Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807055195/hk2364sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807055195/hk2364Isup2.hkl |
CCDC reference: 672864
(2-aminophenyl)(phenyl)methanone was prepared by a method reported recently with a little modification (Zhu et al., 2005). Crystals of (I) suitable for X-ray analysis were obtained by dissolving (2-aminophenyl)(phenyl)methanone (1.0 g, 5.1 mmol) in a solution of hydrochloride acid (5 ml, 1.0 mol/l) and evaporating the solvent slowly at room temperature for about 5 d.
H atoms (for H2O) were located in difference syntheses and refined isotropically [O—H = 0.86 (4) and 0.87 (5) Å, Uiso(H) = 0.10 (2) and 0.11 (2) Å2]. The remaining H atoms were positioned geometrically with N—H = 0.89 Å (for NH3) and C—H = 0.93 Å for aromatic H atoms, and constrained to ride on their parent atoms, with Uiso(H) = xUeq(C,N), where x = 1.2 for aromatic H and x = 1.5 for NH3 H atoms.
Data collection: CAD-4 Software (Enraf–Nonius, 1985); cell refinement: CAD-4 Software (Enraf–Nonius, 1985); 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).
C13H12NO+·Cl−·H2O | F(000) = 528 |
Mr = 251.70 | Dx = 1.315 Mg m−3 |
Monoclinic, P21/c | Mo Kα radiation, λ = 0.71073 Å |
Hall symbol: -P 2ybc | Cell parameters from 25 reflections |
a = 4.771 (1) Å | θ = 9–12° |
b = 17.450 (4) Å | µ = 0.29 mm−1 |
c = 15.277 (3) Å | T = 298 K |
β = 90.50 (3)° | Needle, colorless |
V = 1271.8 (5) Å3 | 0.30 × 0.10 × 0.10 mm |
Z = 4 |
Nonius CAD-4 diffractometer | 1522 reflections with I > 2σ(I) |
Radiation source: fine-focus sealed tube | Rint = 0.065 |
Graphite monochromator | θmax = 26.0°, θmin = 1.8° |
ω/2θ scans | h = −5→5 |
Absorption correction: ψ scan (North et al., 1968) | k = 0→21 |
Tmin = 0.918, Tmax = 0.972 | l = 0→18 |
2786 measured reflections | 3 standard reflections every 120 min |
2479 independent reflections | intensity decay: none |
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)] = 0.068 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.174 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.03 | w = 1/[σ2(Fo2) + (0.07P)2 + 0.6P] where P = (Fo2 + 2Fc2)/3 |
2479 reflections | (Δ/σ)max = 0.001 |
163 parameters | Δρmax = 0.35 e Å−3 |
3 restraints | Δρmin = −0.23 e Å−3 |
C13H12NO+·Cl−·H2O | V = 1271.8 (5) Å3 |
Mr = 251.70 | Z = 4 |
Monoclinic, P21/c | Mo Kα radiation |
a = 4.771 (1) Å | µ = 0.29 mm−1 |
b = 17.450 (4) Å | T = 298 K |
c = 15.277 (3) Å | 0.30 × 0.10 × 0.10 mm |
β = 90.50 (3)° |
Nonius CAD-4 diffractometer | 1522 reflections with I > 2σ(I) |
Absorption correction: ψ scan (North et al., 1968) | Rint = 0.065 |
Tmin = 0.918, Tmax = 0.972 | 3 standard reflections every 120 min |
2786 measured reflections | intensity decay: none |
2479 independent reflections |
R[F2 > 2σ(F2)] = 0.068 | 3 restraints |
wR(F2) = 0.174 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.03 | Δρmax = 0.35 e Å−3 |
2479 reflections | Δρmin = −0.23 e Å−3 |
163 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 | ||
Cl | 1.0018 (2) | 0.34988 (6) | 1.01031 (6) | 0.0466 (3) | |
OW | 0.4922 (7) | 0.56862 (19) | 0.8837 (2) | 0.0602 (9) | |
HWA | 0.366 (8) | 0.591 (3) | 0.914 (3) | 0.10 (2)* | |
HWB | 0.632 (7) | 0.596 (3) | 0.903 (4) | 0.11 (2)* | |
O | −0.0034 (6) | 0.47495 (18) | 0.81909 (19) | 0.0541 (8) | |
N | 0.4887 (6) | 0.41120 (18) | 0.88813 (19) | 0.0394 (8) | |
H0A | 0.6493 | 0.3993 | 0.9149 | 0.059* | |
H0B | 0.3457 | 0.3968 | 0.9213 | 0.059* | |
H0C | 0.4809 | 0.4616 | 0.8794 | 0.059* | |
C1 | 0.6114 (11) | 0.2658 (3) | 0.7154 (3) | 0.0650 (13) | |
H1A | 0.7167 | 0.2215 | 0.7081 | 0.078* | |
C2 | 0.4379 (11) | 0.2909 (3) | 0.6492 (3) | 0.0651 (14) | |
H2A | 0.4250 | 0.2633 | 0.5973 | 0.078* | |
C3 | 0.2834 (10) | 0.3566 (3) | 0.6594 (3) | 0.0585 (12) | |
H3A | 0.1667 | 0.3732 | 0.6141 | 0.070* | |
C4 | 0.2994 (8) | 0.3992 (2) | 0.7374 (2) | 0.0408 (9) | |
C5 | 0.4727 (8) | 0.3716 (2) | 0.8040 (2) | 0.0384 (9) | |
C6 | 0.6292 (9) | 0.3067 (2) | 0.7928 (3) | 0.0516 (11) | |
H6A | 0.7479 | 0.2899 | 0.8375 | 0.062* | |
C7 | 0.1231 (8) | 0.4689 (2) | 0.7509 (3) | 0.0432 (10) | |
C8 | 0.1051 (8) | 0.5295 (3) | 0.6834 (3) | 0.0457 (10) | |
C9 | −0.0827 (10) | 0.5888 (3) | 0.6937 (3) | 0.0626 (13) | |
H9A | −0.2023 | 0.5887 | 0.7415 | 0.075* | |
C10 | −0.0957 (12) | 0.6478 (3) | 0.6347 (4) | 0.0761 (15) | |
H10A | −0.2215 | 0.6877 | 0.6437 | 0.091* | |
C11 | 0.0721 (12) | 0.6489 (3) | 0.5634 (3) | 0.0679 (14) | |
H11A | 0.0594 | 0.6887 | 0.5231 | 0.082* | |
C12 | 0.2563 (13) | 0.5918 (3) | 0.5519 (3) | 0.0771 (16) | |
H12A | 0.3717 | 0.5923 | 0.5032 | 0.093* | |
C13 | 0.2776 (11) | 0.5322 (3) | 0.6115 (3) | 0.0638 (13) | |
H13A | 0.4093 | 0.4937 | 0.6029 | 0.077* |
U11 | U22 | U33 | U12 | U13 | U23 | |
Cl | 0.0380 (5) | 0.0552 (6) | 0.0465 (6) | 0.0004 (5) | 0.0016 (4) | 0.0006 (5) |
OW | 0.0421 (18) | 0.062 (2) | 0.076 (2) | −0.0039 (17) | 0.0082 (17) | −0.0183 (17) |
O | 0.0365 (15) | 0.074 (2) | 0.0516 (18) | 0.0013 (14) | 0.0056 (14) | 0.0060 (15) |
N | 0.0293 (16) | 0.052 (2) | 0.0368 (17) | −0.0025 (15) | 0.0005 (14) | 0.0011 (15) |
C1 | 0.075 (3) | 0.044 (3) | 0.076 (3) | 0.005 (2) | 0.001 (3) | −0.004 (2) |
C2 | 0.089 (4) | 0.050 (3) | 0.057 (3) | −0.008 (3) | 0.006 (3) | −0.014 (2) |
C3 | 0.062 (3) | 0.063 (3) | 0.049 (2) | −0.009 (3) | −0.008 (2) | −0.002 (2) |
C4 | 0.036 (2) | 0.043 (2) | 0.044 (2) | −0.0054 (18) | 0.0012 (17) | 0.0018 (18) |
C5 | 0.035 (2) | 0.041 (2) | 0.039 (2) | −0.0065 (18) | 0.0046 (16) | 0.0012 (17) |
C6 | 0.053 (3) | 0.046 (3) | 0.056 (3) | 0.001 (2) | −0.003 (2) | 0.000 (2) |
C7 | 0.031 (2) | 0.059 (3) | 0.040 (2) | −0.0082 (19) | −0.0008 (17) | 0.000 (2) |
C8 | 0.038 (2) | 0.056 (3) | 0.043 (2) | −0.005 (2) | −0.0028 (18) | 0.002 (2) |
C9 | 0.054 (3) | 0.069 (3) | 0.065 (3) | 0.016 (3) | 0.006 (2) | 0.006 (3) |
C10 | 0.076 (4) | 0.060 (3) | 0.092 (4) | 0.021 (3) | −0.010 (3) | 0.003 (3) |
C11 | 0.093 (4) | 0.050 (3) | 0.060 (3) | −0.006 (3) | −0.017 (3) | 0.006 (3) |
C12 | 0.109 (5) | 0.066 (3) | 0.056 (3) | 0.001 (3) | 0.017 (3) | 0.008 (3) |
C13 | 0.075 (3) | 0.056 (3) | 0.060 (3) | 0.010 (3) | 0.014 (3) | 0.008 (2) |
OW—HWA | 0.86 (4) | C4—C7 | 1.493 (6) |
OW—HWB | 0.87 (5) | C5—C6 | 1.369 (5) |
O—C7 | 1.213 (4) | C6—H6A | 0.9300 |
N—C5 | 1.461 (5) | C7—C8 | 1.480 (6) |
N—H0A | 0.8900 | C8—C13 | 1.379 (6) |
N—H0B | 0.8900 | C8—C9 | 1.379 (6) |
N—H0C | 0.8900 | C9—C10 | 1.369 (7) |
C1—C2 | 1.372 (7) | C9—H9A | 0.9300 |
C1—C6 | 1.383 (6) | C10—C11 | 1.358 (7) |
C1—H1A | 0.9300 | C10—H10A | 0.9300 |
C2—C3 | 1.372 (6) | C11—C12 | 1.341 (7) |
C2—H2A | 0.9300 | C11—H11A | 0.9300 |
C3—C4 | 1.406 (6) | C12—C13 | 1.385 (7) |
C3—H3A | 0.9300 | C12—H12A | 0.9300 |
C4—C5 | 1.391 (5) | C13—H13A | 0.9300 |
HWB—OW—HWA | 96 (3) | C5—C6—H6A | 119.9 |
C5—N—H0A | 109.5 | C1—C6—H6A | 119.9 |
C5—N—H0B | 109.5 | O—C7—C8 | 120.6 (4) |
H0A—N—H0B | 109.5 | O—C7—C4 | 118.4 (4) |
C5—N—H0C | 109.5 | C8—C7—C4 | 121.0 (3) |
H0A—N—H0C | 109.5 | C13—C8—C9 | 117.3 (4) |
H0B—N—H0C | 109.5 | C13—C8—C7 | 123.3 (4) |
C2—C1—C6 | 119.8 (5) | C9—C8—C7 | 119.4 (4) |
C2—C1—H1A | 120.1 | C10—C9—C8 | 120.9 (5) |
C6—C1—H1A | 120.1 | C10—C9—H9A | 119.5 |
C3—C2—C1 | 120.3 (4) | C8—C9—H9A | 119.5 |
C3—C2—H2A | 119.9 | C11—C10—C9 | 121.1 (5) |
C1—C2—H2A | 119.9 | C11—C10—H10A | 119.5 |
C2—C3—C4 | 120.8 (4) | C9—C10—H10A | 119.5 |
C2—C3—H3A | 119.6 | C12—C11—C10 | 119.0 (5) |
C4—C3—H3A | 119.6 | C12—C11—H11A | 120.5 |
C5—C4—C3 | 117.7 (4) | C10—C11—H11A | 120.5 |
C5—C4—C7 | 120.8 (3) | C11—C12—C13 | 121.1 (5) |
C3—C4—C7 | 121.4 (4) | C11—C12—H12A | 119.5 |
C6—C5—C4 | 121.1 (4) | C13—C12—H12A | 119.5 |
C6—C5—N | 118.4 (3) | C8—C13—C12 | 120.6 (5) |
C4—C5—N | 120.4 (3) | C8—C13—H13A | 119.7 |
C5—C6—C1 | 120.2 (4) | C12—C13—H13A | 119.7 |
C6—C1—C2—C3 | 0.4 (8) | C3—C4—C7—C8 | −48.7 (5) |
C1—C2—C3—C4 | −0.1 (7) | O—C7—C8—C13 | 169.0 (4) |
C2—C3—C4—C5 | −1.1 (6) | C4—C7—C8—C13 | −10.3 (6) |
C2—C3—C4—C7 | −177.2 (4) | O—C7—C8—C9 | −7.7 (6) |
C3—C4—C5—C6 | 2.1 (6) | C4—C7—C8—C9 | 173.0 (4) |
C7—C4—C5—C6 | 178.2 (4) | C13—C8—C9—C10 | −0.1 (7) |
C3—C4—C5—N | −177.1 (4) | C7—C8—C9—C10 | 176.9 (5) |
C7—C4—C5—N | −1.0 (5) | C8—C9—C10—C11 | 1.3 (8) |
C4—C5—C6—C1 | −1.8 (6) | C9—C10—C11—C12 | −1.2 (9) |
N—C5—C6—C1 | 177.4 (4) | C10—C11—C12—C13 | −0.1 (8) |
C2—C1—C6—C5 | 0.5 (7) | C9—C8—C13—C12 | −1.2 (7) |
C5—C4—C7—O | −43.9 (5) | C7—C8—C13—C12 | −178.0 (4) |
C3—C4—C7—O | 132.0 (4) | C11—C12—C13—C8 | 1.3 (8) |
C5—C4—C7—C8 | 135.4 (4) |
D—H···A | D—H | H···A | D···A | D—H···A |
N—H0A···Cl | 0.89 | 2.38 | 3.247 (3) | 165 |
N—H0B···Cli | 0.89 | 2.29 | 3.178 (3) | 175 |
N—H0C···OW | 0.89 | 1.87 | 2.748 (5) | 169 |
OW—HWB···Clii | 0.87 (5) | 2.38 (3) | 3.226 (4) | 165 (5) |
OW—HWA···Cliii | 0.86 (4) | 2.35 (4) | 3.204 (4) | 176 (5) |
Symmetry codes: (i) x−1, y, z; (ii) −x+2, −y+1, −z+2; (iii) −x+1, −y+1, −z+2. |
Experimental details
Crystal data | |
Chemical formula | C13H12NO+·Cl−·H2O |
Mr | 251.70 |
Crystal system, space group | Monoclinic, P21/c |
Temperature (K) | 298 |
a, b, c (Å) | 4.771 (1), 17.450 (4), 15.277 (3) |
β (°) | 90.50 (3) |
V (Å3) | 1271.8 (5) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 0.29 |
Crystal size (mm) | 0.30 × 0.10 × 0.10 |
Data collection | |
Diffractometer | Nonius CAD-4 diffractometer |
Absorption correction | ψ scan (North et al., 1968) |
Tmin, Tmax | 0.918, 0.972 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 2786, 2479, 1522 |
Rint | 0.065 |
(sin θ/λ)max (Å−1) | 0.616 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.068, 0.174, 1.03 |
No. of reflections | 2479 |
No. of parameters | 163 |
No. of restraints | 3 |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å−3) | 0.35, −0.23 |
Computer programs: CAD-4 Software (Enraf–Nonius, 1985), 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 |
N—H0A···Cl | 0.89 | 2.38 | 3.247 (3) | 165.4 |
N—H0B···Cli | 0.89 | 2.29 | 3.178 (3) | 174.7 |
N—H0C···OW | 0.89 | 1.87 | 2.748 (5) | 168.7 |
OW—HWB···Clii | 0.87 (5) | 2.38 (3) | 3.226 (4) | 165 (5) |
OW—HWA···Cliii | 0.86 (4) | 2.35 (4) | 3.204 (4) | 176 (5) |
Symmetry codes: (i) x−1, y, z; (ii) −x+2, −y+1, −z+2; (iii) −x+1, −y+1, −z+2. |
(2-aminophenyl)(phenyl)methanone is one of the important monomers, being utilized to synthesize oligomers containing quinoline unit (Shetty et al., 1999). We report herein the crystal structure of the title compound, (I).
In the molecule of (I) (Fig. 1), the bond lengths and angles are within normal ranges (Allen et al., 1987). Rings A (C1—C6) and B (C8—C13) are, of course, planar and they are oriented at a dihedral angle of A/B = 53.62 (3)°.
In the crystal structure, N—H···Cl, N—H···O and O—H···Cl hydrogen bonds (Table 1) link the molecules to form a three dimensional network (Fig. 2), in which they may be effective in the stabilization of the structure.