Crystal structures of three hydrogen-bonded 1:2 compounds of chloranilic acid with 2-pyridone, 3-hy­droxy­pyridine and 4-hyroxypyridine

Gotoh, K.; Ishida, H.

doi:10.1107/S2056989017013536

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ISSN: 2056-9890

Volume 73| Part 10| October 2017| Pages 1546-1550

https://doi.org/10.1107/S2056989017013536

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Crystal structures of three hydrogen-bonded 1:2 compounds of chloranilic acid with 2-pyridone, 3-hydroxypyridine and 4-hyroxypyridine

Kazuma Gotoh ^a and Hiroyuki Ishida ^a ^*

^aDepartment of Chemistry, Faculty of Science, Okayama University, Okayama 700-8530, Japan
^*Correspondence e-mail: ishidah@cc.okayama-u.ac.jp

Edited by A. J. Lough, University of Toronto, Canada (Received 17 September 2017; accepted 21 September 2017; online 29 September 2017)

The crystal structures of the 1:2 compounds of chloranilic acid (systematic name: 2,5-dichloro-3,6-dihydroxy-1,4-benzoquinone) with 2-pyridone, 3-hydroxypyridine and 4-hyroxypyridine, namely, bis(2-pyridone) chloranilic acid, 2C₅H₅NO·C₆H₂Cl₂O₄, (I), bis(3-hydroxypyridinium) chloranilate, 2C₅H₆NO⁺·C₆Cl₂O₄²⁻, (II), and bis(4-hydroxypyridinium) chloranilate, 2C₅H₆NO⁺·C₆Cl₂O₄²⁻, (III), have been determined at 120 K. In the crystal of (I), the base molecule is in the lactam form and no acid–base interaction involving H-atom transfer is observed. The acid molecule lies on an inversion centre and the asymmetric unit consists of one half-molecule of chloranilic acid and one 2-pyridone molecule, which are linked via a short O—H⋯O hydrogen bond. 2-Pyridone molecules form a head-to-head dimer via a pair of N—H⋯O hydrogen bonds, resulting in a tape structure along [201]. In the crystals of (II) and (III), acid–base interactions involving H-atom transfer are observed and the divalent cations lie on an inversion centre. The asymmetric unit of (II) consists of one half of a chloranilate anion and one 3-hydroxypyridinium cation, while that of (III) comprises two independent halves of anions and two 4-hydroxypyridinium cations. The primary intermolecular interaction in (II) is a bifurcated O—H⋯(O,O) hydrogen bond between the cation and the anion. The hydrogen-bonded units are further linked via N—H⋯O hydrogen bonds, forming a layer parallel to the bc plane. In (III), one anion is surrounded by four cations via O—H⋯O and C—H⋯O hydrogen bonds, while the other is surrounded by four cations via N—H⋯O and C—H⋯Cl hydrogen bonds. These interactions link the cations and the anions into a layer parallel to (301).

Keywords: crystal structure; chloranilic acid; 2-pyridone; 3-hydroxypyridine; 4-hyroxypyridine; hydrogen bond.

CCDC references: 1575722; 1575721; 1575720

1. Chemical context

Chloranilic acid, a dibasic acid with hydrogen-bond donor and acceptor groups, appears particularly attractive as a template for generating tightly bound self-assemblies with various pyridine derivatives, as well as a model compound for investigating hydrogen transfer motions in O—H⋯N and N—H⋯O hydrogen-bond systems (Zaman et al., 2004 ; Seliger et al., 2009 ; Asaji et al. 2010 ). In the present study, we have prepared three 1:2 compounds of chloranilic acid with 2-pyridone, 3-hydroxypyridine and 4-hydroxypyridine in order to extend our study of D—H⋯A hydrogen bonding (D = N, O or C; A = N, O or Cl) in chloranilic acid–substituted-pyridine systems (Gotoh et al., 2009a ,b , 2010 ). The crystal structure of the 1:1 compound of chloranilic acid with 3-hydroxypyridine, namely, 3-hydroxypyridinium hydrogen chloranilate monohydrate, has been reported (Gotoh & Ishida, 2009 ).

2. Structural commentary

In compound (I), the base molecule is in the lactam form and no acid-base interaction involving H-atom transfer is observed (Fig. 1). The acid molecule lies on an inversion centre and the asymmetric unit consists of one-half acid molecule and one base molecule, which are linked via a short O—H⋯O hydrogen bond (O2—H2⋯O3; Table 1). The dihedral angle between the acid ring and the base ring is 37.82 (5)°.

Table 1
Hydrogen-bond geometry (Å, °) for (I)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O2—H2⋯O3	0.901 (15)	1.627 (16)	2.4989 (11)	161.9 (19)
N1—H1⋯O3ⁱ	0.893 (16)	1.996 (17)	2.8743 (12)	167.6 (16)
C7—H7⋯Cl1ⁱⁱ	0.95	2.79	3.5122 (13)	134
Symmetry codes: (i) $[-x+2, y, -z+{\script{3\over 2}}]$ ; (ii) -x+2, -y, -z+1.

Figure 1
The molecular structure of compound (I)

, showing the atom-numbering scheme. Displacement ellipsoids are drawn at the 50% probability level and H atoms are shown as small spheres of arbitrary radii. O—H⋯O hydrogen bonds are shown as dashed lines. [Symmetry code: (iii) −x + 1, −y + 1, −z + 1.]

In compound (II), an acid–base interaction involving H-atom transfer is observed. The chloranilate anion is located on an inversion centre and the asymmetric unit contains one-half anion molecule and one cation molecule. The primary intermolecular interaction between the cation and the anion is a bifurcated O—H⋯(O,O) hydrogen bond (O3—H3⋯O2 and O3—H3⋯O1ⁱ; symmetry code as in Table 2) to afford a centrosymmetric 1:2 aggregate of the anion and the cation (Fig. 2). The dihedral angle between the acid ring and the base ring is 72.69 (5)°.

Table 2
Hydrogen-bond geometry (Å, °) for (II)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O3—H3⋯O2	0.852 (17)	1.803 (17)	2.6277 (12)	162.5 (16)
O3—H3⋯O1ⁱ	0.852 (17)	2.438 (17)	2.9738 (12)	121.6 (14)
N1—H1⋯O2ⁱⁱ	0.889 (17)	1.807 (17)	2.6684 (12)	162.6 (16)
C8—H8⋯O1ⁱⁱⁱ	0.95	2.45	3.1481 (13)	130
Symmetry codes: (i) -x+2, -y+1, -z+1; (ii) $[x, -y+{\script{3\over 2}}, z-{\script{1\over 2}}]$ ; (iii) x-1, y, z-1.

Figure 2
The molecular structure of compound (II)

The compound (III) crystallizes with two independent halves of chloranilate anions and two 4-hydroxypyridinium cations in the asymmetric unit (Fig. 3). Although both anions lie on an inversion centre, the hydrogen-bonding schemes around the anions are quite different (Fig. 4); one anion is surrounded by four cations via O—H⋯O and C—H⋯O hydrogen bonds (O5—H5⋯O1ⁱ, O6—H6⋯O2 and C13—H13⋯O2; symmetry code as in Table 3), while the other is surrounded by four cation via N—H⋯O and C—H⋯Cl hydrogen bonds (N1—H1⋯O4, N2—H2⋯O4ⁱⁱ, N2—H2⋯O3ⁱⁱⁱ and C7—H7⋯Cl2; Table 3).

Table 3
Hydrogen-bond geometry (Å, °) for (III)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O5—H5⋯O1ⁱ	0.905 (17)	1.640 (17)	2.5208 (13)	163.2 (17)
O6—H6⋯O2	0.852 (17)	1.800 (17)	2.6510 (13)	177.3 (18)
N1—H1⋯O4	0.919 (17)	1.810 (17)	2.7000 (13)	162.3 (16)
N2—H2⋯O4ⁱⁱ	0.876 (18)	2.156 (17)	2.9603 (14)	152.3 (15)
N2—H2⋯O3ⁱⁱⁱ	0.876 (18)	2.176 (17)	2.8384 (14)	132.1 (14)
C7—H7⋯Cl2	0.95	2.81	3.4540 (12)	126
C12—H12⋯O3^iv	0.95	2.32	3.1541 (14)	146
C13—H13⋯O2	0.95	2.49	3.1685 (14)	128
C16—H16⋯Cl1^v	0.95	2.77	3.4427 (12)	128
Symmetry codes: (i) -x, -y, -z; (ii) x, y+1, z; (iii) -x+3, -y+1, -z+1; (iv) -x+2, -y+1, -z+1; (v) -x+2, -y+1, -z.

Figure 3
The molecular structure of compound (III)

, showing the atom-numbering scheme. Displacement ellipsoids are drawn at the 50% probability level and H atoms are shown as small spheres of arbitrary radii. O—H⋯O, N—H⋯O, C—H⋯Cl and C—H⋯O hydrogen bonds are shown as dashed lines. [Symmetry codes: (i) −x, −y, −z; (vi) −x + 3, −y, −z + 1.]

Figure 4
A partial packing diagram for compound (III)

around two independent chloranilate anions. O—H⋯O, N—H⋯O, C—H⋯Cl and C—H⋯O hydrogen bonds are shown as dashed lines. [Symmetry codes: (i) −x, −y, −z; (iii) −x + 3, −y + 1, −z + 1; (vi) −x + 3, −y, −z + 1; (vii) x, y − 1, z.]

3. Supramolecular features

In the crystal of compound (I), two adjacent 2-pyridone molecules, which are related by a twofold rotation axis, form a head-to-head dimer via a pair of N—H⋯O hydrogen bonds (N1—H1⋯O3ⁱ; symmetry code as in Table 1), as observed in various cocrystals of 2-pyridone (Odani & Matsumoto, 2002 ). The acid and base molecules form an undulating tape structure running along [201] through the above-mentioned O—H⋯O and N—H⋯O hydrogen bonds (Fig. 5). The tapes are stacked along the b axis into a layer structure through a π–π interaction between the pyridine rings [centroid-to-centroid distance = 3.7005 (6) Å and interplanar spacing = 3.4239 (4) Å] and a short C⋯C contact [C2⋯C3^iv = 3.3056 (13) Å; symmetry code: (iv) x, y + 1, z]. A weak C—H⋯Cl interaction formed between the acid and base molecules (C7—H7⋯Cl1ⁱⁱ; Table 1) links the layers. The O—H⋯O hydrogen bond between the acid and base molecules is short [O2⋯O3 = 2.4989 (11) Å], suggesting possible disorder of the H atom in the hydrogen bond, but no distinct evidence of the disorder was observed in the difference Fourier map, nor from the molecular geometry.

Figure 5
A packing diagram for compound (I)

, showing the tape structure formed by O—H⋯O and N—H⋯O hydrogen bonds (dashed lines). H atoms not involved in the interactions have been omitted. [Symmetry codes: (i) −x + 2, y, −z + $[{3\over 2}]$ ; (iii) −x + 1, −y + 1, −z + 1.]

In the crystal of (II), the cation–anion units are further connected by N—H⋯O (N1—H1⋯O2ⁱⁱ; symmetry code as in Table 2 and Fig. 6), forming a layer expanding parallel to the bc plane (Fig. 7). Adjacent layers are connected to each other with a C—H⋯O hydrogen bond (C8—H8⋯O1ⁱⁱⁱ; Table 2) and a short O⋯N contact [O3⋯N1^vi = 3.0430 (12) Å; symmetry code: (vi) −x + 1, y − $[{1\over 2}]$ , −z + $[{1\over 2}]$ ].

Figure 6
A partial packing diagram for compound (II)

around the chloranilate anion. O—H⋯O and N—H⋯O hydrogen bonds are shown as dashed lines. [Symmetry codes: (i) −x + 2, −y + 1, −z + 1; (iv) x, −y + $[{3\over 2}]$ , z + $[{1\over 2}]$ ; (v) −x + 2, y − $[{1\over 2}]$ , −z + $[{1\over 2}]$ .]

Figure 7
A packing diagram for compound (II)

, viewed along the b axis, showing the layer structure formed by O—H⋯O and N—H⋯O hydrogen bonds (dashed lines). H atoms not involved in the interactions have been omitted.

In the crystal of (III), the above-mentioned O—H⋯O, N—H⋯O, C—H⋯O and C—H⋯Cl hydrogen bonds link the cations and anions into a layer parallel to (301) (Fig. 8). Adjacent layers are further linked via weak C—H⋯O and C—H⋯Cl interactions (C12—H12⋯O3^iv and C16—H16⋯Cl1^v; symmetry codes as given in Table 3).

Figure 8
A packing diagram for compound (III)

, showing the hydrogen-bonded network in the layer. O—H⋯O, N—H⋯O, C—H⋯Cl and C—H⋯O hydrogen bonds are shown as dashed lines. H atoms not involved in the hydrogen bonds have been omitted.

4. Database survey

A search of the Cambridge Structural Database (Version 5.38, last update May 2017; Groom et al., 2016 ) for organic crystals of chloranilic acid with substituted pyridines (except for di-, tri- and tetrapyridine derivatives) gave 32 hits. Of these, crystal structures of 16 compounds of chloranilic acid with methyl-substituted pyridines (Adam et al., 2010 ; Łuczyńska et al., 2016 ; Molčanov & Kojić-Prodić, 2010 , and references therein), three compounds of carbamoyl-substituted pyridines (Gotoh et al., 2009a), three compounds of carboxy-substituted pyridines (Gotoh et al., 2009b, and references therein) and three compounds of cyano-substituted pyridines (Gotoh & Ishida, 2012 , and references therein) were reported.

5. Synthesis and crystallization

Single crystals of compound (I) were obtained by slow evaporation from an ethanol solution (120 ml) of chloranilic acid (350 mg) with 2-hydroxypyridine (340 mg) at room temperature. Crystals of compound (II) were obtained by slow evaporation from a methanol solution (400 ml) of chloranilic acid (170 mg) with 3-hydroxypyridine (160 mg) at room temperature. Crystals of compound (III) were obtained by slow diffusion of a methanol solution (20 ml) of 4-hydroxypyridine (160 mg) into an acetonitrile solution (200 ml) of chloranilic acid (170 mg) at room temperature.

6. Refinement

Crystal data, data collection and structure refinement details are summarized in Table 4. All H atoms in compounds (I)–(III) were found in difference Fourier maps. The positions of O- and N-bound H atoms were refined freely, with U_iso(H) = 1.5U_eq(O or N). C-bound H atoms were positioned geometrically (C—H = 0.95 Å) and were treated as riding with U_iso(H) = 1.2U_eq(C).

Table 4
Experimental details

	(I)	(II)	(III)
Crystal data
Chemical formula	2C₅H₅NO·C₆H₂Cl₂O₄	2C₅H₆NO⁺·C₆Cl₂O₄²⁻	2C₅H₆NO⁺·C₆Cl₂O₄²⁻
M_r	399.19	399.19	399.19
Crystal system, space group	Monoclinic, P2/c	Monoclinic, P2₁/c	Triclinic, P $[\overline{1}]$
Temperature (K)	120	120	120
a, b, c (Å)	11.9402 (7), 3.7005 (2), 21.7919 (13)	8.3659 (6), 8.5492 (6), 11.7087 (8)	5.49136 (13), 8.2195 (4), 18.1382 (9)
α, β, γ (°)	90, 121.278 (2), 90	90, 106.968 (3), 90	102.177 (3), 93.952 (3), 95.316 (4)
V (Å³)	822.92 (9)	800.98 (9)	793.52 (6)
Z	2	2	2
Radiation type	Mo Kα	Mo Kα	Mo Kα
μ (mm⁻¹)	0.43	0.45	0.45
Crystal size (mm)	0.39 × 0.36 × 0.21	0.21 × 0.20 × 0.12	0.35 × 0.25 × 0.12

Data collection
Diffractometer	Rigaku R-AXIS RAPIDII	Rigaku R-AXIS RAPIDII	Rigaku R-AXIS RAPIDII
Absorption correction	Multi-scan (ABSCOR; Higashi, 1995 )	Numerical (NUMABS; Higashi, 1999 )	Numerical (NUMABS; Higashi, 1999)
T_min, T_max	0.804, 0.913	0.903, 0.948	0.890, 0.948
No. of measured, independent and observed [I > 2σ(I)] reflections	22767, 2401, 2316	15315, 2329, 2166	12373, 4597, 4124
R_int	0.013	0.017	0.036
(sin θ/λ)_max (Å⁻¹)	0.703	0.703	0.703

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.027, 0.076, 1.06	0.028, 0.075, 1.07	0.030, 0.080, 1.07
No. of reflections	2401	2329	4597
No. of parameters	124	124	247
H-atom treatment	H atoms treated by a mixture of independent and constrained refinement	H atoms treated by a mixture of independent and constrained refinement	H atoms treated by a mixture of independent and constrained refinement
Δρ_max, Δρ_min (e Å⁻³)	0.49, −0.24	0.52, −0.20	0.75, −0.34
Computer programs: RAPID-AUTO (Rigaku, 2006 ), SHELXS97 (Sheldrick, 2008 ), SHELXL2016 (Sheldrick, 2015 ), ORTEP-3 for Windows (Farrugia, 2012 ), CrystalStructure (Rigaku, 2010 ) and PLATON (Spek, 2009 ).

Supporting information

CCDC references: 1575722; 1575721; 1575720

Crystal structure: contains datablocks I, II, III, global. DOI: https://doi.org/10.1107/S2056989017013536/lh5855sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S2056989017013536/lh5855Isup2.hkl

Structure factors: contains datablock II. DOI: https://doi.org/10.1107/S2056989017013536/lh5855IIsup3.hkl

Structure factors: contains datablock III. DOI: https://doi.org/10.1107/S2056989017013536/lh5855IIIsup4.hkl

checkCIF report

Computing details top

For all structures, data collection: RAPID-AUTO (Rigaku, 2006); cell refinement: RAPID-AUTO (Rigaku, 2006); data reduction: RAPID-AUTO (Rigaku, 2006); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL2016 (Sheldrick, 2015); molecular graphics: ORTEP-3 for Windows (Farrugia, 2012). Software used to prepare material for publication: CrystalStructure (Rigaku, 2010), PLATON (Spek, 2009) for (I); CrystalStructure (Rigaku, 2010) and PLATON (Spek, 2009) for (II), (III).

Bis[pyridin-2(1H)-one] 2,5-dichloro-3,6-dihydroxy-1,4-bebzoquinone (I) top

Crystal data top

2C₅H₅NO·C₆H₂Cl₂O₄	F(000) = 408.00
M_r = 399.19	D_x = 1.611 Mg m⁻³
Monoclinic, P2/c	Mo Kα radiation, λ = 0.71075 Å
a = 11.9402 (7) Å	Cell parameters from 20111 reflections
b = 3.7005 (2) Å	θ = 3.3–30.1°
c = 21.7919 (13) Å	µ = 0.43 mm⁻¹
β = 121.278 (2)°	T = 120 K
V = 822.92 (9) Å³	Block, brown
Z = 2	0.39 × 0.36 × 0.21 mm

Data collection top

Rigaku R-AXIS RAPIDII diffractometer	2316 reflections with I > 2σ(I)
Detector resolution: 10.000 pixels mm^-1	R_int = 0.013
ω scans	θ_max = 30.0°, θ_min = 3.4°
Absorption correction: multi-scan (ABSCOR; Higashi, 1995)	h = −16→16
T_min = 0.804, T_max = 0.913	k = −4→5
22767 measured reflections	l = −30→30
2401 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)] = 0.027	Hydrogen site location: mixed
wR(F²) = 0.076	H atoms treated by a mixture of independent and constrained refinement
S = 1.06	w = 1/[σ²(F_o²) + (0.0443P)² + 0.3557P] where P = (F_o² + 2F_c²)/3
2401 reflections	(Δ/σ)_max = 0.001
124 parameters	Δρ_max = 0.49 e Å⁻³
0 restraints	Δρ_min = −0.24 e Å⁻³

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
Cl1	0.60869 (2)	0.78653 (6)	0.40403 (2)	0.01704 (8)
O1	0.33921 (7)	0.8229 (2)	0.37552 (4)	0.02149 (16)
O2	0.75999 (6)	0.4050 (2)	0.54453 (4)	0.01794 (15)
H2	0.8039 (15)	0.289 (4)	0.5870 (8)	0.027*
O3	0.92219 (7)	0.1199 (2)	0.66164 (4)	0.02094 (16)
N1	1.13199 (8)	−0.0736 (2)	0.72858 (4)	0.01604 (16)
H1	1.1281 (13)	−0.016 (4)	0.7672 (8)	0.024*
C1	0.41591 (9)	0.6765 (2)	0.43248 (5)	0.01361 (17)
C2	0.55361 (8)	0.6274 (3)	0.45806 (5)	0.01311 (16)
C3	0.63639 (8)	0.4587 (2)	0.52136 (5)	0.01342 (17)
C4	1.02174 (9)	−0.0153 (3)	0.66317 (5)	0.01563 (17)
C5	1.02800 (9)	−0.1116 (3)	0.60168 (5)	0.01779 (18)
H5	0.953363	−0.080221	0.554948	0.021*
C6	1.14171 (10)	−0.2497 (3)	0.60990 (5)	0.01837 (19)
H6	1.145376	−0.312374	0.568705	0.022*
C7	1.25330 (10)	−0.2995 (3)	0.67902 (5)	0.01870 (19)
H7	1.332337	−0.392760	0.684778	0.022*
C8	1.24515 (9)	−0.2109 (3)	0.73732 (5)	0.01775 (18)
H8	1.318846	−0.245048	0.784277	0.021*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cl1	0.02123 (12)	0.01778 (12)	0.01883 (12)	0.00121 (8)	0.01512 (10)	0.00259 (7)
O1	0.0172 (3)	0.0304 (4)	0.0166 (3)	0.0046 (3)	0.0086 (3)	0.0080 (3)
O2	0.0124 (3)	0.0244 (4)	0.0172 (3)	0.0022 (3)	0.0079 (2)	0.0040 (3)
O3	0.0149 (3)	0.0307 (4)	0.0184 (3)	0.0048 (3)	0.0095 (3)	0.0034 (3)
N1	0.0158 (3)	0.0189 (4)	0.0145 (3)	0.0021 (3)	0.0086 (3)	0.0000 (3)
C1	0.0150 (4)	0.0138 (4)	0.0134 (4)	0.0000 (3)	0.0083 (3)	−0.0005 (3)
C2	0.0150 (4)	0.0139 (4)	0.0139 (4)	0.0000 (3)	0.0098 (3)	0.0002 (3)
C3	0.0139 (4)	0.0137 (4)	0.0143 (4)	−0.0005 (3)	0.0084 (3)	−0.0010 (3)
C4	0.0142 (4)	0.0170 (4)	0.0162 (4)	−0.0005 (3)	0.0083 (3)	0.0012 (3)
C5	0.0178 (4)	0.0207 (4)	0.0146 (4)	−0.0011 (3)	0.0082 (3)	0.0004 (3)
C6	0.0221 (4)	0.0189 (4)	0.0179 (4)	−0.0015 (3)	0.0131 (4)	−0.0018 (3)
C7	0.0184 (4)	0.0190 (4)	0.0211 (4)	0.0023 (3)	0.0119 (4)	−0.0009 (3)
C8	0.0157 (4)	0.0191 (4)	0.0174 (4)	0.0033 (3)	0.0078 (3)	0.0002 (3)

Geometric parameters (Å, º) top

Cl1—C2	1.7233 (9)	C2—C3	1.3614 (12)
O1—C1	1.2217 (11)	C4—C5	1.4256 (13)
O2—C3	1.3033 (10)	C5—C6	1.3726 (14)
O2—H2	0.901 (16)	C5—H5	0.9500
O3—C4	1.2739 (11)	C6—C7	1.4120 (14)
N1—C8	1.3611 (12)	C6—H6	0.9500
N1—C4	1.3648 (11)	C7—C8	1.3636 (14)
N1—H1	0.892 (15)	C7—H7	0.9500
C1—C2	1.4475 (12)	C8—H8	0.9500
C1—C3ⁱ	1.5182 (12)

C3—O2—H2	114.1 (10)	O3—C4—C5	125.24 (8)
C8—N1—C4	123.66 (8)	N1—C4—C5	116.69 (8)
C8—N1—H1	119.5 (9)	C6—C5—C4	120.10 (9)
C4—N1—H1	116.9 (9)	C6—C5—H5	120.0
O1—C1—C2	123.32 (8)	C4—C5—H5	120.0
O1—C1—C3ⁱ	118.05 (8)	C5—C6—C7	120.62 (9)
C2—C1—C3ⁱ	118.63 (7)	C5—C6—H6	119.7
C3—C2—C1	121.99 (8)	C7—C6—H6	119.7
C3—C2—Cl1	121.00 (7)	C8—C7—C6	118.57 (9)
C1—C2—Cl1	117.01 (7)	C8—C7—H7	120.7
O2—C3—C2	122.88 (8)	C6—C7—H7	120.7
O2—C3—C1ⁱ	117.75 (8)	N1—C8—C7	120.35 (9)
C2—C3—C1ⁱ	119.37 (8)	N1—C8—H8	119.8
O3—C4—N1	118.06 (8)	C7—C8—H8	119.8

O1—C1—C2—C3	−179.08 (9)	C8—N1—C4—O3	−178.90 (9)
C3ⁱ—C1—C2—C3	1.18 (15)	C8—N1—C4—C5	1.04 (15)
O1—C1—C2—Cl1	−0.05 (13)	O3—C4—C5—C6	178.84 (10)
C3ⁱ—C1—C2—Cl1	−179.79 (6)	N1—C4—C5—C6	−1.09 (15)
C1—C2—C3—O2	178.46 (9)	C4—C5—C6—C7	0.28 (16)
Cl1—C2—C3—O2	−0.53 (14)	C5—C6—C7—C8	0.64 (16)
C1—C2—C3—C1ⁱ	−1.19 (15)	C4—N1—C8—C7	−0.13 (16)
Cl1—C2—C3—C1ⁱ	179.82 (7)	C6—C7—C8—N1	−0.73 (15)

Symmetry code: (i) −x+1, −y+1, −z+1.

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O2—H2···O3	0.901 (15)	1.627 (16)	2.4989 (11)	161.9 (19)
N1—H1···O3ⁱⁱ	0.893 (16)	1.996 (17)	2.8743 (12)	167.6 (16)
C7—H7···Cl1ⁱⁱⁱ	0.95	2.79	3.5122 (13)	134

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

Bis(3-hyroxypyridinium) 2,5-dichloro-3,6-dioxocyclohexa-1,4-diene-1,4-diolate (II) top

Crystal data top

2C₅H₆NO⁺·C₆Cl₂O₄²⁻	F(000) = 408.00
M_r = 399.19	D_x = 1.655 Mg m⁻³
Monoclinic, P2₁/c	Mo Kα radiation, λ = 0.71075 Å
a = 8.3659 (6) Å	Cell parameters from 13386 reflections
b = 8.5492 (6) Å	θ = 3.0–30.0°
c = 11.7087 (8) Å	µ = 0.45 mm⁻¹
β = 106.968 (3)°	T = 120 K
V = 800.98 (9) Å³	Block, brown
Z = 2	0.21 × 0.20 × 0.12 mm

Data collection top

Rigaku R-AXIS RAPIDII diffractometer	2166 reflections with I > 2σ(I)
Detector resolution: 10.000 pixels mm^-1	R_int = 0.017
ω scans	θ_max = 30.0°, θ_min = 3.0°
Absorption correction: numerical (NUMABS; Higashi, 1999)	h = −11→11
T_min = 0.903, T_max = 0.948	k = −12→12
15315 measured reflections	l = −15→16
2329 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)] = 0.028	Hydrogen site location: mixed
wR(F²) = 0.075	H atoms treated by a mixture of independent and constrained refinement
S = 1.07	w = 1/[σ²(F_o²) + (0.0411P)² + 0.357P] where P = (F_o² + 2F_c²)/3
2329 reflections	(Δ/σ)_max = 0.001
124 parameters	Δρ_max = 0.52 e Å⁻³
0 restraints	Δρ_min = −0.20 e Å⁻³

Special details top

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

	x	y	z	U_iso*/U_eq
Cl1	0.93157 (3)	0.73912 (3)	0.68834 (2)	0.01680 (8)
O1	1.24731 (9)	0.58136 (9)	0.69329 (7)	0.01740 (16)
O2	0.68396 (9)	0.61601 (9)	0.46095 (7)	0.01689 (16)
O3	0.41012 (10)	0.51422 (9)	0.30475 (7)	0.01640 (16)
H3	0.509 (2)	0.5340 (19)	0.3482 (15)	0.025*
N1	0.48820 (11)	0.71217 (11)	0.05541 (8)	0.01529 (17)
H1	0.566 (2)	0.7718 (19)	0.0393 (15)	0.023*
C1	1.13017 (12)	0.54789 (11)	0.60534 (9)	0.01283 (18)
C2	0.96428 (12)	0.60823 (12)	0.58348 (9)	0.01358 (18)
C3	0.83396 (12)	0.56708 (12)	0.48551 (9)	0.01327 (18)
C4	0.51167 (12)	0.66180 (12)	0.16734 (9)	0.01383 (18)
H4	0.609229	0.691448	0.228545	0.017*
C5	0.39288 (12)	0.56593 (11)	0.19388 (9)	0.01309 (18)
C6	0.25163 (13)	0.52430 (13)	0.10152 (10)	0.0171 (2)
H6	0.169400	0.457667	0.116909	0.021*
C7	0.23181 (14)	0.58069 (13)	−0.01295 (10)	0.0192 (2)
H7	0.135178	0.553857	−0.075971	0.023*
C8	0.35290 (14)	0.67593 (13)	−0.03506 (9)	0.0180 (2)
H8	0.340534	0.715121	−0.113094	0.022*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cl1	0.01596 (13)	0.01889 (13)	0.01530 (13)	0.00248 (8)	0.00420 (9)	−0.00478 (8)
O1	0.0143 (3)	0.0210 (4)	0.0144 (3)	0.0017 (3)	0.0004 (3)	−0.0030 (3)
O2	0.0118 (3)	0.0224 (4)	0.0151 (3)	0.0047 (3)	0.0018 (3)	−0.0023 (3)
O3	0.0141 (3)	0.0203 (4)	0.0142 (3)	−0.0010 (3)	0.0032 (3)	0.0034 (3)
N1	0.0148 (4)	0.0160 (4)	0.0155 (4)	−0.0020 (3)	0.0050 (3)	0.0005 (3)
C1	0.0129 (4)	0.0133 (4)	0.0121 (4)	0.0010 (3)	0.0034 (3)	0.0006 (3)
C2	0.0134 (4)	0.0151 (4)	0.0122 (4)	0.0021 (3)	0.0036 (3)	−0.0021 (3)
C3	0.0132 (4)	0.0144 (4)	0.0120 (4)	0.0016 (3)	0.0034 (3)	0.0006 (3)
C4	0.0122 (4)	0.0142 (4)	0.0142 (4)	−0.0007 (3)	0.0025 (3)	0.0001 (3)
C5	0.0121 (4)	0.0127 (4)	0.0144 (4)	0.0010 (3)	0.0037 (3)	0.0001 (3)
C6	0.0129 (4)	0.0180 (5)	0.0194 (5)	−0.0033 (3)	0.0031 (4)	0.0000 (4)
C7	0.0167 (5)	0.0209 (5)	0.0169 (5)	−0.0031 (4)	−0.0001 (4)	−0.0019 (4)
C8	0.0198 (5)	0.0199 (5)	0.0132 (4)	−0.0014 (4)	0.0031 (4)	−0.0005 (4)

Geometric parameters (Å, º) top

Cl1—C2	1.7409 (10)	C2—C3	1.3778 (13)
O1—C1	1.2302 (12)	C4—C5	1.3915 (13)
O2—C3	1.2735 (12)	C4—H4	0.9500
O3—C5	1.3387 (12)	C5—C6	1.3952 (14)
O3—H3	0.850 (18)	C6—C7	1.3880 (15)
N1—C4	1.3384 (13)	C6—H6	0.9500
N1—C8	1.3414 (14)	C7—C8	1.3818 (15)
N1—H1	0.891 (17)	C7—H7	0.9500
C1—C2	1.4319 (13)	C8—H8	0.9500
C1—C3ⁱ	1.5409 (14)

C5—O3—H3	109.0 (11)	N1—C4—H4	120.1
C4—N1—C8	123.22 (9)	C5—C4—H4	120.1
C4—N1—H1	119.0 (11)	O3—C5—C4	121.95 (9)
C8—N1—H1	117.8 (11)	O3—C5—C6	119.64 (9)
O1—C1—C2	124.03 (9)	C4—C5—C6	118.41 (9)
O1—C1—C3ⁱ	117.27 (8)	C7—C6—C5	119.69 (9)
C2—C1—C3ⁱ	118.70 (8)	C7—C6—H6	120.2
C3—C2—C1	123.17 (9)	C5—C6—H6	120.2
C3—C2—Cl1	120.15 (7)	C8—C7—C6	119.88 (9)
C1—C2—Cl1	116.69 (7)	C8—C7—H7	120.1
O2—C3—C2	126.33 (9)	C6—C7—H7	120.1
O2—C3—C1ⁱ	115.54 (8)	N1—C8—C7	118.94 (9)
C2—C3—C1ⁱ	118.13 (8)	N1—C8—H8	120.5
N1—C4—C5	119.86 (9)	C7—C8—H8	120.5

O1—C1—C2—C3	−178.76 (10)	C8—N1—C4—C5	0.55 (16)
C3ⁱ—C1—C2—C3	0.78 (16)	N1—C4—C5—O3	−179.23 (9)
O1—C1—C2—Cl1	1.08 (14)	N1—C4—C5—C6	0.30 (15)
C3ⁱ—C1—C2—Cl1	−179.38 (7)	O3—C5—C6—C7	178.57 (10)
C1—C2—C3—O2	179.87 (10)	C4—C5—C6—C7	−0.97 (15)
Cl1—C2—C3—O2	0.03 (15)	C5—C6—C7—C8	0.83 (17)
C1—C2—C3—C1ⁱ	−0.78 (16)	C4—N1—C8—C7	−0.70 (16)
Cl1—C2—C3—C1ⁱ	179.39 (7)	C6—C7—C8—N1	−0.01 (17)

Symmetry code: (i) −x+2, −y+1, −z+1.

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O3—H3···O2	0.852 (17)	1.803 (17)	2.6277 (12)	162.5 (16)
O3—H3···O1ⁱ	0.852 (17)	2.438 (17)	2.9738 (12)	121.6 (14)
N1—H1···O2ⁱⁱ	0.889 (17)	1.807 (17)	2.6684 (12)	162.6 (16)
C8—H8···O1ⁱⁱⁱ	0.95	2.45	3.1481 (13)	130

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

Bis(4-hyroxypyridinium) 2,5-dichloro-3,6-dioxocyclohexa-1,4-diene-1,4-diolate (III) top

Crystal data top

2C₅H₆NO⁺·C₆Cl₂O₄²⁻	Z = 2
M_r = 399.19	F(000) = 408.00
Triclinic, P1	D_x = 1.671 Mg m⁻³
a = 5.49136 (13) Å	Mo Kα radiation, λ = 0.71075 Å
b = 8.2195 (4) Å	Cell parameters from 11077 reflections
c = 18.1382 (9) Å	θ = 3.0–30.1°
α = 102.177 (3)°	µ = 0.45 mm⁻¹
β = 93.952 (3)°	T = 120 K
γ = 95.316 (4)°	Platelet, brown
V = 793.52 (6) Å³	0.35 × 0.25 × 0.12 mm

Data collection top

Rigaku R-AXIS RAPIDII diffractometer	4124 reflections with I > 2σ(I)
Detector resolution: 10.000 pixels mm^-1	R_int = 0.036
ω scans	θ_max = 30.0°, θ_min = 3.0°
Absorption correction: numerical (NUMABS; Higashi, 1999)	h = −7→7
T_min = 0.890, T_max = 0.948	k = −11→11
12373 measured reflections	l = −25→25
4597 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)] = 0.030	Hydrogen site location: mixed
wR(F²) = 0.080	H atoms treated by a mixture of independent and constrained refinement
S = 1.07	w = 1/[σ²(F_o²) + (0.0406P)² + 0.3136P] where P = (F_o² + 2F_c²)/3
4597 reflections	(Δ/σ)_max = 0.001
247 parameters	Δρ_max = 0.75 e Å⁻³
0 restraints	Δρ_min = −0.34 e Å⁻³

Special details top

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

	x	y	z	U_iso*/U_eq
Cl1	0.42856 (5)	0.16233 (3)	−0.07860 (2)	0.01668 (7)
Cl2	1.13911 (5)	0.28348 (3)	0.52483 (2)	0.01730 (7)
O1	0.03685 (16)	−0.10701 (11)	−0.14946 (5)	0.02014 (18)
O2	0.33010 (15)	0.24516 (10)	0.08473 (5)	0.01729 (17)
O3	1.55337 (16)	0.23416 (11)	0.62981 (5)	0.01865 (17)
O4	1.14201 (15)	0.00027 (10)	0.38854 (5)	0.01586 (16)
O5	0.18017 (16)	0.33437 (10)	0.25526 (5)	0.01818 (17)
H5	0.118 (3)	0.263 (2)	0.2115 (10)	0.027*
O6	0.74923 (17)	0.40347 (11)	0.05992 (5)	0.02044 (18)
H6	0.617 (3)	0.350 (2)	0.0681 (11)	0.031*
N1	0.76255 (18)	0.16991 (12)	0.35832 (6)	0.01695 (19)
H1	0.896 (3)	0.128 (2)	0.3779 (10)	0.025*
N2	1.04584 (18)	0.71260 (12)	0.25721 (6)	0.01696 (19)
H2	1.114 (3)	0.777 (2)	0.2998 (10)	0.025*
C1	0.02618 (19)	−0.05358 (13)	−0.08002 (6)	0.01355 (19)
C2	0.19204 (19)	0.07509 (13)	−0.03554 (6)	0.01332 (19)
C3	0.18242 (19)	0.13365 (13)	0.04220 (6)	0.01289 (19)
C4	1.52060 (19)	0.12916 (13)	0.56903 (6)	0.01293 (19)
C5	1.33437 (19)	0.12624 (13)	0.51055 (6)	0.01346 (19)
C6	1.30221 (19)	0.00728 (13)	0.44252 (6)	0.01271 (19)
C7	0.6571 (2)	0.30150 (14)	0.39505 (7)	0.0178 (2)
H7	0.719110	0.355184	0.445342	0.021*
C8	0.4617 (2)	0.35945 (14)	0.36116 (7)	0.0169 (2)
H8	0.390102	0.453256	0.387366	0.020*
C9	0.3693 (2)	0.27801 (13)	0.28719 (6)	0.0141 (2)
C10	0.4863 (2)	0.14337 (14)	0.24949 (6)	0.0169 (2)
H10	0.430463	0.088006	0.198898	0.020*
C11	0.6819 (2)	0.09297 (15)	0.28659 (7)	0.0180 (2)
H11	0.761693	0.002289	0.261273	0.022*
C12	0.8247 (2)	0.62477 (14)	0.25631 (6)	0.0169 (2)
H12	0.743357	0.635815	0.301370	0.020*
C13	0.7170 (2)	0.51997 (14)	0.19096 (6)	0.0152 (2)
H13	0.560916	0.459117	0.190415	0.018*
C14	0.8392 (2)	0.50334 (13)	0.12492 (6)	0.0145 (2)
C15	1.0695 (2)	0.59750 (15)	0.12741 (7)	0.0178 (2)
H15	1.155223	0.590054	0.083294	0.021*
C16	1.1663 (2)	0.69955 (15)	0.19462 (7)	0.0181 (2)
H16	1.321913	0.762460	0.197088	0.022*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cl1	0.01602 (12)	0.01837 (13)	0.01388 (12)	−0.00454 (9)	0.00310 (9)	0.00181 (9)
Cl2	0.01776 (13)	0.01555 (12)	0.01668 (13)	0.00527 (9)	−0.00194 (9)	−0.00109 (9)
O1	0.0204 (4)	0.0252 (4)	0.0108 (4)	−0.0062 (3)	0.0022 (3)	−0.0016 (3)
O2	0.0165 (4)	0.0179 (4)	0.0136 (4)	−0.0054 (3)	−0.0007 (3)	−0.0014 (3)
O3	0.0202 (4)	0.0181 (4)	0.0140 (4)	0.0038 (3)	−0.0031 (3)	−0.0038 (3)
O4	0.0164 (4)	0.0164 (4)	0.0129 (4)	0.0021 (3)	−0.0034 (3)	0.0005 (3)
O5	0.0183 (4)	0.0175 (4)	0.0162 (4)	0.0037 (3)	−0.0050 (3)	−0.0004 (3)
O6	0.0196 (4)	0.0230 (4)	0.0135 (4)	−0.0083 (3)	0.0008 (3)	−0.0029 (3)
N1	0.0157 (4)	0.0177 (4)	0.0181 (5)	0.0022 (3)	−0.0003 (4)	0.0057 (4)
N2	0.0177 (4)	0.0173 (4)	0.0128 (4)	−0.0016 (3)	−0.0028 (4)	−0.0006 (3)
C1	0.0126 (4)	0.0151 (5)	0.0117 (5)	−0.0008 (4)	0.0003 (4)	0.0014 (4)
C2	0.0118 (4)	0.0151 (4)	0.0121 (5)	−0.0025 (4)	0.0018 (4)	0.0023 (4)
C3	0.0120 (4)	0.0131 (4)	0.0126 (5)	−0.0004 (3)	0.0000 (4)	0.0019 (4)
C4	0.0134 (4)	0.0129 (4)	0.0116 (5)	0.0001 (4)	0.0011 (4)	0.0012 (4)
C5	0.0135 (4)	0.0128 (4)	0.0133 (5)	0.0028 (4)	−0.0001 (4)	0.0007 (4)
C6	0.0122 (4)	0.0124 (4)	0.0126 (5)	−0.0005 (3)	−0.0001 (4)	0.0020 (4)
C7	0.0200 (5)	0.0153 (5)	0.0162 (5)	0.0000 (4)	−0.0032 (4)	0.0016 (4)
C8	0.0196 (5)	0.0141 (5)	0.0154 (5)	0.0020 (4)	−0.0011 (4)	0.0003 (4)
C9	0.0144 (4)	0.0131 (4)	0.0146 (5)	0.0000 (4)	0.0006 (4)	0.0032 (4)
C10	0.0201 (5)	0.0171 (5)	0.0125 (5)	0.0027 (4)	0.0010 (4)	0.0012 (4)
C11	0.0197 (5)	0.0180 (5)	0.0170 (5)	0.0045 (4)	0.0043 (4)	0.0034 (4)
C12	0.0170 (5)	0.0198 (5)	0.0129 (5)	0.0010 (4)	0.0016 (4)	0.0015 (4)
C13	0.0132 (4)	0.0164 (5)	0.0147 (5)	−0.0011 (4)	0.0008 (4)	0.0019 (4)
C14	0.0149 (5)	0.0137 (4)	0.0129 (5)	−0.0006 (4)	−0.0006 (4)	0.0002 (4)
C15	0.0156 (5)	0.0205 (5)	0.0148 (5)	−0.0039 (4)	0.0023 (4)	0.0001 (4)
C16	0.0146 (5)	0.0191 (5)	0.0181 (5)	−0.0032 (4)	−0.0001 (4)	0.0010 (4)

Geometric parameters (Å, º) top

Cl1—C2	1.7363 (11)	C4—C5	1.4165 (14)
Cl2—C5	1.7438 (11)	C4—C6ⁱⁱ	1.5426 (15)
O1—C1	1.2508 (13)	C5—C6	1.3924 (15)
O2—C3	1.2532 (12)	C7—C8	1.3722 (16)
O3—C4	1.2390 (13)	C7—H7	0.9500
O4—C6	1.2586 (13)	C8—C9	1.4035 (15)
O5—C9	1.3223 (13)	C8—H8	0.9500
O5—H5	0.907 (18)	C9—C10	1.4065 (16)
O6—C14	1.3208 (13)	C10—C11	1.3703 (16)
O6—H6	0.852 (19)	C10—H10	0.9500
N1—C11	1.3456 (15)	C11—H11	0.9500
N1—C7	1.3469 (15)	C12—C13	1.3693 (15)
N1—H1	0.918 (18)	C12—H12	0.9500
N2—C16	1.3430 (16)	C13—C14	1.4009 (16)
N2—C12	1.3511 (15)	C13—H13	0.9500
N2—H2	0.877 (18)	C14—C15	1.4126 (15)
C1—C2	1.3997 (14)	C15—C16	1.3671 (15)
C1—C3ⁱ	1.5410 (15)	C15—H15	0.9500
C2—C3	1.3970 (15)	C16—H16	0.9500

C9—O5—H5	111.3 (11)	C8—C7—H7	119.4
C14—O6—H6	107.1 (13)	C7—C8—C9	118.99 (11)
C11—N1—C7	120.85 (10)	C7—C8—H8	120.5
C11—N1—H1	114.5 (11)	C9—C8—H8	120.5
C7—N1—H1	124.6 (11)	O5—C9—C8	118.46 (10)
C16—N2—C12	121.30 (10)	O5—C9—C10	122.89 (10)
C16—N2—H2	119.3 (12)	C8—C9—C10	118.62 (10)
C12—N2—H2	119.4 (12)	C11—C10—C9	119.23 (10)
O1—C1—C2	123.43 (10)	C11—C10—H10	120.4
O1—C1—C3ⁱ	117.79 (9)	C9—C10—H10	120.4
C2—C1—C3ⁱ	118.79 (9)	N1—C11—C10	121.03 (11)
C3—C2—C1	123.56 (10)	N1—C11—H11	119.5
C3—C2—Cl1	118.10 (8)	C10—C11—H11	119.5
C1—C2—Cl1	118.31 (8)	N2—C12—C13	120.52 (11)
O2—C3—C2	125.93 (10)	N2—C12—H12	119.7
O2—C3—C1ⁱ	116.43 (9)	C13—C12—H12	119.7
C2—C3—C1ⁱ	117.64 (9)	C12—C13—C14	119.37 (10)
O3—C4—C5	124.83 (10)	C12—C13—H13	120.3
O3—C4—C6ⁱⁱ	116.58 (9)	C14—C13—H13	120.3
C5—C4—C6ⁱⁱ	118.59 (9)	O6—C14—C13	123.08 (10)
C6—C5—C4	123.72 (10)	O6—C14—C15	118.05 (10)
C6—C5—Cl2	118.75 (8)	C13—C14—C15	118.87 (10)
C4—C5—Cl2	117.52 (8)	C16—C15—C14	118.63 (11)
O4—C6—C5	126.22 (10)	C16—C15—H15	120.7
O4—C6—C4ⁱⁱ	116.09 (9)	C14—C15—H15	120.7
C5—C6—C4ⁱⁱ	117.69 (9)	N2—C16—C15	121.29 (10)
N1—C7—C8	121.23 (11)	N2—C16—H16	119.4
N1—C7—H7	119.4	C15—C16—H16	119.4

O1—C1—C2—C3	−179.19 (11)	C11—N1—C7—C8	1.17 (18)
C3ⁱ—C1—C2—C3	1.29 (18)	N1—C7—C8—C9	0.81 (18)
O1—C1—C2—Cl1	−1.30 (16)	C7—C8—C9—O5	179.64 (10)
C3ⁱ—C1—C2—Cl1	179.17 (7)	C7—C8—C9—C10	−2.23 (17)
C1—C2—C3—O2	178.00 (11)	O5—C9—C10—C11	179.80 (10)
Cl1—C2—C3—O2	0.11 (16)	C8—C9—C10—C11	1.75 (17)
C1—C2—C3—C1ⁱ	−1.27 (17)	C7—N1—C11—C10	−1.68 (17)
Cl1—C2—C3—C1ⁱ	−179.16 (7)	C9—C10—C11—N1	0.18 (17)
O3—C4—C5—C6	179.64 (11)	C16—N2—C12—C13	−0.23 (17)
C6ⁱⁱ—C4—C5—C6	−0.41 (17)	N2—C12—C13—C14	0.54 (17)
O3—C4—C5—Cl2	0.75 (16)	C12—C13—C14—O6	179.17 (11)
C6ⁱⁱ—C4—C5—Cl2	−179.29 (7)	C12—C13—C14—C15	−0.92 (17)
C4—C5—C6—O4	−179.11 (10)	O6—C14—C15—C16	−179.08 (11)
Cl2—C5—C6—O4	−0.23 (16)	C13—C14—C15—C16	1.01 (17)
C4—C5—C6—C4ⁱⁱ	0.40 (17)	C12—N2—C16—C15	0.33 (18)
Cl2—C5—C6—C4ⁱⁱ	179.28 (7)	C14—C15—C16—N2	−0.72 (18)

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

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O5—H5···O1ⁱ	0.905 (17)	1.640 (17)	2.5208 (13)	163.2 (17)
O6—H6···O2	0.852 (17)	1.800 (17)	2.6510 (13)	177.3 (18)
N1—H1···O4	0.919 (17)	1.810 (17)	2.7000 (13)	162.3 (16)
N2—H2···O4ⁱⁱⁱ	0.876 (18)	2.156 (17)	2.9603 (14)	152.3 (15)
N2—H2···O3^iv	0.876 (18)	2.176 (17)	2.8384 (14)	132.1 (14)
C7—H7···Cl2	0.95	2.81	3.4540 (12)	126
C12—H12···O3^v	0.95	2.32	3.1541 (14)	146
C13—H13···O2	0.95	2.49	3.1685 (14)	128
C16—H16···Cl1^vi	0.95	2.77	3.4427 (12)	128

Symmetry codes: (i) −x, −y, −z; (iii) x, y+1, z; (iv) −x+3, −y+1, −z+1; (v) −x+2, −y+1, −z+1; (vi) −x+2, −y+1, −z.

References

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Volume 73| Part 10| October 2017| Pages 1546-1550

https://doi.org/10.1107/S2056989017013536

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

Crystal structures of three hydrogen-bonded 1:2 compounds of chloranilic acid with 2-pyridone, 3-hy­dr­oxy­pyridine and 4-hyroxypyridine

1. Chemical context

2. Structural commentary

3. Supra­molecular features

4. Database survey

5. Synthesis and crystallization

6. Refinement

Supporting information

References

research communications

Crystal structures of three hydrogen-bonded 1:2 compounds of chloranilic acid with 2-pyridone, 3-hydroxypyridine and 4-hyroxypyridine

3. Supramolecular features