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

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ISSN: 2056-9890

Poly[(μ4-3-carb­­oxy­pyrazine-2-carboxyl­ato)(μ4-nitrato)dilithium]

aInstitute of Nuclear Chemistry and Technology, ul. Dorodna 16, 03-195 Warszawa, Poland
*Correspondence e-mail: j.leciejewicz@ichtj.waw.pl

(Received 9 December 2012; accepted 13 December 2012; online 19 December 2012)

In the title compound, [Li2(C6H3N2O4)2(NO3)]n, the two symmetry-independent LiI ions are each in a trigonal–bipyramidal coordination and are bridged by N,O-bonding ligands, forming mol­ecular ribbons propagating in [010]. Each LiI ion is also coordinated by two O atoms from nitrate ions, connecting the ribbons into a three-dimensional network. Very strong intra­molecular O—H⋯O hydrogen bonds occur between the carboxyl and the carboxylate group.

Related literature

For three structures of lithium(I) complexes with pyrazine-2,3-dicarboxyl­ate and water ligands, see: Tombul et al. (2008[Tombul, M., Güven, K. & Büyükgüngör, O. (2008). Acta Cryst. E64, m491-m492.]); Tombul & Güven (2009)[Tombul, M. & Guven, K. (2009). Acta Cryst. E65, m1704-m1705.]; Starosta & Leciejewicz (2011[Starosta, W. & Leciejewicz, J. (2011). Acta Cryst. E67, m1133-m1134.]). For structures of calcium(II) complexes with the title ligand, see: Ptasiewicz-Bąk & Leciejewicz (1997[Ptasiewicz-Bąk, H. & Leciejewicz, J. (1997). Pol. J. Chem. 71, 1603-1610.]); Starosta & Leciejewicz (2004[Starosta, W. & Leciejewicz, J. (2004). J. Coord. Chem. 57, 1151-1156.], 2005a[Starosta, W. & Leciejewicz, J. (2005a). J. Coord. Chem. 58, 891-898.],b[Starosta, W. & Leciejewicz, J. (2005b). J. Coord. Chem. 58, 963-968.]).

[Scheme 1]

Experimental

Crystal data
  • [Li2(C6H3N2O4)2(NO3)]

  • Mr = 241.99

  • Monoclinic, P 21

  • a = 4.6273 (1) Å

  • b = 15.8565 (3) Å

  • c = 6.1719 (2) Å

  • β = 95.598 (2)°

  • V = 450.69 (2) Å3

  • Z = 2

  • Mo Kα radiation

  • μ = 0.16 mm−1

  • T = 293 K

  • 0.20 × 0.14 × 0.12 mm

Data collection
  • Agilent SuperNova (Dual, Cu at zero, Eos) diffractometer

  • Absorption correction: multi-scan (CrysAlis PRO; Agilent, 2011[Agilent (2011). CrysAlis PRO. Agilent Technologies, Yarnton, England.]) Tmin = 0.936, Tmax = 1.000

  • 4032 measured reflections

  • 2572 independent reflections

  • 2401 reflections with I > 2σ(I)

  • Rint = 0.015

Refinement
  • R[F2 > 2σ(F2)] = 0.036

  • wR(F2) = 0.084

  • S = 1.10

  • 2572 reflections

  • 167 parameters

  • 1 restraint

  • H atoms treated by a mixture of independent and constrained refinement

  • Δρmax = 0.21 e Å−3

  • Δρmin = −0.20 e Å−3

Table 1
Selected bond lengths (Å)

Li1—O1 2.086 (3)
Li1—O5 2.005 (3)
Li1—N1 2.158 (3)
Li1—O7i 1.994 (3)
Li1—O3ii 1.999 (3)
Li2—N4 2.176 (3)
Li2—O1iii 1.989 (3)
Li2—O5iv 2.014 (3)
Li2—O6v 2.040 (4)
Li2—O3 2.086 (3)
Symmetry codes: (i) x+1, y, z; (ii) [-x+1, y+{\script{1\over 2}}, -z+1]; (iii) [-x+1, y-{\script{1\over 2}}, -z+1]; (iv) [-x+1, y-{\script{1\over 2}}, -z]; (v) [-x, y-{\script{1\over 2}}, -z].

Table 2
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A DA D—H⋯A
O2—H1⋯O4 1.07 (4) 1.34 (4) 2.3955 (19) 170 (4)

Data collection: CrysAlis PRO (Agilent, 2011[Agilent (2011). CrysAlis PRO. Agilent Technologies, Yarnton, England.]); cell refinement: CrysAlis PRO; data reduction: CrysAlis PRO; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); molecular graphics: SHELXTL (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); software used to prepare material for publication: SHELXTL.

Supporting information


Comment top

Pyrazine-2,3-dicarboxylate dianion shows large versality in forming coordination compounds with metal ions. Depending on the adopted chemical synthesis procedures, compounds with a number of different polymeric structures have been observed, as for example, in the case of the Ca(II) ion (Ptasiewicz-Bąk & Leciejewicz, 1997; Starosta & Leciejewicz, 2004, 2005a, 2005b). Polymeric structures of three LiI complexes with the title ligand have been reported (Tombul et al., 2008; Tombul & Güven, 2009; Starosta & Leciejewicz, 2011). Recently we have obtained a new compund with the title ligand. The asymmetric unit of the title compound contains two symmetry independent LiI ions. Each shows a distorted trigonal-bipyramidal coordination geometry. The Li1 ion is coordinated by ligand N1,O1 bonding group, a carboxylato O3ii atom from the adjacent ligand and O5 and O7i atoms from two different nitrate ions. The O1, O5, O7i atoms form a base, the Li1 ion is 0.1572 (3) Å out of this plane; N1 and O3ii atoms are at the axial positions. The same coordination geometry shows the Li2 ion which is situated 0.3616 (3) Å out of the equatorial plane composed of N4, O1iii and O6v atoms, while the O3 and O5iv atoms form the apices. The observed Li—O and Li—N bond distances are typical of LiI complexes with diazine carboxylate ligands. Ligand carboxylate O2 and O4 atoms remain coordination inactive. Fourier maps indicate clearly, that the O2 atom is protonated acting as a donor in a low-barrier intramolecular hydrogen bond of 2.3955 (19) Å to the O4 atom suggesting a partial proton transfer(Table 2). The ligand is monovalent and with the nitrate anion maintains the charge balance in the structure. Pyrazine ring is planar with r.m.s. of 0.0051 (2) Å; carboxylate groups C7/O1/O2 and C8/O3/O4 form with it dihedral angles of 8.4 (1)° and 12.5 (1)°, respectively. Ligand molecule bridges metal ions in µ4 mode. Li1 and Li2 ions are chelated by both N,O groups of a ligand and bidentate O1ii and O3iiatoms [Fig. 1]. A dimeric moiety Li1/O1/L2ii/O3iii constitutes a link in a bridging pathway formed by ligand molecules, giving rise to molecular ribbons propagating in the [010] direction. A nitrate anion with r.m.s. of 0.0016 (1) Å acts also in the µ4 mode and forms the other bridging pathway: while the O6 atom coordinates the Li2v and the O7 atom - the Li1iv ion, the O5 atom acts as bidentate bridging to the Li1 and Li2iii ions giving rise to a three-dimensional framework (Fig. 2).

Related literature top

For three structures of lithium(I) complexes with pyrazine-2,3-dicarboxylate and water ligands, see: Tombul et al. (2008); Tombul & Güven (2009); Starosta & Leciejewicz (2011). For structures of calcium(II) complexes with the title ligand, see: Ptasiewicz-Bąk & Leciejewicz (1997); Starosta & Leciejewicz (2004, 2005a,b).

Experimental top

An aqueous solution containing 1 mmol of lithium(I) nitrate and 1 mmol of pyrazine-2,3-dicarboxylic acid dihydrate was boiled with stirring under reflux for 6 h. After cooling to room temperature three drops of 1 N nitric acid were added to maintain pH of 5. Then the solution was left to evaporate to dryness. Deposited single crystal plates were washed with cold ethanol and dried in the air.

Refinement top

The hydrogen atom of carboxylate group was located in a difference map and was refined independently with an isotropic displacement parameter. H atoms bonded to pyrazine ring C atoms were placed in calculated positions with C—H = 0.93 and 0.96 Å and treated as riding on the parent atoms with Uiso(H)= 1.2Ueq(C).

Computing details top

Data collection: CrysAlis PRO (Agilent, 2011); cell refinement: CrysAlis PRO (Agilent, 2011); data reduction: CrysAlis PRO (Agilent, 2011); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures top
[Figure 1] Fig. 1. A fragment of the structure of the title compound with atom labelling scheme and 50% probability displacement ellipsoids. Symmetry code: (i) x + 1, y, z; (ii) -x + 1, y + 1/2, -z + 2; (iii) -x + 1, y - 1/2, -z + 2; (iv) -x + 1, y - 1/2, -z + 1; (v) -x, y - 1/2, -z + 1.
[Figure 2] Fig. 2. The packing of molecular ribbons in the structure of the title compound showing nitrate bridging mode.
Poly[(µ4-3-carboxypyrazine-2-carboxylato)(µ4-nitrato)dilithium] top
Crystal data top
[Li2(C6H3N2O4)2(NO3)]F(000) = 242
Mr = 241.99Dx = 1.783 Mg m3
Monoclinic, P21Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2ybCell parameters from 2509 reflections
a = 4.6273 (1) Åθ = 3.3–30.7°
b = 15.8565 (3) ŵ = 0.16 mm1
c = 6.1719 (2) ÅT = 293 K
β = 95.598 (2)°Block, colourless
V = 450.69 (2) Å30.20 × 0.14 × 0.12 mm
Z = 2
Data collection top
Agilent SuperNova (Dual, Cu at zero, Eos)
diffractometer
2572 independent reflections
Radiation source: SuperNova (Mo) X-ray Source2401 reflections with I > 2σ(I)
Mirror monochromatorRint = 0.015
Detector resolution: 16.0131 pixels mm-1θmax = 30.7°, θmin = 3.3°
ω scansh = 56
Absorption correction: multi-scan
(CrysAlis PRO; Agilent, 2011)
k = 2122
Tmin = 0.936, Tmax = 1.000l = 58
4032 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)] = 0.036Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.084H atoms treated by a mixture of independent and constrained refinement
S = 1.10 w = 1/[σ2(Fo2) + (0.0337P)2 + 0.0702P]
where P = (Fo2 + 2Fc2)/3
2572 reflections(Δ/σ)max < 0.001
167 parametersΔρmax = 0.21 e Å3
1 restraintΔρmin = 0.20 e Å3
Crystal data top
[Li2(C6H3N2O4)2(NO3)]V = 450.69 (2) Å3
Mr = 241.99Z = 2
Monoclinic, P21Mo Kα radiation
a = 4.6273 (1) ŵ = 0.16 mm1
b = 15.8565 (3) ÅT = 293 K
c = 6.1719 (2) Å0.20 × 0.14 × 0.12 mm
β = 95.598 (2)°
Data collection top
Agilent SuperNova (Dual, Cu at zero, Eos)
diffractometer
2572 independent reflections
Absorption correction: multi-scan
(CrysAlis PRO; Agilent, 2011)
2401 reflections with I > 2σ(I)
Tmin = 0.936, Tmax = 1.000Rint = 0.015
4032 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0361 restraint
wR(F2) = 0.084H atoms treated by a mixture of independent and constrained refinement
S = 1.10Δρmax = 0.21 e Å3
2572 reflectionsΔρmin = 0.20 e Å3
167 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
O10.5316 (3)0.40681 (8)0.6101 (2)0.0322 (3)
O50.4586 (3)0.48672 (8)0.0630 (2)0.0297 (3)
C20.4874 (4)0.27654 (10)0.4273 (3)0.0223 (3)
N40.5051 (4)0.14644 (9)0.2348 (2)0.0279 (3)
N10.6499 (3)0.31421 (9)0.2871 (2)0.0278 (3)
N20.1867 (3)0.47658 (9)0.0539 (2)0.0243 (3)
O20.2330 (4)0.31513 (9)0.7378 (3)0.0427 (4)
C80.2425 (4)0.13507 (11)0.5462 (3)0.0261 (3)
C30.4152 (4)0.19074 (10)0.4027 (3)0.0228 (3)
O70.0838 (3)0.43786 (9)0.2022 (3)0.0393 (3)
O60.0354 (3)0.50501 (10)0.1046 (2)0.0388 (3)
C50.6615 (4)0.18550 (12)0.0970 (3)0.0326 (4)
H50.72230.15590.02050.039*
C70.4118 (4)0.33782 (11)0.6048 (3)0.0267 (3)
C60.7368 (5)0.27000 (11)0.1245 (3)0.0338 (4)
H60.85000.29570.02690.041*
Li10.7058 (7)0.44849 (19)0.3298 (5)0.0289 (6)
Li20.3903 (7)0.0133 (2)0.2244 (5)0.0300 (6)
O30.2524 (3)0.05895 (8)0.5143 (2)0.0329 (3)
O40.1008 (4)0.16985 (8)0.6880 (3)0.0444 (4)
H10.153 (8)0.252 (2)0.713 (6)0.093 (11)*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
O10.0444 (8)0.0222 (6)0.0311 (7)0.0058 (6)0.0086 (6)0.0054 (5)
O50.0184 (5)0.0402 (7)0.0307 (6)0.0033 (5)0.0045 (4)0.0052 (5)
C20.0242 (7)0.0194 (7)0.0236 (7)0.0013 (6)0.0044 (6)0.0004 (6)
N40.0352 (8)0.0224 (7)0.0275 (8)0.0012 (6)0.0092 (6)0.0022 (6)
N10.0337 (8)0.0208 (6)0.0303 (8)0.0019 (6)0.0103 (6)0.0006 (6)
N20.0223 (6)0.0230 (6)0.0285 (7)0.0014 (5)0.0073 (5)0.0009 (5)
O20.0596 (9)0.0274 (6)0.0463 (9)0.0092 (7)0.0320 (7)0.0110 (6)
C80.0308 (9)0.0230 (8)0.0249 (9)0.0012 (7)0.0039 (7)0.0008 (6)
C30.0237 (8)0.0214 (7)0.0239 (8)0.0003 (6)0.0050 (6)0.0017 (6)
O70.0332 (7)0.0416 (8)0.0461 (8)0.0019 (6)0.0197 (6)0.0144 (6)
O60.0280 (7)0.0479 (8)0.0392 (7)0.0007 (6)0.0036 (6)0.0101 (6)
C50.0433 (10)0.0271 (9)0.0301 (9)0.0005 (8)0.0173 (8)0.0051 (7)
C70.0322 (9)0.0217 (7)0.0265 (8)0.0010 (6)0.0045 (7)0.0022 (6)
C60.0426 (11)0.0258 (8)0.0356 (10)0.0016 (8)0.0171 (8)0.0032 (7)
Li10.0342 (16)0.0249 (14)0.0288 (15)0.0009 (12)0.0097 (12)0.0000 (12)
Li20.0382 (16)0.0234 (13)0.0287 (15)0.0015 (13)0.0052 (13)0.0008 (12)
O30.0495 (8)0.0207 (6)0.0293 (6)0.0037 (5)0.0085 (6)0.0027 (5)
O40.0629 (10)0.0275 (7)0.0488 (9)0.0113 (7)0.0359 (8)0.0059 (6)
Geometric parameters (Å, º) top
O1—C71.225 (2)O2—C71.273 (2)
O1—Li2i1.989 (3)O2—H11.07 (4)
Li1—O12.086 (3)C8—O31.224 (2)
O5—N21.2643 (18)C8—O41.269 (2)
Li1—O52.005 (3)C8—C31.530 (2)
Li1—N12.158 (3)O7—Li1iv1.994 (3)
Li1—O7ii1.994 (3)O6—Li2v2.040 (4)
Li1—O3i1.999 (3)C5—C61.391 (3)
O5—Li2iii2.014 (3)C5—H50.9300
C2—N11.341 (2)C6—H60.9300
C2—C31.406 (2)Li1—Li2i3.011 (4)
C2—C71.530 (2)Li2—O1vi1.989 (3)
N4—C51.324 (2)Li2—O5vii2.014 (3)
N4—C31.351 (2)Li2—O6viii2.040 (4)
Li2—N42.176 (3)Li2—O32.086 (3)
N1—C61.319 (2)Li2—Li1vi3.011 (4)
N2—O61.231 (2)O3—Li1vi1.999 (3)
N2—O71.2359 (19)O4—H11.34 (4)
C7—O1—Li2i146.19 (15)C5—C6—H6119.5
C7—O1—Li1118.12 (15)O7ii—Li1—O3i102.51 (15)
Li2i—O1—Li195.24 (14)O7ii—Li1—O598.83 (14)
N2—O5—Li1118.93 (13)O3i—Li1—O598.69 (14)
N2—O5—Li2iii114.63 (14)O7ii—Li1—O1136.49 (18)
Li1—O5—Li2iii124.59 (14)O3i—Li1—O184.57 (13)
N1—C2—C3120.27 (14)O5—Li1—O1122.78 (17)
N1—C2—C7111.15 (14)O7ii—Li1—N188.16 (13)
C3—C2—C7128.55 (15)O3i—Li1—N1158.15 (18)
C5—N4—C3118.59 (14)O5—Li1—N198.41 (14)
C5—N4—Li2125.60 (15)O1—Li1—N174.76 (11)
C3—N4—Li2115.76 (14)O7ii—Li1—Li2i127.08 (16)
C6—N1—C2119.08 (15)O3i—Li1—Li2i43.67 (9)
C6—N1—Li1125.14 (14)O5—Li1—Li2i121.60 (15)
C2—N1—Li1115.41 (13)O1—Li1—Li2i41.13 (9)
O6—N2—O7122.70 (15)N1—Li1—Li2i114.95 (13)
O6—N2—O5118.37 (14)O1vi—Li2—O5vii102.31 (15)
O7—N2—O5118.93 (15)O1vi—Li2—O6viii104.59 (16)
C7—O2—H1114 (2)O5vii—Li2—O6viii94.18 (14)
O3—C8—O4124.69 (17)O1vi—Li2—O384.81 (13)
O3—C8—C3116.47 (15)O5vii—Li2—O3171.64 (18)
O4—C8—C3118.83 (14)O6viii—Li2—O388.17 (14)
N4—C3—C2119.89 (14)O1vi—Li2—N4141.01 (18)
N4—C3—C8111.18 (14)O5vii—Li2—N497.16 (14)
C2—C3—C8128.92 (14)O6viii—Li2—N4107.32 (15)
N2—O7—Li1iv131.81 (15)O3—Li2—N474.49 (12)
N2—O6—Li2v139.98 (15)O1vi—Li2—Li1vi43.63 (9)
N4—C5—C6121.23 (16)O5vii—Li2—Li1vi145.93 (15)
N4—C5—H5119.4O6viii—Li2—Li1vi94.92 (13)
C6—C5—H5119.4O3—Li2—Li1vi41.41 (9)
O1—C7—O2123.79 (16)N4—Li2—Li1vi111.21 (14)
O1—C7—C2116.83 (15)C8—O3—Li1vi142.15 (15)
O2—C7—C2119.38 (15)C8—O3—Li2119.94 (14)
N1—C6—C5120.92 (17)Li1vi—O3—Li294.92 (14)
N1—C6—H6119.5C8—O4—H1113.8 (17)
C3—C2—N1—C61.0 (3)N2—O5—Li1—Li2i57.2 (2)
C7—C2—N1—C6179.39 (16)Li2iii—O5—Li1—Li2i139.21 (19)
C3—C2—N1—Li1174.35 (15)C7—O1—Li1—O7ii88.5 (3)
C7—C2—N1—Li17.3 (2)Li2i—O1—Li1—O7ii97.2 (3)
Li1—O5—N2—O6175.52 (16)C7—O1—Li1—O3i168.99 (15)
Li2iii—O5—N2—O619.3 (2)Li2i—O1—Li1—O3i5.28 (15)
Li1—O5—N2—O75.3 (2)C7—O1—Li1—O572.1 (2)
Li2iii—O5—N2—O7159.91 (16)Li2i—O1—Li1—O5102.13 (19)
C5—N4—C3—C20.3 (3)C7—O1—Li1—N118.14 (18)
Li2—N4—C3—C2177.86 (16)Li2i—O1—Li1—N1167.59 (13)
C5—N4—C3—C8179.02 (17)C7—O1—Li1—Li2i174.3 (2)
Li2—N4—C3—C81.4 (2)C6—N1—Li1—O7ii34.8 (2)
N1—C2—C3—N41.3 (3)C2—N1—Li1—O7ii152.34 (15)
C7—C2—C3—N4179.31 (17)C6—N1—Li1—O3i155.0 (4)
N1—C2—C3—C8177.86 (17)C2—N1—Li1—O3i32.2 (6)
C7—C2—C3—C80.2 (3)C6—N1—Li1—O563.8 (2)
O3—C8—C3—N412.0 (2)C2—N1—Li1—O5109.00 (16)
O4—C8—C3—N4167.97 (17)C6—N1—Li1—O1174.35 (17)
O3—C8—C3—C2167.18 (17)C2—N1—Li1—O112.80 (17)
O4—C8—C3—C212.8 (3)C6—N1—Li1—Li2i165.38 (18)
O6—N2—O7—Li1iv32.3 (3)C2—N1—Li1—Li2i21.8 (2)
O5—N2—O7—Li1iv148.58 (19)C5—N4—Li2—O1vi112.0 (3)
O7—N2—O6—Li2v1.3 (3)C3—N4—Li2—O1vi65.4 (3)
O5—N2—O6—Li2v179.55 (19)C5—N4—Li2—O5vii7.8 (2)
C3—N4—C5—C60.9 (3)C3—N4—Li2—O5vii174.83 (14)
Li2—N4—C5—C6176.40 (18)C5—N4—Li2—O6viii104.4 (2)
Li2i—O1—C7—O29.4 (4)C3—N4—Li2—O6viii78.16 (19)
Li1—O1—C7—O2160.34 (19)C5—N4—Li2—O3172.54 (18)
Li2i—O1—C7—C2170.2 (2)C3—N4—Li2—O34.88 (16)
Li1—O1—C7—C220.1 (2)C5—N4—Li2—Li1vi153.02 (18)
N1—C2—C7—O17.9 (2)C3—N4—Li2—Li1vi24.4 (2)
C3—C2—C7—O1170.27 (18)O4—C8—O3—Li1vi43.1 (4)
N1—C2—C7—O2172.51 (18)C3—C8—O3—Li1vi136.9 (2)
C3—C2—C7—O29.3 (3)O4—C8—O3—Li2162.41 (19)
C2—N1—C6—C50.2 (3)C3—C8—O3—Li217.6 (2)
Li1—N1—C6—C5172.44 (19)O1vi—Li2—O3—C8159.34 (16)
N4—C5—C6—N11.2 (3)O5vii—Li2—O3—C810.7 (14)
N2—O5—Li1—O7ii158.55 (14)O6viii—Li2—O3—C895.84 (18)
Li2iii—O5—Li1—O7ii5.1 (2)N4—Li2—O3—C812.71 (19)
N2—O5—Li1—O3i97.24 (17)Li1vi—Li2—O3—C8164.6 (2)
Li2iii—O5—Li1—O3i99.13 (17)O1vi—Li2—O3—Li1vi5.27 (15)
N2—O5—Li1—O18.1 (2)O5vii—Li2—O3—Li1vi153.9 (13)
Li2iii—O5—Li1—O1171.75 (15)O6viii—Li2—O3—Li1vi99.55 (14)
N2—O5—Li1—N169.12 (17)N4—Li2—O3—Li1vi151.90 (13)
Li2iii—O5—Li1—N194.52 (18)
Symmetry codes: (i) x+1, y+1/2, z+1; (ii) x+1, y, z; (iii) x+1, y+1/2, z; (iv) x1, y, z; (v) x, y+1/2, z; (vi) x+1, y1/2, z+1; (vii) x+1, y1/2, z; (viii) x, y1/2, z.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O2—H1···O41.07 (4)1.34 (4)2.3955 (19)170 (4)

Experimental details

Crystal data
Chemical formula[Li2(C6H3N2O4)2(NO3)]
Mr241.99
Crystal system, space groupMonoclinic, P21
Temperature (K)293
a, b, c (Å)4.6273 (1), 15.8565 (3), 6.1719 (2)
β (°) 95.598 (2)
V3)450.69 (2)
Z2
Radiation typeMo Kα
µ (mm1)0.16
Crystal size (mm)0.20 × 0.14 × 0.12
Data collection
DiffractometerAgilent SuperNova (Dual, Cu at zero, Eos)
diffractometer
Absorption correctionMulti-scan
(CrysAlis PRO; Agilent, 2011)
Tmin, Tmax0.936, 1.000
No. of measured, independent and
observed [I > 2σ(I)] reflections
4032, 2572, 2401
Rint0.015
(sin θ/λ)max1)0.719
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.036, 0.084, 1.10
No. of reflections2572
No. of parameters167
No. of restraints1
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å3)0.21, 0.20

Computer programs: CrysAlis PRO (Agilent, 2011), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008).

Selected bond lengths (Å) top
Li1—O12.086 (3)Li2—N42.176 (3)
Li1—O52.005 (3)Li2—O1iii1.989 (3)
Li1—N12.158 (3)Li2—O5iv2.014 (3)
Li1—O7i1.994 (3)Li2—O6v2.040 (4)
Li1—O3ii1.999 (3)Li2—O32.086 (3)
Symmetry codes: (i) x+1, y, z; (ii) x+1, y+1/2, z+1; (iii) x+1, y1/2, z+1; (iv) x+1, y1/2, z; (v) x, y1/2, z.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O2—H1···O41.07 (4)1.34 (4)2.3955 (19)170 (4)
 

References

First citationAgilent (2011). CrysAlis PRO. Agilent Technologies, Yarnton, England.
First citationPtasiewicz-Bąk, H. & Leciejewicz, J. (1997). Pol. J. Chem. 71, 1603–1610.
First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals
First citationStarosta, W. & Leciejewicz, J. (2004). J. Coord. Chem. 57, 1151–1156.  Web of Science CSD CrossRef CAS
First citationStarosta, W. & Leciejewicz, J. (2005a). J. Coord. Chem. 58, 891–898.  Web of Science CSD CrossRef CAS
First citationStarosta, W. & Leciejewicz, J. (2005b). J. Coord. Chem. 58, 963–968.  Web of Science CSD CrossRef CAS
First citationStarosta, W. & Leciejewicz, J. (2011). Acta Cryst. E67, m1133–m1134.  Web of Science CSD CrossRef CAS IUCr Journals
First citationTombul, M. & Guven, K. (2009). Acta Cryst. E65, m1704–m1705.  Web of Science CSD CrossRef CAS IUCr Journals
First citationTombul, M., Güven, K. & Büyükgüngör, O. (2008). Acta Cryst. E64, m491–m492.  Web of Science CSD CrossRef CAS IUCr Journals

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