supplementary materials


HTML versionpdf versioncif file3d viewstructure factorssupplementary materialsCIF check reportsimilar papers Open access

bi2365 scheme

Acta Cryst. (2009). E65, o1267    [ doi:10.1107/S1600536809016778 ]

1,2-Dibenzoylhydrazine-dimethylformamide (3/1)

Q.-P. He, H.-G. Li, G.-B. Wang, F.-L. Fu and M.-S. Liu

Abstract top

The title compound, 3C14H12N2O2·C3H7NO, was synthesized by reaction of benzoyl chloride with hydrazine hydrate under microwave irradition. The asymmetric unit comprises three 1,2-dibenzoylhydrazine molecules and one dimethylformamide molecule. The 1,2-dibenzoylhydrazine molecules are linked by pairs of N-H...O hydrogen bonds into chains propagating along [010].

Comment top

In recent years, high-speed synthesis using microwave radiation has attracted considerable attention, and some important reviews in the study of microwave-assisted organic synthesis have been published (Galema, 1997). We describe in this paper a user-friendly microwave irradiation protocol for the synthesis of the title compound, and its crystal structure.

In the crystal structure, the asymmetric unit comprises three 1,2-dibenzoylhydrazine molecules and one dimethylformamide solvent molecule. The bond lengths and angles are normal and comparable to those in the unsolvated crystal structure of 1,2-dibenzoylhydrazine (Shanmuga Sundara Raj et al., 2000). Molecules are linked by N—H···O hydrogen bonds between the amide H and carbonyl O atoms, forming ten-membered rings, into chains propagating along [010]. the dimethylformamide molecules lie between these chains.

Related literature top

For background literature concerning microwave-assisted synthesis, see: Galema (1997). For the unsolvated crystal structure of 1,2-dibenzoylhydrazine, see: Shanmuga Sundara Raj et al. (2000).

Experimental top

Benzoyl chloride (0.5 mmol) and hydrazine hydrate (0.5 mmol) were mixed in a 50 ml flask. After microwave irradiation for 5 min at 275 W, then cooling to room temperature, the resulting mixture was washed with 10 ml water to yield a white product. The crude product was recrystallised from ethanol to afford the title compound as a crystalline solid. Elemental analysis calculated for C45H43N7O7: C 68.08, H 5.46, N 12.35%; found: C 68.24, H 5.68, N 12.28%.

Refinement top

All H atoms were placed in idealized positions (C—H = 0.93–0.96 Å, N—H 0.86 Å) and constrained to ride on their parent atoms, with Uiso(H) = 1.2 or 1.5 Ueq(C/N). The crystal diffracted relatively weakly and data are truncated to 1.00 Å resolution, with ca 60% of data observed at the 2σ(I) level. The structure is therefore of relatively low precision.

Computing details top

Data collection: SMART (Siemens, 1996); cell refinement: SAINT (Siemens, 1996); data reduction: SAINT (Siemens, 1996); 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. The content of asymmetric unit of the title compound showing the atomic numbering scheme and 30% probability displacement ellipsoids.The solvent molecular is omitted for clarity.
1,2-Dibenzoylhydrazine–dimethylformamide (3/1) top
Crystal data top
3C14H12N2O2·C3H7NOZ = 2
Mr = 793.86F000 = 836
Triclinic, P1Dx = 1.283 Mg m−3
Hall symbol: -P 1Mo Kα radiation
λ = 0.71073 Å
a = 10.7666 (12) ÅCell parameters from 1452 reflections
b = 11.4615 (13) Åθ = 2.3–21.0º
c = 18.100 (2) ŵ = 0.09 mm−1
α = 100.127 (2)ºT = 298 K
β = 96.084 (2)ºNeedle, colourless
γ = 108.382 (3)º0.50 × 0.32 × 0.27 mm
V = 2055.2 (4) Å3
Data collection top
Bruker SMART APEX CCD
diffractometer		4163 independent reflections
Radiation source: fine-focus sealed tube2487 reflections with I > 2σ(I)
Monochromator: graphiteRint = 0.075
T = 298 Kθmax = 20.8º
φ and ω scansθmin = 2.0º
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)		h = −10→10
Tmin = 0.957, Tmax = 0.977k = −11→11
6846 measured reflectionsl = −10→18
Refinement top
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.120H-atom parameters constrained
wR(F2) = 0.359  w = 1/[σ2(Fo2) + (0.2P)2]
where P = (Fo2 + 2Fc2)/3
S = 1.14(Δ/σ)max = 0.001
4163 reflectionsΔρmax = 0.66 e Å−3
534 parametersΔρmin = −0.52 e Å−3
Primary atom site location: structure-invariant direct methodsExtinction correction: none
Crystal data top
3C14H12N2O2·C3H7NOγ = 108.382 (3)º
Mr = 793.86V = 2055.2 (4) Å3
Triclinic, P1Z = 2
a = 10.7666 (12) ÅMo Kα
b = 11.4615 (13) ŵ = 0.09 mm−1
c = 18.100 (2) ÅT = 298 K
α = 100.127 (2)º0.50 × 0.32 × 0.27 mm
β = 96.084 (2)º
Data collection top
Bruker SMART APEX CCD
diffractometer		4163 independent reflections
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)		2487 reflections with I > 2σ(I)
Tmin = 0.957, Tmax = 0.977Rint = 0.075
6846 measured reflectionsθmax = 20.8º
Refinement top
R[F2 > 2σ(F2)] = 0.120534 parameters
wR(F2) = 0.359H-atom parameters constrained
S = 1.14Δρmax = 0.66 e Å−3
4163 reflectionsΔρmin = −0.52 e Å−3
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
N10.1213 (7)0.7581 (6)0.2502 (4)0.0367 (18)
H10.08270.81320.25850.044*
N20.1953 (7)0.7353 (7)0.3099 (4)0.0373 (19)
H20.16420.66710.32570.045*
N30.1123 (6)0.3584 (6)0.2436 (4)0.0377 (19)
H30.09580.28270.21840.045*
N40.2312 (6)0.4518 (6)0.2435 (4)0.0364 (18)
H40.23160.50890.21840.044*
N50.1935 (7)0.1264 (6)0.3108 (4)0.0368 (18)
H50.23420.20620.32680.044*
N60.2322 (7)0.0597 (6)0.2525 (4)0.0354 (18)
H60.27660.01170.26190.042*
N70.380 (3)0.619 (2)0.8906 (19)0.200 (10)
O10.1675 (7)0.6159 (6)0.1659 (3)0.0541 (18)
O20.3604 (6)0.9179 (6)0.3238 (3)0.0472 (17)
O30.0421 (6)0.4918 (6)0.3186 (4)0.0495 (17)
O40.3487 (5)0.3746 (6)0.3198 (3)0.0460 (16)
O50.0327 (6)−0.0487 (6)0.3225 (3)0.0491 (17)
O60.1339 (7)0.1356 (6)0.1664 (3)0.0550 (18)
O70.5384 (19)0.6803 (19)1.0039 (13)0.241 (8)
C10.1106 (9)0.6927 (8)0.1791 (5)0.036 (2)
C20.0228 (9)0.7136 (8)0.1180 (5)0.040 (2)
C30.0276 (11)0.6610 (10)0.0446 (6)0.062 (3)
H3A0.08730.61870.03590.074*
C4−0.0520 (15)0.6694 (11)−0.0146 (6)0.077 (4)
H4A−0.04520.6346−0.06380.093*
C5−0.1417 (14)0.7274 (14)−0.0044 (7)0.082 (4)
H5A−0.19770.7307−0.04620.099*
C6−0.1506 (11)0.7816 (12)0.0676 (8)0.080 (4)
H6A−0.21320.82080.07530.095*
C7−0.0630 (10)0.7770 (10)0.1300 (6)0.059 (3)
H7−0.06420.81730.17910.071*
C80.3152 (9)0.8189 (8)0.3433 (4)0.032 (2)
C90.3875 (8)0.7849 (8)0.4068 (4)0.034 (2)
C100.3335 (9)0.6761 (9)0.4323 (5)0.042 (2)
H100.24860.62100.40990.050*
C110.4055 (10)0.6491 (11)0.4910 (5)0.058 (3)
H110.37090.57390.50660.070*
C120.5278 (11)0.7334 (12)0.5261 (6)0.069 (3)
H120.57460.71860.56760.083*
C130.5791 (11)0.8381 (12)0.4996 (7)0.079 (4)
H130.66420.89300.52170.095*
C140.5094 (9)0.8667 (10)0.4404 (5)0.059 (3)
H140.54590.94090.42420.071*
C150.0250 (8)0.3862 (9)0.2823 (5)0.034 (2)
C16−0.1008 (8)0.2810 (8)0.2787 (5)0.037 (2)
C17−0.1390 (9)0.1684 (10)0.2308 (6)0.061 (3)
H17−0.08480.15360.19620.073*
C18−0.2547 (12)0.0737 (11)0.2306 (8)0.088 (4)
H18−0.2788−0.00210.19490.106*
C19−0.3312 (12)0.0886 (12)0.2797 (7)0.079 (4)
H19−0.40760.02250.28050.094*
C20−0.2992 (11)0.2016 (14)0.3301 (7)0.096 (5)
H20−0.35580.21500.36350.115*
C21−0.1791 (10)0.2973 (11)0.3306 (6)0.072 (3)
H21−0.15320.37260.36690.086*
C220.3466 (8)0.4540 (8)0.2825 (5)0.028 (2)
C230.4680 (8)0.5553 (8)0.2778 (5)0.035 (2)
C240.5759 (9)0.5837 (11)0.3321 (6)0.060 (3)
H240.57330.53760.36970.073*
C250.6887 (10)0.6805 (12)0.3313 (7)0.075 (3)
H250.76040.70210.37060.091*
C260.7002 (11)0.7455 (12)0.2764 (8)0.078 (4)
H260.77960.80800.27550.093*
C270.5919 (13)0.7169 (12)0.2219 (8)0.090 (4)
H270.59640.76150.18340.108*
C280.4764 (10)0.6236 (11)0.2228 (6)0.064 (3)
H280.40270.60640.18560.077*
C290.0926 (8)0.0672 (9)0.3427 (5)0.034 (2)
C300.0563 (8)0.1458 (8)0.4058 (4)0.031 (2)
C310.1238 (9)0.2727 (9)0.4328 (5)0.043 (2)
H310.19560.31290.41120.052*
C320.0865 (10)0.3404 (11)0.4910 (6)0.060 (3)
H320.13100.42680.50740.072*
C33−0.0139 (11)0.2833 (13)0.5246 (6)0.069 (3)
H33−0.03570.32950.56560.082*
C34−0.0833 (14)0.1591 (14)0.4992 (7)0.090 (4)
H34−0.15460.12040.52170.108*
C35−0.0472 (10)0.0886 (10)0.4387 (6)0.063 (3)
H35−0.09430.00290.42120.076*
C360.2001 (9)0.0699 (8)0.1802 (5)0.036 (2)
C370.2514 (9)0.0059 (8)0.1209 (5)0.040 (2)
C380.3468 (10)−0.0487 (10)0.1344 (6)0.060 (3)
H380.3815−0.04600.18420.072*
C390.3899 (14)−0.1055 (13)0.0763 (9)0.097 (4)
H390.4526−0.14350.08610.116*
C400.342 (2)−0.1079 (14)0.0027 (10)0.109 (5)
H400.3763−0.1423−0.03730.131*
C410.2433 (19)−0.0595 (15)−0.0117 (7)0.103 (5)
H410.2061−0.0657−0.06170.123*
C420.2011 (12)−0.0039 (10)0.0458 (6)0.065 (3)
H420.13510.03000.03520.079*
C430.410 (3)0.596 (3)0.962 (2)0.211 (14)
H430.35330.53260.98040.253*
C440.486 (3)0.704 (2)0.8626 (15)0.210 (11)
H44A0.49080.78900.88130.315*
H44B0.46850.68390.80790.315*
H44C0.56900.69440.88020.315*
C450.252 (3)0.556 (2)0.8505 (16)0.214 (12)
H45A0.20290.49920.87830.321*
H45B0.25580.51020.80150.321*
H45C0.20960.61680.84380.321*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
N10.046 (4)0.032 (4)0.037 (5)0.022 (4)−0.004 (3)0.012 (4)
N20.047 (5)0.030 (4)0.035 (4)0.014 (4)−0.007 (4)0.015 (3)
N30.032 (4)0.018 (4)0.053 (5)−0.001 (4)0.006 (4)0.001 (3)
N40.028 (4)0.024 (4)0.055 (5)0.003 (4)0.005 (4)0.017 (3)
N50.055 (5)0.021 (4)0.036 (4)0.013 (4)0.014 (4)0.009 (3)
N60.055 (5)0.029 (4)0.032 (4)0.021 (4)0.017 (4)0.012 (3)
N70.137 (19)0.131 (18)0.30 (3)0.011 (15)0.05 (2)0.01 (2)
O10.076 (5)0.049 (4)0.050 (4)0.038 (4)0.008 (3)0.016 (3)
O20.046 (4)0.033 (4)0.058 (4)0.007 (3)−0.005 (3)0.021 (3)
O30.048 (4)0.026 (4)0.068 (4)0.006 (3)0.014 (3)0.004 (3)
O40.038 (4)0.038 (4)0.060 (4)0.006 (3)0.001 (3)0.025 (3)
O50.051 (4)0.028 (4)0.062 (4)0.006 (3)0.020 (3)0.003 (3)
O60.086 (5)0.049 (4)0.043 (4)0.043 (4)0.005 (3)0.011 (3)
O70.176 (15)0.178 (17)0.33 (2)0.041 (14)0.001 (15)0.025 (16)
C10.048 (6)0.021 (5)0.038 (6)0.006 (5)0.002 (4)0.011 (4)
C20.048 (6)0.022 (5)0.049 (6)0.012 (5)−0.008 (5)0.016 (5)
C30.088 (8)0.046 (7)0.044 (7)0.028 (6)−0.015 (6)−0.005 (5)
C40.113 (10)0.069 (9)0.042 (7)0.032 (8)−0.014 (7)0.002 (6)
C50.089 (9)0.095 (10)0.057 (9)0.025 (8)−0.014 (7)0.031 (7)
C60.065 (8)0.096 (10)0.103 (11)0.051 (7)0.012 (7)0.044 (8)
C70.059 (7)0.069 (8)0.053 (6)0.028 (6)−0.002 (5)0.018 (5)
C80.047 (6)0.019 (5)0.033 (5)0.016 (5)0.005 (5)0.006 (4)
C90.037 (6)0.034 (6)0.033 (5)0.017 (5)−0.001 (4)0.004 (4)
C100.040 (5)0.046 (6)0.035 (5)0.012 (5)−0.004 (4)0.013 (5)
C110.054 (7)0.068 (7)0.055 (6)0.016 (6)−0.004 (5)0.037 (6)
C120.066 (8)0.083 (9)0.062 (7)0.026 (7)−0.009 (6)0.036 (7)
C130.068 (8)0.068 (9)0.087 (9)0.014 (7)−0.037 (7)0.024 (7)
C140.046 (6)0.052 (7)0.064 (7)0.004 (6)−0.013 (6)0.009 (6)
C150.029 (5)0.026 (6)0.045 (5)0.006 (5)−0.003 (4)0.010 (5)
C160.026 (5)0.037 (6)0.039 (5)0.002 (5)−0.001 (4)0.008 (5)
C170.031 (6)0.045 (7)0.084 (8)−0.012 (5)0.002 (5)0.012 (6)
C180.069 (8)0.056 (8)0.100 (10)−0.033 (7)0.014 (8)0.018 (7)
C190.056 (8)0.068 (9)0.079 (9)−0.021 (7)−0.003 (7)0.019 (7)
C200.061 (8)0.103 (12)0.093 (9)−0.022 (8)0.033 (7)0.021 (9)
C210.046 (7)0.077 (9)0.066 (7)−0.004 (6)0.008 (6)−0.001 (6)
C220.026 (5)0.023 (5)0.036 (5)0.008 (4)0.004 (4)0.010 (4)
C230.026 (5)0.033 (5)0.045 (5)0.008 (4)0.010 (5)0.011 (5)
C240.034 (6)0.075 (8)0.065 (7)0.005 (6)0.006 (5)0.027 (6)
C250.049 (7)0.068 (8)0.081 (8)−0.013 (6)0.003 (6)0.010 (7)
C260.050 (8)0.067 (9)0.097 (9)−0.005 (6)0.018 (7)0.013 (8)
C270.070 (9)0.083 (10)0.104 (10)−0.006 (8)0.012 (8)0.053 (8)
C280.041 (6)0.074 (8)0.079 (7)0.005 (6)0.009 (5)0.046 (7)
C290.038 (5)0.029 (6)0.039 (5)0.015 (5)0.007 (4)0.010 (5)
C300.039 (5)0.030 (6)0.026 (5)0.013 (4)0.006 (4)0.009 (4)
C310.045 (6)0.042 (7)0.040 (5)0.015 (5)0.010 (4)0.001 (5)
C320.061 (7)0.057 (7)0.058 (7)0.023 (6)0.014 (6)−0.004 (6)
C330.076 (8)0.072 (9)0.057 (7)0.031 (7)0.025 (6)−0.009 (6)
C340.109 (10)0.088 (11)0.098 (9)0.045 (9)0.073 (8)0.031 (8)
C350.067 (7)0.054 (7)0.070 (7)0.015 (6)0.040 (6)0.012 (6)
C360.053 (6)0.021 (5)0.038 (6)0.011 (5)0.014 (5)0.013 (4)
C370.045 (6)0.035 (6)0.038 (6)0.007 (5)0.013 (4)0.008 (4)
C380.063 (7)0.076 (8)0.052 (6)0.038 (6)0.022 (5)0.010 (6)
C390.116 (11)0.104 (11)0.093 (11)0.063 (9)0.048 (9)0.017 (9)
C400.160 (15)0.077 (11)0.089 (13)0.028 (11)0.070 (11)0.008 (9)
C410.165 (15)0.091 (11)0.060 (9)0.050 (11)0.024 (9)0.022 (8)
C420.115 (9)0.050 (7)0.045 (7)0.039 (7)0.028 (7)0.016 (5)
C430.16 (3)0.13 (2)0.31 (4)0.020 (19)0.04 (3)0.00 (3)
C440.17 (2)0.14 (2)0.29 (3)0.017 (17)0.06 (2)0.00 (2)
C450.15 (2)0.14 (2)0.30 (3)0.001 (17)0.02 (2)0.01 (2)
Geometric parameters (Å, °) top
N1—C11.344 (10)C17—C181.369 (14)
N1—N21.385 (9)C17—H170.930
N1—H10.860C18—C191.298 (16)
N2—C81.342 (10)C18—H180.930
N2—H20.860C19—C201.366 (17)
N3—C151.313 (10)C19—H190.930
N3—N41.385 (9)C20—C211.405 (15)
N3—H30.860C20—H200.930
N4—C221.353 (10)C21—H210.930
N4—H40.860C22—C231.472 (12)
N5—C291.333 (10)C23—C241.352 (12)
N5—N61.372 (9)C23—C281.363 (12)
N5—H50.860C24—C251.366 (14)
N6—C361.352 (10)C24—H240.930
N6—H60.860C25—C261.337 (16)
N7—C431.38 (3)C25—H250.930
N7—C451.39 (3)C26—C271.357 (15)
N7—C441.45 (3)C26—H260.930
O1—C11.226 (10)C27—C281.365 (15)
O2—C81.215 (9)C27—H270.930
O3—C151.219 (10)C28—H280.930
O4—C221.229 (9)C29—C301.492 (11)
O5—C291.247 (10)C30—C351.357 (12)
O6—C361.227 (10)C30—C311.375 (11)
O7—C431.45 (3)C31—C321.369 (13)
C1—C21.480 (12)C31—H310.930
C2—C71.356 (13)C32—C331.341 (14)
C2—C31.372 (13)C32—H320.930
C3—C41.337 (14)C33—C341.350 (16)
C3—H3A0.930C33—H330.930
C4—C51.345 (16)C34—C351.408 (15)
C4—H4A0.930C34—H340.930
C5—C61.368 (16)C35—H350.930
C5—H5A0.930C36—C371.450 (12)
C6—C71.412 (15)C37—C421.381 (13)
C6—H6A0.930C37—C381.383 (13)
C7—H70.930C38—C391.340 (15)
C8—C91.497 (12)C38—H380.930
C9—C141.351 (12)C39—C401.369 (19)
C9—C101.380 (12)C39—H390.930
C10—C111.386 (12)C40—C411.37 (2)
C10—H100.930C40—H400.930
C11—C121.369 (14)C41—C421.321 (18)
C11—H110.930C41—H410.930
C12—C131.347 (15)C42—H420.930
C12—H120.930C43—H430.930
C13—C141.389 (14)C44—H44A0.960
C13—H130.930C44—H44B0.960
C14—H140.930C44—H44C0.960
C15—C161.488 (12)C45—H45A0.960
C16—C171.335 (13)C45—H45B0.960
C16—C211.354 (12)C45—H45C0.960
C1—N1—N2118.9 (7)C16—C21—C20120.7 (11)
C1—N1—H1120.5C16—C21—H21119.7
N2—N1—H1120.5C20—C21—H21119.7
C8—N2—N1120.5 (7)O4—C22—N4121.0 (7)
C8—N2—H2119.7O4—C22—C23122.2 (7)
N1—N2—H2119.7N4—C22—C23116.8 (8)
C15—N3—N4119.7 (6)C24—C23—C28118.5 (9)
C15—N3—H3120.1C24—C23—C22117.9 (8)
N4—N3—H3120.1C28—C23—C22123.6 (8)
C22—N4—N3120.8 (7)C23—C24—C25119.5 (10)
C22—N4—H4119.6C23—C24—H24120.2
N3—N4—H4119.6C25—C24—H24120.2
C29—N5—N6119.9 (7)C26—C25—C24122.7 (11)
C29—N5—H5120.1C26—C25—H25118.6
N6—N5—H5120.1C24—C25—H25118.6
C36—N6—N5119.5 (7)C25—C26—C27117.6 (11)
C36—N6—H6120.2C25—C26—H26121.2
N5—N6—H6120.2C27—C26—H26121.2
C43—N7—C45118 (3)C26—C27—C28120.9 (12)
C43—N7—C44118 (3)C26—C27—H27119.6
C45—N7—C44125 (3)C28—C27—H27119.6
O1—C1—N1121.5 (8)C23—C28—C27120.7 (10)
O1—C1—C2121.5 (8)C23—C28—H28119.7
N1—C1—C2117.0 (8)C27—C28—H28119.7
C7—C2—C3118.9 (8)O5—C29—N5122.2 (7)
C7—C2—C1124.6 (9)O5—C29—C30120.9 (8)
C3—C2—C1116.4 (9)N5—C29—C30116.9 (8)
C4—C3—C2121.2 (11)C35—C30—C31118.7 (8)
C4—C3—H3A119.4C35—C30—C29118.3 (8)
C2—C3—H3A119.4C31—C30—C29123.0 (8)
C3—C4—C5121.2 (11)C32—C31—C30120.7 (9)
C3—C4—H4A119.4C32—C31—H31119.6
C5—C4—H4A119.4C30—C31—H31119.6
C4—C5—C6119.9 (11)C33—C32—C31120.5 (10)
C4—C5—H5A120.0C33—C32—H32119.7
C6—C5—H5A120.0C31—C32—H32119.7
C5—C6—C7118.9 (11)C32—C33—C34120.4 (10)
C5—C6—H6A120.5C32—C33—H33119.8
C7—C6—H6A120.5C34—C33—H33119.8
C2—C7—C6119.7 (10)C33—C34—C35119.6 (10)
C2—C7—H7120.2C33—C34—H34120.2
C6—C7—H7120.2C35—C34—H34120.2
O2—C8—N2121.4 (7)C30—C35—C34120.0 (10)
O2—C8—C9122.3 (8)C30—C35—H35120.0
N2—C8—C9116.3 (8)C34—C35—H35120.0
C14—C9—C10120.1 (8)O6—C36—N6120.5 (8)
C14—C9—C8117.3 (9)O6—C36—C37121.5 (8)
C10—C9—C8122.6 (8)N6—C36—C37118.0 (9)
C9—C10—C11120.1 (8)C42—C37—C38117.1 (9)
C9—C10—H10120.0C42—C37—C36118.7 (9)
C11—C10—H10120.0C38—C37—C36124.2 (9)
C12—C11—C10119.8 (10)C39—C38—C37120.6 (11)
C12—C11—H11120.1C39—C38—H38119.7
C10—C11—H11120.1C37—C38—H38119.7
C13—C12—C11119.0 (9)C38—C39—C40120.4 (13)
C13—C12—H12120.5C38—C39—H39119.8
C11—C12—H12120.5C40—C39—H39119.8
C12—C13—C14122.2 (10)C41—C40—C39119.7 (13)
C12—C13—H13118.9C41—C40—H40120.2
C14—C13—H13118.9C39—C40—H40120.2
C9—C14—C13118.8 (10)C42—C41—C40119.5 (13)
C9—C14—H14120.6C42—C41—H41120.3
C13—C14—H14120.6C40—C41—H41120.3
O3—C15—N3123.3 (7)C41—C42—C37122.6 (12)
O3—C15—C16120.3 (8)C41—C42—H42118.7
N3—C15—C16116.4 (8)C37—C42—H42118.7
C17—C16—C21117.0 (9)N7—C43—O7113 (4)
C17—C16—C15124.9 (8)N7—C43—H43123.4
C21—C16—C15118.0 (8)O7—C43—H43123.4
C16—C17—C18122.8 (11)N7—C44—H44A109.5
C16—C17—H17118.6N7—C44—H44B109.5
C18—C17—H17118.6H44A—C44—H44B109.5
C19—C18—C17120.7 (12)N7—C44—H44C109.5
C19—C18—H18119.6H44A—C44—H44C109.5
C17—C18—H18119.6H44B—C44—H44C109.5
C18—C19—C20119.9 (11)N7—C45—H45A109.5
C18—C19—H19120.1N7—C45—H45B109.5
C20—C19—H19120.1H45A—C45—H45B109.5
C19—C20—C21118.8 (12)N7—C45—H45C109.5
C19—C20—H20120.6H45A—C45—H45C109.5
C21—C20—H20120.6H45B—C45—H45C109.5
Hydrogen-bond geometry (Å, °) top
D—H···AD—HH···AD···AD—H···A
N1—H1···O5i0.862.042.846 (9)156
N6—H6···O2ii0.862.012.826 (9)157
N2—H2···O30.862.002.800 (9)155
N3—H3···O60.861.962.778 (10)158
N4—H4···O10.861.922.743 (9)160
N5—H5···O40.861.972.774 (9)155
Symmetry codes: (i) x, y+1, z; (ii) x, y−1, z.
Table 1
Hydrogen-bond geometry (Å, °) top
D—H···AD—HH···AD···AD—H···A
N1—H1···O5i0.862.042.846 (9)156
N6—H6···O2ii0.862.012.826 (9)157
N2—H2···O30.862.002.800 (9)155
N3—H3···O60.861.962.778 (10)158
N4—H4···O10.861.922.743 (9)160
N5—H5···O40.861.972.774 (9)155
Symmetry codes: (i) x, y+1, z; (ii) x, y−1, z.
Acknowledgements top

This project was supported by the Foundation of Liaocheng University (grant No. X071013).

references
References top

Galema, S. A. (1997). Chem. Soc. Rev. 26, 233–238.

Shanmuga Sundara Raj, S., Yamin, B. M., Boshaala, A. M. A., Tarafder, M. T. H., Crouse, K. A. & Fun, H.-K. (2000). Acta Cryst. C56, 1011–1012.

Sheldrick, G. M. (1996). SADABS. University of Göttingen, Germany.

Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122.

Siemens (1996). SMART and SAINT. Siemens Analytical X-Ray Systems, Inc., Madison, Wisconsin, USA.