Issue contents
Download PDF of article
Download CIF
3D view
Navigation
Highlighting
Dictionary of Crystallography reference
IUPAC Gold Book reference
more ...
Download citation
FormatBIBTeX
EndNote
RefMan
Refer
Medline
CIF
SGML
Plain Text
share
Previous article
Next article
Previous article
Issue contents
Download PDF of article
Download CIF
3D view
Navigation
Highlighting
Dictionary of Crystallography reference
IUPAC Gold Book reference
more ...
Download citation
FormatBIBTeX
EndNote
RefMan
Refer
Medline
CIF
SGML
Plain Text
share
Next article

organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 67| Part 1| January 2011| Page o235
https://doi.org/10.1107/S1600536810053390

2-Methyl­imidazolium picrate

Grzegorz Dutkiewicz,a S. Samshuddin,b B. Narayana,b H. S. Yathirajanc and Maciej Kubickia*

aDepartment of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, 60-780 Poznań, Poland, bDepartment of Studies in Chemistry, Mangalore University, Mangalagangotri 574 199, India, and cDepartment of Studies in Chemistry, University of Mysore, Manasagangotri, Mysore 570 006, India
*Correspondence e-mail: mkubicki@amu.edu.pl

(Received 16 December 2010; accepted 20 December 2010; online 24 December 2010)

In both ionic components of the title salt, C4H7N2+·C6H2N3O7−, the rings are approximately planar; the maximum deviation from the mean plane is an order of magnitude larger in the picrate ring [0.0289 (10) Å] than in the imidazolium ring [0.0028 (10) Å. The nitro groups are twisted with respect to the six-atom ring plane; the NO2 groups next to the oxide O atom, at the 2- and 6-positions, are twisted more [by 53.59 (9) and 18.46 (12)°] than the NO2 group at the 4-postition, for which the twist angle is 7.28 (16)°. In the crystal, N—H⋯O hydrogen bonds, in which the hydroxyl O atom acts as a double acceptor and one of the O atoms from a nitro group acts as an additional acceptor, connect mol­ecules into chains along the c-axis direction. Relatively short C—H⋯O contacts and π–π inter­actions between symmetry-related six-membered rings [centroid–centroid distances = 3.5938 (10) and 3.6223 (10) Å] also occur.

Related literature

For the crystal structure of imidazolium picrate, see: Soriano-García et al. (1990[Soriano-García, M., Schatz-Levine, M., Toscano, R. A. & Villena Iribe, R. (1990). Acta Cryst. C46, 1556-1558.]). For the structures of picrates of some other imidazole derivatives, see, for example: Nardelli et al. (1987[Nardelli, M., Pelizzi, G., Vitali, F., Bordi, F., Plazzi, P. V. & Vitali, T. (1987). Acta Cryst. C43, 507-514.]); Du & Zhao (2003[Du, M. & Zhao, X.-J. (2003). Acta Cryst. E59, o1898-o1900.]); MacDonald et al. (2005[MacDonald, J., Yigit, M. V. & Mychajlonka, K. (2005). Cryst. Growth Des. 5, 2248-2255.]); Pi et al. (2009[Pi, M., Liu, X.-L., Xu, J.-J. & Jin, C.-M. (2009). Acta Cryst. E65, o2386.]).

[Scheme 1]

Experimental

Crystal data

  • C4H7N2+·C6H2N3O7−

  • Mr = 311.22

  • Monoclinic, P 21 /c

  • a = 7.0983 (9) Å

  • b = 21.644 (2) Å

  • c = 8.1583 (9) Å

  • β = 100.327 (12)°

  • V = 1233.1 (2) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 0.15 mm−1

  • T = 295 K

  • 0.3 × 0.2 × 0.2 mm
Data collection

  • Oxford Diffraction Xcalibur Eos diffractometer

  • Absorption correction: multi-scan (CrysAlis PRO; Oxford Diffraction, 2009[Oxford Diffraction (2009). CrysAlis PRO. Oxford Diffraction Ltd, Yarnton, Oxfordshire, England.]) Tmin = 0.964, Tmax = 1.000

  • 4778 measured reflections

  • 2483 independent reflections

  • 1792 reflections with I > 2σ(I)

  • Rint = 0.014
Refinement

  • R[F2 > 2σ(F2)] = 0.039

  • wR(F2) = 0.101

  • S = 1.03

  • 2483 reflections

  • 235 parameters

  • All H-atom parameters refined

  • Δρmax = 0.30 e Å−3

  • Δρmin = −0.27 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A D⋯A D—H⋯A
C5—H5⋯O21i 0.911 (19) 2.478 (19) 3.378 (2) 169.4 (16)
N11—H11⋯O1 0.89 (2) 1.95 (2) 2.8357 (19) 172.9 (19)
N13—H13⋯O1ii 0.86 (2) 2.09 (2) 2.819 (2) 143 (2)
N13—H13⋯O22ii 0.86 (2) 2.14 (2) 2.782 (2) 131.3 (19)
Symmetry codes: (i) x, y, z-1; (ii) [x, -y+{\script{3\over 2}}, z-{\script{1\over 2}}].

Data collection: CrysAlis PRO (Oxford Diffraction, 2009[Oxford Diffraction (2009). CrysAlis PRO. Oxford Diffraction Ltd, Yarnton, Oxfordshire, England.]); cell refinement: CrysAlis PRO; data reduction: CrysAlis PRO; program(s) used to solve structure: SIR92 (Altomare et al., 1993[Altomare, A., Cascarano, G., Giacovazzo, C. & Guagliardi, A. (1993). J. Appl. Cryst. 26, 343-350.]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); molecular graphics: Stereochemical Workstation Operation Manual. (Siemens, 1989[Siemens (1989). Stereochemical Workstation Operation Manual. Siemens Analytical X-ray Instruments Inc., Madison, Wisconsin, USA.]); software used to prepare material for publication: SHELXL97.

Supporting information

Crystal structure: contains datablocks I, global. DOI: https://doi.org/10.1107/S1600536810053390/dn2638sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536810053390/dn2638Isup2.hkl

checkCIF report


Comment top

The imidazole nucleus appears in a number of naturally occurring products like amino acid histidine and purines which comprise many of the most important bases in nucleic acids. Imidazole derivatives deal with a broad spectrum of pharmacological activities. The crystal structures of some imidazolium picrates have been reported, for instance imidazolium picrate itself (Soriano-García et al. (1990); also two solvates (hydrate and ethanolate) of 2-aminohistamine dipicrate (Nardelli et al.,1987), 4-hydroxymethylimidazolium picrate (Du & Zhao, 2003), two polymorphs of betaine bis(diimidazolium) dipicrate (MacDonald et al., 2005) and 3-benzyl-1-methyl-imidazolium picrate (Pi et al., 2009).

The title compound, 2-methylimidazolium picrate (2-methyl-1H-imidazol-3-ium 2,4,6-trinitrophenolate, Scheme 1) crystallizes with two ionic components, as proved by successful location and refinement of hydrogen atoms at both imiadzole nitrogen atoms as well as by the bond length pattern. Both cyclic fragments are in a good approximation planar. As might be expected, the deviations from the least-squares plane are by an order of magnitude smaller in the imidazolium ring (maximum 0.0028 (10) Å) than in a six-atom ring of picrate anion (0.0289 (10) Å). The two rings make a dihedral angle of 60.28 (7)°. The nitro groups are twisted with respect to the ring plane; the dihedral angles are larger for the substituents ortho- with respect to the C=O- group (18.46 (12)° and 53.59 (9)°) than for the para-group, which is 7.28 (16)°.

The ionic fragments are conneced by relatively short N—H···O hydrogen bonds. One of N—H groups acts as a donor in almost linear hydrogen bond, while the other is involved in the bifurcated N—H···O bonds, in which O1 atom and one of nitro group O atoms act as acceptors. These two bonds are of similar lengths and therefore they deviate significantly from linearity. These hydrogen bonds, together with relatively short C—H···O contacts connect the cations and anions into a layer in which one can find the C12(6) chains, created only by N—H···O hydrogen bonds and R45(21) rings, in which all contacts are involved (Fig. 2).

The layers related by centers of symmetry are additionally connected by quite short π–π stacking interactions between six-membered rings. The distances between the centers of consecutive rings in a stack are 3.594Å and 3.621Å, but if the parallel shift is taken into account the distances between the planes are 3.48Å and 3.27Å (Fig. 3). It should be noted, however, that the parallel shift is in these cases 1.00Å and 1.50Å, respectively, which might suggest weak π–π stacking in the first case but edge-to-edge kind of interaction in the second.

Related literature top

For the crystal structure of imidazolium picrate, see: Soriano-García et al. (1990). For the structures of picrates of some other imidazole derivatives, see, for example: Nardelli et al. (1987); Du & Zhao (2003); MacDonald et al. (2005);Pi et al. (2009).

Experimental top

2-Methyl imidazole (0.82 g, 0.01 mol) was dissolved in 25 ml of ethanol. Picric acid (2.29 g, 0.01 mol) was dissolved in 15 ml of water. Both the solutions were mixed and to this, 5 ml of 5M HCl was added and stirred for few minutes. The formed complex (I) was filtered and dried. Good quality crystals were grown from ethanol solution by slow evaporation (m. p.: 483 K). Composition: Found (Calculated): C: 38.50 (38.59); H: 2.88 (2.91); N: 22.45 (22.50).

Refinement top

Hydrogen atoms were located in difference Fourier maps and isotropically refined.

Structure description top

The imidazole nucleus appears in a number of naturally occurring products like amino acid histidine and purines which comprise many of the most important bases in nucleic acids. Imidazole derivatives deal with a broad spectrum of pharmacological activities. The crystal structures of some imidazolium picrates have been reported, for instance imidazolium picrate itself (Soriano-García et al. (1990); also two solvates (hydrate and ethanolate) of 2-aminohistamine dipicrate (Nardelli et al.,1987), 4-hydroxymethylimidazolium picrate (Du & Zhao, 2003), two polymorphs of betaine bis(diimidazolium) dipicrate (MacDonald et al., 2005) and 3-benzyl-1-methyl-imidazolium picrate (Pi et al., 2009).

The title compound, 2-methylimidazolium picrate (2-methyl-1H-imidazol-3-ium 2,4,6-trinitrophenolate, Scheme 1) crystallizes with two ionic components, as proved by successful location and refinement of hydrogen atoms at both imiadzole nitrogen atoms as well as by the bond length pattern. Both cyclic fragments are in a good approximation planar. As might be expected, the deviations from the least-squares plane are by an order of magnitude smaller in the imidazolium ring (maximum 0.0028 (10) Å) than in a six-atom ring of picrate anion (0.0289 (10) Å). The two rings make a dihedral angle of 60.28 (7)°. The nitro groups are twisted with respect to the ring plane; the dihedral angles are larger for the substituents ortho- with respect to the C=O- group (18.46 (12)° and 53.59 (9)°) than for the para-group, which is 7.28 (16)°.

The ionic fragments are conneced by relatively short N—H···O hydrogen bonds. One of N—H groups acts as a donor in almost linear hydrogen bond, while the other is involved in the bifurcated N—H···O bonds, in which O1 atom and one of nitro group O atoms act as acceptors. These two bonds are of similar lengths and therefore they deviate significantly from linearity. These hydrogen bonds, together with relatively short C—H···O contacts connect the cations and anions into a layer in which one can find the C12(6) chains, created only by N—H···O hydrogen bonds and R45(21) rings, in which all contacts are involved (Fig. 2).

The layers related by centers of symmetry are additionally connected by quite short π–π stacking interactions between six-membered rings. The distances between the centers of consecutive rings in a stack are 3.594Å and 3.621Å, but if the parallel shift is taken into account the distances between the planes are 3.48Å and 3.27Å (Fig. 3). It should be noted, however, that the parallel shift is in these cases 1.00Å and 1.50Å, respectively, which might suggest weak π–π stacking in the first case but edge-to-edge kind of interaction in the second.

For the crystal structure of imidazolium picrate, see: Soriano-García et al. (1990). For the structures of picrates of some other imidazole derivatives, see, for example: Nardelli et al. (1987); Du & Zhao (2003); MacDonald et al. (2005);Pi et al. (2009).

Computing details top

Data collection: CrysAlis PRO (Oxford Diffraction, 2009); cell refinement: CrysAlis PRO (Oxford Diffraction, 2009); data reduction: CrysAlis PRO (Oxford Diffraction, 2009); program(s) used to solve structure: SIR92 (Altomare et al., 1993); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: Stereochemical Workstation Operation Manual. (Siemens, 1989); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008).

Figures top
[Figure 1] Fig. 1. Anisotropic ellipsoid representation of the compound I together with atom labelling scheme. The ellipsoids are drawn at the 50% probability level, hydrogen atoms are depicted as spheres with arbitrary radii; hydrogen bond is shown as dashed line/
[Figure 2] Fig. 2. The layer of molecules of I as seen approximately along x direction; hydrogen bonds are shown as dashed lines. Syzmmetry codes: (i) x,3/2 - y,-1/2 + z; (ii) x,y,-1 + z; (iii) x,3/2 - y,-3/2 + z.
[Figure 3] Fig. 3. Two layers related by the center of symmetry; hydrogen bonds and π–π contacts are shown as dashed lines.
2-methyl-1H-imidazol-3-ium 2,4,6-trinitrophenolate top
Crystal data top
C4H7N2+·C6H2N3O7−F(000) = 640
Mr = 311.22Dx = 1.676 Mg m−3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybcCell parameters from 2592 reflections
a = 7.0983 (9) Åθ = 2.9–28.2°
b = 21.644 (2) ŵ = 0.15 mm−1
c = 8.1583 (9) ÅT = 295 K
β = 100.327 (12)°Block, yellow
V = 1233.1 (2) Å30.3 × 0.2 × 0.2 mm
Z = 4
Data collection top
Oxford Diffraction Xcalibur Eos
diffractometer		2483 independent reflections
Radiation source: Enhance (Mo) X-ray Source1792 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.014
Detector resolution: 16.1544 pixels mm-1θmax = 28.2°, θmin = 2.9°
ω scansh = −8→9
Absorption correction: multi-scan
(CrysAlis PRO; Oxford Diffraction, 2009)		k = −15→28
Tmin = 0.964, Tmax = 1.000l = −10→10
4778 measured reflections
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.039Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.101All H-atom parameters refined
S = 1.03 w = 1/[σ2(Fo2) + (0.060P)2]
where P = (Fo2 + 2Fc2)/3
2483 reflections(Δ/σ)max = 0.001
235 parametersΔρmax = 0.30 e Å−3
0 restraintsΔρmin = −0.27 e Å−3
Crystal data top
C4H7N2+·C6H2N3O7−V = 1233.1 (2) Å3
Mr = 311.22Z = 4
Monoclinic, P21/cMo Kα radiation
a = 7.0983 (9) ŵ = 0.15 mm−1
b = 21.644 (2) ÅT = 295 K
c = 8.1583 (9) Å0.3 × 0.2 × 0.2 mm
β = 100.327 (12)°
Data collection top
Oxford Diffraction Xcalibur Eos
diffractometer		2483 independent reflections
Absorption correction: multi-scan
(CrysAlis PRO; Oxford Diffraction, 2009)		1792 reflections with I > 2σ(I)
Tmin = 0.964, Tmax = 1.000Rint = 0.014
4778 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0390 restraints
wR(F2) = 0.101All H-atom parameters refined
S = 1.03Δρmax = 0.30 e Å−3
2483 reflectionsΔρmin = −0.27 e Å−3
235 parameters
Special details top

Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.

Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
C10.3265 (2)0.93118 (8)0.60988 (19)0.0241 (4)
O10.38378 (17)0.88003 (5)0.67241 (14)0.0347 (3)
C20.2787 (2)0.98440 (7)0.70037 (19)0.0253 (4)
N20.2874 (2)0.98159 (7)0.88019 (17)0.0358 (4)
O210.2016 (3)1.02077 (8)0.94412 (17)0.0716 (5)
O220.3770 (3)0.94120 (7)0.96128 (17)0.0656 (5)
C30.2171 (2)1.03981 (8)0.6272 (2)0.0266 (4)
H30.189 (2)1.0723 (8)0.691 (2)0.028 (5)*
C40.1956 (2)1.04630 (8)0.4569 (2)0.0267 (4)
N40.1304 (2)1.10493 (7)0.38329 (19)0.0348 (4)
O410.1247 (2)1.11171 (7)0.23347 (17)0.0615 (5)
O420.08086 (19)1.14506 (6)0.47167 (17)0.0479 (4)
C50.2260 (2)0.99677 (8)0.3565 (2)0.0272 (4)
H50.205 (3)0.9999 (9)0.243 (2)0.041 (5)*
C60.2876 (2)0.94228 (7)0.43176 (19)0.0248 (4)
N60.3054 (2)0.89003 (7)0.32303 (17)0.0310 (3)
O610.45451 (19)0.86075 (6)0.34477 (16)0.0436 (4)
O620.1676 (2)0.87781 (7)0.21488 (17)0.0537 (4)
N110.5304 (2)0.76346 (7)0.59823 (18)0.0353 (4)
H110.491 (3)0.8016 (10)0.617 (3)0.054 (6)*
C120.4264 (2)0.72364 (8)0.49579 (19)0.0310 (4)
C12A0.2238 (3)0.73045 (13)0.4178 (3)0.0484 (5)
H12A0.163 (5)0.6936 (15)0.401 (4)0.129 (13)*
H12B0.155 (4)0.7574 (13)0.480 (3)0.094 (9)*
H12C0.213 (4)0.7461 (14)0.318 (4)0.111 (11)*
N130.5382 (2)0.67629 (7)0.47868 (18)0.0341 (4)
H130.506 (3)0.6450 (11)0.416 (3)0.056 (7)*
C140.7165 (3)0.68530 (9)0.5723 (2)0.0377 (4)
H140.811 (3)0.6565 (10)0.574 (2)0.046 (6)*
C150.7118 (3)0.74005 (9)0.6470 (2)0.0391 (5)
H150.808 (3)0.7634 (10)0.719 (3)0.057 (6)*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
C10.0225 (7)0.0236 (9)0.0259 (8)0.0002 (7)0.0035 (6)0.0003 (7)
O10.0505 (7)0.0247 (7)0.0282 (6)0.0088 (6)0.0053 (5)0.0019 (5)
C20.0274 (8)0.0263 (9)0.0219 (8)−0.0003 (7)0.0038 (6)0.0000 (7)
N20.0501 (9)0.0318 (9)0.0252 (7)0.0080 (7)0.0062 (7)−0.0004 (7)
O210.1138 (13)0.0717 (12)0.0334 (7)0.0473 (10)0.0244 (8)0.0002 (8)
O220.1215 (14)0.0427 (9)0.0296 (7)0.0315 (9)0.0057 (8)0.0062 (7)
C30.0266 (8)0.0239 (9)0.0299 (9)0.0008 (7)0.0070 (7)−0.0040 (8)
C40.0280 (8)0.0209 (9)0.0321 (9)0.0018 (7)0.0077 (7)0.0050 (7)
N40.0378 (8)0.0286 (9)0.0385 (8)0.0024 (7)0.0084 (7)0.0083 (7)
O410.1011 (12)0.0457 (9)0.0393 (8)0.0197 (8)0.0173 (8)0.0183 (7)
O420.0632 (9)0.0264 (7)0.0563 (9)0.0118 (6)0.0165 (7)0.0024 (7)
C50.0292 (8)0.0304 (10)0.0223 (8)−0.0002 (7)0.0052 (7)0.0037 (8)
C60.0261 (8)0.0239 (9)0.0250 (8)−0.0007 (7)0.0067 (6)−0.0028 (7)
N60.0395 (8)0.0282 (8)0.0265 (7)−0.0004 (7)0.0093 (6)−0.0008 (6)
O610.0498 (8)0.0378 (8)0.0451 (8)0.0136 (7)0.0134 (6)−0.0063 (6)
O620.0563 (8)0.0575 (10)0.0419 (8)−0.0018 (7)−0.0060 (7)−0.0211 (7)
N110.0479 (9)0.0240 (8)0.0329 (8)−0.0010 (8)0.0044 (7)−0.0042 (7)
C120.0424 (10)0.0252 (9)0.0256 (8)−0.0034 (8)0.0067 (7)−0.0002 (7)
C12A0.0426 (12)0.0519 (15)0.0477 (12)−0.0025 (11)0.0000 (10)0.0012 (12)
N130.0501 (9)0.0230 (8)0.0293 (8)−0.0043 (7)0.0077 (7)−0.0044 (7)
C140.0426 (11)0.0329 (11)0.0381 (10)0.0036 (9)0.0084 (9)0.0046 (9)
C150.0416 (10)0.0374 (12)0.0356 (10)−0.0071 (9)−0.0005 (8)0.0006 (9)
Geometric parameters (Å, º) top
C1—O11.2557 (19)N6—O611.2193 (18)
C1—C21.441 (2)N6—O621.2226 (19)
C1—C61.450 (2)N11—C121.329 (2)
C2—C31.376 (2)N11—C151.375 (2)
C2—N21.459 (2)N11—H110.89 (2)
N2—O221.2067 (19)C12—N131.319 (2)
N2—O211.2145 (19)C12—C12A1.472 (3)
C3—C41.377 (2)C12A—H12A0.91 (3)
C3—H30.918 (18)C12A—H12B0.96 (3)
C4—C51.389 (2)C12A—H12C0.87 (3)
C4—N41.444 (2)N13—C141.370 (2)
N4—O421.2200 (19)N13—H130.86 (2)
N4—O411.2245 (19)C14—C151.336 (3)
C5—C61.365 (2)C14—H140.92 (2)
C5—H50.911 (19)C15—H150.96 (2)
C6—N61.457 (2)
O1—C1—C2125.83 (14)O61—N6—O62123.62 (15)
O1—C1—C6122.88 (14)O61—N6—C6118.85 (14)
C2—C1—C6111.17 (14)O62—N6—C6117.53 (14)
C3—C2—C1124.06 (14)C12—N11—C15109.23 (16)
C3—C2—N2115.19 (14)C12—N11—H11123.3 (13)
C1—C2—N2120.72 (14)C15—N11—H11126.7 (13)
O22—N2—O21121.74 (15)N13—C12—N11107.04 (16)
O22—N2—C2120.29 (14)N13—C12—C12A126.31 (18)
O21—N2—C2117.97 (15)N11—C12—C12A126.64 (18)
C2—C3—C4119.73 (16)C12—C12A—H12A112 (2)
C2—C3—H3120.5 (11)C12—C12A—H12B112.4 (16)
C4—C3—H3119.7 (11)H12A—C12A—H12B110 (2)
C3—C4—C5121.00 (15)C12—C12A—H12C111 (2)
C3—C4—N4118.57 (15)H12A—C12A—H12C104 (3)
C5—C4—N4120.34 (15)H12B—C12A—H12C107 (3)
O42—N4—O41122.90 (16)C12—N13—C14110.12 (16)
O42—N4—C4118.99 (15)C12—N13—H13125.4 (15)
O41—N4—C4118.10 (15)C14—N13—H13124.5 (15)
C6—C5—C4118.21 (15)C15—C14—N13106.55 (17)
C6—C5—H5120.2 (12)C15—C14—H14132.4 (13)
C4—C5—H5121.6 (12)N13—C14—H14121.0 (13)
C5—C6—C1125.60 (15)C14—C15—N11107.06 (17)
C5—C6—N6116.91 (14)C14—C15—H15132.4 (13)
C1—C6—N6117.40 (14)N11—C15—H15120.5 (13)
O1—C1—C2—C3179.72 (16)C4—C5—C6—C1−0.5 (2)
C6—C1—C2—C3−4.2 (2)C4—C5—C6—N6175.84 (13)
O1—C1—C2—N2−2.4 (2)O1—C1—C6—C5−179.73 (16)
C6—C1—C2—N2173.62 (14)C2—C1—C6—C54.1 (2)
C3—C2—N2—O22−163.80 (17)O1—C1—C6—N63.9 (2)
C1—C2—N2—O2218.2 (2)C2—C1—C6—N6−172.26 (13)
C3—C2—N2—O2116.4 (2)C5—C6—N6—O61129.43 (16)
C1—C2—N2—O21−161.61 (17)C1—C6—N6—O61−53.90 (19)
C1—C2—C3—C40.9 (2)C5—C6—N6—O62−51.0 (2)
N2—C2—C3—C4−177.07 (14)C1—C6—N6—O62125.64 (17)
C2—C3—C4—C53.3 (2)C15—N11—C12—N13−0.36 (19)
C2—C3—C4—N4179.90 (14)C15—N11—C12—C12A178.83 (19)
C3—C4—N4—O42−6.2 (2)N11—C12—N13—C140.53 (19)
C5—C4—N4—O42170.49 (15)C12A—C12—N13—C14−178.67 (18)
C3—C4—N4—O41174.92 (16)C12—N13—C14—C15−0.49 (19)
C5—C4—N4—O41−8.4 (2)N13—C14—C15—N110.25 (19)
C3—C4—C5—C6−3.4 (2)C12—N11—C15—C140.1 (2)
N4—C4—C5—C6−179.99 (15)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
C5—H5···O21i0.911 (19)2.478 (19)3.378 (2)169.4 (16)
N11—H11···O10.89 (2)1.95 (2)2.8357 (19)172.9 (19)
N13—H13···O1ii0.86 (2)2.09 (2)2.819 (2)143 (2)
N13—H13···O22ii0.86 (2)2.14 (2)2.782 (2)131.3 (19)
Symmetry codes: (i) x, y, z−1; (ii) x, −y+3/2, z−1/2.

Experimental details

Crystal data
Chemical formulaC4H7N2+·C6H2N3O7−
Mr311.22
Crystal system, space groupMonoclinic, P21/c
Temperature (K)295
a, b, c (Å)7.0983 (9), 21.644 (2), 8.1583 (9)
β (°) 100.327 (12)
V (Å3)1233.1 (2)
Z4
Radiation typeMo Kα
µ (mm−1)0.15
Crystal size (mm)0.3 × 0.2 × 0.2
Data collection
DiffractometerOxford Diffraction Xcalibur Eos
Absorption correctionMulti-scan
(CrysAlis PRO; Oxford Diffraction, 2009)
Tmin, Tmax0.964, 1.000
No. of measured, independent and
observed [I > 2σ(I)] reflections		4778, 2483, 1792
Rint0.014
(sin θ/λ)max (Å−1)0.665
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.039, 0.101, 1.03
No. of reflections2483
No. of parameters235
H-atom treatmentAll H-atom parameters refined
Δρmax, Δρmin (e Å−3)0.30, −0.27

Computer programs: CrysAlis PRO (Oxford Diffraction, 2009), SIR92 (Altomare et al., 1993), SHELXL97 (Sheldrick, 2008), Stereochemical Workstation Operation Manual. (Siemens, 1989).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
C5—H5···O21i0.911 (19)2.478 (19)3.378 (2)169.4 (16)
N11—H11···O10.89 (2)1.95 (2)2.8357 (19)172.9 (19)
N13—H13···O1ii0.86 (2)2.09 (2)2.819 (2)143 (2)
N13—H13···O22ii0.86 (2)2.14 (2)2.782 (2)131.3 (19)
Symmetry codes: (i) x, y, z−1; (ii) x, −y+3/2, z−1/2.
 

Acknowledgements

SS thanks Mangalore University for the research facilities

References

First citationAltomare, A., Cascarano, G., Giacovazzo, C. & Guagliardi, A. (1993). J. Appl. Cryst. 26, 343–350.  CrossRef Web of Science IUCr Journals Google Scholar
 First citationDu, M. & Zhao, X.-J. (2003). Acta Cryst. E59, o1898–o1900.  Web of Science CSD CrossRef CAS IUCr Journals Google Scholar
 First citationMacDonald, J., Yigit, M. V. & Mychajlonka, K. (2005). Cryst. Growth Des. 5, 2248–2255.  Web of Science CSD CrossRef CAS Google Scholar
 First citationNardelli, M., Pelizzi, G., Vitali, F., Bordi, F., Plazzi, P. V. & Vitali, T. (1987). Acta Cryst. C43, 507–514.  CSD CrossRef CAS Web of Science IUCr Journals Google Scholar
 First citationOxford Diffraction (2009). CrysAlis PRO. Oxford Diffraction Ltd, Yarnton, Oxfordshire, England.  Google Scholar
 First citationPi, M., Liu, X.-L., Xu, J.-J. & Jin, C.-M. (2009). Acta Cryst. E65, o2386.  Web of Science CSD CrossRef IUCr Journals Google Scholar
 First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationSiemens (1989). Stereochemical Workstation Operation Manual. Siemens Analytical X-ray Instruments Inc., Madison, Wisconsin, USA.  Google Scholar
 First citationSoriano-García, M., Schatz-Levine, M., Toscano, R. A. & Villena Iribe, R. (1990). Acta Cryst. C46, 1556–1558.  CSD CrossRef Web of Science IUCr Journals Google Scholar

This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 67| Part 1| January 2011| Page o235
https://doi.org/10.1107/S1600536810053390
Follow Acta Cryst. E
Sign up for e-alerts
E-alerts
Follow Acta Cryst. on Twitter
Twitter
Follow us on facebook
Facebook
Sign up for RSS feeds
RSS