N-[4-(Phenyl­imino­meth­yl)phen­yl]acetamide 0.67-hydrate

Mahmud, T.; Thebo, K.H.; Rehman, R.; Malik, M.A.; Helliwell, M.

doi:10.1107/S1600536810039656

organic compounds

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ISSN: 2056-9890

Volume 66| Part 11| November 2010| Page o2781

https://doi.org/10.1107/S1600536810039656

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N-[4-(Phenyliminomethyl)phenyl]acetamide 0.67-hydrate

Tariq Mahmud,^a ^* Khalid H. Thebo,^b Rabia Rehman,^a Mohammad A. Malik ^b and Madeleine Helliwell ^b

^aInstitute of Chemistry, University of the Punjab, Lahore 54590, Pakistan, and ^bSchool of Chemistry and School of Materials, The University of Manchester, Oxford Road, Manchester M13 9PL, England
^*Correspondence e-mail: tariqmeer30@hotmail.com

(Received 20 September 2010; accepted 4 October 2010; online 9 October 2010)

The title compound, C₁₅H₁₄N₂O·0.67H₂O, was prepared by the reaction of 4-acetoaminebenzaldehyde and aniline. The asymmetric unit contains six organic molecules and four water molecules. The dihedral angles between the aromatic ring planes in each organic molecule vary from 42.4 (2) to 53.8 (2)°. In the crystal, an extensive network of intermolecular N—H⋯O, O—H⋯N and O—H⋯O hydrogen bonds link the molecules into [010] chains.

Related literature

For background to polydentate Schiff bases in coordination chemistry, see: Souza et al. (1985 ); Dixit et al. (2009 ). For information on their uses as stereospecific catalysts, see: Kureshy et al. (1999 ); Aoyama et al. (1986 ).

Experimental

Crystal data

C₁₅H₁₄N₂O·0.67H₂O
M_r = 250.29
Monoclinic, P 2₁ /c
a = 21.328 (4) Å
b = 17.797 (3) Å
c = 23.021 (4) Å
β = 117.244 (4)°
V = 7769 (3) Å³
Z = 24
Mo Kα radiation
μ = 0.09 mm⁻¹
T = 100 K
0.60 × 0.35 × 0.10 mm

Data collection

Bruker SMART CCD diffractometer
40121 measured reflections
13696 independent reflections
4483 reflections with I > 2σ(I)
R_int = 0.113

Refinement

R[F² > 2σ(F²)] = 0.055
wR(F²) = 0.119
S = 0.76
13696 reflections
1057 parameters
23 restraints
H atoms treated by a mixture of independent and constrained refinement
Δρ_max = 0.34 e Å⁻³
Δρ_min = −0.21 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1N⋯O1S	0.88 (2)	2.00 (2)	2.872 (5)	173 (4)
N3—H3N⋯O2S	0.87 (2)	1.99 (2)	2.859 (5)	173 (4)
N5—H5N⋯O4S	0.86 (2)	2.09 (2)	2.919 (5)	163 (4)
N7—H7N⋯O3S	0.86 (2)	2.03 (2)	2.858 (5)	161 (4)
N9—H9N⋯O4	0.87 (2)	2.10 (2)	2.929 (5)	158 (4)
N11—H11N⋯O2	0.87 (2)	2.16 (3)	2.947 (5)	151 (4)
O1S—H1O⋯N4	0.83 (2)	2.29 (3)	2.939 (5)	136 (4)
O1S—H2O⋯O5	0.88 (2)	1.88 (2)	2.764 (5)	173 (4)
O2S—H3O⋯N2	0.85 (2)	2.16 (2)	3.006 (5)	177 (4)
O2S—H4O⋯O3	0.86 (2)	1.96 (2)	2.781 (5)	160 (5)
O3S—H5O⋯N6ⁱ	0.85 (2)	2.33 (3)	3.001 (5)	136 (3)
O3S—H6O⋯O1ⁱ	0.89 (2)	1.90 (2)	2.778 (4)	172 (4)
O4S—H7O⋯N8ⁱⁱ	0.87 (2)	2.09 (2)	2.954 (5)	171 (4)
O4S—H8O⋯O6ⁱⁱ	0.98 (2)	1.76 (2)	2.726 (5)	170 (4)
Symmetry codes: (i) x, y+1, z; (ii) x, y-1, z.

Data collection: SMART (Bruker, 2001 ); cell refinement: SAINT (Bruker, 2002 ); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009 ); software used to prepare material for publication: SHELXTL and PLATON.

Supporting information

Crystal structure: contains datablocks global, I. DOI: https://doi.org/10.1107/S1600536810039656/hb5642sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536810039656/hb5642Isup2.hkl

checkCIF report

Comment top

Polydentate Schiff base ligands are widely used in the preparation of transition metal complexes (Souza et al., 1985). Some such complexes possess binding sites and cavities for various cations, anions and organic molecules (Dixit et al., 2009). In addition, Schiff base metal complexes can be effective as stereospecific catalysts for oxidation (Kureshy et al., 1999), reduction (Aoyama et al., 1986) and other transformations in organic and inorganic chemistry. The title Schiff base compound was synthesized from 4-acetoaminebenzaldehyde and aniline as a potential ligand for the preparation of transition metal complexes.

The asymmetric unit contains six molecules of 4-acetylaminobenzylidine aniline (I) and four water molecules. Figure 1 shows a plot of one of the molecules of (I). The dihedral angles between the two aromatic ring planes in each molecule of (I) vary from 42.4 (2) to 53.8 (2)° (Table 2). The six molecules in the asymetric unit are arranged in pairs, one above the other. There are possible π-stacking interactions between the carbonyl group of each molecule in the pair with the central phenyl group of the molecule above or below it, with carbonyl O and C atoms to aromatic ring distances varying from 3.002 (4) to 3.421 (4) Å and 3.191 (6) to 3.492 (6) Å, respectively (Table 3, Figure 2). The paired molecules are further linked to one another by O—H···N and O—H···O hydrogen bonds from two water molecules, one at each side of the pair (Table 1, Figure 2). Each pair of molecules is linked to adjacent pairs on either side by N—H···O contacts (Table 3), either to water O atoms (i.e. the N1—H1···O1S, N3—H3···O2S, N5—H5···O4S and N7—H7···O3S contacts) or to a carbonyl oxygen of the next molecule (i.e. the N11—H11···O2 and the N9—H9···O4 contacts). In this way, the pairs of molecules are linked into chains along b, as shown in Figure 2.

Related literature top

For background to polydentate Schiff bases in coordination chemistry, see: Souza et al. (1985); Dixit et al. (2009). For information on their uses as stereospecific catalysts, see: Kureshy et al. (1999); Aoyama et al. (1986).

Experimental top

0.0163 g (1.0 mmol) of 4-acetoaminebenzaldehyde and 0.0911 ml (1.0 mmol) of aniline were dissolved in 10.0 ml 95% ethanol separately. Both solutions were mixed in 100 ml round bottom flask. The mixture was refluxed for two hours at 423 K. It was then recrystallized by using a mixture of acetonitrile, methanol and water in the ratio 1: 3: 4 respectively.

Structure description top

For background to polydentate Schiff bases in coordination chemistry, see: Souza et al. (1985); Dixit et al. (2009). For information on their uses as stereospecific catalysts, see: Kureshy et al. (1999); Aoyama et al. (1986).

Computing details top

Data collection: SMART (Bruker, 2001); cell refinement: SAINT (Bruker, 2002); data reduction: SAINT (Bruker, 2002); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009); software used to prepare material for publication: SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009).

Figures top

	Fig. 1. Plot of one molecule of (I) with ellipsoids drawn at the 50% probability level.
	Fig. 2. Plot showing the packing arrangement of the crystal structure of (I) viewed down a showing pairs of molecules linked to each other by hydrogen bonding interactions, to form a chain along b. Only H atoms involved in hydrogen bonding are shown. Symmetry codes: (c) x, y+1, z; (e) x, y-1, z.

N-[4-(Phenyliminomethyl)phenyl]acetamide 0.67-hydrate top

Crystal data top

C₁₅H₁₄N₂O·0.67H₂O	F(000) = 3184
M_r = 250.29	D_x = 1.284 Mg m⁻³
Monoclinic, P2₁/c	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybc	Cell parameters from 766 reflections
a = 21.328 (4) Å	θ = 2.9–24.5°
b = 17.797 (3) Å	µ = 0.09 mm⁻¹
c = 23.021 (4) Å	T = 100 K
β = 117.244 (4)°	Plate, colourless
V = 7769 (3) Å³	0.60 × 0.35 × 0.10 mm
Z = 24

Data collection top

Bruker SMART CCD diffractometer	4483 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tube	R_int = 0.113
Graphite monochromator	θ_max = 25.0°, θ_min = 2.1°
phi and ω scans	h = −25→24
40121 measured reflections	k = −20→21
13696 independent reflections	l = −27→26

Refinement top

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)] = 0.055	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.119	H atoms treated by a mixture of independent and constrained refinement
S = 0.76	w = 1/[σ²(F_o²) + (0.0147P)²] where P = (F_o² + 2F_c²)/3
13696 reflections	(Δ/σ)_max = 0.001
1057 parameters	Δρ_max = 0.34 e Å⁻³
23 restraints	Δρ_min = −0.21 e Å⁻³

Crystal data top

C₁₅H₁₄N₂O·0.67H₂O	V = 7769 (3) Å³
M_r = 250.29	Z = 24
Monoclinic, P2₁/c	Mo Kα radiation
a = 21.328 (4) Å	µ = 0.09 mm⁻¹
b = 17.797 (3) Å	T = 100 K
c = 23.021 (4) Å	0.60 × 0.35 × 0.10 mm
β = 117.244 (4)°

Data collection top

Bruker SMART CCD diffractometer	4483 reflections with I > 2σ(I)
40121 measured reflections	R_int = 0.113
13696 independent reflections

Refinement top

R[F² > 2σ(F²)] = 0.055	23 restraints
wR(F²) = 0.119	H atoms treated by a mixture of independent and constrained refinement
S = 0.76	Δρ_max = 0.34 e Å⁻³
13696 reflections	Δρ_min = −0.21 e Å⁻³
1057 parameters

Special details top

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds 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

	x	y	z	U_iso*/U_eq
O1	0.18362 (17)	0.05033 (18)	0.33952 (15)	0.0264 (9)
N1	0.1999 (2)	0.1750 (2)	0.3278 (2)	0.0174 (10)
H1N	0.2190 (19)	0.2159 (14)	0.3501 (16)	0.021*
N2	0.1041 (2)	0.2783 (2)	0.03041 (18)	0.0190 (11)
C1	0.2263 (2)	0.1271 (2)	0.43504 (19)	0.0220 (12)
H1A	0.1854	0.1353	0.4429	0.033*
H1B	0.2568	0.1716	0.4489	0.033*
H1C	0.2528	0.0833	0.4600	0.033*
C2	0.2016 (2)	0.1134 (3)	0.3628 (2)	0.0169 (12)
C3	0.1748 (2)	0.1801 (3)	0.2598 (2)	0.0175 (12)
C4	0.1439 (2)	0.1227 (3)	0.2154 (2)	0.0221 (13)
H4	0.1389	0.0742	0.2301	0.027*
C5	0.1203 (2)	0.1357 (3)	0.1500 (2)	0.0239 (13)
H5	0.0995	0.0955	0.1201	0.029*
C6	0.1259 (2)	0.2050 (3)	0.1263 (2)	0.0151 (12)
C7	0.1558 (2)	0.2640 (3)	0.1704 (2)	0.0212 (13)
H7	0.1602	0.3124	0.1552	0.025*
C8	0.1792 (2)	0.2516 (3)	0.2364 (2)	0.0201 (12)
H8	0.1985	0.2921	0.2662	0.024*
C9	0.1008 (3)	0.2157 (3)	0.0562 (2)	0.0221 (13)
H9	0.0809	0.1738	0.0282	0.027*
C10	0.0809 (3)	0.2823 (3)	−0.0384 (2)	0.0203 (13)
C11	0.0973 (2)	0.2264 (3)	−0.0729 (2)	0.0203 (12)
H11	0.1219	0.1822	−0.0512	0.024*
C12	0.0771 (2)	0.2368 (3)	−0.1387 (2)	0.0235 (13)
H12	0.0881	0.1994	−0.1621	0.028*
C13	0.0411 (3)	0.3008 (3)	−0.1708 (2)	0.0245 (14)
H13	0.0280	0.3075	−0.2159	0.029*
C14	0.0244 (3)	0.3552 (3)	−0.1371 (2)	0.0244 (14)
H14	−0.0010	0.3988	−0.1593	0.029*
C15	0.0447 (3)	0.3462 (3)	−0.0713 (2)	0.0213 (13)
H15	0.0338	0.3841	−0.0483	0.026*
O2	0.31874 (18)	0.63435 (18)	0.16385 (15)	0.0252 (9)
N3	0.2971 (2)	0.5096 (2)	0.16793 (19)	0.0168 (10)
H3N	0.2778 (19)	0.4694 (15)	0.1456 (17)	0.020*
N4	0.3898 (2)	0.3942 (2)	0.46400 (18)	0.0209 (11)
C16	0.2677 (2)	0.5655 (3)	0.0640 (2)	0.0287 (13)
H16A	0.2327	0.6048	0.0415	0.043*
H16B	0.2454	0.5161	0.0508	0.043*
H16C	0.3063	0.5697	0.0522	0.043*
C17	0.2961 (2)	0.5746 (3)	0.1357 (2)	0.0203 (12)
C18	0.3253 (2)	0.4967 (3)	0.2350 (2)	0.0182 (12)
C19	0.3067 (2)	0.4306 (3)	0.2562 (2)	0.0196 (12)
H19	0.2764	0.3954	0.2249	0.024*
C20	0.3318 (2)	0.4156 (3)	0.3219 (2)	0.0183 (12)
H20	0.3191	0.3699	0.3351	0.022*
C21	0.3753 (2)	0.4664 (3)	0.3694 (2)	0.0192 (13)
C22	0.3943 (2)	0.5310 (3)	0.3481 (2)	0.0209 (13)
H22	0.4247	0.5658	0.3798	0.025*
C23	0.3710 (2)	0.5473 (3)	0.2821 (2)	0.0203 (12)
H23	0.3857	0.5920	0.2693	0.024*
C24	0.4008 (2)	0.4543 (3)	0.4389 (2)	0.0210 (13)
H24	0.4274	0.4933	0.4678	0.025*
C25	0.4151 (3)	0.3917 (3)	0.5331 (2)	0.0202 (13)
C26	0.4487 (3)	0.3259 (3)	0.5653 (2)	0.0233 (13)
H26	0.4567	0.2862	0.5419	0.028*
C27	0.4705 (3)	0.3189 (3)	0.6320 (3)	0.0276 (14)
H27	0.4939	0.2745	0.6542	0.033*
C28	0.4581 (2)	0.3768 (3)	0.6666 (2)	0.0268 (14)
H28	0.4728	0.3716	0.7121	0.032*
C29	0.4245 (2)	0.4418 (3)	0.6343 (2)	0.0273 (14)
H29	0.4163	0.4812	0.6579	0.033*
C30	0.4025 (2)	0.4500 (3)	0.5670 (2)	0.0241 (13)
H30	0.3792	0.4945	0.5449	0.029*
O3	0.32175 (18)	0.27632 (18)	0.16364 (15)	0.0270 (9)
N5	0.3035 (2)	0.1528 (2)	0.1761 (2)	0.0240 (11)
H5N	0.293 (2)	0.1107 (14)	0.1558 (18)	0.029*
N6	0.3977 (2)	0.0503 (2)	0.47430 (19)	0.0223 (11)
C31	0.2754 (2)	0.1980 (2)	0.0682 (2)	0.0255 (13)
H31A	0.2408	0.2364	0.0428	0.038*
H31B	0.2531	0.1483	0.0575	0.038*
H31C	0.3149	0.1993	0.0574	0.038*
C32	0.3021 (3)	0.2130 (3)	0.1394 (2)	0.0251 (13)
C33	0.3298 (2)	0.1451 (3)	0.2438 (2)	0.0178 (12)
C34	0.3252 (2)	0.0740 (3)	0.2680 (2)	0.0241 (13)
H34	0.3065	0.0327	0.2388	0.029*
C35	0.3475 (2)	0.0640 (3)	0.3333 (2)	0.0204 (13)
H35	0.3442	0.0154	0.3487	0.025*
C36	0.3749 (2)	0.1224 (3)	0.3781 (2)	0.0182 (12)
C37	0.3796 (2)	0.1938 (3)	0.3543 (2)	0.0227 (13)
H37	0.3982	0.2348	0.3837	0.027*
C38	0.3571 (2)	0.2049 (3)	0.2877 (2)	0.0229 (13)
H38	0.3604	0.2534	0.2721	0.028*
C39	0.3986 (2)	0.1140 (3)	0.4476 (2)	0.0220 (13)
H39	0.4154	0.1571	0.4748	0.026*
C40	0.4198 (2)	0.0468 (3)	0.5425 (2)	0.0184 (12)
C41	0.4593 (2)	−0.0158 (3)	0.5761 (2)	0.0224 (13)
H41	0.4716	−0.0527	0.5532	0.027*
C42	0.4807 (3)	−0.0249 (3)	0.6421 (2)	0.0233 (13)
H42	0.5087	−0.0671	0.6645	0.028*
C43	0.4617 (2)	0.0272 (3)	0.6757 (2)	0.0244 (13)
H43	0.4753	0.0205	0.7208	0.029*
C44	0.4223 (2)	0.0896 (3)	0.6427 (2)	0.0237 (13)
H44	0.4097	0.1261	0.6656	0.028*
C45	0.4015 (2)	0.0987 (3)	0.5769 (2)	0.0225 (12)
H45	0.3741	0.1414	0.5548	0.027*
O4	0.17838 (17)	0.69595 (16)	0.33253 (15)	0.0282 (8)
N7	0.2032 (2)	0.8216 (2)	0.3298 (2)	0.0213 (11)
H7N	0.216 (2)	0.8614 (16)	0.3537 (17)	0.026*
N8	0.1046 (2)	0.9396 (2)	0.03385 (18)	0.0231 (10)
C46	0.2345 (2)	0.7620 (2)	0.43357 (19)	0.0301 (13)
H46A	0.1969	0.7642	0.4468	0.045*
H46B	0.2638	0.8073	0.4488	0.045*
H46C	0.2638	0.7175	0.4529	0.045*
C47	0.2022 (2)	0.7574 (3)	0.3598 (2)	0.0212 (12)
C48	0.1736 (2)	0.8347 (2)	0.2619 (2)	0.0154 (11)
C49	0.1905 (2)	0.9016 (2)	0.2411 (2)	0.0194 (11)
H49	0.2206	0.9364	0.2729	0.023*
C50	0.1653 (2)	0.9189 (3)	0.1764 (2)	0.0211 (12)
H50	0.1779	0.9650	0.1637	0.025*
C51	0.1202 (2)	0.8678 (3)	0.1287 (2)	0.0211 (13)
C52	0.1005 (3)	0.8029 (3)	0.1492 (2)	0.0235 (13)
H52	0.0685	0.7692	0.1175	0.028*
C53	0.1264 (2)	0.7862 (3)	0.2149 (2)	0.0241 (13)
H53	0.1119	0.7415	0.2278	0.029*
C54	0.0920 (3)	0.8812 (3)	0.0589 (2)	0.0255 (13)
H54	0.0620	0.8439	0.0300	0.031*
C55	0.0762 (3)	0.9445 (3)	−0.0355 (2)	0.0214 (13)
C56	0.0460 (2)	1.0108 (3)	−0.0670 (2)	0.0284 (14)
H56	0.0433	1.0518	−0.0419	0.034*
C57	0.0195 (3)	1.0197 (3)	−0.1337 (2)	0.0290 (14)
H57	−0.0021	1.0656	−0.1540	0.035*
C58	0.0249 (2)	0.9607 (3)	−0.1710 (2)	0.0277 (13)
H58	0.0077	0.9661	−0.2168	0.033*
C59	0.0555 (2)	0.8945 (3)	−0.1400 (2)	0.0279 (14)
H59	0.0600	0.8544	−0.1651	0.034*
C60	0.0800 (2)	0.8846 (3)	−0.0738 (2)	0.0235 (12)
H60	0.0993	0.8376	−0.0540	0.028*
O5	0.17220 (17)	0.41264 (18)	0.32528 (15)	0.0268 (9)
N9	0.1768 (2)	0.5360 (2)	0.30192 (19)	0.0212 (10)
H9N	0.186 (2)	0.5795 (13)	0.3216 (17)	0.025*
N10	0.0890 (2)	0.6160 (2)	0.0028 (2)	0.0278 (11)
C61	0.2153 (2)	0.4991 (2)	0.4143 (2)	0.0312 (14)
H61A	0.1866	0.4763	0.4329	0.047*
H61B	0.2144	0.5539	0.4181	0.047*
H61C	0.2639	0.4811	0.4382	0.047*
C62	0.1860 (3)	0.4777 (3)	0.3438 (2)	0.0225 (13)
C63	0.1546 (2)	0.5338 (3)	0.2337 (2)	0.0234 (13)
C64	0.1207 (2)	0.4740 (3)	0.1929 (2)	0.0242 (13)
H64	0.1115	0.4291	0.2100	0.029*
C65	0.1004 (2)	0.4807 (3)	0.1266 (2)	0.0255 (13)
H65	0.0781	0.4391	0.0989	0.031*
C66	0.1113 (2)	0.5452 (3)	0.0990 (2)	0.0219 (13)
C67	0.1455 (2)	0.6046 (3)	0.1412 (2)	0.0248 (13)
H67	0.1541	0.6497	0.1240	0.030*
C68	0.1668 (2)	0.5993 (3)	0.2069 (2)	0.0206 (13)
H68	0.1902	0.6406	0.2346	0.025*
C69	0.0883 (2)	0.5532 (3)	0.0296 (2)	0.0252 (13)
H69	0.0720	0.5098	0.0027	0.030*
C70	0.0689 (3)	0.6184 (3)	−0.0650 (2)	0.0228 (13)
C71	0.0906 (2)	0.5658 (3)	−0.0972 (2)	0.0278 (13)
H71	0.1185	0.5240	−0.0739	0.033*
C72	0.0718 (3)	0.5742 (3)	−0.1622 (2)	0.0303 (13)
H72	0.0873	0.5386	−0.1836	0.036*
C73	0.0302 (3)	0.6346 (3)	−0.1970 (2)	0.0300 (14)
H73	0.0166	0.6400	−0.2422	0.036*
C74	0.0087 (3)	0.6869 (3)	−0.1652 (2)	0.0321 (14)
H74	−0.0201	0.7280	−0.1888	0.039*
C75	0.0287 (3)	0.6797 (3)	−0.0999 (2)	0.0250 (14)
H75	0.0151	0.7167	−0.0782	0.030*
O6	0.32500 (17)	0.91894 (19)	0.17329 (16)	0.0318 (9)
N11	0.3190 (2)	0.7942 (2)	0.1974 (2)	0.0313 (11)
H11N	0.303 (2)	0.7515 (15)	0.1780 (19)	0.038*
N12	0.4177 (2)	0.7185 (2)	0.4983 (2)	0.0247 (11)
C76	0.2809 (2)	0.8298 (2)	0.0847 (2)	0.0339 (13)
H76A	0.3195	0.8270	0.0729	0.051*
H76B	0.2463	0.8672	0.0573	0.051*
H76C	0.2580	0.7806	0.0781	0.051*
C77	0.3103 (3)	0.8524 (3)	0.1566 (2)	0.0237 (13)
C78	0.3446 (2)	0.7961 (3)	0.2651 (2)	0.0218 (12)
C79	0.3814 (2)	0.8570 (3)	0.3046 (2)	0.0268 (14)
H79	0.3905	0.9010	0.2862	0.032*
C80	0.4041 (3)	0.8512 (3)	0.3707 (2)	0.0250 (13)
H80	0.4277	0.8928	0.3977	0.030*
C81	0.3938 (2)	0.7863 (3)	0.4002 (2)	0.0227 (13)
C82	0.3566 (2)	0.7262 (3)	0.3592 (2)	0.0260 (13)
H82	0.3482	0.6818	0.3774	0.031*
C83	0.3323 (2)	0.7318 (3)	0.2930 (2)	0.0272 (13)
H83	0.3067	0.6912	0.2657	0.033*
C84	0.4202 (2)	0.7804 (3)	0.4706 (2)	0.0277 (14)
H84	0.4399	0.8236	0.4969	0.033*
C85	0.4417 (3)	0.7169 (3)	0.5663 (2)	0.0263 (13)
C86	0.4285 (2)	0.7739 (3)	0.6005 (2)	0.0284 (14)
H86	0.4042	0.8179	0.5780	0.034*
C87	0.4501 (2)	0.7675 (3)	0.6665 (2)	0.0311 (14)
H87	0.4403	0.8067	0.6892	0.037*
C88	0.4860 (3)	0.7042 (3)	0.7001 (2)	0.0324 (14)
H88	0.5016	0.7003	0.7458	0.039*
C89	0.4991 (3)	0.6464 (3)	0.6666 (2)	0.0321 (14)
H89	0.5238	0.6028	0.6894	0.039*
C90	0.4764 (3)	0.6522 (3)	0.6004 (2)	0.0287 (14)
H90	0.4843	0.6117	0.5776	0.034*
O1S	0.25984 (18)	0.30429 (19)	0.40922 (16)	0.0264 (9)
H1O	0.3019 (11)	0.307 (2)	0.417 (2)	0.040*
H2O	0.2331 (19)	0.3415 (17)	0.3852 (18)	0.040*
O2S	0.22697 (18)	0.38491 (18)	0.08542 (16)	0.0281 (9)
H3O	0.1920 (16)	0.356 (2)	0.0685 (18)	0.042*
H4O	0.2586 (19)	0.351 (2)	0.102 (2)	0.042*
O3S	0.27737 (17)	0.94103 (17)	0.41746 (15)	0.0292 (8)
H5O	0.3144 (15)	0.958 (2)	0.417 (2)	0.044*
H6O	0.2460 (18)	0.9762 (19)	0.3956 (19)	0.044*
O4S	0.23815 (18)	0.02510 (18)	0.08989 (16)	0.0360 (9)
H7O	0.2016 (16)	−0.004 (2)	0.0729 (19)	0.054*
H8O	0.2736 (18)	−0.010 (2)	0.1188 (18)	0.054*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
O1	0.030 (2)	0.021 (2)	0.024 (2)	−0.0057 (17)	0.0088 (16)	0.0027 (17)
N1	0.018 (2)	0.010 (2)	0.023 (3)	−0.0049 (19)	0.0082 (19)	−0.0028 (19)
N2	0.015 (2)	0.027 (3)	0.016 (3)	−0.007 (2)	0.0076 (19)	−0.010 (2)
C1	0.024 (3)	0.024 (3)	0.017 (3)	−0.002 (2)	0.008 (2)	−0.003 (2)
C2	0.010 (3)	0.016 (3)	0.025 (3)	0.001 (2)	0.008 (2)	−0.002 (2)
C3	0.016 (3)	0.022 (3)	0.015 (3)	0.007 (2)	0.007 (2)	0.003 (2)
C4	0.021 (3)	0.016 (3)	0.027 (3)	−0.003 (2)	0.009 (2)	0.002 (2)
C5	0.024 (3)	0.027 (3)	0.016 (3)	−0.007 (2)	0.006 (2)	−0.007 (2)
C6	0.013 (3)	0.016 (3)	0.012 (3)	0.001 (2)	0.002 (2)	−0.002 (2)
C7	0.024 (3)	0.021 (3)	0.022 (3)	−0.001 (2)	0.012 (2)	0.001 (2)
C8	0.017 (3)	0.017 (3)	0.024 (3)	−0.003 (2)	0.008 (2)	−0.008 (2)
C9	0.016 (3)	0.021 (3)	0.029 (3)	−0.003 (3)	0.011 (3)	−0.007 (3)
C10	0.016 (3)	0.024 (3)	0.024 (3)	−0.007 (2)	0.012 (2)	−0.003 (3)
C11	0.013 (3)	0.024 (3)	0.023 (3)	0.002 (2)	0.006 (2)	0.001 (2)
C12	0.020 (3)	0.031 (3)	0.017 (3)	−0.006 (2)	0.007 (2)	−0.009 (2)
C13	0.024 (3)	0.036 (4)	0.013 (3)	−0.004 (3)	0.008 (2)	−0.002 (3)
C14	0.022 (3)	0.024 (3)	0.023 (3)	−0.002 (3)	0.005 (2)	0.007 (3)
C15	0.018 (3)	0.025 (3)	0.021 (3)	−0.002 (3)	0.009 (2)	−0.006 (3)
O2	0.033 (2)	0.018 (2)	0.025 (2)	−0.0072 (17)	0.0134 (16)	−0.0051 (17)
N3	0.021 (3)	0.013 (2)	0.011 (2)	−0.0001 (19)	0.0037 (19)	−0.0033 (19)
N4	0.022 (3)	0.022 (3)	0.018 (3)	0.003 (2)	0.009 (2)	0.006 (2)
C16	0.029 (3)	0.028 (3)	0.031 (3)	−0.001 (2)	0.016 (3)	0.004 (3)
C17	0.018 (3)	0.024 (3)	0.021 (3)	0.001 (2)	0.011 (2)	0.006 (3)
C18	0.018 (3)	0.020 (3)	0.023 (3)	−0.004 (2)	0.014 (2)	−0.006 (2)
C19	0.015 (3)	0.024 (3)	0.018 (3)	−0.004 (2)	0.006 (2)	−0.005 (2)
C20	0.024 (3)	0.008 (3)	0.027 (3)	−0.002 (2)	0.016 (2)	−0.003 (2)
C21	0.015 (3)	0.019 (3)	0.027 (3)	0.002 (2)	0.012 (2)	0.004 (3)
C22	0.021 (3)	0.014 (3)	0.019 (3)	−0.002 (2)	0.002 (2)	−0.004 (2)
C23	0.024 (3)	0.016 (3)	0.020 (3)	−0.001 (2)	0.010 (2)	0.001 (2)
C24	0.012 (3)	0.026 (3)	0.023 (3)	−0.002 (2)	0.007 (2)	−0.007 (3)
C25	0.015 (3)	0.021 (3)	0.021 (3)	−0.006 (2)	0.006 (2)	0.000 (3)
C26	0.024 (3)	0.023 (3)	0.024 (3)	−0.007 (3)	0.011 (2)	−0.003 (3)
C27	0.021 (3)	0.027 (3)	0.034 (4)	−0.003 (3)	0.011 (3)	0.006 (3)
C28	0.017 (3)	0.043 (4)	0.017 (3)	−0.002 (3)	0.005 (2)	0.006 (3)
C29	0.023 (3)	0.032 (3)	0.025 (3)	−0.004 (2)	0.010 (2)	−0.007 (3)
C30	0.023 (3)	0.024 (3)	0.022 (3)	−0.006 (2)	0.008 (2)	−0.004 (2)
O3	0.031 (2)	0.019 (2)	0.027 (2)	−0.0077 (17)	0.0102 (16)	−0.0071 (17)
N5	0.028 (3)	0.021 (3)	0.025 (3)	0.000 (2)	0.013 (2)	−0.006 (2)
N6	0.021 (2)	0.019 (3)	0.027 (3)	0.0032 (19)	0.0101 (19)	0.003 (2)
C31	0.021 (3)	0.029 (3)	0.029 (3)	−0.005 (2)	0.013 (2)	−0.001 (2)
C32	0.018 (3)	0.032 (4)	0.029 (3)	0.000 (3)	0.013 (2)	0.002 (3)
C33	0.015 (3)	0.016 (3)	0.025 (3)	−0.003 (2)	0.010 (2)	−0.006 (2)
C34	0.026 (3)	0.024 (3)	0.023 (3)	0.000 (2)	0.011 (2)	0.002 (2)
C35	0.020 (3)	0.014 (3)	0.031 (3)	0.001 (2)	0.015 (2)	−0.003 (3)
C36	0.015 (3)	0.022 (3)	0.021 (3)	0.000 (2)	0.011 (2)	0.004 (2)
C37	0.016 (3)	0.020 (3)	0.032 (3)	−0.001 (2)	0.011 (2)	−0.005 (2)
C38	0.025 (3)	0.016 (3)	0.034 (3)	0.001 (2)	0.019 (3)	−0.001 (2)
C39	0.016 (3)	0.018 (3)	0.033 (3)	−0.001 (2)	0.012 (2)	−0.006 (3)
C40	0.012 (3)	0.019 (3)	0.020 (3)	−0.002 (2)	0.004 (2)	0.004 (2)
C41	0.021 (3)	0.020 (3)	0.028 (3)	−0.006 (2)	0.013 (2)	−0.004 (2)
C42	0.021 (3)	0.023 (3)	0.031 (3)	0.004 (2)	0.016 (3)	0.001 (3)
C43	0.017 (3)	0.032 (3)	0.022 (3)	−0.002 (3)	0.007 (2)	0.000 (3)
C44	0.017 (3)	0.029 (3)	0.026 (3)	−0.004 (2)	0.011 (2)	−0.013 (3)
C45	0.021 (3)	0.017 (3)	0.029 (3)	−0.004 (2)	0.011 (2)	−0.002 (2)
O4	0.037 (2)	0.0192 (19)	0.029 (2)	−0.0047 (17)	0.0163 (17)	−0.0014 (17)
N7	0.023 (3)	0.017 (3)	0.024 (3)	−0.006 (2)	0.011 (2)	−0.005 (2)
N8	0.021 (2)	0.025 (3)	0.021 (3)	−0.001 (2)	0.0082 (19)	−0.001 (2)
C46	0.029 (3)	0.034 (3)	0.025 (3)	−0.006 (3)	0.011 (2)	0.001 (3)
C47	0.022 (3)	0.018 (3)	0.031 (3)	−0.006 (2)	0.018 (2)	−0.010 (3)
C48	0.014 (3)	0.013 (3)	0.018 (3)	0.004 (2)	0.006 (2)	0.002 (2)
C49	0.028 (3)	0.012 (3)	0.019 (3)	−0.004 (2)	0.011 (2)	−0.004 (2)
C50	0.017 (3)	0.021 (3)	0.025 (3)	−0.007 (2)	0.009 (2)	−0.005 (2)
C51	0.020 (3)	0.028 (3)	0.015 (3)	0.003 (2)	0.008 (2)	−0.003 (2)
C52	0.017 (3)	0.026 (3)	0.025 (3)	−0.003 (2)	0.008 (2)	−0.004 (3)
C53	0.018 (3)	0.025 (3)	0.026 (3)	−0.008 (2)	0.006 (2)	−0.006 (2)
C54	0.017 (3)	0.019 (3)	0.039 (4)	−0.004 (2)	0.012 (3)	−0.010 (3)
C55	0.019 (3)	0.020 (3)	0.025 (3)	−0.004 (2)	0.010 (2)	−0.005 (3)
C56	0.023 (3)	0.032 (3)	0.036 (4)	0.005 (3)	0.019 (3)	0.003 (3)
C57	0.030 (3)	0.029 (3)	0.031 (4)	0.002 (3)	0.016 (3)	0.007 (3)
C58	0.026 (3)	0.035 (3)	0.025 (3)	−0.001 (2)	0.013 (2)	0.004 (3)
C59	0.021 (3)	0.036 (3)	0.028 (3)	−0.006 (2)	0.012 (2)	−0.009 (3)
C60	0.019 (3)	0.020 (3)	0.028 (3)	−0.005 (2)	0.008 (2)	0.004 (2)
O5	0.032 (2)	0.016 (2)	0.031 (2)	0.0005 (17)	0.0135 (17)	0.0008 (18)
N9	0.024 (2)	0.010 (2)	0.032 (3)	−0.001 (2)	0.015 (2)	−0.005 (2)
N10	0.031 (3)	0.022 (3)	0.036 (3)	0.005 (2)	0.021 (2)	−0.001 (2)
C61	0.030 (3)	0.029 (3)	0.033 (3)	0.002 (3)	0.013 (3)	−0.003 (3)
C62	0.016 (3)	0.028 (3)	0.027 (3)	0.002 (3)	0.012 (2)	−0.003 (3)
C63	0.016 (3)	0.030 (3)	0.028 (3)	0.000 (2)	0.013 (2)	0.001 (3)
C64	0.019 (3)	0.019 (3)	0.031 (3)	−0.004 (2)	0.008 (2)	0.003 (3)
C65	0.021 (3)	0.027 (3)	0.026 (3)	−0.002 (2)	0.008 (2)	−0.008 (3)
C66	0.014 (3)	0.021 (3)	0.030 (3)	−0.004 (2)	0.010 (2)	−0.004 (3)
C67	0.023 (3)	0.024 (3)	0.032 (3)	0.002 (2)	0.015 (2)	0.008 (3)
C68	0.017 (3)	0.015 (3)	0.036 (3)	−0.008 (2)	0.018 (3)	−0.015 (3)
C69	0.020 (3)	0.030 (3)	0.022 (3)	0.000 (2)	0.007 (2)	−0.003 (3)
C70	0.019 (3)	0.026 (3)	0.022 (3)	−0.003 (2)	0.009 (2)	−0.002 (2)
C71	0.018 (3)	0.032 (3)	0.033 (3)	0.007 (2)	0.013 (2)	−0.004 (3)
C72	0.031 (3)	0.032 (3)	0.027 (3)	0.003 (3)	0.013 (2)	0.000 (2)
C73	0.025 (3)	0.044 (4)	0.023 (3)	−0.002 (3)	0.014 (2)	0.002 (3)
C74	0.027 (3)	0.033 (3)	0.040 (4)	0.005 (3)	0.018 (3)	0.014 (3)
C75	0.030 (3)	0.017 (3)	0.035 (4)	−0.001 (2)	0.022 (3)	−0.002 (3)
O6	0.030 (2)	0.029 (2)	0.036 (2)	−0.0012 (18)	0.0143 (17)	−0.0042 (19)
N11	0.025 (3)	0.032 (3)	0.033 (3)	−0.002 (2)	0.009 (2)	−0.003 (2)
N12	0.023 (3)	0.017 (3)	0.035 (3)	−0.002 (2)	0.015 (2)	−0.003 (2)
C76	0.032 (3)	0.041 (3)	0.027 (3)	0.004 (3)	0.012 (2)	−0.005 (3)
C77	0.016 (3)	0.017 (3)	0.033 (3)	0.003 (2)	0.007 (2)	0.000 (3)
C78	0.023 (3)	0.021 (3)	0.020 (3)	0.004 (2)	0.009 (2)	−0.005 (2)
C79	0.024 (3)	0.024 (3)	0.033 (3)	0.001 (2)	0.014 (3)	−0.008 (3)
C80	0.022 (3)	0.018 (3)	0.032 (3)	−0.004 (2)	0.010 (2)	−0.008 (3)
C81	0.015 (3)	0.021 (3)	0.033 (3)	−0.002 (2)	0.012 (3)	−0.009 (3)
C82	0.022 (3)	0.023 (3)	0.038 (3)	−0.002 (2)	0.017 (3)	−0.008 (3)
C83	0.025 (3)	0.022 (3)	0.037 (4)	−0.003 (2)	0.016 (3)	0.004 (3)
C84	0.021 (3)	0.025 (3)	0.042 (4)	0.002 (2)	0.019 (3)	−0.008 (3)
C85	0.021 (3)	0.024 (3)	0.037 (3)	−0.004 (2)	0.016 (3)	−0.006 (3)
C86	0.025 (3)	0.016 (3)	0.044 (4)	0.005 (2)	0.016 (3)	0.005 (3)
C87	0.026 (3)	0.033 (3)	0.032 (3)	0.005 (2)	0.012 (2)	−0.002 (3)
C88	0.034 (3)	0.030 (3)	0.036 (3)	0.004 (3)	0.019 (3)	0.004 (3)
C89	0.034 (3)	0.028 (3)	0.040 (4)	0.004 (3)	0.022 (3)	0.005 (3)
C90	0.029 (3)	0.015 (3)	0.045 (4)	0.003 (2)	0.020 (3)	0.003 (3)
O1S	0.026 (2)	0.022 (2)	0.028 (2)	−0.0022 (17)	0.0093 (18)	0.0002 (16)
O2S	0.027 (2)	0.025 (2)	0.029 (2)	−0.0046 (16)	0.0093 (18)	−0.0038 (17)
O3S	0.031 (2)	0.023 (2)	0.034 (2)	−0.0034 (16)	0.0147 (18)	−0.0014 (16)
O4S	0.039 (2)	0.027 (2)	0.035 (2)	−0.0100 (18)	0.0113 (18)	−0.0014 (17)

Geometric parameters (Å, º) top

O1—C2	1.227 (5)	N8—C54	1.277 (6)
N1—C2	1.350 (6)	N8—C55	1.427 (6)
N1—C3	1.407 (6)	C46—C47	1.515 (6)
N1—H1N	0.877 (17)	C46—H46A	0.9800
N2—C9	1.279 (6)	C46—H46B	0.9800
N2—C10	1.429 (6)	C46—H46C	0.9800
C1—C2	1.517 (6)	C48—C53	1.390 (6)
C1—H1A	0.9800	C48—C49	1.392 (6)
C1—H1B	0.9800	C49—C50	1.368 (6)
C1—H1C	0.9800	C49—H49	0.9500
C3—C4	1.381 (6)	C50—C51	1.410 (6)
C3—C8	1.403 (6)	C50—H50	0.9500
C4—C5	1.370 (6)	C51—C52	1.384 (6)
C4—H4	0.9500	C51—C54	1.454 (6)
C5—C6	1.377 (6)	C52—C53	1.384 (6)
C5—H5	0.9500	C52—H52	0.9500
C6—C7	1.395 (6)	C53—H53	0.9500
C6—C9	1.461 (7)	C54—H54	0.9500
C7—C8	1.382 (6)	C55—C56	1.379 (6)
C7—H7	0.9500	C55—C60	1.410 (6)
C8—H8	0.9500	C56—C57	1.381 (6)
C9—H9	0.9500	C56—H56	0.9500
C10—C15	1.388 (6)	C57—C58	1.393 (6)
C10—C11	1.415 (6)	C57—H57	0.9500
C11—C12	1.383 (6)	C58—C59	1.378 (6)
C11—H11	0.9500	C58—H58	0.9500
C12—C13	1.385 (6)	C59—C60	1.379 (6)
C12—H12	0.9500	C59—H59	0.9500
C13—C14	1.386 (6)	C60—H60	0.9500
C13—H13	0.9500	O5—C62	1.222 (5)
C14—C15	1.382 (6)	N9—C62	1.368 (6)
C14—H14	0.9500	N9—C63	1.418 (6)
C15—H15	0.9500	N9—H9N	0.873 (17)
O2—C17	1.224 (5)	N10—C69	1.280 (6)
N3—C17	1.368 (6)	N10—C70	1.418 (6)
N3—C18	1.396 (6)	C61—C62	1.499 (6)
N3—H3N	0.868 (17)	C61—H61A	0.9800
N4—C24	1.286 (6)	C61—H61B	0.9800
N4—C25	1.427 (6)	C61—H61C	0.9800
C16—C17	1.485 (6)	C63—C64	1.385 (6)
C16—H16A	0.9800	C63—C68	1.399 (6)
C16—H16B	0.9800	C64—C65	1.390 (6)
C16—H16C	0.9800	C64—H64	0.9500
C18—C19	1.400 (6)	C65—C66	1.381 (6)
C18—C23	1.402 (6)	C65—H65	0.9500
C19—C20	1.379 (6)	C66—C67	1.393 (6)
C19—H19	0.9500	C66—C69	1.449 (6)
C20—C21	1.394 (6)	C67—C68	1.369 (6)
C20—H20	0.9500	C67—H67	0.9500
C21—C22	1.381 (6)	C68—H68	0.9500
C21—C24	1.452 (6)	C69—H69	0.9500
C22—C23	1.396 (6)	C70—C75	1.393 (6)
C22—H22	0.9500	C70—C71	1.398 (6)
C23—H23	0.9500	C71—C72	1.367 (6)
C24—H24	0.9500	C71—H71	0.9500
C25—C26	1.397 (6)	C72—C73	1.392 (6)
C25—C30	1.397 (6)	C72—H72	0.9500
C26—C27	1.391 (7)	C73—C74	1.386 (6)
C26—H26	0.9500	C73—H73	0.9500
C27—C28	1.399 (6)	C74—C75	1.367 (6)
C27—H27	0.9500	C74—H74	0.9500
C28—C29	1.384 (6)	C75—H75	0.9500
C28—H28	0.9500	O6—C77	1.240 (5)
C29—C30	1.405 (6)	N11—C77	1.353 (6)
C29—H29	0.9500	N11—C78	1.396 (6)
C30—H30	0.9500	N11—H11N	0.867 (18)
O3—C32	1.242 (5)	N12—C84	1.285 (6)
N5—C32	1.357 (6)	N12—C85	1.406 (6)
N5—C33	1.401 (6)	C76—C77	1.531 (6)
N5—H5N	0.857 (17)	C76—H76A	0.9800
N6—C39	1.294 (6)	C76—H76B	0.9800
N6—C40	1.419 (6)	C76—H76C	0.9800
C31—C32	1.493 (6)	C78—C83	1.395 (6)
C31—H31A	0.9800	C78—C79	1.402 (6)
C31—H31B	0.9800	C79—C80	1.374 (6)
C31—H31C	0.9800	C79—H79	0.9500
C33—C38	1.398 (6)	C80—C81	1.406 (6)
C33—C34	1.404 (6)	C80—H80	0.9500
C34—C35	1.364 (6)	C81—C82	1.406 (6)
C34—H34	0.9500	C81—C84	1.457 (6)
C35—C36	1.391 (6)	C82—C83	1.370 (6)
C35—H35	0.9500	C82—H82	0.9500
C36—C37	1.406 (6)	C83—H83	0.9500
C36—C39	1.449 (6)	C84—H84	0.9500
C37—C38	1.395 (6)	C85—C86	1.392 (6)
C37—H37	0.9500	C85—C90	1.399 (6)
C38—H38	0.9500	C86—C87	1.377 (6)
C39—H39	0.9500	C86—H86	0.9500
C40—C45	1.384 (6)	C87—C88	1.381 (6)
C40—C41	1.398 (6)	C87—H87	0.9500
C41—C42	1.382 (6)	C88—C89	1.389 (6)
C41—H41	0.9500	C88—H88	0.9500
C42—C43	1.383 (6)	C89—C90	1.374 (6)
C42—H42	0.9500	C89—H89	0.9500
C43—C44	1.389 (6)	C90—H90	0.9500
C43—H43	0.9500	O1S—H1O	0.832 (19)
C44—C45	1.380 (6)	O1S—H2O	0.884 (18)
C44—H44	0.9500	O2S—H3O	0.845 (18)
C45—H45	0.9500	O2S—H4O	0.857 (19)
O4—C47	1.247 (5)	O3S—H5O	0.848 (18)
N7—C47	1.341 (6)	O3S—H6O	0.886 (18)
N7—C48	1.411 (6)	O4S—H7O	0.870 (19)
N7—H7N	0.860 (18)	O4S—H8O	0.977 (19)

C2—N1—C3	127.5 (4)	C48—N7—H7N	115 (3)
C2—N1—H1N	117 (3)	C54—N8—C55	119.1 (4)
C3—N1—H1N	116 (3)	C47—C46—H46A	109.5
C9—N2—C10	119.5 (4)	C47—C46—H46B	109.5
C2—C1—H1A	109.5	H46A—C46—H46B	109.5
C2—C1—H1B	109.5	C47—C46—H46C	109.5
H1A—C1—H1B	109.5	H46A—C46—H46C	109.5
C2—C1—H1C	109.5	H46B—C46—H46C	109.5
H1A—C1—H1C	109.5	O4—C47—N7	126.0 (4)
H1B—C1—H1C	109.5	O4—C47—C46	118.9 (4)
O1—C2—N1	124.4 (4)	N7—C47—C46	115.1 (4)
O1—C2—C1	120.6 (4)	C53—C48—C49	118.2 (4)
N1—C2—C1	115.0 (4)	C53—C48—N7	123.9 (4)
C4—C3—C8	118.7 (4)	C49—C48—N7	117.8 (4)
C4—C3—N1	125.8 (5)	C50—C49—C48	122.2 (4)
C8—C3—N1	115.4 (5)	C50—C49—H49	118.9
C5—C4—C3	119.9 (5)	C48—C49—H49	118.9
C5—C4—H4	120.0	C49—C50—C51	119.4 (4)
C3—C4—H4	120.0	C49—C50—H50	120.3
C4—C5—C6	122.2 (5)	C51—C50—H50	120.3
C4—C5—H5	118.9	C52—C51—C50	118.6 (4)
C6—C5—H5	118.9	C52—C51—C54	118.4 (5)
C5—C6—C7	118.6 (4)	C50—C51—C54	123.0 (5)
C5—C6—C9	120.1 (5)	C51—C52—C53	121.3 (5)
C7—C6—C9	121.4 (5)	C51—C52—H52	119.4
C8—C7—C6	119.7 (5)	C53—C52—H52	119.4
C8—C7—H7	120.1	C52—C53—C48	120.2 (5)
C6—C7—H7	120.1	C52—C53—H53	119.9
C7—C8—C3	120.8 (5)	C48—C53—H53	119.9
C7—C8—H8	119.6	N8—C54—C51	124.5 (5)
C3—C8—H8	119.6	N8—C54—H54	117.8
N2—C9—C6	123.7 (5)	C51—C54—H54	117.8
N2—C9—H9	118.1	C56—C55—C60	117.6 (4)
C6—C9—H9	118.1	C56—C55—N8	119.9 (5)
C15—C10—C11	119.3 (5)	C60—C55—N8	122.4 (5)
C15—C10—N2	118.0 (5)	C55—C56—C57	122.6 (5)
C11—C10—N2	122.6 (5)	C55—C56—H56	118.7
C12—C11—C10	119.2 (5)	C57—C56—H56	118.7
C12—C11—H11	120.4	C56—C57—C58	119.4 (5)
C10—C11—H11	120.4	C56—C57—H57	120.3
C11—C12—C13	120.9 (5)	C58—C57—H57	120.3
C11—C12—H12	119.5	C59—C58—C57	118.6 (5)
C13—C12—H12	119.5	C59—C58—H58	120.7
C12—C13—C14	119.8 (5)	C57—C58—H58	120.7
C12—C13—H13	120.1	C58—C59—C60	122.0 (5)
C14—C13—H13	120.1	C58—C59—H59	119.0
C15—C14—C13	120.1 (5)	C60—C59—H59	119.0
C15—C14—H14	119.9	C59—C60—C55	119.6 (5)
C13—C14—H14	119.9	C59—C60—H60	120.2
C14—C15—C10	120.7 (5)	C55—C60—H60	120.2
C14—C15—H15	119.7	C62—N9—C63	128.8 (4)
C10—C15—H15	119.7	C62—N9—H9N	112 (3)
C17—N3—C18	129.1 (4)	C63—N9—H9N	119 (3)
C17—N3—H3N	119 (3)	C69—N10—C70	119.4 (5)
C18—N3—H3N	112 (3)	C62—C61—H61A	109.5
C24—N4—C25	118.2 (4)	C62—C61—H61B	109.5
C17—C16—H16A	109.5	H61A—C61—H61B	109.5
C17—C16—H16B	109.5	C62—C61—H61C	109.5
H16A—C16—H16B	109.5	H61A—C61—H61C	109.5
C17—C16—H16C	109.5	H61B—C61—H61C	109.5
H16A—C16—H16C	109.5	O5—C62—N9	122.7 (5)
H16B—C16—H16C	109.5	O5—C62—C61	122.2 (5)
O2—C17—N3	122.9 (4)	N9—C62—C61	115.1 (4)
O2—C17—C16	122.9 (5)	C64—C63—C68	119.2 (4)
N3—C17—C16	114.1 (4)	C64—C63—N9	125.3 (5)
N3—C18—C19	118.4 (4)	C68—C63—N9	115.5 (5)
N3—C18—C23	123.0 (4)	C63—C64—C65	118.8 (5)
C19—C18—C23	118.6 (4)	C63—C64—H64	120.6
C20—C19—C18	121.0 (5)	C65—C64—H64	120.6
C20—C19—H19	119.5	C66—C65—C64	122.9 (5)
C18—C19—H19	119.5	C66—C65—H65	118.6
C19—C20—C21	121.3 (5)	C64—C65—H65	118.6
C19—C20—H20	119.4	C65—C66—C67	117.1 (4)
C21—C20—H20	119.4	C65—C66—C69	122.9 (5)
C22—C21—C20	117.4 (4)	C67—C66—C69	120.0 (5)
C22—C21—C24	119.5 (5)	C68—C67—C66	121.4 (5)
C20—C21—C24	123.1 (5)	C68—C67—H67	119.3
C21—C22—C23	122.9 (5)	C66—C67—H67	119.3
C21—C22—H22	118.5	C67—C68—C63	120.6 (5)
C23—C22—H22	118.5	C67—C68—H68	119.7
C22—C23—C18	118.8 (5)	C63—C68—H68	119.7
C22—C23—H23	120.6	N10—C69—C66	122.9 (5)
C18—C23—H23	120.6	N10—C69—H69	118.5
N4—C24—C21	124.4 (5)	C66—C69—H69	118.5
N4—C24—H24	117.8	C75—C70—C71	119.0 (5)
C21—C24—H24	117.8	C75—C70—N10	117.0 (5)
C26—C25—C30	120.5 (5)	C71—C70—N10	123.9 (5)
C26—C25—N4	117.3 (5)	C72—C71—C70	120.3 (5)
C30—C25—N4	121.9 (5)	C72—C71—H71	119.9
C27—C26—C25	119.5 (5)	C70—C71—H71	119.9
C27—C26—H26	120.2	C71—C72—C73	120.3 (5)
C25—C26—H26	120.2	C71—C72—H72	119.9
C26—C27—C28	120.5 (5)	C73—C72—H72	119.9
C26—C27—H27	119.7	C74—C73—C72	119.6 (5)
C28—C27—H27	119.7	C74—C73—H73	120.2
C29—C28—C27	119.7 (5)	C72—C73—H73	120.2
C29—C28—H28	120.1	C75—C74—C73	120.3 (5)
C27—C28—H28	120.1	C75—C74—H74	119.9
C28—C29—C30	120.6 (5)	C73—C74—H74	119.9
C28—C29—H29	119.7	C74—C75—C70	120.6 (5)
C30—C29—H29	119.7	C74—C75—H75	119.7
C25—C30—C29	119.1 (5)	C70—C75—H75	119.7
C25—C30—H30	120.4	C77—N11—C78	128.0 (4)
C29—C30—H30	120.4	C77—N11—H11N	115 (3)
C32—N5—C33	130.9 (4)	C78—N11—H11N	117 (3)
C32—N5—H5N	115 (3)	C84—N12—C85	119.5 (5)
C33—N5—H5N	113 (3)	C77—C76—H76A	109.5
C39—N6—C40	119.6 (4)	C77—C76—H76B	109.5
C32—C31—H31A	109.5	H76A—C76—H76B	109.5
C32—C31—H31B	109.5	C77—C76—H76C	109.5
H31A—C31—H31B	109.5	H76A—C76—H76C	109.5
C32—C31—H31C	109.5	H76B—C76—H76C	109.5
H31A—C31—H31C	109.5	O6—C77—N11	125.5 (5)
H31B—C31—H31C	109.5	O6—C77—C76	120.4 (5)
O3—C32—N5	121.9 (5)	N11—C77—C76	114.0 (4)
O3—C32—C31	122.5 (5)	C83—C78—N11	115.8 (5)
N5—C32—C31	115.6 (4)	C83—C78—C79	120.2 (5)
C38—C33—N5	123.4 (5)	N11—C78—C79	124.0 (5)
C38—C33—C34	118.8 (5)	C80—C79—C78	117.9 (5)
N5—C33—C34	117.7 (4)	C80—C79—H79	121.1
C35—C34—C33	120.1 (5)	C78—C79—H79	121.1
C35—C34—H34	120.0	C79—C80—C81	122.9 (5)
C33—C34—H34	120.0	C79—C80—H80	118.6
C34—C35—C36	122.5 (5)	C81—C80—H80	118.6
C34—C35—H35	118.8	C80—C81—C82	117.8 (5)
C36—C35—H35	118.8	C80—C81—C84	122.0 (5)
C35—C36—C37	117.8 (4)	C82—C81—C84	120.2 (5)
C35—C36—C39	124.0 (5)	C83—C82—C81	120.0 (5)
C37—C36—C39	118.2 (5)	C83—C82—H82	120.0
C38—C37—C36	120.4 (5)	C81—C82—H82	120.0
C38—C37—H37	119.8	C82—C83—C78	121.1 (5)
C36—C37—H37	119.8	C82—C83—H83	119.4
C37—C38—C33	120.4 (5)	C78—C83—H83	119.4
C37—C38—H38	119.8	N12—C84—C81	122.1 (5)
C33—C38—H38	119.8	N12—C84—H84	119.0
N6—C39—C36	122.7 (5)	C81—C84—H84	119.0
N6—C39—H39	118.6	C86—C85—C90	118.3 (5)
C36—C39—H39	118.6	C86—C85—N12	123.3 (5)
C45—C40—C41	118.2 (5)	C90—C85—N12	118.2 (5)
C45—C40—N6	124.5 (5)	C87—C86—C85	120.8 (5)
C41—C40—N6	117.2 (5)	C87—C86—H86	119.6
C42—C41—C40	120.9 (5)	C85—C86—H86	119.6
C42—C41—H41	119.6	C86—C87—C88	120.3 (5)
C40—C41—H41	119.6	C86—C87—H87	119.8
C41—C42—C43	120.2 (5)	C88—C87—H87	119.8
C41—C42—H42	119.9	C87—C88—C89	119.7 (5)
C43—C42—H42	119.9	C87—C88—H88	120.2
C42—C43—C44	119.3 (5)	C89—C88—H88	120.2
C42—C43—H43	120.3	C90—C89—C88	120.1 (5)
C44—C43—H43	120.3	C90—C89—H89	120.0
C45—C44—C43	120.3 (5)	C88—C89—H89	120.0
C45—C44—H44	119.8	C89—C90—C85	120.8 (5)
C43—C44—H44	119.8	C89—C90—H90	119.6
C44—C45—C40	121.1 (5)	C85—C90—H90	119.6
C44—C45—H45	119.5	H1O—O1S—H2O	114 (4)
C40—C45—H45	119.5	H3O—O2S—H4O	97 (4)
C47—N7—C48	127.3 (4)	H5O—O3S—H6O	102 (4)
C47—N7—H7N	117 (3)	H7O—O4S—H8O	100 (4)

C3—N1—C2—O1	3.4 (8)	C48—N7—C47—O4	4.7 (8)
C3—N1—C2—C1	−175.3 (4)	C48—N7—C47—C46	−176.3 (4)
C2—N1—C3—C4	3.3 (8)	C47—N7—C48—C53	13.3 (8)
C2—N1—C3—C8	179.8 (4)	C47—N7—C48—C49	−169.6 (4)
C8—C3—C4—C5	2.1 (7)	C53—C48—C49—C50	−3.6 (7)
N1—C3—C4—C5	178.5 (5)	N7—C48—C49—C50	179.2 (4)
C3—C4—C5—C6	−0.4 (8)	C48—C49—C50—C51	0.3 (7)
C4—C5—C6—C7	−0.8 (8)	C49—C50—C51—C52	2.9 (7)
C4—C5—C6—C9	179.2 (5)	C49—C50—C51—C54	−179.0 (4)
C5—C6—C7—C8	0.2 (7)	C50—C51—C52—C53	−2.8 (7)
C9—C6—C7—C8	−179.8 (4)	C54—C51—C52—C53	178.9 (5)
C6—C7—C8—C3	1.6 (7)	C51—C52—C53—C48	−0.4 (8)
C4—C3—C8—C7	−2.7 (7)	C49—C48—C53—C52	3.6 (7)
N1—C3—C8—C7	−179.5 (4)	N7—C48—C53—C52	−179.3 (4)
C10—N2—C9—C6	177.3 (5)	C55—N8—C54—C51	177.2 (5)
C5—C6—C9—N2	179.9 (5)	C52—C51—C54—N8	178.1 (5)
C7—C6—C9—N2	−0.1 (8)	C50—C51—C54—N8	−0.1 (8)
C9—N2—C10—C15	141.4 (5)	C54—N8—C55—C56	136.3 (5)
C9—N2—C10—C11	−42.8 (7)	C54—N8—C55—C60	−46.3 (7)
C15—C10—C11—C12	0.2 (7)	C60—C55—C56—C57	0.5 (7)
N2—C10—C11—C12	−175.6 (5)	N8—C55—C56—C57	178.0 (5)
C10—C11—C12—C13	−0.1 (7)	C55—C56—C57—C58	−1.8 (8)
C11—C12—C13—C14	−0.6 (8)	C56—C57—C58—C59	1.1 (7)
C12—C13—C14—C15	1.2 (8)	C57—C58—C59—C60	1.0 (7)
C13—C14—C15—C10	−1.1 (8)	C58—C59—C60—C55	−2.4 (7)
C11—C10—C15—C14	0.4 (7)	C56—C55—C60—C59	1.6 (7)
N2—C10—C15—C14	176.3 (5)	N8—C55—C60—C59	−175.8 (5)
C18—N3—C17—O2	−3.6 (8)	C63—N9—C62—O5	−3.4 (8)
C18—N3—C17—C16	174.1 (5)	C63—N9—C62—C61	175.7 (4)
C17—N3—C18—C19	166.2 (5)	C62—N9—C63—C64	17.4 (8)
C17—N3—C18—C23	−13.3 (8)	C62—N9—C63—C68	−164.6 (4)
N3—C18—C19—C20	−178.6 (4)	C68—C63—C64—C65	0.5 (7)
C23—C18—C19—C20	0.9 (7)	N9—C63—C64—C65	178.4 (5)
C18—C19—C20—C21	1.2 (7)	C63—C64—C65—C66	−1.4 (8)
C19—C20—C21—C22	−2.2 (7)	C64—C65—C66—C67	1.3 (7)
C19—C20—C21—C24	177.7 (4)	C64—C65—C66—C69	−178.1 (5)
C20—C21—C22—C23	1.1 (7)	C65—C66—C67—C68	−0.5 (7)
C24—C21—C22—C23	−178.8 (5)	C69—C66—C67—C68	179.0 (5)
C21—C22—C23—C18	1.0 (8)	C66—C67—C68—C63	−0.3 (7)
N3—C18—C23—C22	177.5 (4)	C64—C63—C68—C67	0.3 (7)
C19—C18—C23—C22	−2.0 (7)	N9—C63—C68—C67	−177.8 (4)
C25—N4—C24—C21	−176.9 (5)	C70—N10—C69—C66	176.9 (5)
C22—C21—C24—N4	−175.6 (5)	C65—C66—C69—N10	169.5 (5)
C20—C21—C24—N4	4.6 (8)	C67—C66—C69—N10	−9.9 (8)
C24—N4—C25—C26	−136.0 (5)	C69—N10—C70—C75	140.5 (5)
C24—N4—C25—C30	48.7 (7)	C69—N10—C70—C71	−43.5 (7)
C30—C25—C26—C27	−0.8 (7)	C75—C70—C71—C72	−0.7 (8)
N4—C25—C26—C27	−176.1 (4)	N10—C70—C71—C72	−176.7 (5)
C25—C26—C27—C28	0.8 (8)	C70—C71—C72—C73	−0.8 (8)
C26—C27—C28—C29	−0.5 (8)	C71—C72—C73—C74	0.9 (8)
C27—C28—C29—C30	0.2 (8)	C72—C73—C74—C75	0.6 (8)
C26—C25—C30—C29	0.5 (7)	C73—C74—C75—C70	−2.2 (8)
N4—C25—C30—C29	175.6 (4)	C71—C70—C75—C74	2.2 (8)
C28—C29—C30—C25	−0.2 (7)	N10—C70—C75—C74	178.5 (5)
C33—N5—C32—O3	−5.6 (8)	C78—N11—C77—O6	1.1 (8)
C33—N5—C32—C31	174.5 (5)	C78—N11—C77—C76	−180.0 (4)
C32—N5—C33—C38	4.7 (8)	C77—N11—C78—C83	165.0 (5)
C32—N5—C33—C34	−178.3 (5)	C77—N11—C78—C79	−16.0 (8)
C38—C33—C34—C35	−0.3 (7)	C83—C78—C79—C80	−0.5 (7)
N5—C33—C34—C35	−177.5 (4)	N11—C78—C79—C80	−179.5 (5)
C33—C34—C35—C36	0.4 (7)	C78—C79—C80—C81	2.1 (7)
C34—C35—C36—C37	−0.4 (7)	C79—C80—C81—C82	−2.2 (7)
C34—C35—C36—C39	179.5 (5)	C79—C80—C81—C84	178.0 (5)
C35—C36—C37—C38	0.2 (7)	C80—C81—C82—C83	0.7 (7)
C39—C36—C37—C38	−179.6 (4)	C84—C81—C82—C83	−179.5 (4)
C36—C37—C38—C33	−0.2 (7)	C81—C82—C83—C78	0.8 (7)
N5—C33—C38—C37	177.2 (5)	N11—C78—C83—C82	178.2 (4)
C34—C33—C38—C37	0.2 (7)	C79—C78—C83—C82	−0.9 (7)
C40—N6—C39—C36	−178.1 (5)	C85—N12—C84—C81	−177.8 (5)
C35—C36—C39—N6	1.7 (8)	C80—C81—C84—N12	−172.3 (5)
C37—C36—C39—N6	−178.5 (4)	C82—C81—C84—N12	7.9 (7)
C39—N6—C40—C45	42.9 (7)	C84—N12—C85—C86	40.9 (7)
C39—N6—C40—C41	−140.8 (5)	C84—N12—C85—C90	−143.9 (5)
C45—C40—C41—C42	−1.2 (7)	C90—C85—C86—C87	1.3 (7)
N6—C40—C41—C42	−177.7 (4)	N12—C85—C86—C87	176.5 (5)
C40—C41—C42—C43	1.7 (8)	C85—C86—C87—C88	0.5 (8)
C41—C42—C43—C44	−1.6 (8)	C86—C87—C88—C89	−1.2 (8)
C42—C43—C44—C45	1.1 (7)	C87—C88—C89—C90	−0.1 (8)
C43—C44—C45—C40	−0.7 (7)	C88—C89—C90—C85	1.9 (8)
C41—C40—C45—C44	0.7 (7)	C86—C85—C90—C89	−2.5 (8)
N6—C40—C45—C44	176.9 (5)	N12—C85—C90—C89	−178.0 (5)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1N···O1S	0.88 (2)	2.00 (2)	2.872 (5)	173 (4)
N3—H3N···O2S	0.87 (2)	1.99 (2)	2.859 (5)	173 (4)
N5—H5N···O4S	0.86 (2)	2.09 (2)	2.919 (5)	163 (4)
N7—H7N···O3S	0.86 (2)	2.03 (2)	2.858 (5)	161 (4)
N9—H9N···O4	0.87 (2)	2.10 (2)	2.929 (5)	158 (4)
N11—H11N···O2	0.87 (2)	2.16 (3)	2.947 (5)	151 (4)
O1S—H1O···N4	0.83 (2)	2.29 (3)	2.939 (5)	136 (4)
O1S—H2O···O5	0.88 (2)	1.88 (2)	2.764 (5)	173 (4)
O2S—H3O···N2	0.85 (2)	2.16 (2)	3.006 (5)	177 (4)
O2S—H4O···O3	0.86 (2)	1.96 (2)	2.781 (5)	160 (5)
O3S—H5O···N6ⁱ	0.85 (2)	2.33 (3)	3.001 (5)	136 (3)
O3S—H6O···O1ⁱ	0.89 (2)	1.90 (2)	2.778 (4)	172 (4)
O4S—H7O···N8ⁱⁱ	0.87 (2)	2.09 (2)	2.954 (5)	171 (4)
O4S—H8O···O6ⁱⁱ	0.98 (2)	1.76 (2)	2.726 (5)	170 (4)

Symmetry codes: (i) x, y+1, z; (ii) x, y−1, z.

Experimental details

Crystal data
Chemical formula	C₁₅H₁₄N₂O·0.67H₂O
M_r	250.29
Crystal system, space group	Monoclinic, P2₁/c
Temperature (K)	100
a, b, c (Å)	21.328 (4), 17.797 (3), 23.021 (4)
β (°)	117.244 (4)
V (Å³)	7769 (3)
Z	24
Radiation type	Mo Kα
µ (mm⁻¹)	0.09
Crystal size (mm)	0.60 × 0.35 × 0.10

Data collection
Diffractometer	Bruker SMART CCD
Absorption correction	–
No. of measured, independent and observed [I > 2σ(I)] reflections	40121, 13696, 4483
R_int	0.113
(sin θ/λ)_max (Å⁻¹)	0.595

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.055, 0.119, 0.76
No. of reflections	13696
No. of parameters	1057
No. of restraints	23
H-atom treatment	H atoms treated by a mixture of independent and constrained refinement
Δρ_max, Δρ_min (e Å⁻³)	0.34, −0.21

Computer programs: SMART (Bruker, 2001), SAINT (Bruker, 2002), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2009).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1N···O1S	0.877 (17)	1.999 (19)	2.872 (5)	173 (4)
N3—H3N···O2S	0.868 (17)	1.994 (19)	2.859 (5)	173 (4)
N5—H5N···O4S	0.857 (17)	2.09 (2)	2.919 (5)	163 (4)
N7—H7N···O3S	0.860 (18)	2.03 (2)	2.858 (5)	161 (4)
N9—H9N···O4	0.873 (17)	2.10 (2)	2.929 (5)	158 (4)
N11—H11N···O2	0.867 (18)	2.16 (3)	2.947 (5)	151 (4)
O1S—H1O···N4	0.832 (19)	2.29 (3)	2.939 (5)	136 (4)
O1S—H2O···O5	0.884 (18)	1.88 (2)	2.764 (5)	173 (4)
O2S—H3O···N2	0.845 (18)	2.161 (19)	3.006 (5)	177 (4)
O2S—H4O···O3	0.857 (19)	1.96 (2)	2.781 (5)	160 (5)
O3S—H5O···N6ⁱ	0.848 (18)	2.33 (3)	3.001 (5)	136 (3)
O3S—H6O···O1ⁱ	0.886 (18)	1.90 (2)	2.778 (4)	172 (4)
O4S—H7O···N8ⁱⁱ	0.870 (19)	2.09 (2)	2.954 (5)	171 (4)
O4S—H8O···O6ⁱⁱ	0.977 (19)	1.76 (2)	2.726 (5)	170 (4)

Symmetry codes: (i) x, y+1, z; (ii) x, y−1, z.

Dihedral angles (°) between the aromatic rings in each molecule of (I) top

Plane–plane	Dihedral angle
P1–P2	42.4 (2)
P3–P4	52.8 (2)
P5–P6	43.7 (2)
P7–P8	48.0 (2)
P9–P10	53.8 (2)
P11–P12	48.1 (2)

Planes P1–P12 are those through the C3–C9, C10–C15, C18–C23, C25–C30, C33–C38, C40–C45, C48–C53, C55–C60, C63–C68, C70–C75, C78–C83 and C85-C90 rings, respectively.

Intermolecular distances (Å) of the atoms of the carbonyl groups to the aromatic ring between the paired molecules top

Atom···plane	Distances
O1···P5, C2···P5	3.375 (4), 3.427 (6)
O2···P9, C17···P9	3.061 (4), 3.191 (6)
O3···P1, C32···P1	3.421 (4), 3.492 (6)
O4···P11, C47···P11	3.073 (4), 3.236 (6)
O5···P3, C62···P3	3.002 (4), 3.448 (6)
O6···P7, C77···P7	3.036 (4), 3.470 (6)

Planes P1, P3, P5, P7, P9 and P11 are those through the C3–C9, C18–C23, C33–C38, C48–C53, C63–C68 and C78–C83 rings, respectively.

Acknowledgements

The authors thank the University of the Punjab and the Higher Education Commission (HEC), Government of Pakistan, for financial support, and are also grateful to the School of Chemistry, The University of Manchester, England, for providing research facilities.

References

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