Crystal structure of a mixed-ligand dinuclear Ba—Zn complex with 2-meth­oxy­ethanol having tri­phenyl­acetate and chloride bridges

Utko, J.; Sobocińska, M.; Dobrzyńska, D.; Lis, T.

doi:10.1107/S2056989015011226

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ISSN: 2056-9890

Volume 71| Part 7| July 2015| Pages 791-794

doi:10.1107/S2056989015011226

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Crystal structure of a mixed-ligand dinuclear Ba—Zn complex with 2-methoxyethanol having triphenylacetate and chloride bridges

Józef Utko,^a Maria Sobocińska,^a ^* Danuta Dobrzyńska ^b and Tadeusz Lis ^a

^aFaculty of Chemistry, University of Wrocław, 14 Joliot-Curie St, 50-383 Wrocław, Poland, and ^bFaculty of Chemistry, Wrocław University of Technology, 27 Wybrzeże Wyspiańskiego, 50-370 Wrocław, Poland
^*Correspondence e-mail: maria.sobocinska@chem.uni.wroc.pl

Edited by G. Smith, Queensland University of Technology, Australia (Received 29 April 2015; accepted 9 June 2015; online 17 June 2015)

The dinuclear barium–zinc complex, μ-chlorido-1:2κ²Cl:Cl-chlorido-2κCl-bis(2-methoxyethanol-1κO)bis(2-methoxyethanol-1κ²O,O′)bis(μ-triphenylacetato-1:2κ²O:O′)bariumzinc, [BaZn(C₂₀H₁₅O₂)₂Cl₂(C₃H₈O₂)₄], has been synthesized by the reaction of barium triphenylacetate, anhydrous zinc chloride and 2-methoxyethanol in the presence of toluene. The barium and zinc metal cations in the dinuclear complex are linked via one chloride anion and carboxylate O atoms of the triphenylacetate ligands, giving a Ba⋯Zn separation of 3.9335 (11) Å. The irregular nine-coordinate BaO₈Cl coordination centres comprise eight O-atom donors, six of them from 2-methoxyethanol ligands (four from two bidentate O,O′-chelate interactions and two from monodentate interactions), two from bridging triphenylacetate ligands and one from a bridging Cl donor. The distorted tetrahedral coordination sphere of zinc comprises two O-atom donors from the triphenylacetate ligands and two Cl donors (one bridging and one terminal). In the crystal, O—H⋯Cl, O—H⋯O and C—H⋯Cl intermolecular interactions form a layered structure, lying parallel to (001).

Keywords: crystal structure; Ba–Zn dinuclear complex; triphenylacetate ligand; 2-methoxyethanol; hydrogen bonding.

CCDC reference: 1405801

1. Chemical context

Only a few polynuclear heterometallic compounds containing barium and zinc connected by carboxylate bridges are known (Akine et al., 2006 , 2009 , 2010 ; Zhang et al., 2012 ; Bo et al., 2013 ). We have been studying the reactions of the triphenylacetate anion with metal salts and we have obtained several anhydrous polynuclear Mn^II triphenylacetate-containing clusters (Utko et al., 2014 ). The complexes with some metals (for example: Fe, Ni, Cu, Ru, Rh, Ag) are reported in the literature (Yamanaka et al., 1993 ; Cotton et al., 1994 ; Akhbari & Morsali, 2010 ; Barberis et al., 2001 ; Cadiou et al., 2002 ; Do & Lippard, 2011 ). However, among polynuclear complexes with triphenylacetate ligands, dinuclear Ba–Zn representatives have not previously been reported. In the present work, we aimed to create a mixed-ligand compound containing zinc and barium cations, using barium triphenylacetate as a means of displacing chlorine atoms from zinc chloride. This procedure for removal of chlorine using triphenylacetate was successfully carried out in a reaction leading to the formation of a mixed-metal complex with a [Ba₄Ti₂] core (Kosińska-Klähn et al., 2014 ). In the present paper we report the synthesis and structural characterization of a dinuclear Ba–Zn complex, namely μ-chlorido-1:2κ²Cl:Cl-chlorido-2κCl-bis(2-methoxyethanol-1κO)bis(2-methoxyethanol-1κ²O,O′)bis(μ-triphenylacetato-1:2κ²O:O′)bariumzinc, (I), and the structure is discussed herein.

2. Structural commentary

In the structure of (I), the asymmetric unit contains one dinuclear complex of [BaZn(Ph₃CCOO)₂(CH₃OCH₂CH₂OH)₄Cl₂] (Fig. 1), in which the dinuclear [BaZn]⁴⁺ cationic core is bridged by two carboxylate arms of the triphenylacetate ligands in a κ¹:κ¹:μ² coordination mode and by one bridging chlorine atom (μ₂-Cl). The Ba⋯Zn distance in the dinuclear complex is 3.9335 (11) Å. Oxygen atoms have the largest contribution to the filling of the coordination sphere of barium [Ba—O bond-length range, 2.6925 (19)– 2.985 (2) Å; Table 1]. Barium is bonded to one bridging chloride atom (μ₂-Cl), two O-atoms of two carboxylate groups and also to six O atoms from the 2-methoxyethanol ligands (four from two bidentate O,O¹-chelate interactions and two from monodentate interactions). 2-Methoxyethanol is coordinated only to the Ba²⁺ cation. The coordination mode is achieved in two different ways. Two terminal molecules representing an κ¹:κ¹ mode form two five-membered rings completed by the barium atom. Two other molecules of 2-methoxyethanol coordinate to Ba only through the hydroxyl O atoms.

Table 1
Selected bond lengths (Å)

Ba—O3	2.6925 (19)	Ba—O2G	2.985 (2)
Ba—O1	2.7073 (19)	Ba—Cl1	3.1118 (11)
Ba—O1J	2.7572 (19)	Zn—O2	1.9682 (17)
Ba—O1H	2.783 (2)	Zn—O4	1.9683 (18)
Ba—O2J	2.7908 (19)	Zn—Cl1	2.2595 (10)
Ba—O1G	2.799 (2)	Zn—Cl2	2.2653 (9)
Ba—O1I	2.810 (2)

Figure 1
The molecular structure of the title complex, with displacement ellipsoids drawn at the 50% probability level. Dashed lines represent intra-complex hydrogen bonds. C-bonded H atoms have been omitted for clarity.

Zinc is four-coordinated with a distorted tetrahedral ZnO₂Cl₂ stereochemistry (Table 1), with Zn—Cl1 (bridging) = 2.2595 (10) Å and Zn—Cl2 (monodentate) = 2.2653 (9) Å and Zn—O (both from the bridging triphenylacetate groups = 1.96817 (2) and 1.9683 (18) Å). A comparison with other structurally characterized mixed-metallic zinc–barium complexes reveals that the Zn–Cl–Ba linkage has been observed for the first time in the present compound. There are only a few compounds containing both of these metals and only one is a dimeric structure, with a distance between the atoms of 3.629 (2) Å, significantly shorter than in the title complex [3.9335 (11) Å], but zinc and barium are connected only via bridging oxygen atoms (μ₂-O) from organic ligands (Van Veggel et al., 1989 ). Also, in other structures without carboxylate bridges, the Zn⋯Ba distances are often much shorter than in the title complex with values in the range 3.4325 (5) to 4.850 (3) Å (Westerhausen et al., 2001 , 2006 ; Baggio et al., 2004 ; John et al., 2008 ). In those cases where the oxygen atom (μ₂-O) and also carboxylates connect zinc and barium, the Zn⋯Ba distance is not longer than 3.638 (1) Å (Akine et al., 2006, 2009, 2010). In a polymeric structure where zinc and barium cations are bridged via two carboxylate arms and also via one molecule of water, the distance between them is 4.0208 (5) Å (Zhang et al., 2012).

3. Supramolecular features

In the crystal, there are intramolecular O—H⋯O hydrogen bonds (Table 2). One is formed between a hydroxyl group O1I and an O-atom acceptor from the ether atom (O2H) of a 2-methoxyethanol ligand, the second is formed between a hydroxyl group O1H and an O-atom acceptor from a carboxyl group (O3) of a Ph₃CCOO⁻ ligand (Fig. 1). The presence of electronegative atoms (oxygen and chlorine) also leads to the occurrence of intermolecular hydrogen bonds in the crystal structure. The neighbouring dinuclear molecules interact through O—H⋯O, O—H⋯Cl and C—H⋯Cl hydrogen bonds. The first one occurs between the hydroxyl group O1G and an ether O-atom acceptor O2Iⁱ, the second occurs between the hydroxyl group O1J and the terminal chlorine atom Cl2ⁱⁱⁱ. In the third interaction, the H-donor atom is from a 2-methoxyethanol carbon (C2I), with the bridging chlorine atom (Cl1I)ⁱⁱ acting as the H-atom acceptor (for symmetry codes, see Table 2). A two-dimensional network structure is generated (Fig. 2), lying parallel to (001).

Table 2
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O1G—H1G⋯O2Iⁱ	0.84	1.91	2.728 (3)	163
O1I—H1I⋯O2H	0.84	1.99	2.817 (3)	170
C2I—H2I2⋯Cl1ⁱⁱ	0.99	2.81	3.660 (3)	144
O1J—H1J⋯Cl2ⁱⁱⁱ	0.84	2.17	3.012 (2)	174
Symmetry codes: (i) x-1, y, z; (ii) x+1, y, z; (iii) x, y+1, z.

Figure 2
Part of the crystal structure of the complex. Dashed lines represent intra- and intermolecular hydrogen bonds. C-bonded H atoms not involved in hydrogen bonding have been omitted for clarity. For symmetry codes, see Table 2

4. Synthesis and crystallization

For the preparation of Ba(Ph₃CCOO)₂, a mixture of metallic barium (0.521 g, 3.8 mmol), triphenylacetic acid (2.209 g, 7.66 mmol), C₆H₅CH₃ (50 ml) and THF (10 ml) was stirred at 363–373 K for 24 h until all the metal had reacted. The solution, which included a white precipitate, was concentrated to about 20 ml and then hexane (50 ml) was added while stirring, which led to further precipitation. The product was filtered on a Schlenk flask (yield: 2.520 g, 93.26%). Elemental analysis (%) calculated for Ba(Ph₃CCOO)₂: C 67.48, H 5.38, Ba 19.29; found: C 67.56, H 5.51, Ba 19.44. Solid ZnCl₂ (0.273 g, 2.0 mmol) and Ba(Ph₃CCOO)₂ (1.426 g, 2.0 mmol) were then added to a solution of CH₃OCH₂CH₂OH (30 ml) and C₆H₅CH₃ (15 ml) and the resulting mixture was stirred under a nitrogen atmosphere for 24 h. The solution was filtered and then concentrated to about 20 ml. Afterwards 20 ml of hexane was funneled into the reaction solution, leading to the creation of two layers and the mixture was left to crystallize at room temperature. After one week, colorless crystals suitable for the X-ray experiment were obtained (1.289 g, yield: 55.83%). Knowledge of the molecular structure of the final product enables representation of the chemical equation for the reaction as: ZnCl₂ + Ba((C₆H₅)₃CCOO)₂ + 4 (CH₃OCH₂CH₂OH) → [BaZnCl₂[(C₆H₅)₃CCOO]₂(CH₃OCH₂CH₂OH)₄]. Elemental analysis: (%) calculated for the complex: C 54.14, H 5.38, Cl 6.3, Zn 5.67, Ba 11.91; found: C 52.94, H 5.67, Zn 5.48, Ba 11.24.

5. Refinement details

Crystal data, data collection and structure refinement details are summarized in Table 3. All C-bonded H atoms were positioned geometrically and treated as riding atoms: methyl H atoms were constrained to an ideal geometry, with C—H = 0.98 Å and U_iso(H) = 1.5U_eq(C); the remaining H atoms were afixed to C atoms, with Csp²—H = 0.95 Å and Csp³—H = 0.99 Å, and with U_iso(H) = 1.2U_eq(C). The locations of H atoms of the hydroxyl groups were determined from a difference-Fourier map and finally constrained to ride on their parent atoms, with O—H = 0.84 Å and U_iso(H) = 1.5U_eq(O).

Table 3
Experimental details

Crystal data
Chemical formula	[BaZn(C₂₀H₁₅O₂)₂Cl₂(C₃H₈O₂)₄]
M_r	1152.62
Crystal system, space group	Triclinic, P $[\overline{1}]$
Temperature (K)	100
a, b, c (Å)	9.706 (3), 10.643 (3), 25.073 (6)
α, β, γ (°)	89.62 (3), 89.26 (3), 82.73 (3)
V (Å³)	2569.0 (12)
Z	2
Radiation type	Mo Kα
μ (mm⁻¹)	1.39
Crystal size (mm)	0.31 × 0.23 × 0.21

Data collection
Diffractometer	Oxford Diffraction KM-4-CCD
Absorption correction	Analytical [CrysAlis RED (Oxford Diffraction, 2010 $[Oxford Diffraction (2010). CrysAlis CCD and CrysAlis RED. Oxford Diffraction Ltd., Yarnton, England.]$ ), based on expressions derived by Clark & Reid (1995 )]
T_min, T_max	0.687, 0.780
No. of measured, independent and observed [I > 2σ(I)] reflections	24098, 12296, 10742
R_int	0.025
(sin θ/λ)_max (Å⁻¹)	0.705

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.035, 0.100, 1.14
No. of reflections	12296
No. of parameters	617
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.89, −0.57
Computer programs: CrysAlis CCD and CrysAlis RED (Oxford Diffraction, 2010 $[Oxford Diffraction (2010). CrysAlis CCD and CrysAlis RED. Oxford Diffraction Ltd., Yarnton, England.]$ ), SHELXS97 and SHELXTL (Sheldrick, 2008 ) and SHELXL2013 (Sheldrick, 2015 ).

Supporting information

CCDC reference: 1405801

Crystal structure: contains datablocks I, publication_text. DOI: 10.1107/S2056989015011226/zs2332sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S2056989015011226/zs2332Isup2.hkl

checkCIF report

Chemical context top

\ Only a few polynuclear heterometallic compounds containing barium and zinc connected by carboxylate bridges are known (Akine et al., 2006, 2009, 2010; Zhang et al., 2012; Bo et al., 2013). We have been studying the reactions of the triphenylacetate anion with metal salts and we have obtained several anhydrous polynuclear Mn^II triphenylacetate-containing clusters (Utko et al., 2014). The complexes with some metals (for example: Fe, Ni, Cu, Ru, Rh, Ag) are reported in the literature (Yamanaka et al., 1993; Cotton et al., 1994; Akhbari & Morsali, 2010; Barberis et al., 2001; Cadiou et al., 2002; Do & Lippard, 2011). However, among polynuclear complexes with triphenylacetate ligands, Ba–Zn clusters have not previously been reported. In the present work, we aimed to create a mixed-ligand compound containing zinc and barium metals, using barium triphenylacetate as a means of displacing chlorine atoms from zinc chloride. This procedure for removal of chlorine using triphenylacetate was successfully carried out in a reaction leading to the formation of a mixed-metal complex with a [Ba₄Ti₂] core (Kosińska-Klähn et al., 2014). In the present paper we report the synthesis and structural characterization of a dinuclear Ba–Zn complex, namely µ-chlorido-1:2κ²Cl:Cl-chlorido-2κCl-bis(2-\ methoxyethanol-1κO)bis(2-methoxyethanol-1κ²O,O')\ bis(µ-triphenylacetato-1:2κ²O:O')bariumzinc, (I), and the structure is discussed herein.

Structural commentary top

In the structure of (I), the asymmetric unit contains one dinuclear complex of [BaZn(Ph₃CCOO)₂(CH₃OCH₂CH₂OH)₄Cl₂] (Fig. 1), in which the dinuclear [BaZn]⁴⁺ cationic core is bridged by two carboxylate arms of the triphenylacetate ligands in a η¹:η¹:µ² coordination mode and by one bridging chlorine atom (µ₂-Cl). To the best of our knowledge, the (µ₂-Cl) bridge between zinc and barium has been found for the first time in the structure of the title compound. The Ba···Zn distance in this dimer is 3.9335 (11) Å. Oxygen atoms have the largest contribution to the filling of the coordination sphere of barium [Ba—O bond-length range, 2.6925 (19)– 2.985 (2) Å; Table 1]. Barium is bonded to one bridging chloride atom (µ₂-Cl), two O-atoms of two carboxylate groups and also to six O atoms from the 2-methoxyethanol ligands (four from two bidentate O,O¹ chelate interactions and two from monodentate interactions). 2-Methoxyethanol is coordinated only to the Ba atom. The coordination mode is achieved in two different ways. Two terminal molecules representing an η¹:η¹ mode form two five-membered rings completed by the barium atom. Two other molecules of 2-methoxyethanol coordinate to Ba only through the hydroxyl O atoms.

Zinc is four-coordinated with a distorted tetrahedral ZnO₂Cl₂ stereochemistry (Table 1), with Zn—Cl1 (bridging) = 2.2595 (10) Å and Zn—Cl2 (monodentate) = 2.2653 (9) Å and Zn—O (both from the bridging triphenylacetate groups = 1.96817 (2) and 1.9683 (18) Å). A comparison with other structurally characterized mixed-metallic zinc–barium complexes reveals that the Zn–Cl–Ba linkage has been observed for the first time in the present compound. There are only a few compounds containing both of these metals and only one is a dinuclear structure, with a distance between the atoms of 3.629 (2) Å, significantly shorter than in the title complex [3.9335 (11) Å], but zinc and barium are connected only via bridging oxygen atoms (µ₂-O) from organic ligands (Van Veggel et al., 1989). Also, in other structures without carboxylate bridges, the Zn···Ba distances are often much shorter than in the title complex with values in the range 3.4325 (5) to 4.850 (3) Å (Westerhausen et al., 2001, 2006; Baggio et al., 2004; Łukasz et al., 2008). In those cases where the oxygen atom (µ₂-O) and also carboxylates connect zinc and barium, the Zn···Ba distance is not longer than 3.638 (1) Å (Akine et al., 2006, 2009, 2010). In a polymeric structure where zinc and barium atoms are bridged via two carboxylate arms and also via one molecule of water, the distance between them is 4.0208 (5) Å (Zhang et al., 2012).

Supramolecular features top

In the crystal, there are intramolecular O—H···O hydrogen bonds (Table 2). One is formed between a hydroxyl group O1I and an O-atom acceptor from the ether group (O2H) of a 2-methoxyethanol ligand, the second is formed between a hydroxyl group O1H and an O-atom acceptor from a carboxyl group (O3) of a Ph₃CCOO^- ligand (Fig. 2). The presence of electronegative atoms (oxygen and chlorine) also leads to the occurrence of intermolecular hydrogen bonds in the crystal structure. The neighbouring dinuclear molecules interact through O—H···O, O—H···Cl and C—H···Cl hydrogen bonds. The first one occurs between the hydroxyl group O1G and an ether O-atom acceptor O2Iⁱ, the second occurs between the hydroxyl group O1J and the terminal chlorine atom Cl2ⁱⁱⁱ. In the third interaction, the H-donor atom is from a 2-methoxyethanol carbon (C2I), with the bridging chlorine atom (Cl1I)ⁱⁱ acting as the H-atom acceptor (for symmetry codes, see Table 2). A two-dimensional network structure is generated (Fig. 3), lying parallel to (001).

Synthesis and crystallization top

For the preparation of Ba(Ph₃CCOO)₂, a mixture of metallic barium (0.521 g, 3.8 mmol), triphenylacetic acid (2.209 g, 7.66 mmol), C₆H₅CH₃ (50 ml) and THF (10 ml) was stirred at 363– 373 K for 24 hours until all the metal had reacted. The solution, which included a white precipitate, was concentrated to about 20 ml and then hexane (50 ml) was added while stirring, which led to further precipitation. The product was filtered on a Schlenk flask (yield: 2.520 g, 93.26%). Elemental analysis (%) calculated for Ba(Ph₃CCOO)₂: C 67.48, H 5.38, Ba 19.29; found: C 67.56, H 5.51, Ba 19.44. Solid ZnCl₂ (0.273 g, 2.0 mmol) and Ba(Ph₃CCOO)₂ (1.426 g, 2.0 mmol) were then added to a solution of CH₃OCH₂CH₂OH (30 ml) and C₆H₅CH₃ (15 ml) and the resulting mixture was stirred under a nitrogen atmosphere for 24 hours. The solution was filtered and then concentrated to about 20 ml. Afterwards 20 ml of hexane was funneled into the reaction solution, leading to the creation of two layers and the mixture was left to crystallize at room temperature. After one week, colorless crystals suitable for the X-ray experiment were obtained (1.289 g, yield: 55.83%). Knowledge of the molecular structure of the final product enables representation of the chemical equation for the reaction as: ZnCl₂ + Ba((C₆H₅)₃CCOO)₂ + 4 (CH₃OCH₂CH₂OH) → [BaZnCl₂((C₆H₅)₃CCOO)₂(CH₃OCH₂CH₂OH)₄]. Elemental analysis: (%) calculated for the complex: C 54.14, H 5.38, Cl 6.3, Zn 5.67, Ba 11.91; found: C 52.94, H 5.67, Zn 5.48, Ba 11.24.

Refinement details top

Related literature top

For related literature, see: Akhbari & Morsali (2010); Akine et al. (2006, 2009, 2010); Baggio et al. (2004); Barberis et al. (2001); Bo et al. (2013); Cadiou et al. (2002); Cotton et al. (1994); Do & Lippard (2011); Łukasz et al. (2008); Kosińska-Klähn, Łukasz, Drąg-Jarząbek, Utko, Petrus, Jerzykiewicz & Sobota (2014); Utko et al. (2014); Veggel et al. (1989); Westerhausen et al. (2001, 2006); Yamanaka et al. (1993); Zhang et al. (2012).

Computing details top

Data collection: CrysAlis CCD (Oxford Diffraction, 2010); cell refinement: CrysAlis CCD (Oxford Diffraction, 2010); data reduction: CrysAlis RED (Oxford Diffraction, 2010); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL2013 (Sheldrick, 2015); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXL2013 (Sheldrick, 2015).

Figures top

	Fig. 1. The molecular structure of the title complex, with displacement ellipsoids drawn at the 50% probability level. Dashed lines represent intra-complex hydrogen bonds. C-bonded H atoms have been omitted for clarity.
	Fig. 2. Part of the crystal structure of the complex. Dashed lines represent intra- and intermolecular hydrogen bonds. C-bonded H atoms not involved in hydrogen bonding have been omitted for clarity. For symmetry codes, see Table 2.

µ-Chlorido-1:2κ²Cl:Cl-chlorido-2κCl-bis(2-methoxyethanol-1κO)bis(2-methoxyethanol-1κ²O,O')bis(µ-triphenylacetato-1:2κ²O:O')bariumzinc top

Crystal data top

[BaZn(C₂₀H₁₅O₂)₂Cl₂(C₃H₈O₂)₄]	Z = 2
M_r = 1152.62	F(000) = 1180
Triclinic, P1	D_x = 1.490 Mg m⁻³
a = 9.706 (3) Å	Mo Kα radiation, λ = 0.71073 Å
b = 10.643 (3) Å	Cell parameters from 17769 reflections
c = 25.073 (6) Å	θ = 2–31°
α = 89.62 (3)°	µ = 1.39 mm⁻¹
β = 89.26 (3)°	T = 100 K
γ = 82.73 (3)°	Block, colorless
V = 2569.0 (12) Å³	0.31 × 0.23 × 0.21 mm

Data collection top

Oxford Diffraction KM-4-CCD diffractometer	10742 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tube	R_int = 0.025
ω scans	θ_max = 30.1°, θ_min = 2.8°
Absorption correction: analytical [CrysAlis RED (Oxford Diffraction, 2010), based on expressions derived by Clark & Reid (1995)]	h = −12→12
T_min = 0.687, T_max = 0.780	k = −13→13
24098 measured reflections	l = −33→35
12296 independent reflections

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)] = 0.035	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.100	H-atom parameters constrained
S = 1.14	w = 1/[σ²(F_o²) + (0.064P)²] where P = (F_o² + 2F_c²)/3
12296 reflections	(Δ/σ)_max = 0.001
617 parameters	Δρ_max = 0.89 e Å⁻³
0 restraints	Δρ_min = −0.57 e Å⁻³

Crystal data top

[BaZn(C₂₀H₁₅O₂)₂Cl₂(C₃H₈O₂)₄]	γ = 82.73 (3)°
M_r = 1152.62	V = 2569.0 (12) Å³
Triclinic, P1	Z = 2
a = 9.706 (3) Å	Mo Kα radiation
b = 10.643 (3) Å	µ = 1.39 mm⁻¹
c = 25.073 (6) Å	T = 100 K
α = 89.62 (3)°	0.31 × 0.23 × 0.21 mm
β = 89.26 (3)°

Data collection top

Oxford Diffraction KM-4-CCD diffractometer	12296 independent reflections
Absorption correction: analytical [CrysAlis RED (Oxford Diffraction, 2010), based on expressions derived by Clark & Reid (1995)]	10742 reflections with I > 2σ(I)
T_min = 0.687, T_max = 0.780	R_int = 0.025
24098 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.035	0 restraints
wR(F²) = 0.100	H-atom parameters constrained
S = 1.14	Δρ_max = 0.89 e Å⁻³
12296 reflections	Δρ_min = −0.57 e Å⁻³
617 parameters

Special details top

Experimental. The O-bonded H atoms were found from a difference-Fourier map. These H atoms were included in the refinement with constraint:;finally with instruction Afix 3.

Absorption correction: CrysAlis RED (Oxford Diffraction, 2010), employing an analytical numeric absorption correction using a multifaceted crystal model based on expressions derived by R.C. Clark & J.S. Reid (Clark & Reid, 1995).

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
Ba	0.13461 (2)	0.39066 (2)	0.25149 (2)	0.01587 (5)
Zn	0.09859 (3)	0.02666 (2)	0.25185 (2)	0.01406 (7)
Cl1	−0.07279 (6)	0.19070 (6)	0.25860 (3)	0.02295 (13)
Cl2	−0.00737 (6)	−0.14768 (6)	0.23751 (2)	0.02093 (12)
O1	0.24715 (19)	0.19812 (16)	0.31457 (7)	0.0202 (4)
O2	0.20140 (18)	−0.00059 (16)	0.31895 (6)	0.0178 (3)
C1	0.2527 (2)	0.0946 (2)	0.33730 (9)	0.0147 (4)
C2	0.3316 (2)	0.0704 (2)	0.39131 (9)	0.0131 (4)
C1A	0.3078 (2)	0.1863 (2)	0.42871 (9)	0.0141 (4)
C2A	0.3301 (3)	0.3070 (2)	0.41065 (9)	0.0196 (5)
H2A	0.3540	0.3190	0.3743	0.024*
C3A	0.3179 (3)	0.4090 (2)	0.44516 (10)	0.0238 (5)
H3A	0.3340	0.4900	0.4321	0.029*
C4A	0.2824 (3)	0.3948 (2)	0.49867 (10)	0.0247 (5)
H4A	0.2729	0.4654	0.5220	0.030*
C5A	0.2613 (3)	0.2763 (2)	0.51715 (10)	0.0222 (5)
H5A	0.2372	0.2648	0.5535	0.027*
C6A	0.2752 (3)	0.1736 (2)	0.48271 (9)	0.0180 (5)
H6A	0.2621	0.0923	0.4963	0.022*
C1B	0.2833 (2)	−0.0447 (2)	0.41952 (9)	0.0148 (4)
C2B	0.3746 (3)	−0.1460 (2)	0.43841 (9)	0.0175 (5)
H2B	0.4712	−0.1488	0.4311	0.021*
C3B	0.3268 (3)	−0.2436 (2)	0.46791 (10)	0.0217 (5)
H3B	0.3907	−0.3120	0.4805	0.026*
C4B	0.1867 (3)	−0.2410 (2)	0.47891 (10)	0.0233 (5)
H4B	0.1543	−0.3071	0.4993	0.028*
C5B	0.0933 (3)	−0.1414 (2)	0.46006 (10)	0.0208 (5)
H5B	−0.0033	−0.1393	0.4673	0.025*
C6B	0.1418 (3)	−0.0450 (2)	0.43054 (9)	0.0177 (5)
H6B	0.0773	0.0224	0.4175	0.021*
C1C	0.4882 (2)	0.0448 (2)	0.37655 (9)	0.0144 (4)
C2C	0.5884 (3)	0.0737 (2)	0.41205 (9)	0.0187 (5)
H2C	0.5599	0.1150	0.4446	0.022*
C3C	0.7289 (3)	0.0433 (2)	0.40100 (10)	0.0216 (5)
H3C	0.7955	0.0634	0.4259	0.026*
C4C	0.7723 (3)	−0.0164 (3)	0.35348 (10)	0.0233 (5)
H4C	0.8684	−0.0380	0.3458	0.028*
C5C	0.6735 (3)	−0.0441 (3)	0.31737 (10)	0.0256 (6)
H5C	0.7023	−0.0844	0.2847	0.031*
C6C	0.5329 (3)	−0.0136 (2)	0.32859 (10)	0.0203 (5)
H6C	0.4664	−0.0327	0.3034	0.024*
O3	0.2094 (2)	0.22740 (16)	0.17158 (7)	0.0244 (4)
O4	0.22946 (18)	0.02259 (16)	0.19108 (6)	0.0195 (4)
C3	0.2431 (3)	0.1152 (2)	0.16032 (9)	0.0167 (5)
C4	0.3131 (2)	0.0801 (2)	0.10490 (9)	0.0164 (4)
C1D	0.3201 (3)	0.2003 (2)	0.07098 (9)	0.0189 (5)
C2D	0.4423 (3)	0.2304 (3)	0.04765 (10)	0.0245 (5)
H2D	0.5275	0.1794	0.0551	0.029*
C3D	0.4417 (4)	0.3342 (3)	0.01355 (11)	0.0335 (7)
H3D	0.5264	0.3524	−0.0024	0.040*
C4D	0.3199 (4)	0.4111 (3)	0.00251 (12)	0.0355 (7)
H4D	0.3198	0.4817	−0.0208	0.043*
C5D	0.1979 (4)	0.3830 (3)	0.02615 (12)	0.0356 (7)
H5D	0.1133	0.4356	0.0194	0.043*
C6D	0.1978 (3)	0.2785 (3)	0.05973 (11)	0.0253 (5)
H6D	0.1128	0.2601	0.0753	0.030*
C1E	0.4604 (2)	0.0178 (2)	0.11792 (9)	0.0175 (5)
C2E	0.5232 (3)	−0.0894 (2)	0.09188 (9)	0.0201 (5)
H2E	0.4725	−0.1297	0.0663	0.024*
C3E	0.6595 (3)	−0.1387 (3)	0.10280 (10)	0.0248 (5)
H3E	0.7010	−0.2120	0.0845	0.030*
C4E	0.7351 (3)	−0.0822 (3)	0.13997 (11)	0.0281 (6)
H4E	0.8285	−0.1159	0.1470	0.034*
C5E	0.6736 (3)	0.0245 (3)	0.16711 (11)	0.0283 (6)
H5E	0.7244	0.0634	0.1931	0.034*
C6E	0.5379 (3)	0.0737 (3)	0.15608 (10)	0.0248 (5)
H6E	0.4964	0.1466	0.1747	0.030*
C1F	0.2325 (2)	−0.0103 (2)	0.07292 (9)	0.0167 (5)
C2F	0.2503 (3)	−0.0153 (3)	0.01745 (10)	0.0249 (5)
H2F	0.3067	0.0402	0.0005	0.030*
C3F	0.1875 (3)	−0.0990 (3)	−0.01334 (10)	0.0277 (6)
H3F	0.2015	−0.1000	−0.0509	0.033*
C4F	0.1055 (3)	−0.1806 (3)	0.00986 (11)	0.0296 (6)
H4F	0.0646	−0.2398	−0.0110	0.036*
C5F	0.0841 (3)	−0.1744 (3)	0.06440 (12)	0.0351 (7)
H5F	0.0253	−0.2285	0.0809	0.042*
C6F	0.1463 (3)	−0.0909 (3)	0.09569 (11)	0.0279 (6)
H6F	0.1298	−0.0890	0.1331	0.034*
O1G	−0.12372 (19)	0.54119 (18)	0.25180 (8)	0.0257 (4)
H1G	−0.1790	0.5348	0.2774	0.039*
C1G	−0.1947 (3)	0.5900 (3)	0.20479 (11)	0.0276 (6)
H1G1	−0.2228	0.6823	0.2081	0.033*
H1G2	−0.2792	0.5484	0.1996	0.033*
C2G	−0.0963 (3)	0.5630 (3)	0.15848 (12)	0.0299 (6)
H2G1	−0.1454	0.5896	0.1251	0.036*
H2G2	−0.0186	0.6142	0.1621	0.036*
O2G	−0.0411 (2)	0.43219 (19)	0.15458 (8)	0.0293 (4)
C3G	−0.1399 (4)	0.3533 (3)	0.13765 (13)	0.0390 (7)
H3G1	−0.2184	0.3603	0.1629	0.058*
H3G2	−0.0962	0.2652	0.1363	0.058*
H3G3	−0.1732	0.3802	0.1021	0.058*
O1H	0.2695 (2)	0.4717 (2)	0.16137 (8)	0.0352 (5)
H1H	0.2743	0.4048	0.1435	0.053*
C1H	0.3414 (4)	0.5586 (3)	0.13328 (13)	0.0425 (8)
H1H1	0.2929	0.5839	0.0996	0.051*
H1H2	0.4365	0.5188	0.1243	0.051*
C2H	0.3480 (4)	0.6720 (3)	0.16707 (13)	0.0366 (7)
H2H1	0.3783	0.7415	0.1452	0.044*
H2H2	0.2549	0.7013	0.1823	0.044*
O2H	0.4452 (2)	0.63873 (17)	0.20935 (8)	0.0255 (4)
C3H	0.4607 (3)	0.7504 (3)	0.23808 (13)	0.0328 (6)
H3H1	0.4842	0.8161	0.2132	0.049*
H3H2	0.5352	0.7320	0.2641	0.049*
H3H3	0.3735	0.7801	0.2568	0.049*
O1I	0.40709 (19)	0.43145 (18)	0.27599 (8)	0.0280 (4)
H1I	0.4267	0.4943	0.2583	0.042*
C1I	0.5361 (3)	0.3481 (3)	0.27592 (12)	0.0294 (6)
H1I1	0.5877	0.3600	0.2423	0.035*
H1I2	0.5162	0.2591	0.2773	0.035*
C2I	0.6245 (3)	0.3723 (3)	0.32224 (12)	0.0327 (6)
H2I1	0.5721	0.3626	0.3558	0.039*
H2I2	0.7083	0.3088	0.3224	0.039*
O2I	0.6661 (2)	0.4974 (2)	0.31999 (8)	0.0334 (5)
C3I	0.5953 (4)	0.5833 (4)	0.35674 (13)	0.0435 (8)
H3I1	0.4962	0.5968	0.3482	0.065*
H3I2	0.6334	0.6642	0.3546	0.065*
H3I3	0.6070	0.5485	0.3929	0.065*
O1J	0.1679 (2)	0.62932 (17)	0.28717 (7)	0.0235 (4)
H1J	0.1135	0.6889	0.2740	0.035*
C1J	0.1615 (3)	0.6484 (3)	0.34373 (11)	0.0279 (6)
H1J1	0.1530	0.7403	0.3513	0.033*
H1J2	0.2487	0.6079	0.3599	0.033*
C2J	0.0403 (3)	0.5938 (3)	0.36864 (11)	0.0273 (6)
H2J1	0.0414	0.6034	0.4079	0.033*
H2J2	−0.0479	0.6391	0.3552	0.033*
O2J	0.0511 (2)	0.46206 (17)	0.35502 (7)	0.0238 (4)
C3J	−0.0263 (3)	0.3905 (3)	0.38985 (11)	0.0300 (6)
H3J1	0.0141	0.3877	0.4255	0.045*
H3J2	−0.0234	0.3041	0.3762	0.045*
H3J3	−0.1229	0.4304	0.3918	0.045*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Ba	0.01883 (8)	0.01347 (8)	0.01522 (8)	−0.00166 (5)	−0.00076 (5)	−0.00073 (5)
Zn	0.01664 (14)	0.01436 (14)	0.01128 (12)	−0.00221 (10)	−0.00157 (10)	−0.00034 (9)
Cl1	0.0179 (3)	0.0180 (3)	0.0328 (3)	−0.0018 (2)	−0.0001 (2)	−0.0005 (2)
Cl2	0.0215 (3)	0.0179 (3)	0.0242 (3)	−0.0053 (2)	−0.0049 (2)	−0.0010 (2)
O1	0.0276 (9)	0.0181 (8)	0.0157 (8)	−0.0051 (7)	−0.0059 (7)	0.0044 (6)
O2	0.0229 (9)	0.0175 (8)	0.0136 (7)	−0.0042 (7)	−0.0039 (7)	−0.0004 (6)
C1	0.0158 (11)	0.0151 (11)	0.0127 (10)	0.0005 (8)	0.0001 (8)	−0.0002 (8)
C2	0.0152 (11)	0.0121 (10)	0.0123 (10)	−0.0030 (8)	−0.0005 (8)	0.0006 (8)
C1A	0.0126 (10)	0.0153 (11)	0.0144 (10)	−0.0010 (8)	−0.0017 (8)	−0.0021 (8)
C2A	0.0262 (13)	0.0184 (12)	0.0150 (10)	−0.0057 (10)	−0.0037 (9)	0.0002 (9)
C3A	0.0340 (15)	0.0139 (12)	0.0234 (12)	−0.0017 (10)	−0.0070 (11)	−0.0015 (9)
C4A	0.0302 (14)	0.0203 (13)	0.0227 (12)	0.0013 (10)	−0.0057 (11)	−0.0065 (10)
C5A	0.0237 (13)	0.0279 (13)	0.0149 (11)	−0.0028 (10)	−0.0008 (9)	−0.0042 (9)
C6A	0.0220 (12)	0.0181 (11)	0.0143 (10)	−0.0039 (9)	0.0004 (9)	−0.0018 (9)
C1B	0.0211 (12)	0.0128 (10)	0.0110 (9)	−0.0042 (9)	−0.0008 (8)	−0.0018 (8)
C2B	0.0221 (12)	0.0152 (11)	0.0152 (10)	−0.0018 (9)	−0.0033 (9)	−0.0012 (8)
C3B	0.0323 (14)	0.0147 (11)	0.0184 (11)	−0.0040 (10)	−0.0043 (10)	0.0012 (9)
C4B	0.0373 (15)	0.0184 (12)	0.0168 (11)	−0.0131 (11)	0.0029 (10)	0.0005 (9)
C5B	0.0230 (12)	0.0228 (12)	0.0183 (11)	−0.0097 (10)	0.0045 (9)	−0.0038 (9)
C6B	0.0196 (12)	0.0166 (11)	0.0162 (10)	0.0000 (9)	0.0012 (9)	−0.0021 (9)
C1C	0.0163 (11)	0.0136 (10)	0.0132 (10)	−0.0013 (8)	0.0016 (8)	0.0017 (8)
C2C	0.0203 (12)	0.0227 (12)	0.0132 (10)	−0.0032 (10)	0.0005 (9)	−0.0014 (9)
C3C	0.0178 (12)	0.0271 (13)	0.0203 (11)	−0.0046 (10)	−0.0033 (9)	0.0023 (10)
C4C	0.0151 (12)	0.0284 (14)	0.0255 (13)	−0.0003 (10)	0.0047 (10)	0.0026 (10)
C5C	0.0244 (13)	0.0321 (15)	0.0200 (12)	−0.0027 (11)	0.0071 (10)	−0.0068 (10)
C6C	0.0188 (12)	0.0251 (13)	0.0176 (11)	−0.0045 (10)	0.0009 (9)	−0.0061 (9)
O3	0.0364 (11)	0.0157 (9)	0.0210 (9)	−0.0033 (8)	0.0081 (8)	−0.0044 (7)
O4	0.0247 (9)	0.0196 (9)	0.0141 (8)	−0.0032 (7)	0.0025 (7)	0.0011 (6)
C3	0.0184 (11)	0.0199 (12)	0.0123 (10)	−0.0040 (9)	0.0000 (9)	0.0000 (8)
C4	0.0180 (11)	0.0159 (11)	0.0154 (10)	−0.0028 (9)	−0.0002 (9)	0.0007 (8)
C1D	0.0248 (13)	0.0197 (12)	0.0131 (10)	−0.0059 (10)	−0.0019 (9)	−0.0012 (9)
C2D	0.0304 (14)	0.0247 (13)	0.0199 (12)	−0.0092 (11)	0.0040 (10)	−0.0016 (10)
C3D	0.0497 (19)	0.0309 (15)	0.0241 (13)	−0.0219 (13)	0.0011 (13)	0.0016 (11)
C4D	0.061 (2)	0.0227 (14)	0.0263 (14)	−0.0173 (14)	−0.0104 (14)	0.0082 (11)
C5D	0.0477 (19)	0.0240 (14)	0.0355 (16)	−0.0046 (13)	−0.0183 (14)	0.0061 (12)
C6D	0.0279 (14)	0.0238 (13)	0.0243 (12)	−0.0033 (11)	−0.0052 (11)	0.0025 (10)
C1E	0.0178 (11)	0.0209 (12)	0.0139 (10)	−0.0038 (9)	0.0010 (9)	0.0019 (9)
C2E	0.0226 (13)	0.0230 (12)	0.0147 (10)	−0.0039 (10)	0.0004 (9)	0.0022 (9)
C3E	0.0239 (13)	0.0275 (14)	0.0221 (12)	0.0002 (11)	−0.0008 (10)	0.0024 (10)
C4E	0.0201 (13)	0.0392 (16)	0.0241 (13)	−0.0008 (11)	−0.0027 (10)	0.0097 (11)
C5E	0.0267 (14)	0.0383 (16)	0.0215 (12)	−0.0105 (12)	−0.0067 (11)	−0.0003 (11)
C6E	0.0246 (13)	0.0297 (14)	0.0213 (12)	−0.0077 (11)	−0.0010 (10)	−0.0029 (10)
C1F	0.0172 (11)	0.0178 (11)	0.0149 (10)	−0.0014 (9)	−0.0021 (9)	−0.0023 (8)
C2F	0.0316 (14)	0.0273 (14)	0.0173 (11)	−0.0092 (11)	0.0010 (10)	−0.0006 (10)
C3F	0.0324 (15)	0.0331 (15)	0.0179 (12)	−0.0053 (12)	−0.0009 (11)	−0.0021 (10)
C4F	0.0280 (14)	0.0361 (16)	0.0270 (13)	−0.0120 (12)	−0.0045 (11)	−0.0082 (11)
C5F	0.0407 (17)	0.0426 (18)	0.0274 (14)	−0.0269 (14)	0.0036 (13)	−0.0037 (12)
C6F	0.0339 (15)	0.0336 (15)	0.0189 (12)	−0.0143 (12)	0.0023 (11)	−0.0029 (10)
O1G	0.0219 (9)	0.0263 (10)	0.0283 (10)	−0.0015 (7)	−0.0003 (8)	0.0034 (8)
C1G	0.0227 (13)	0.0237 (13)	0.0357 (15)	0.0000 (11)	−0.0055 (11)	0.0048 (11)
C2G	0.0265 (14)	0.0283 (14)	0.0341 (15)	−0.0010 (11)	−0.0035 (12)	0.0108 (11)
O2G	0.0281 (10)	0.0294 (10)	0.0291 (10)	0.0013 (8)	−0.0033 (8)	0.0011 (8)
C3G	0.0416 (18)	0.0429 (18)	0.0327 (16)	−0.0052 (14)	−0.0105 (14)	−0.0042 (13)
O1H	0.0540 (14)	0.0334 (11)	0.0229 (10)	−0.0244 (10)	0.0042 (9)	−0.0042 (8)
C1H	0.056 (2)	0.049 (2)	0.0284 (15)	−0.0296 (17)	0.0075 (14)	−0.0014 (13)
C2H	0.0457 (19)	0.0329 (16)	0.0339 (16)	−0.0152 (14)	−0.0050 (14)	0.0050 (12)
O2H	0.0266 (10)	0.0213 (9)	0.0286 (10)	−0.0032 (7)	−0.0051 (8)	−0.0014 (7)
C3H	0.0376 (17)	0.0208 (14)	0.0404 (16)	−0.0056 (12)	0.0005 (13)	−0.0063 (12)
O1I	0.0222 (10)	0.0286 (10)	0.0338 (10)	−0.0052 (8)	−0.0057 (8)	0.0094 (8)
C1I	0.0243 (14)	0.0274 (14)	0.0356 (15)	−0.0003 (11)	0.0037 (11)	−0.0007 (11)
C2I	0.0244 (14)	0.0381 (17)	0.0343 (15)	0.0004 (12)	−0.0005 (12)	0.0103 (13)
O2I	0.0245 (10)	0.0441 (13)	0.0321 (11)	−0.0066 (9)	0.0032 (8)	−0.0031 (9)
C3I	0.046 (2)	0.055 (2)	0.0287 (15)	−0.0026 (16)	−0.0039 (14)	−0.0069 (14)
O1J	0.0294 (10)	0.0184 (9)	0.0221 (9)	0.0001 (7)	−0.0021 (8)	−0.0024 (7)
C1J	0.0347 (15)	0.0243 (14)	0.0251 (13)	−0.0052 (11)	−0.0037 (11)	−0.0033 (10)
C2J	0.0327 (15)	0.0253 (14)	0.0231 (12)	−0.0003 (11)	0.0020 (11)	−0.0073 (10)
O2J	0.0286 (10)	0.0231 (9)	0.0194 (8)	−0.0025 (8)	0.0035 (7)	0.0005 (7)
C3J	0.0266 (14)	0.0391 (16)	0.0253 (13)	−0.0084 (12)	0.0014 (11)	0.0032 (11)

Geometric parameters (Å, º) top

Ba—O3	2.6925 (19)	C1E—C2E	1.387 (3)
Ba—O1	2.7073 (19)	C1E—C6E	1.405 (3)
Ba—O1J	2.7572 (19)	C2E—C3E	1.389 (4)
Ba—O1H	2.783 (2)	C2E—H2E	0.9500
Ba—O2J	2.7908 (19)	C3E—C4E	1.381 (4)
Ba—O1G	2.799 (2)	C3E—H3E	0.9500
Ba—O1I	2.810 (2)	C4E—C5E	1.392 (4)
Ba—O2G	2.985 (2)	C4E—H4E	0.9500
Ba—Cl1	3.1118 (11)	C5E—C6E	1.385 (4)
Ba—Zn	3.9335 (11)	C5E—H5E	0.9500
Zn—O2	1.9682 (17)	C6E—H6E	0.9500
Zn—O4	1.9683 (18)	C1F—C6F	1.388 (4)
Zn—Cl1	2.2595 (10)	C1F—C2F	1.400 (3)
Zn—Cl2	2.2653 (9)	C2F—C3F	1.386 (4)
O1—C1	1.233 (3)	C2F—H2F	0.9500
O2—C1	1.275 (3)	C3F—C4F	1.372 (4)
C1—C2	1.568 (3)	C3F—H3F	0.9500
C2—C1B	1.531 (3)	C4F—C5F	1.381 (4)
C2—C1A	1.547 (3)	C4F—H4F	0.9500
C2—C1C	1.550 (3)	C5F—C6F	1.388 (4)
C1A—C6A	1.396 (3)	C5F—H5F	0.9500
C1A—C2A	1.401 (3)	C6F—H6F	0.9500
C2A—C3A	1.385 (3)	O1G—C1G	1.434 (3)
C2A—H2A	0.9500	O1G—H1G	0.8397
C3A—C4A	1.393 (4)	C1G—C2G	1.500 (4)
C3A—H3A	0.9500	C1G—H1G1	0.9900
C4A—C5A	1.380 (4)	C1G—H1G2	0.9900
C4A—H4A	0.9500	C2G—O2G	1.431 (3)
C5A—C6A	1.390 (3)	C2G—H2G1	0.9900
C5A—H5A	0.9500	C2G—H2G2	0.9900
C6A—H6A	0.9500	O2G—C3G	1.422 (4)
C1B—C2B	1.391 (3)	C3G—H3G1	0.9800
C1B—C6B	1.397 (3)	C3G—H3G2	0.9800
C2B—C3B	1.394 (3)	C3G—H3G3	0.9800
C2B—H2B	0.9500	O1H—C1H	1.407 (4)
C3B—C4B	1.381 (4)	O1H—H1H	0.8402
C3B—H3B	0.9500	C1H—C2H	1.487 (4)
C4B—C5B	1.389 (4)	C1H—H1H1	0.9900
C4B—H4B	0.9500	C1H—H1H2	0.9900
C5B—C6B	1.388 (3)	C2H—O2H	1.440 (4)
C5B—H5B	0.9500	C2H—H2H1	0.9900
C6B—H6B	0.9500	C2H—H2H2	0.9900
C1C—C2C	1.390 (3)	O2H—C3H	1.419 (3)
C1C—C6C	1.396 (3)	C3H—H3H1	0.9800
C2C—C3C	1.386 (3)	C3H—H3H2	0.9800
C2C—H2C	0.9500	C3H—H3H3	0.9800
C3C—C4C	1.390 (4)	O1I—C1I	1.440 (3)
C3C—H3C	0.9500	O1I—H1I	0.8399
C4C—C5C	1.387 (4)	C1I—C2I	1.496 (4)
C4C—H4C	0.9500	C1I—H1I1	0.9900
C5C—C6C	1.388 (4)	C1I—H1I2	0.9900
C5C—H5C	0.9500	C2I—O2I	1.439 (4)
C6C—H6C	0.9500	C2I—H2I1	0.9900
O3—C3	1.232 (3)	C2I—H2I2	0.9900
O4—C3	1.266 (3)	O2I—C3I	1.412 (4)
C3—C4	1.565 (3)	C3I—H3I1	0.9800
C4—C1E	1.536 (3)	C3I—H3I2	0.9800
C4—C1D	1.540 (3)	C3I—H3I3	0.9800
C4—C1F	1.549 (3)	O1J—C1J	1.433 (3)
C1D—C2D	1.388 (4)	O1J—H1J	0.8403
C1D—C6D	1.391 (4)	C1J—C2J	1.503 (4)
C2D—C3D	1.392 (4)	C1J—H1J1	0.9900
C2D—H2D	0.9500	C1J—H1J2	0.9900
C3D—C4D	1.380 (5)	C2J—O2J	1.436 (3)
C3D—H3D	0.9500	C2J—H2J1	0.9900
C4D—C5D	1.383 (5)	C2J—H2J2	0.9900
C4D—H4D	0.9500	O2J—C3J	1.424 (3)
C5D—C6D	1.390 (4)	C3J—H3J1	0.9800
C5D—H5D	0.9500	C3J—H3J2	0.9800
C6D—H6D	0.9500	C3J—H3J3	0.9800

O3—Ba—O1	84.08 (6)	C4D—C3D—H3D	119.5
O3—Ba—O1J	142.04 (6)	C2D—C3D—H3D	119.5
O1—Ba—O1J	114.85 (6)	C3D—C4D—C5D	118.6 (3)
O3—Ba—O1H	60.16 (6)	C3D—C4D—H4D	120.7
O1—Ba—O1H	122.95 (7)	C5D—C4D—H4D	120.7
O1J—Ba—O1H	82.35 (6)	C4D—C5D—C6D	120.7 (3)
O3—Ba—O2J	155.84 (6)	C4D—C5D—H5D	119.7
O1—Ba—O2J	74.87 (6)	C6D—C5D—H5D	119.7
O1J—Ba—O2J	60.31 (6)	C5D—C6D—C1D	121.2 (3)
O1H—Ba—O2J	142.49 (6)	C5D—C6D—H6D	119.4
O3—Ba—O1G	120.96 (6)	C1D—C6D—H6D	119.4
O1—Ba—O1G	133.04 (6)	C2E—C1E—C6E	118.1 (2)
O1J—Ba—O1G	71.05 (6)	C2E—C1E—C4	122.6 (2)
O1H—Ba—O1G	103.93 (7)	C6E—C1E—C4	119.3 (2)
O2J—Ba—O1G	68.94 (6)	C1E—C2E—C3E	120.8 (2)
O3—Ba—O1I	95.18 (7)	C1E—C2E—H2E	119.6
O1—Ba—O1I	71.58 (6)	C3E—C2E—H2E	119.6
O1J—Ba—O1I	63.80 (6)	C4E—C3E—C2E	120.7 (3)
O1H—Ba—O1I	69.50 (7)	C4E—C3E—H3E	119.7
O2J—Ba—O1I	89.38 (6)	C2E—C3E—H3E	119.7
O1G—Ba—O1I	134.83 (6)	C3E—C4E—C5E	119.6 (3)
O3—Ba—O2G	65.59 (6)	C3E—C4E—H4E	120.2
O1—Ba—O2G	139.45 (6)	C5E—C4E—H4E	120.2
O1J—Ba—O2G	105.51 (6)	C6E—C5E—C4E	119.7 (3)
O1H—Ba—O2G	64.98 (6)	C6E—C5E—H5E	120.2
O2J—Ba—O2G	125.48 (6)	C4E—C5E—H5E	120.2
O1G—Ba—O2G	57.15 (6)	C5E—C6E—C1E	121.2 (3)
O1I—Ba—O2G	134.31 (6)	C5E—C6E—H6E	119.4
O3—Ba—Cl1	74.73 (5)	C1E—C6E—H6E	119.4
O1—Ba—Cl1	71.96 (5)	C6F—C1F—C2F	117.0 (2)
O1J—Ba—Cl1	140.95 (4)	C6F—C1F—C4	124.4 (2)
O1H—Ba—Cl1	128.16 (5)	C2F—C1F—C4	118.6 (2)
O2J—Ba—Cl1	87.39 (5)	C3F—C2F—C1F	121.7 (2)
O1G—Ba—Cl1	77.39 (5)	C3F—C2F—H2F	119.2
O1I—Ba—Cl1	142.95 (4)	C1F—C2F—H2F	119.2
O2G—Ba—Cl1	74.38 (5)	C4F—C3F—C2F	120.7 (2)
O3—Ba—Zn	53.90 (4)	C4F—C3F—H3F	119.6
O1—Ba—Zn	48.34 (4)	C2F—C3F—H3F	119.6
O1J—Ba—Zn	160.81 (4)	C3F—C4F—C5F	118.2 (3)
O1H—Ba—Zn	113.88 (5)	C3F—C4F—H4F	120.9
O2J—Ba—Zn	102.37 (5)	C5F—C4F—H4F	120.9
O1G—Ba—Zn	112.26 (5)	C4F—C5F—C6F	121.6 (3)
O1I—Ba—Zn	110.85 (5)	C4F—C5F—H5F	119.2
O2G—Ba—Zn	91.21 (5)	C6F—C5F—H5F	119.2
Cl1—Ba—Zn	35.01 (2)	C1F—C6F—C5F	120.7 (2)
O2—Zn—O4	110.00 (8)	C1F—C6F—H6F	119.6
O2—Zn—Cl1	111.30 (6)	C5F—C6F—H6F	119.6
O4—Zn—Cl1	118.74 (6)	C1G—O1G—Ba	124.47 (16)
O2—Zn—Cl2	107.44 (6)	C1G—O1G—H1G	111.8
O4—Zn—Cl2	102.14 (6)	Ba—O1G—H1G	119.0
Cl1—Zn—Cl2	106.19 (3)	O1G—C1G—C2G	107.4 (2)
O2—Zn—Ba	91.95 (6)	O1G—C1G—H1G1	110.2
O4—Zn—Ba	83.59 (6)	C2G—C1G—H1G1	110.2
Cl1—Zn—Ba	52.20 (3)	O1G—C1G—H1G2	110.2
Cl2—Zn—Ba	156.02 (2)	C2G—C1G—H1G2	110.2
Zn—Cl1—Ba	92.79 (3)	H1G1—C1G—H1G2	108.5
C1—O1—Ba	155.72 (16)	O2G—C2G—C1G	113.0 (2)
C1—O2—Zn	116.35 (15)	O2G—C2G—H2G1	109.0
O1—C1—O2	124.3 (2)	C1G—C2G—H2G1	109.0
O1—C1—C2	120.6 (2)	O2G—C2G—H2G2	109.0
O2—C1—C2	115.06 (19)	C1G—C2G—H2G2	109.0
C1B—C2—C1A	109.37 (18)	H2G1—C2G—H2G2	107.8
C1B—C2—C1C	110.82 (18)	C3G—O2G—C2G	113.5 (2)
C1A—C2—C1C	108.82 (18)	C3G—O2G—Ba	125.66 (17)
C1B—C2—C1	109.40 (18)	C2G—O2G—Ba	102.89 (15)
C1A—C2—C1	112.19 (18)	O2G—C3G—H3G1	109.5
C1C—C2—C1	106.20 (17)	O2G—C3G—H3G2	109.5
C6A—C1A—C2A	117.2 (2)	H3G1—C3G—H3G2	109.5
C6A—C1A—C2	121.6 (2)	O2G—C3G—H3G3	109.5
C2A—C1A—C2	121.0 (2)	H3G1—C3G—H3G3	109.5
C3A—C2A—C1A	120.8 (2)	H3G2—C3G—H3G3	109.5
C3A—C2A—H2A	119.6	C1H—O1H—Ba	152.75 (18)
C1A—C2A—H2A	119.6	C1H—O1H—H1H	108.3
C2A—C3A—C4A	121.1 (2)	Ba—O1H—H1H	98.5
C2A—C3A—H3A	119.5	O1H—C1H—C2H	109.1 (3)
C4A—C3A—H3A	119.5	O1H—C1H—H1H1	109.9
C5A—C4A—C3A	118.8 (2)	C2H—C1H—H1H1	109.9
C5A—C4A—H4A	120.6	O1H—C1H—H1H2	109.9
C3A—C4A—H4A	120.6	C2H—C1H—H1H2	109.9
C4A—C5A—C6A	120.2 (2)	H1H1—C1H—H1H2	108.3
C4A—C5A—H5A	119.9	O2H—C2H—C1H	108.8 (3)
C6A—C5A—H5A	119.9	O2H—C2H—H2H1	109.9
C5A—C6A—C1A	121.9 (2)	C1H—C2H—H2H1	109.9
C5A—C6A—H6A	119.0	O2H—C2H—H2H2	109.9
C1A—C6A—H6A	119.0	C1H—C2H—H2H2	109.9
C2B—C1B—C6B	117.7 (2)	H2H1—C2H—H2H2	108.3
C2B—C1B—C2	123.1 (2)	C3H—O2H—C2H	108.2 (2)
C6B—C1B—C2	119.1 (2)	O2H—C3H—H3H1	109.5
C1B—C2B—C3B	121.2 (2)	O2H—C3H—H3H2	109.5
C1B—C2B—H2B	119.4	H3H1—C3H—H3H2	109.5
C3B—C2B—H2B	119.4	O2H—C3H—H3H3	109.5
C4B—C3B—C2B	120.1 (2)	H3H1—C3H—H3H3	109.5
C4B—C3B—H3B	119.9	H3H2—C3H—H3H3	109.5
C2B—C3B—H3B	119.9	C1I—O1I—Ba	131.91 (16)
C3B—C4B—C5B	119.8 (2)	C1I—O1I—H1I	103.1
C3B—C4B—H4B	120.1	Ba—O1I—H1I	108.4
C5B—C4B—H4B	120.1	O1I—C1I—C2I	111.8 (2)
C6B—C5B—C4B	119.6 (2)	O1I—C1I—H1I1	109.3
C6B—C5B—H5B	120.2	C2I—C1I—H1I1	109.3
C4B—C5B—H5B	120.2	O1I—C1I—H1I2	109.3
C5B—C6B—C1B	121.6 (2)	C2I—C1I—H1I2	109.3
C5B—C6B—H6B	119.2	H1I1—C1I—H1I2	107.9
C1B—C6B—H6B	119.2	O2I—C2I—C1I	111.8 (2)
C2C—C1C—C6C	118.1 (2)	O2I—C2I—H2I1	109.3
C2C—C1C—C2	120.7 (2)	C1I—C2I—H2I1	109.3
C6C—C1C—C2	121.0 (2)	O2I—C2I—H2I2	109.3
C3C—C2C—C1C	121.4 (2)	C1I—C2I—H2I2	109.3
C3C—C2C—H2C	119.3	H2I1—C2I—H2I2	107.9
C1C—C2C—H2C	119.3	C3I—O2I—C2I	114.1 (3)
C2C—C3C—C4C	120.0 (2)	O2I—C3I—H3I1	109.5
C2C—C3C—H3C	120.0	O2I—C3I—H3I2	109.5
C4C—C3C—H3C	120.0	H3I1—C3I—H3I2	109.5
C5C—C4C—C3C	119.2 (2)	O2I—C3I—H3I3	109.5
C5C—C4C—H4C	120.4	H3I1—C3I—H3I3	109.5
C3C—C4C—H4C	120.4	H3I2—C3I—H3I3	109.5
C4C—C5C—C6C	120.6 (2)	C1J—O1J—Ba	116.81 (15)
C4C—C5C—H5C	119.7	C1J—O1J—H1J	105.9
C6C—C5C—H5C	119.7	Ba—O1J—H1J	115.3
C5C—C6C—C1C	120.7 (2)	O1J—C1J—C2J	111.5 (2)
C5C—C6C—H6C	119.7	O1J—C1J—H1J1	109.3
C1C—C6C—H6C	119.7	C2J—C1J—H1J1	109.3
C3—O3—Ba	144.65 (16)	O1J—C1J—H1J2	109.3
C3—O4—Zn	125.09 (16)	C2J—C1J—H1J2	109.3
O3—C3—O4	125.0 (2)	H1J1—C1J—H1J2	108.0
O3—C3—C4	119.3 (2)	O2J—C2J—C1J	108.4 (2)
O4—C3—C4	115.6 (2)	O2J—C2J—H2J1	110.0
C1E—C4—C1D	110.1 (2)	C1J—C2J—H2J1	110.0
C1E—C4—C1F	111.38 (19)	O2J—C2J—H2J2	110.0
C1D—C4—C1F	107.84 (18)	C1J—C2J—H2J2	110.0
C1E—C4—C3	105.03 (18)	H2J1—C2J—H2J2	108.4
C1D—C4—C3	110.38 (19)	C3J—O2J—C2J	113.4 (2)
C1F—C4—C3	112.12 (19)	C3J—O2J—Ba	124.66 (16)
C2D—C1D—C6D	117.8 (2)	C2J—O2J—Ba	118.34 (15)
C2D—C1D—C4	122.9 (2)	O2J—C3J—H3J1	109.5
C6D—C1D—C4	119.2 (2)	O2J—C3J—H3J2	109.5
C1D—C2D—C3D	120.9 (3)	H3J1—C3J—H3J2	109.5
C1D—C2D—H2D	119.5	O2J—C3J—H3J3	109.5
C3D—C2D—H2D	119.5	H3J1—C3J—H3J3	109.5
C4D—C3D—C2D	120.9 (3)	H3J2—C3J—H3J3	109.5

Ba—O1—C1—O2	31.5 (5)	O4—C3—C4—C1D	178.6 (2)
Ba—O1—C1—C2	−151.1 (3)	O3—C3—C4—C1F	−123.7 (2)
Zn—O2—C1—O1	−3.5 (3)	O4—C3—C4—C1F	58.3 (3)
Zn—O2—C1—C2	178.94 (14)	C1E—C4—C1D—C2D	11.6 (3)
O1—C1—C2—C1B	161.4 (2)	C1F—C4—C1D—C2D	−110.1 (3)
O2—C1—C2—C1B	−21.0 (3)	C3—C4—C1D—C2D	127.2 (2)
O1—C1—C2—C1A	39.8 (3)	C1E—C4—C1D—C6D	−173.1 (2)
O2—C1—C2—C1A	−142.6 (2)	C1F—C4—C1D—C6D	65.2 (3)
O1—C1—C2—C1C	−79.0 (3)	C3—C4—C1D—C6D	−57.6 (3)
O2—C1—C2—C1C	98.7 (2)	C6D—C1D—C2D—C3D	−0.9 (4)
C1B—C2—C1A—C6A	12.2 (3)	C4—C1D—C2D—C3D	174.4 (2)
C1C—C2—C1A—C6A	−109.0 (2)	C1D—C2D—C3D—C4D	0.8 (4)
C1—C2—C1A—C6A	133.8 (2)	C2D—C3D—C4D—C5D	0.1 (4)
C1B—C2—C1A—C2A	−173.5 (2)	C3D—C4D—C5D—C6D	−0.9 (4)
C1C—C2—C1A—C2A	65.3 (3)	C4D—C5D—C6D—C1D	0.8 (4)
C1—C2—C1A—C2A	−51.9 (3)	C2D—C1D—C6D—C5D	0.1 (4)
C6A—C1A—C2A—C3A	−1.0 (4)	C4—C1D—C6D—C5D	−175.4 (2)
C2—C1A—C2A—C3A	−175.6 (2)	C1D—C4—C1E—C2E	−103.2 (3)
C1A—C2A—C3A—C4A	−0.3 (4)	C1F—C4—C1E—C2E	16.4 (3)
C2A—C3A—C4A—C5A	0.9 (4)	C3—C4—C1E—C2E	138.0 (2)
C3A—C4A—C5A—C6A	−0.1 (4)	C1D—C4—C1E—C6E	74.1 (3)
C4A—C5A—C6A—C1A	−1.3 (4)	C1F—C4—C1E—C6E	−166.3 (2)
C2A—C1A—C6A—C5A	1.8 (4)	C3—C4—C1E—C6E	−44.7 (3)
C2—C1A—C6A—C5A	176.3 (2)	C6E—C1E—C2E—C3E	−0.9 (4)
C1A—C2—C1B—C2B	−108.0 (2)	C4—C1E—C2E—C3E	176.4 (2)
C1C—C2—C1B—C2B	12.0 (3)	C1E—C2E—C3E—C4E	0.3 (4)
C1—C2—C1B—C2B	128.7 (2)	C2E—C3E—C4E—C5E	0.6 (4)
C1A—C2—C1B—C6B	67.2 (3)	C3E—C4E—C5E—C6E	−0.8 (4)
C1C—C2—C1B—C6B	−172.85 (19)	C4E—C5E—C6E—C1E	0.1 (4)
C1—C2—C1B—C6B	−56.1 (3)	C2E—C1E—C6E—C5E	0.7 (4)
C6B—C1B—C2B—C3B	−0.9 (3)	C4—C1E—C6E—C5E	−176.7 (2)
C2—C1B—C2B—C3B	174.4 (2)	C1E—C4—C1F—C6F	92.9 (3)
C1B—C2B—C3B—C4B	0.0 (4)	C1D—C4—C1F—C6F	−146.2 (3)
C2B—C3B—C4B—C5B	0.6 (4)	C3—C4—C1F—C6F	−24.4 (3)
C3B—C4B—C5B—C6B	−0.3 (4)	C1E—C4—C1F—C2F	−84.8 (3)
C4B—C5B—C6B—C1B	−0.6 (4)	C1D—C4—C1F—C2F	36.1 (3)
C2B—C1B—C6B—C5B	1.1 (3)	C3—C4—C1F—C2F	157.8 (2)
C2—C1B—C6B—C5B	−174.3 (2)	C6F—C1F—C2F—C3F	−1.6 (4)
C1B—C2—C1C—C2C	−89.5 (3)	C4—C1F—C2F—C3F	176.3 (2)
C1A—C2—C1C—C2C	30.8 (3)	C1F—C2F—C3F—C4F	−0.1 (4)
C1—C2—C1C—C2C	151.7 (2)	C2F—C3F—C4F—C5F	1.8 (5)
C1B—C2—C1C—C6C	87.1 (3)	C3F—C4F—C5F—C6F	−1.9 (5)
C1A—C2—C1C—C6C	−152.6 (2)	C2F—C1F—C6F—C5F	1.5 (4)
C1—C2—C1C—C6C	−31.7 (3)	C4—C1F—C6F—C5F	−176.2 (3)
C6C—C1C—C2C—C3C	−1.3 (4)	C4F—C5F—C6F—C1F	0.2 (5)
C2—C1C—C2C—C3C	175.4 (2)	Ba—O1G—C1G—C2G	−8.8 (3)
C1C—C2C—C3C—C4C	0.4 (4)	O1G—C1G—C2G—O2G	54.1 (3)
C2C—C3C—C4C—C5C	0.5 (4)	C1G—C2G—O2G—C3G	71.7 (3)
C3C—C4C—C5C—C6C	−0.5 (4)	C1G—C2G—O2G—Ba	−67.0 (2)
C4C—C5C—C6C—C1C	−0.4 (4)	Ba—O1H—C1H—C2H	−4.1 (7)
C2C—C1C—C6C—C5C	1.2 (4)	O1H—C1H—C2H—O2H	72.7 (4)
C2—C1C—C6C—C5C	−175.4 (2)	C1H—C2H—O2H—C3H	174.4 (2)
Ba—O3—C3—O4	13.4 (5)	Ba—O1I—C1I—C2I	−140.4 (2)
Ba—O3—C3—C4	−164.39 (19)	O1I—C1I—C2I—O2I	−63.6 (3)
Zn—O4—C3—O3	22.2 (3)	C1I—C2I—O2I—C3I	105.6 (3)
Zn—O4—C3—C4	−159.98 (15)	Ba—O1J—C1J—C2J	−46.1 (3)
O3—C3—C4—C1E	115.2 (2)	O1J—C1J—C2J—O2J	56.2 (3)
O4—C3—C4—C1E	−62.8 (3)	C1J—C2J—O2J—C3J	159.6 (2)
O3—C3—C4—C1D	−3.4 (3)	C1J—C2J—O2J—Ba	−40.8 (3)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O1G—H1G···O2Iⁱ	0.84	1.91	2.728 (3)	163
O1H—H1H···O3	0.84	2.17	2.746 (3)	125
O1I—H1I···O2H	0.84	1.99	2.817 (3)	170
C2I—H2I2···Cl1ⁱⁱ	0.99	2.81	3.660 (3)	144
O1J—H1J···Cl2ⁱⁱⁱ	0.84	2.17	3.012 (2)	174

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

Selected bond lengths (Å) top

Ba—O3	2.6925 (19)	Ba—O2G	2.985 (2)
Ba—O1	2.7073 (19)	Ba—Cl1	3.1118 (11)
Ba—O1J	2.7572 (19)	Zn—O2	1.9682 (17)
Ba—O1H	2.783 (2)	Zn—O4	1.9683 (18)
Ba—O2J	2.7908 (19)	Zn—Cl1	2.2595 (10)
Ba—O1G	2.799 (2)	Zn—Cl2	2.2653 (9)
Ba—O1I	2.810 (2)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O1G—H1G···O2Iⁱ	0.84	1.91	2.728 (3)	163
O1I—H1I···O2H	0.84	1.99	2.817 (3)	170
C2I—H2I2···Cl1ⁱⁱ	0.99	2.81	3.660 (3)	144
O1J—H1J···Cl2ⁱⁱⁱ	0.84	2.17	3.012 (2)	174

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

Experimental details

Crystal data
Chemical formula	[BaZn(C₂₀H₁₅O₂)₂Cl₂(C₃H₈O₂)₄]
M_r	1152.62
Crystal system, space group	Triclinic, P1
Temperature (K)	100
a, b, c (Å)	9.706 (3), 10.643 (3), 25.073 (6)
α, β, γ (°)	89.62 (3), 89.26 (3), 82.73 (3)
V (Å³)	2569.0 (12)
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	1.39
Crystal size (mm)	0.31 × 0.23 × 0.21

Data collection
Diffractometer	Oxford Diffraction KM-4-CCD diffractometer
Absorption correction	Analytical [CrysAlis RED (Oxford Diffraction, 2010), based on expressions derived by Clark & Reid (1995)]
T_min, T_max	0.687, 0.780
No. of measured, independent and observed [I > 2σ(I)] reflections	24098, 12296, 10742
R_int	0.025
(sin θ/λ)_max (Å⁻¹)	0.705

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.035, 0.100, 1.14
No. of reflections	12296
No. of parameters	617
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.89, −0.57

Computer programs: CrysAlis CCD (Oxford Diffraction, 2010), CrysAlis RED (Oxford Diffraction, 2010), SHELXS97 (Sheldrick, 2008), SHELXL2013 (Sheldrick, 2015), SHELXTL (Sheldrick, 2008).

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Volume 71| Part 7| July 2015| Pages 791-794

doi:10.1107/S2056989015011226

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research communications\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Crystal structure of a mixed-ligand dinuclear Ba—Zn complex with 2-meth­­oxy­ethanol having tri­phenyl­acetate and chloride bridges

1. Chemical context

2. Structural commentary

3. Supra­molecular features

4. Synthesis and crystallization

5. Refinement details

Supporting information

References

research communications

Crystal structure of a mixed-ligand dinuclear Ba—Zn complex with 2-methoxyethanol having triphenylacetate and chloride bridges

3. Supramolecular features