Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807054840/hk2358sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807054840/hk2358Isup2.hkl |
CCDC reference: 672849
For the preparation of the title compound, acryloyl chloride (1.1 ml) containing diphenylpicrylhydrazyl polymerization inhibitor (0.01%) and sodium hydroxide solution [0.61 g, in H2O (5 ml)] were added dropwise simultaneously over a 30 min period to a well stirred aqueous solution of glycylglycine [2.0 g, in H2O (30 ml)] and sodium hydroxide [0.61 g, in H2O (5 ml)], and then stirred 1 h more. The reaction of the mixture was kept at 273 K in an ice-water bath. The solution was acidified to pH = 2 with 6 N HCl and the resulting solid was filtered off and crystallized from ethanol (95%) (yield; 63%, m.p. 421–423 K).
H atoms (for H2O) were located in difference syntheses and constrained to ride on their parent atom [O—H = 0.8543, 0.8553 Å and Uiso(H) = 1.2Ueq(O)]. The remaining H atoms were positioned geometrically, with N—H = 0.86 Å (for NH), O—H = 0.82 Å (for OH) and C—H = 0.93, 0.93 and 0.97 Å, for aromatic and methylene H atoms and constrained to ride on their parent atoms, with Uiso(H) = xUeq(C,N,O), where x = 1.5 for OH H and x = 1.2 for all other H atoms.
Data collection: CAD-4 Software (Enraf–Nonius, 1989); cell refinement: CAD-4 Software (Enraf–Nonius, 1989); data reduction: XCAD4 (Harms & Wocadlo, 1995); program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: SHELXTL (Bruker, 2000); software used to prepare material for publication: SHELXTL (Bruker, 2000).
C7H10N2O4·H2O | F(000) = 432 |
Mr = 204.19 | Dx = 1.403 Mg m−3 |
Monoclinic, P21/n | Melting point: 422 K |
Hall symbol: -P 2yn | Mo Kα radiation, λ = 0.71073 Å |
a = 13.332 (3) Å | Cell parameters from 25 reflections |
b = 5.149 (1) Å | θ = 9–13° |
c = 14.458 (3) Å | µ = 0.12 mm−1 |
β = 103.09 (3)° | T = 294 K |
V = 966.7 (4) Å3 | Block, colorless |
Z = 4 | 0.40 × 0.10 × 0.10 mm |
Enraf–Nonius CAD-4 diffractometer | 1424 reflections with I > 2σ(I) |
Radiation source: fine-focus sealed tube | Rint = 0.052 |
Graphite monochromator | θmax = 25.9°, θmin = 1.9° |
ω/2θ scans | h = 0→16 |
Absorption correction: ψ scan (North et al., 1968) | k = 0→6 |
Tmin = 0.954, Tmax = 0.988 | l = −17→17 |
1959 measured reflections | 3 standard reflections every 120 min |
1875 independent reflections | intensity decay: none |
Refinement on F2 | Secondary atom site location: difference Fourier map |
Least-squares matrix: full | Hydrogen site location: inferred from neighbouring sites |
R[F2 > 2σ(F2)] = 0.053 | H-atom parameters constrained |
wR(F2) = 0.163 | w = 1/[σ2(Fo2) + (0.1P)2 + 0.2P] where P = (Fo2 + 2Fc2)/3 |
S = 1.03 | (Δ/σ)max < 0.001 |
1875 reflections | Δρmax = 0.20 e Å−3 |
127 parameters | Δρmin = −0.26 e Å−3 |
0 restraints | Extinction correction: SHELXL97 |
Primary atom site location: structure-invariant direct methods | Extinction coefficient: 0.028 (5) |
C7H10N2O4·H2O | V = 966.7 (4) Å3 |
Mr = 204.19 | Z = 4 |
Monoclinic, P21/n | Mo Kα radiation |
a = 13.332 (3) Å | µ = 0.12 mm−1 |
b = 5.149 (1) Å | T = 294 K |
c = 14.458 (3) Å | 0.40 × 0.10 × 0.10 mm |
β = 103.09 (3)° |
Enraf–Nonius CAD-4 diffractometer | 1424 reflections with I > 2σ(I) |
Absorption correction: ψ scan (North et al., 1968) | Rint = 0.052 |
Tmin = 0.954, Tmax = 0.988 | 3 standard reflections every 120 min |
1959 measured reflections | intensity decay: none |
1875 independent reflections |
R[F2 > 2σ(F2)] = 0.053 | 0 restraints |
wR(F2) = 0.163 | H-atom parameters constrained |
S = 1.03 | Δρmax = 0.20 e Å−3 |
1875 reflections | Δρmin = −0.26 e Å−3 |
127 parameters |
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. |
x | y | z | Uiso*/Ueq | ||
OW | 0.23119 (13) | 1.4675 (4) | 0.32683 (15) | 0.0778 (7) | |
HWA | 0.1700 | 1.5204 | 0.3028 | 0.093* | |
HWB | 0.2821 | 1.5271 | 0.3067 | 0.093* | |
O1 | −0.09533 (11) | 0.1547 (3) | 0.75924 (12) | 0.0549 (5) | |
O2 | 0.22255 (11) | 0.4246 (3) | 0.68108 (11) | 0.0471 (4) | |
O3 | 0.26156 (12) | 1.1329 (4) | 0.45810 (13) | 0.0596 (5) | |
H3A | 0.2427 | 1.2454 | 0.4178 | 0.089* | |
O4 | 0.09464 (11) | 1.1214 (3) | 0.46083 (12) | 0.0524 (5) | |
N1 | 0.06626 (12) | 0.2081 (4) | 0.73869 (12) | 0.0394 (4) | |
H1A | 0.1293 | 0.1580 | 0.7550 | 0.047* | |
N2 | 0.12573 (12) | 0.7266 (3) | 0.59002 (12) | 0.0401 (5) | |
H2A | 0.0655 | 0.7923 | 0.5697 | 0.048* | |
C1 | −0.0148 (2) | −0.2397 (8) | 0.8963 (3) | 0.1003 (14) | |
H1B | −0.0855 | −0.2131 | 0.8852 | 0.120* | |
H1C | 0.0166 | −0.3632 | 0.9403 | 0.120* | |
C2 | 0.03980 (18) | −0.1049 (5) | 0.85048 (17) | 0.0520 (6) | |
H2B | 0.1103 | −0.1356 | 0.8630 | 0.062* | |
C3 | −0.00320 (16) | 0.0949 (4) | 0.77944 (15) | 0.0392 (5) | |
C4 | 0.03959 (15) | 0.4106 (4) | 0.66844 (15) | 0.0408 (5) | |
H4A | 0.0015 | 0.5463 | 0.6919 | 0.049* | |
H4B | −0.0036 | 0.3403 | 0.6107 | 0.049* | |
C5 | 0.13773 (14) | 0.5225 (4) | 0.64742 (14) | 0.0352 (5) | |
C6 | 0.21375 (16) | 0.8398 (5) | 0.56131 (17) | 0.0463 (6) | |
H6A | 0.2508 | 0.7044 | 0.5363 | 0.056* | |
H6B | 0.2601 | 0.9146 | 0.6164 | 0.056* | |
C7 | 0.18165 (15) | 1.0451 (4) | 0.48762 (15) | 0.0386 (5) |
U11 | U22 | U33 | U12 | U13 | U23 | |
OW | 0.0528 (11) | 0.0893 (15) | 0.1042 (16) | 0.0224 (10) | 0.0447 (10) | 0.0482 (13) |
O1 | 0.0335 (8) | 0.0620 (11) | 0.0732 (11) | 0.0044 (7) | 0.0204 (7) | 0.0196 (9) |
O2 | 0.0321 (8) | 0.0464 (9) | 0.0635 (10) | 0.0015 (7) | 0.0121 (7) | 0.0119 (8) |
O3 | 0.0356 (9) | 0.0713 (12) | 0.0752 (12) | 0.0008 (8) | 0.0194 (8) | 0.0283 (10) |
O4 | 0.0324 (9) | 0.0629 (11) | 0.0634 (10) | 0.0051 (7) | 0.0144 (7) | 0.0182 (8) |
N1 | 0.0292 (9) | 0.0432 (10) | 0.0472 (9) | −0.0002 (7) | 0.0116 (7) | 0.0040 (8) |
N2 | 0.0290 (9) | 0.0410 (10) | 0.0515 (10) | 0.0013 (7) | 0.0116 (7) | 0.0072 (8) |
C1 | 0.0625 (19) | 0.128 (3) | 0.117 (3) | 0.017 (2) | 0.0358 (19) | 0.078 (3) |
C2 | 0.0392 (12) | 0.0551 (15) | 0.0633 (15) | 0.0032 (10) | 0.0147 (11) | 0.0164 (12) |
C3 | 0.0325 (10) | 0.0421 (12) | 0.0456 (11) | −0.0012 (9) | 0.0141 (9) | 0.0001 (9) |
C4 | 0.0332 (11) | 0.0448 (12) | 0.0457 (11) | −0.0024 (9) | 0.0114 (9) | 0.0029 (10) |
C5 | 0.0295 (10) | 0.0375 (11) | 0.0389 (10) | −0.0028 (8) | 0.0088 (8) | −0.0052 (9) |
C6 | 0.0320 (11) | 0.0467 (13) | 0.0614 (13) | 0.0004 (9) | 0.0130 (9) | 0.0124 (11) |
C7 | 0.0308 (10) | 0.0410 (11) | 0.0453 (12) | −0.0047 (9) | 0.0116 (8) | −0.0014 (9) |
OW—HWA | 0.8553 | N2—H2A | 0.8600 |
OW—HWB | 0.8543 | C1—C2 | 1.292 (4) |
O1—C3 | 1.235 (3) | C1—H1B | 0.9300 |
O2—C5 | 1.233 (2) | C1—H1C | 0.9300 |
O3—C7 | 1.314 (2) | C2—C3 | 1.475 (3) |
O3—H3A | 0.8200 | C2—H2B | 0.9300 |
O4—C7 | 1.203 (2) | C4—C5 | 1.522 (3) |
N1—C3 | 1.338 (3) | C4—H4A | 0.9700 |
N1—C4 | 1.443 (3) | C4—H4B | 0.9700 |
N1—H1A | 0.8600 | C6—C7 | 1.493 (3) |
N2—C5 | 1.326 (3) | C6—H6A | 0.9700 |
N2—C6 | 1.452 (3) | C6—H6B | 0.9700 |
HWA—OW—HWB | 120.4 | N1—C4—H4A | 109.8 |
C3—N1—C4 | 122.67 (17) | C5—C4—H4A | 109.8 |
C3—N1—H1A | 118.7 | N1—C4—H4B | 109.8 |
C4—N1—H1A | 118.7 | C5—C4—H4B | 109.8 |
C2—C1—H1B | 120.0 | H4A—C4—H4B | 108.3 |
C2—C1—H1C | 120.0 | O2—C5—N2 | 122.73 (18) |
H1B—C1—H1C | 120.0 | O2—C5—C4 | 121.30 (19) |
C5—N2—C6 | 120.40 (17) | N2—C5—C4 | 115.96 (17) |
C5—N2—H2A | 119.8 | N2—C6—C7 | 111.62 (18) |
C6—N2—H2A | 119.8 | N2—C6—H6A | 109.3 |
C1—C2—C3 | 123.8 (2) | C7—C6—H6A | 109.3 |
C1—C2—H2B | 118.1 | N2—C6—H6B | 109.3 |
C3—C2—H2B | 118.1 | C7—C6—H6B | 109.3 |
C7—O3—H3A | 109.5 | H6A—C6—H6B | 108.0 |
O1—C3—N1 | 122.5 (2) | O4—C7—O3 | 125.2 (2) |
O1—C3—C2 | 123.19 (19) | O4—C7—C6 | 124.11 (19) |
N1—C3—C2 | 114.31 (18) | O3—C7—C6 | 110.66 (18) |
N1—C4—C5 | 109.16 (16) | ||
C4—N1—C3—O1 | 0.5 (3) | C6—N2—C5—C4 | −176.70 (19) |
C4—N1—C3—C2 | −179.1 (2) | N1—C4—C5—O2 | 6.8 (3) |
C1—C2—C3—O1 | 1.7 (5) | N1—C4—C5—N2 | −174.33 (17) |
C1—C2—C3—N1 | −178.6 (3) | C5—N2—C6—C7 | 172.89 (18) |
C3—N1—C4—C5 | 171.95 (18) | N2—C6—C7—O4 | 5.4 (3) |
C6—N2—C5—O2 | 2.2 (3) | N2—C6—C7—O3 | −175.83 (19) |
D—H···A | D—H | H···A | D···A | D—H···A |
OW—HWA···O1i | 0.86 | 2.05 | 2.755 (3) | 140 |
N1—H1A···O2ii | 0.86 | 2.32 | 3.150 (2) | 163 |
N2—H2A···O4i | 0.86 | 2.13 | 2.968 (2) | 166 |
C2—H2B···O2ii | 0.93 | 2.47 | 3.305 (3) | 149 |
Symmetry codes: (i) −x, −y+2, −z+1; (ii) −x+1/2, y−1/2, −z+3/2. |
Experimental details
Crystal data | |
Chemical formula | C7H10N2O4·H2O |
Mr | 204.19 |
Crystal system, space group | Monoclinic, P21/n |
Temperature (K) | 294 |
a, b, c (Å) | 13.332 (3), 5.149 (1), 14.458 (3) |
β (°) | 103.09 (3) |
V (Å3) | 966.7 (4) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 0.12 |
Crystal size (mm) | 0.40 × 0.10 × 0.10 |
Data collection | |
Diffractometer | Enraf–Nonius CAD-4 diffractometer |
Absorption correction | ψ scan (North et al., 1968) |
Tmin, Tmax | 0.954, 0.988 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 1959, 1875, 1424 |
Rint | 0.052 |
(sin θ/λ)max (Å−1) | 0.615 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.053, 0.163, 1.03 |
No. of reflections | 1875 |
No. of parameters | 127 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.20, −0.26 |
Computer programs: CAD-4 Software (Enraf–Nonius, 1989), XCAD4 (Harms & Wocadlo, 1995), SHELXS97 (Sheldrick, 1997), SHELXL97 (Sheldrick, 1997), SHELXTL (Bruker, 2000).
D—H···A | D—H | H···A | D···A | D—H···A |
OW—HWA···O1i | 0.86 | 2.05 | 2.755 (3) | 140 |
N1—H1A···O2ii | 0.86 | 2.32 | 3.150 (2) | 163 |
N2—H2A···O4i | 0.86 | 2.13 | 2.968 (2) | 166 |
C2—H2B···O2ii | 0.93 | 2.47 | 3.305 (3) | 149 |
Symmetry codes: (i) −x, −y+2, −z+1; (ii) −x+1/2, y−1/2, −z+3/2. |
N-acryloylglycylglycine(I) is one of the useful synthetic intermediates and free radical addition monomers. The crystal structure determination of the title compound, (I), has been carried out in order to elucidate its molecular conformation.
In the molecule of the title compound, (I), (Fig.1) the bond lengths and angles are within normal ranges (Allen et al., 1987). The main chain of the molecule is nearly planar.
In the crystal structure, O—H···O, N—H···O and C—H···O hydrogen bonds (Table 1) link the molecules into a three dimensional network, in which they may be effective in the stabilization of the structure.