Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536803005166/cv6166sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536803005166/cv6166Isup2.hkl |
CCDC reference: 209940
Key indicators
- Single-crystal X-ray study
- T = 293 K
- Mean (C-C) = 0.003 Å
- R factor = 0.040
- wR factor = 0.110
- Data-to-parameter ratio = 9.6
checkCIF results
No syntax errors found ADDSYM reports no extra symmetry
Alert Level A:
PLAT_305 Alert A Isolated Hydrogen Atom (Outside Bond Range ??) <H(3')
Alert Level B:
REFLT_03 From the CIF: _diffrn_reflns_theta_max 65.10 From the CIF: _reflns_number_total 2212 TEST2: Reflns within _diffrn_reflns_theta_max Count of symmetry unique reflns 2466 Completeness (_total/calc) 89.70% Alert B: < 90% complete (theta max?) PLAT_420 Alert B D-H Without Acceptor O(2) - >H(3) ?
Alert Level C:
REFNR_01 Alert C Ratio of reflections to parameters is < 10 for a centrosymmetric structure sine(theta)/lambda 0.5883 Proportion of unique data used 1.0000 Ratio reflections to parameters 9.5758 THETM_01 Alert C The value of sine(theta_max)/wavelength is less than 0.590 Calculated sin(theta_max)/wavelength = 0.5883 General Notes
ABSTM_02 When printed, the submitted absorption T values will be replaced by the scaled T values. Since the ratio of scaled T's is identical to the ratio of reported T values, the scaling does not imply a change to the absorption corrections used in the study. Ratio of Tmax expected/reported 1.127 Tmax scaled 0.835 Tmin scaled 0.613
1 Alert Level A = Potentially serious problem
2 Alert Level B = Potential problem
2 Alert Level C = Please check
Crystals of the title compound suitable for X-ray crystal structure analysis were obtained by slow crystallization of the yellow–green reaction mixture containing copper(II) sulfate (0.0926 g CuSO4·5H2O, 0.37 mmol), 3,5-dinitrosalicylic acid (0.2811 g, 0.74 mmol) and nicotinamide (0.186 g, 1.52 mmol) in water solution (50 ml) in an Erlenmayer flask at room temperature for three months.
The O atom of the hydroxide group is disordered, occupying two statistic positions represented by O3 and O3' with occupancy factors of 0.758 (5) and 0.242 (5), respectively. Atom O3 was refined anisotropically and O3' isotropically. The crystal structure of the title compound was also recalculated by two other ways. For atom O3 (anisotropic refinement) in a single position, R1 = 0.0707 for 1631 reflections and Δρmax = 1.58 e Å−3. For statistically distributed atom O3 (isotropically refined), R1 and Δρmax were 0.0444 and 0.43 e Å−3, respectively. The H atoms were placed in calculated positions, except for H3, which was located from a difference Fourier map.
Data collection: Syntax P21 Software (Syntex, 1974); cell refinement: Syntax P21 Software; data reduction: XP21 (Pavelčík, 1993); program(s) used to solve structure: SHELXS86 (Sheldrick, 1985); program(s) used to refine structure: SHELXL93 (Sheldrick, 1994); molecular graphics: ORTEP (Johnson, 1965); software used to prepare material for publication: SHELXL93.
C6H7N2O+·C7H3N2O7− | Dx = 1.617 Mg m−3 |
Mr = 350.25 | Melting point: 458 K |
Monoclinic, P21/n | Cu Kα radiation, λ = 1.54180 Å |
a = 4.740 (1) Å | Cell parameters from 25 reflections |
b = 21.968 (4) Å | θ = 4.5–11.8° |
c = 13.858 (3) Å | µ = 1.20 mm−1 |
β = 94.62 (3)° | T = 293 K |
V = 1438.3 (5) Å3 | Needle, yellow |
Z = 4 | 0.40 × 0.20 × 0.15 mm |
F(000) = 720 |
Syntex P21 diffractometer | 1631 reflections with I > 2˘I) |
Radiation source: fine-focus sealed tube | Rint = 0.031 |
Graphite monochromator | θmax = 65.1°, θmin = 3.8° |
θ–2θ scans | h = −5→2 |
Absorption correction: ψ scan (North et al., 1968) | k = 0→25 |
Tmin = 0.544, Tmax = 0.741 | l = −16→16 |
3511 measured reflections | 2 standard reflections every 100 reflections |
2212 independent reflections | intensity decay: 15% |
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)] = 0.040 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.110 | H-atom parameters constrained |
S = 1.07 | w = 1/[σ2(Fo2) + (0.0618P)2 + 0.1656P] where P = (Fo2 + 2Fc2)/3 |
2212 reflections | (Δ/σ)max < 0.001 |
231 parameters | Δρmax = 0.15 e Å−3 |
0 restraints | Δρmin = −0.18 e Å−3 |
C6H7N2O+·C7H3N2O7− | V = 1438.3 (5) Å3 |
Mr = 350.25 | Z = 4 |
Monoclinic, P21/n | Cu Kα radiation |
a = 4.740 (1) Å | µ = 1.20 mm−1 |
b = 21.968 (4) Å | T = 293 K |
c = 13.858 (3) Å | 0.40 × 0.20 × 0.15 mm |
β = 94.62 (3)° |
Syntex P21 diffractometer | 1631 reflections with I > 2˘I) |
Absorption correction: ψ scan (North et al., 1968) | Rint = 0.031 |
Tmin = 0.544, Tmax = 0.741 | 2 standard reflections every 100 reflections |
3511 measured reflections | intensity decay: 15% |
2212 independent reflections |
R[F2 > 2σ(F2)] = 0.040 | 0 restraints |
wR(F2) = 0.110 | H-atom parameters constrained |
S = 1.07 | Δρmax = 0.15 e Å−3 |
2212 reflections | Δρmin = −0.18 e Å−3 |
231 parameters |
x | y | z | Uiso*/Ueq | Occ. (<1) | |
O1 | 0.1009 (3) | 0.61448 (7) | 0.90611 (10) | 0.0531 (4) | |
O2 | 0.0081 (4) | 0.67232 (7) | 0.77654 (11) | 0.0593 (5) | |
O3 | 0.2416 (5) | 0.65338 (10) | 0.62978 (14) | 0.0598 (8) | 0.756 (5) |
O3' | 0.4525 (12) | 0.5346 (3) | 0.9078 (4) | 0.049 (2)* | 0.244 (5) |
O4 | 0.4483 (6) | 0.61849 (12) | 0.47593 (14) | 0.0961 (8) | |
O5 | 0.7735 (6) | 0.55335 (13) | 0.48105 (16) | 0.1091 (9) | |
O6 | 1.0494 (4) | 0.44392 (8) | 0.76707 (17) | 0.0766 (6) | |
O7 | 0.8103 (5) | 0.44969 (9) | 0.89099 (14) | 0.0822 (6) | |
O8 | −0.4078 (3) | 0.80338 (7) | 0.72734 (10) | 0.0483 (4) | |
N1 | 0.5982 (5) | 0.58166 (9) | 0.51934 (13) | 0.0545 (5) | |
N2 | 0.8625 (4) | 0.46639 (8) | 0.81108 (15) | 0.0527 (5) | |
N3 | 0.0148 (4) | 0.84673 (9) | 0.76834 (12) | 0.0486 (5) | |
N4 | 0.2075 (4) | 0.82145 (8) | 0.48136 (11) | 0.0417 (4) | |
C1 | 0.3446 (4) | 0.59331 (8) | 0.76774 (13) | 0.0374 (4) | |
C2 | 0.3772 (4) | 0.60750 (8) | 0.67004 (13) | 0.0401 (4) | |
C3 | 0.5656 (5) | 0.57173 (9) | 0.62151 (14) | 0.0421 (5) | |
C4 | 0.7235 (5) | 0.52589 (9) | 0.66740 (15) | 0.0440 (5) | |
C5 | 0.6888 (4) | 0.51422 (8) | 0.76299 (15) | 0.0409 (5) | |
C6 | 0.4990 (4) | 0.54693 (8) | 0.81421 (13) | 0.0396 (4) | |
C7 | 0.1375 (5) | 0.62926 (9) | 0.82058 (14) | 0.0429 (5) | |
C8 | −0.0685 (4) | 0.80166 (8) | 0.61132 (13) | 0.0349 (4) | |
C9 | 0.1295 (4) | 0.83650 (8) | 0.56883 (13) | 0.0378 (4) | |
C10 | 0.1022 (5) | 0.77346 (10) | 0.43197 (14) | 0.0487 (5) | |
C11 | −0.0966 (5) | 0.73825 (10) | 0.47096 (16) | 0.0551 (6) | |
C12 | −0.1842 (5) | 0.75225 (9) | 0.56066 (15) | 0.0445 (5) | |
C13 | −0.1675 (4) | 0.81733 (9) | 0.70847 (13) | 0.0372 (4) | |
H3 | 0.1131 | 0.6712 | 0.7090 | 0.050* | 0.76 |
H3' | 0.2913 | 0.5630 | 0.9303 | 0.050* | 0.24 |
H4 | 0.8527 | 0.5034 | 0.6347 | 0.050* | |
H6 | 0.4753 | 0.5377 | 0.8786 | 0.050* | |
H9 | 0.2072 | 0.8702 | 0.6011 | 0.050* | |
H10 | 0.1642 | 0.7639 | 0.3716 | 0.050* | |
H11 | −0.1711 | 0.7047 | 0.4365 | 0.050* | |
H12 | −0.3232 | 0.7291 | 0.5869 | 0.050* | |
H31 | −0.0332 | 0.8576 | 0.8245 | 0.050* | |
H32 | 0.1790 | 0.8558 | 0.7509 | 0.050* | |
H41 | 0.3310 | 0.8441 | 0.4561 | 0.050* |
U11 | U22 | U33 | U12 | U13 | U23 | |
O1 | 0.0586 (10) | 0.0660 (9) | 0.0370 (8) | 0.0080 (7) | 0.0174 (7) | 0.0003 (6) |
O2 | 0.0709 (11) | 0.0599 (10) | 0.0490 (9) | 0.0242 (8) | 0.0169 (8) | 0.0055 (7) |
O3 | 0.0790 (17) | 0.0604 (13) | 0.0404 (12) | 0.0208 (11) | 0.0076 (10) | 0.0139 (9) |
O4 | 0.130 (2) | 0.1174 (17) | 0.0435 (10) | 0.0287 (15) | 0.0240 (11) | 0.0298 (11) |
O5 | 0.141 (2) | 0.136 (2) | 0.0572 (11) | 0.0480 (17) | 0.0518 (13) | 0.0005 (12) |
O6 | 0.0665 (12) | 0.0561 (10) | 0.1099 (16) | 0.0213 (8) | 0.0242 (11) | 0.0127 (10) |
O7 | 0.1089 (17) | 0.0757 (12) | 0.0615 (11) | 0.0250 (11) | 0.0040 (10) | 0.0258 (10) |
O8 | 0.0393 (8) | 0.0639 (9) | 0.0435 (8) | −0.0026 (7) | 0.0150 (6) | 0.0048 (7) |
N1 | 0.0757 (14) | 0.0542 (10) | 0.0358 (9) | −0.0080 (10) | 0.0176 (9) | −0.0021 (8) |
N2 | 0.0538 (12) | 0.0398 (9) | 0.0637 (12) | 0.0015 (8) | 0.0007 (9) | 0.0045 (8) |
N3 | 0.0428 (11) | 0.0746 (12) | 0.0295 (8) | −0.0067 (8) | 0.0102 (7) | −0.0069 (8) |
N4 | 0.0417 (10) | 0.0534 (9) | 0.0311 (8) | 0.0005 (7) | 0.0096 (7) | 0.0053 (7) |
C1 | 0.0409 (11) | 0.0397 (9) | 0.0321 (9) | −0.0041 (8) | 0.0064 (8) | −0.0003 (8) |
C2 | 0.0496 (12) | 0.0386 (10) | 0.0324 (9) | −0.0002 (8) | 0.0049 (8) | 0.0023 (8) |
C3 | 0.0543 (13) | 0.0419 (10) | 0.0314 (9) | −0.0057 (9) | 0.0105 (8) | −0.0014 (8) |
C4 | 0.0484 (12) | 0.0377 (10) | 0.0478 (11) | −0.0021 (9) | 0.0157 (9) | −0.0046 (9) |
C5 | 0.0440 (12) | 0.0337 (9) | 0.0450 (10) | −0.0011 (8) | 0.0033 (8) | 0.0027 (8) |
C6 | 0.0462 (12) | 0.0409 (10) | 0.0317 (9) | −0.0060 (8) | 0.0039 (8) | 0.0037 (7) |
C7 | 0.0485 (12) | 0.0455 (10) | 0.0358 (10) | −0.0021 (9) | 0.0114 (9) | −0.0042 (8) |
C8 | 0.0333 (10) | 0.0410 (10) | 0.0306 (8) | 0.0020 (8) | 0.0043 (7) | 0.0033 (7) |
C9 | 0.0394 (12) | 0.0433 (10) | 0.0309 (9) | −0.0001 (8) | 0.0039 (8) | −0.0004 (7) |
C10 | 0.0579 (14) | 0.0574 (13) | 0.0316 (9) | 0.0061 (10) | 0.0079 (9) | −0.0058 (9) |
C11 | 0.0684 (16) | 0.0495 (11) | 0.0470 (12) | −0.0050 (11) | 0.0031 (11) | −0.0125 (9) |
C12 | 0.0484 (12) | 0.0419 (10) | 0.0436 (11) | −0.0073 (9) | 0.0050 (9) | 0.0001 (9) |
C13 | 0.0392 (12) | 0.0419 (10) | 0.0310 (9) | 0.0049 (8) | 0.0069 (8) | 0.0059 (7) |
O1—C7 | 1.254 (2) | C1—C2 | 1.410 (3) |
O2—C7 | 1.258 (3) | C1—C7 | 1.497 (3) |
O3—C2 | 1.297 (3) | C2—C3 | 1.402 (3) |
O4—N1 | 1.205 (3) | C3—C4 | 1.379 (3) |
O5—N1 | 1.196 (3) | C4—C5 | 1.372 (3) |
O6—N2 | 1.220 (3) | C4—H4 | 0.9317 |
O7—N2 | 1.211 (3) | C5—C6 | 1.390 (3) |
O8—C13 | 1.228 (2) | C6—H6 | 0.9302 |
N1—C3 | 1.453 (3) | C8—C9 | 1.379 (3) |
N2—C5 | 1.462 (3) | C8—C12 | 1.382 (3) |
N3—C13 | 1.318 (3) | C8—C13 | 1.501 (2) |
N3—H31 | 0.8622 | C9—H9 | 0.9256 |
N3—H32 | 0.8565 | C10—C11 | 1.364 (3) |
N4—C9 | 1.337 (3) | C10—H10 | 0.9324 |
N4—C10 | 1.332 (3) | C11—C12 | 1.377 (3) |
N4—H41 | 0.8637 | C11—H11 | 0.9317 |
C1—C6 | 1.383 (3) | C12—H12 | 0.9299 |
C7—O1—H3' | 106.6 | C4—C5—C6 | 121.96 (19) |
C7—O2—H3 | 99.2 | C4—C5—N2 | 117.87 (18) |
C2—O3—H3 | 96.6 | C6—C5—N2 | 120.16 (18) |
C6—O3'—H3' | 109.9 | O3'—C6—C1 | 118.1 (3) |
C6—O3'—H6 | 5.5 | O3'—C6—C5 | 123.0 (3) |
H3'—O3'—H6 | 115.0 | C1—C6—C5 | 118.88 (17) |
O5—N1—O4 | 122.0 (2) | O3'—C6—H6 | 2.6 |
O5—N1—C3 | 119.1 (2) | C1—C6—H6 | 120.5 |
O4—N1—C3 | 118.8 (2) | C5—C6—H6 | 120.7 |
O7—N2—O6 | 123.0 (2) | O1—C7—O2 | 123.63 (18) |
O7—N2—C5 | 119.1 (2) | O1—C7—C1 | 118.15 (19) |
O6—N2—C5 | 117.9 (2) | O2—C7—C1 | 118.22 (17) |
C13—N3—H31 | 119.8 | C9—C8—C12 | 118.35 (17) |
C13—N3—H32 | 120.1 | C9—C8—C13 | 121.89 (17) |
H31—N3—H32 | 120.1 | C12—C8—C13 | 119.73 (17) |
C9—N4—C10 | 122.82 (17) | N4—C9—C8 | 119.81 (18) |
C9—N4—H41 | 118.1 | N4—C9—H9 | 120.5 |
C10—N4—H41 | 119.1 | C8—C9—H9 | 119.7 |
C6—C1—C2 | 121.02 (18) | N4—C10—C11 | 119.19 (18) |
C6—C1—C7 | 120.29 (17) | N4—C10—H10 | 120.5 |
C2—C1—C7 | 118.68 (18) | C11—C10—H10 | 120.3 |
O3—C2—C3 | 122.82 (18) | C10—C11—C12 | 119.95 (19) |
O3—C2—C1 | 119.74 (19) | C10—C11—H11 | 119.4 |
C3—C2—C1 | 117.40 (18) | C12—C11—H11 | 120.7 |
C4—C3—C2 | 122.08 (17) | C8—C12—C11 | 119.87 (19) |
C4—C3—N1 | 117.56 (19) | C8—C12—H12 | 119.7 |
C2—C3—N1 | 120.35 (19) | C11—C12—H12 | 120.4 |
C5—C4—C3 | 118.61 (18) | O8—C13—N3 | 124.10 (18) |
C5—C4—H4 | 120.3 | O8—C13—C8 | 119.74 (18) |
C3—C4—H4 | 121.0 | N3—C13—C8 | 116.15 (17) |
C6—C1—C2—O3 | −176.2 (2) | C2—C1—C6—C5 | 0.1 (3) |
C7—C1—C2—O3 | 4.2 (3) | C7—C1—C6—C5 | 179.73 (18) |
C6—C1—C2—C3 | 1.7 (3) | C4—C5—C6—O3' | 177.2 (3) |
C7—C1—C2—C3 | −177.91 (18) | N2—C5—C6—O3' | −3.8 (4) |
O3—C2—C3—C4 | 175.2 (2) | C4—C5—C6—C1 | −1.2 (3) |
C1—C2—C3—C4 | −2.6 (3) | N2—C5—C6—C1 | 177.80 (18) |
O3—C2—C3—N1 | −5.5 (3) | C6—C1—C7—O1 | −2.8 (3) |
C1—C2—C3—N1 | 176.67 (18) | C2—C1—C7—O1 | 176.84 (19) |
O5—N1—C3—C4 | −5.6 (3) | C6—C1—C7—O2 | 177.76 (19) |
O4—N1—C3—C4 | 174.8 (2) | C2—C1—C7—O2 | −2.6 (3) |
O5—N1—C3—C2 | 175.1 (2) | C10—N4—C9—C8 | −0.1 (3) |
O4—N1—C3—C2 | −4.5 (3) | C12—C8—C9—N4 | −1.0 (3) |
C2—C3—C4—C5 | 1.6 (3) | C13—C8—C9—N4 | −178.76 (17) |
N1—C3—C4—C5 | −177.70 (18) | C9—N4—C10—C11 | 0.9 (3) |
C3—C4—C5—C6 | 0.4 (3) | N4—C10—C11—C12 | −0.5 (3) |
C3—C4—C5—N2 | −178.65 (17) | C9—C8—C12—C11 | 1.3 (3) |
O7—N2—C5—C4 | −170.3 (2) | C13—C8—C12—C11 | 179.13 (19) |
O6—N2—C5—C4 | 7.7 (3) | C10—C11—C12—C8 | −0.6 (3) |
O7—N2—C5—C6 | 10.7 (3) | C9—C8—C13—O8 | 150.58 (19) |
O6—N2—C5—C6 | −171.4 (2) | C12—C8—C13—O8 | −27.2 (3) |
C2—C1—C6—O3' | −178.4 (3) | C9—C8—C13—N3 | −28.4 (3) |
C7—C1—C6—O3' | 1.2 (4) | C12—C8—C13—N3 | 153.80 (19) |
D—H···A | D—H | H···A | D···A | D—H···A |
N3—H31···O4i | 0.86 | 2.17 | 3.018 (2) | 167 |
N3—H32···O8ii | 0.86 | 2.32 | 2.995 (2) | 136 |
N3—H32···O6iii | 0.86 | 2.35 | 3.038 (3) | 138 |
N4—H41···O1iv | 0.86 | 1.76 | 2.619 (2) | 176 |
Symmetry codes: (i) x−1/2, −y+3/2, z+1/2; (ii) x+1, y, z; (iii) −x+3/2, y+1/2, −z+3/2; (iv) x+1/2, −y+3/2, z−1/2. |
Experimental details
Crystal data | |
Chemical formula | C6H7N2O+·C7H3N2O7− |
Mr | 350.25 |
Crystal system, space group | Monoclinic, P21/n |
Temperature (K) | 293 |
a, b, c (Å) | 4.740 (1), 21.968 (4), 13.858 (3) |
β (°) | 94.62 (3) |
V (Å3) | 1438.3 (5) |
Z | 4 |
Radiation type | Cu Kα |
µ (mm−1) | 1.20 |
Crystal size (mm) | 0.40 × 0.20 × 0.15 |
Data collection | |
Diffractometer | Syntex P21 diffractometer |
Absorption correction | ψ scan (North et al., 1968) |
Tmin, Tmax | 0.544, 0.741 |
No. of measured, independent and observed [I > 2˘I)] reflections | 3511, 2212, 1631 |
Rint | 0.031 |
(sin θ/λ)max (Å−1) | 0.588 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.040, 0.110, 1.07 |
No. of reflections | 2212 |
No. of parameters | 231 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.15, −0.18 |
Computer programs: Syntax P21 Software (Syntex, 1974), Syntax P21 Software, XP21 (Pavelčík, 1993), SHELXS86 (Sheldrick, 1985), SHELXL93 (Sheldrick, 1994), ORTEP (Johnson, 1965), SHELXL93.
O1—C7 | 1.254 (2) | C1—C6 | 1.383 (3) |
O2—C7 | 1.258 (3) | C1—C2 | 1.410 (3) |
O3—C2 | 1.297 (3) | C1—C7 | 1.497 (3) |
O4—N1 | 1.205 (3) | C2—C3 | 1.402 (3) |
O5—N1 | 1.196 (3) | C3—C4 | 1.379 (3) |
O6—N2 | 1.220 (3) | C4—C5 | 1.372 (3) |
O7—N2 | 1.211 (3) | C5—C6 | 1.390 (3) |
O8—C13 | 1.228 (2) | C8—C9 | 1.379 (3) |
N1—C3 | 1.453 (3) | C8—C12 | 1.382 (3) |
N2—C5 | 1.462 (3) | C8—C13 | 1.501 (2) |
N3—C13 | 1.318 (3) | C10—C11 | 1.364 (3) |
N4—C9 | 1.337 (3) | C11—C12 | 1.377 (3) |
N4—C10 | 1.332 (3) | ||
O5—N1—O4 | 122.0 (2) | C4—C5—C6 | 121.96 (19) |
O5—N1—C3 | 119.1 (2) | C4—C5—N2 | 117.87 (18) |
O4—N1—C3 | 118.8 (2) | C6—C5—N2 | 120.16 (18) |
O7—N2—O6 | 123.0 (2) | O1—C7—O2 | 123.63 (18) |
O7—N2—C5 | 119.1 (2) | O1—C7—C1 | 118.15 (19) |
O6—N2—C5 | 117.9 (2) | O2—C7—C1 | 118.22 (17) |
C9—N4—C10 | 122.82 (17) | C9—C8—C12 | 118.35 (17) |
C6—C1—C2 | 121.02 (18) | C9—C8—C13 | 121.89 (17) |
C6—C1—C7 | 120.29 (17) | C12—C8—C13 | 119.73 (17) |
C2—C1—C7 | 118.68 (18) | N4—C9—C8 | 119.81 (18) |
O3—C2—C3 | 122.82 (18) | N4—C10—C11 | 119.19 (18) |
O3—C2—C1 | 119.74 (19) | C10—C11—C12 | 119.95 (19) |
C3—C2—C1 | 117.40 (18) | C8—C12—C11 | 119.87 (19) |
C4—C3—C2 | 122.08 (17) | O8—C13—N3 | 124.10 (18) |
C4—C3—N1 | 117.56 (19) | O8—C13—C8 | 119.74 (18) |
C2—C3—N1 | 120.35 (19) | N3—C13—C8 | 116.15 (17) |
C5—C4—C3 | 118.61 (18) |
D—H···A | D—H | H···A | D···A | D—H···A |
N3—H31···O4i | 0.86 | 2.17 | 3.018 (2) | 167 |
N3—H32···O8ii | 0.86 | 2.32 | 2.995 (2) | 136 |
N3—H32···O6iii | 0.86 | 2.35 | 3.038 (3) | 138 |
N4—H41···O1iv | 0.86 | 1.76 | 2.619 (2) | 176 |
Symmetry codes: (i) x−1/2, −y+3/2, z+1/2; (ii) x+1, y, z; (iii) −x+3/2, y+1/2, −z+3/2; (iv) x+1/2, −y+3/2, z−1/2. |
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As part of our study of new copper(II) complexes with 3,5-dinitrosalicylate anions and nicotinamide, the title compound, (I), was prepared. Later, the same compound were also prepared by reaction of nicotinamide with 3,5-dinitrosalicylic acid in water solution. To our knowledge, salt formation is typical for 3,5-dinitrosalicylic acid, e.g. with 3-amino-1,2,4-triazole (Smith et al., 1996) or even with different aminobenzoic acids (Smith et al., 1995).
Neighbouring protonated molecules of nicotinamide and 3,5-dinitrosalicylate anions form dimers via hydrogen bonds N4—H41···O1iv (see Table 2). Additional hydrogen bonds are formed by the amide H atoms of the nicotinamide cation and by the O atom of the nitro groups of the salicylate anion (Table 2). Atom H3 forms an intramolecular hydrogen bond with atoms O2 and O3. Atom O3 is statistically distributed between two positions.