYOU01, YAFYOU02 and YAFYOU03; Pazderski et al., 2004a and Bhosekar et al., 2007 ). Finally, the Cd compounds CdCl₂(C₄H₄N₂) (AZABUY; Pazderski et al., 2004b ), CdBr₂(C₄H₄N₂) and CdI₂(C₄H₄N₂) have also been reported (refcodes to be assigned; Näther & Jess, 2023 ).

5. Physical characterization

The experimental powder pattern of the title compound agrees closely with that calculated from the single crystal data, which proves that a pure compound was obtained (Fig. S1). The thermal properties were investigated by differential thermoanalysis and thermogravimetry (DTA–TG) under an air atmosphere. Upon heating, only one mass loss is observed, which is accompanied by an endothermic event in the DTA curve (Fig. S2). The experimental mass loss of 27.4% is much lower than that calculated for the removal of one pyridazine ligand (38.2%), indicating that the pyridazine ligands are not completely removed. This is supported by the fact that the TG curve still decreases upon further heating. In the DTA curve, a successive endothermic and exothermic event is observed, which points to the decomposition of this compound (Fig. S2).

The title compounds were also characterized by magnetic measurements. The temperature dependence of the susceptibility was measured in the range 2–300 K under an applied magnetic field of 1000 Oe. Upon cooling, a maximum is observed at 3.0 K, indicating an antiferromagnetic transition (Fig. S3). The data were analyzed using a Curie–Weiss law, leading to a magnetic moment of 5.0 µ_B, which is higher than expected for a Co^II cation in a high-spin 3d⁷ configuration. The Weiss constant of −8 K suggests predominant antiferromagnetic interactions, but it must be kept in mind that these values are frequently too high because of the strong spin–orbit coupling of Co^II. Additional field-dependent measurements at 2 K indicate metamagnetic behavior with no saturation even at high fields, as previously observed for the linear chain compound CoCl₂(C₄H₄N₂)₂ (Fig. S4; Foner et al., 1975).

6. Synthesis and crystallization

Synthesis

CoCl₂·6H₂O and pyridazine were purchased from Sigma Aldrich and pyridazine from Alfa Aesar. All chemicals were used without further purification.

Pink-colored crystals were obtained by the reaction of 1 mmol of Co(NCS)₂ (237.9 mg) and 1 mmol (72 µl) of pyridazine in 1 ml of demineralized water. The reaction mixture was heated in a sealed glass vessel at 388 K for 2 d, leading to the formation of crystals suitable for single-crystal X-ray analysis. An IR spectrum of the title compound can be found in Fig. S5.

Experimental details

The IR spectrum was measured using an ATI Mattson Genesis Series FTIR Spectrometer, control software: WINFIRST, from ATI Mattson.

The PXRD measurement was performed with Cu Kα₁ radiation (λ = 1.540598 Å) using a Stoe Transmission Powder Diffraction System (STADI P) equipped with a MYTHEN 1K detector and a Johansson-type Ge(111) monochromator.

Thermogravimetry and differential thermoanalysis (TG–DTA) measurements were performed in a dynamic air atmosphere in Al₂O₃ crucibles using a STA-PT 1000 thermobalance from Linseis. The instrument was calibrated using standard reference materials.

Magnetic measurements were performed using a Quantum Design PPMS equipped with a 7 T magnet, using samples mounted in a gelatine capsule.

7. Refinement

Crystal data, data collection and structure refinement details are summarized in Table 3. The C—H hydrogen atoms were positioned with idealized geometry and refined as riding atoms with U_iso(H) = 1.2 U_eq(C).

Table 3
Experimental details

Crystal data
Chemical formula	[CoCl₂(C₄H₄N₂)]
M_r	209.92
Crystal system, space group	Orthorhombic, Imma
Temperature (K)	100
a, b, c (Å)	6.6935 (1), 7.2024 (1), 12.7978 (2)
V (Å³)	616.97 (2)
Z	4
Radiation type	Cu Kα
μ (mm⁻¹)	28.91
Crystal size (mm)	0.1 × 0.08 × 0.08

Data collection
Diffractometer	XtaLAB Synergy, Dualflex, HyPix
Absorption correction	Multi-scan (CrysAlis PRO; Rigaku OD, 2022 $[Rigaku OD (2022). CrysAlis PRO. Rigaku Oxford Diffraction.]$ )
T_min, T_max	0.316, 1.000
No. of measured, independent and observed [I > 2σ(I)] reflections	3164, 395, 386
R_int	0.027
(sin θ/λ)_max (Å⁻¹)	0.639

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.020, 0.058, 1.07
No. of reflections	395
No. of parameters	30
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.64, −0.34
Computer programs: CrysAlis PRO (Rigaku OD, 2022 $[Rigaku OD (2022). CrysAlis PRO. Rigaku Oxford Diffraction.]$ ), SHELXT2014 (Sheldrick, 2015a ), SHELXL2016 (Sheldrick, 2015b ), DIAMOND (Brandenburg, 1999 ) and publCIF (Westrip, 2010 ).

Supporting information

CCDC reference: 2287781

Crystal structure: contains datablock I. DOI: https://doi.org/10.1107/S2056989023007065/hb8073sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S2056989023007065/hb8073Isup2.hkl

Fig. S1. Experimental (top) and calculated (bottom) powder pattern of the title compound. DOI: https://doi.org/10.1107/S2056989023007065/hb8073sup3.png

Fig. S2. DTG (top), TG (middle) and DTA curve (bottom) for the title compound measured with 8C in air atmosphere. DOI: https://doi.org/10.1107/S2056989023007065/hb8073sup4.png

Fig. S3. Magnetic susceptibility as function of temperature measured for the title compound at 1000 Oe. DOI: https://doi.org/10.1107/S2056989023007065/hb8073sup5.png

Fig. S4. Field dependence of the magnetization measured for the title compound at 2 K. DOI: https://doi.org/10.1107/S2056989023007065/hb8073sup6.png

Fig. S5. IR spectrum of the title compound. The wave numbers of the most prominent vibrations are given. DOI: https://doi.org/10.1107/S2056989023007065/hb8073sup7.png

checkCIF report

Computing details top

Data collection: CrysAlis PRO (Rigaku OD, 2022); cell refinement: CrysAlis PRO (Rigaku OD, 2022); data reduction: CrysAlis PRO (Rigaku OD, 2022); program(s) used to solve structure: SHELXT2014 (Sheldrick, 2015a); program(s) used to refine structure: SHELXL2016 (Sheldrick, 2015b); molecular graphics: DIAMOND (Brandenburg, 1999); software used to prepare material for publication: publCIF (Westrip, 2010).

catena-poly[cobalt(II)-di-µ-chlorido-µ-pyridazine-κ²N¹:N²] top

Crystal data top

[CoCl₂(C₄H₄N₂)]	D_x = 2.260 Mg m⁻³
M_r = 209.92	Cu Kα radiation, λ = 1.54184 Å
Orthorhombic, Imma	Cell parameters from 2503 reflections
a = 6.6935 (1) Å	θ = 6.9–78.2°
b = 7.2024 (1) Å	µ = 28.91 mm⁻¹
c = 12.7978 (2) Å	T = 100 K
V = 616.97 (2) Å³	Block, pink
Z = 4	0.1 × 0.08 × 0.08 mm
F(000) = 412

Data collection top

XtaLAB Synergy, Dualflex, HyPix diffractometer	395 independent reflections
Radiation source: micro-focus sealed X-ray tube, PhotonJet (Cu) X-ray Source	386 reflections with I > 2σ(I)
Mirror monochromator	R_int = 0.027
Detector resolution: 10.0000 pixels mm^-1	θ_max = 80.2°, θ_min = 6.9°
ω scans	h = −8→8
Absorption correction: multi-scan (CrysAlis PRO; Rigaku OD, 2022)	k = −8→8
T_min = 0.316, T_max = 1.000	l = −16→15
3164 measured reflections

Refinement top

Refinement on F²	Hydrogen site location: inferred from neighbouring sites
Least-squares matrix: full	H-atom parameters constrained
R[F² > 2σ(F²)] = 0.020	w = 1/[σ²(F_o²) + (0.039P)² + 0.9618P] where P = (F_o² + 2F_c²)/3
wR(F²) = 0.058	(Δ/σ)_max < 0.001
S = 1.07	Δρ_max = 0.64 e Å⁻³
395 reflections	Δρ_min = −0.34 e Å⁻³
30 parameters	Extinction correction: SHELXL2016 (Sheldrick, 2015b), Fc^*=kFc[1+0.001xFc²λ³/sin(2θ)]^-1/4
0 restraints	Extinction coefficient: 0.0016 (3)
Primary atom site location: dual

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²) top

	x	y	z	U_iso*/U_eq
Co1	0.250000	0.250000	0.250000	0.0069 (2)
Cl1	0.500000	0.47804 (8)	0.19118 (4)	0.0089 (2)
N1	0.3991 (3)	0.250000	0.39687 (15)	0.0082 (4)
C1	0.3025 (4)	0.250000	0.48765 (19)	0.0126 (5)
H1	0.160605	0.250000	0.486369	0.015*
C2	0.3973 (4)	0.250000	0.58452 (17)	0.0112 (5)
H2	0.323309	0.250000	0.647854	0.013*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Co1	0.0036 (3)	0.0111 (3)	0.0062 (3)	0.000	−0.00030 (17)	0.000
Cl1	0.0060 (3)	0.0108 (3)	0.0099 (3)	0.000	0.000	0.00073 (17)
N1	0.0052 (9)	0.0107 (9)	0.0087 (8)	0.000	0.0001 (7)	0.000
C1	0.0076 (11)	0.0184 (12)	0.0118 (11)	0.000	0.0020 (10)	0.000
C2	0.0103 (12)	0.0142 (11)	0.0090 (11)	0.000	−0.0005 (9)	0.000

Geometric parameters (Å, º) top

Co1—N1	2.1282 (19)	N1—C1	1.330 (3)
Co1—N1ⁱ	2.1282 (19)	N1—N1ⁱⁱ	1.350 (4)
Co1—Cl1	2.4626 (4)	C1—C2	1.393 (3)
Co1—Cl1ⁱ	2.4626 (4)	C1—H1	0.9500
Co1—Cl1ⁱⁱ	2.4626 (4)	C2—C2ⁱⁱ	1.374 (5)
Co1—Cl1ⁱⁱⁱ	2.4626 (4)	C2—H2	0.9500

N1—Co1—N1ⁱ	180.0	Cl1ⁱ—Co1—Cl1ⁱⁱⁱ	83.66 (2)
N1—Co1—Cl1	87.21 (4)	Cl1ⁱⁱ—Co1—Cl1ⁱⁱⁱ	180.0
N1ⁱ—Co1—Cl1	92.79 (4)	Co1—Cl1—Co1ⁱⁱ	85.611 (17)
N1—Co1—Cl1ⁱ	92.79 (4)	C1—N1—N1ⁱⁱ	119.10 (15)
N1ⁱ—Co1—Cl1ⁱ	87.21 (4)	C1—N1—Co1	122.93 (17)
Cl1—Co1—Cl1ⁱ	180.0	N1ⁱⁱ—N1—Co1	117.97 (5)
N1—Co1—Cl1ⁱⁱ	87.21 (4)	N1—C1—C2	123.8 (3)
N1ⁱ—Co1—Cl1ⁱⁱ	92.79 (4)	N1—C1—H1	118.1
Cl1—Co1—Cl1ⁱⁱ	83.66 (2)	C2—C1—H1	118.1
Cl1ⁱ—Co1—Cl1ⁱⁱ	96.34 (2)	C2ⁱⁱ—C2—C1	117.11 (16)
N1—Co1—Cl1ⁱⁱⁱ	92.79 (4)	C2ⁱⁱ—C2—H2	121.4
N1ⁱ—Co1—Cl1ⁱⁱⁱ	87.21 (4)	C1—C2—H2	121.4
Cl1—Co1—Cl1ⁱⁱⁱ	96.34 (2)

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

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C2—H2···Cl1^iv	0.95	2.97	3.574 (2)	123

Symmetry code: (iv) x−1/2, y−1/2, z+1/2.

Acknowledgements

Financial support by the State of Schleswig-Holstein is gratefully acknowledged.

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