Crystal structure of 1,4-bis-[5-(2-meth-oxy-phen-yl)-2H-tetra-zol-2-yl]butane.

The title compound, C20H22N8O2, was synthesized by the coupling reaction of a sodium tetra-zolate salt and di-bromo-butane in a molar ratio of 2:1. The reaction can produce several possible regioisomers and the title compound was separated as the major product. The X-ray crystallographic study confirmed that the title compound crystallizes in the monoclinic P21/c space group and possesses a bridging butyl-ene group that connects two identical phenyl tetra-zole moieties. The butyl-ene group is attached not to the first but the second nitro-gen atoms of both tetra-zole rings. The dihedral angles between the phenyl groups and the adjacent tetra-zolyl rings are 5.32 (6) and 15.37 (7)°. In the crystal, the mol-ecules form centrosymmetric dimers through C-H⋯O hydrogen bonds between a C-H group of the butyl-ene linker and the O atom of a meth-oxy group. © Byun et al. 2019.

Chemical context

Tetra­zole ligands have four nitro­gen atoms in their five-membered rings and the lone pairs of these nitro­gen atoms are useful for coordination bonds with metal ions (Zhao et al., 2008 ▸). Tetra­zole has a variety of binding modes with metal ions, which results in the unusual formation of high-dimensional metal–organic frameworks (MOFs) or coordination polymers (Karaghiosoff et al., 2009 ▸; Liu et al., 2013 ▸). Valuable mono-, bis- and polytetra­zole ligands for the formation of MOFs and coordination polymers have been also reported (Boland et al., 2013 ▸; Fan et al., 2016 ▸; Tăbăcaru et al., 2018 ▸; Zhao et al., 2016 ▸). As an extension of a project on the study of self-assembly behaviour in solution, we designed a di­tetra­zolyl chelate ligand possessing a butane bridge. It is worth noting that tetra­zole has two different resonance structures in which the hydrogen atoms are located at either the N1 or N2 positions. In many cases, this results in the formation of several products (Lee et al., 2017 ▸). It is therefore essential to study the mol­ecular structure of synthesized tetra­zole complexes by X-ray crystallography.

The title compound was isolated as an inter­mediate in the middle of the synthetic route for a chelate ligand. The reaction between the sodium salt of tetra­zole and 1,4-di­bromo­butane gave three isomeric products (Fig. 1 ▸). Using column chromatography, the major product was isolated and its mol­ecular structure was determined unambiguously by X-ray crystallography. This compound is a useful precursor for the synthesis of dinuclear metal complexes with the expectation of synergetic effects of two metal centers (Fig. 2 ▸). Herein, we report the synthesis and crystal structure of this compound.

Figure 1

Synthesis of the title compound (I).

Figure 2

Synthetic route of the desired dinuclear metal complexes from the title compound (I).

Structural commentary

The reaction yielded three isomeric products as described in Section 5, Synthesis and crystallization, and the structural analysis confirms the formation of the desired major product. The mol­ecular structure of the title compound is shown in Fig. 3 ▸. There are no unusual bond lengths or angles. The title compound possesses two identical phenyl tetra­zole fragments, connected by a butyl (C17–C20) bridge. The butyl group is attached to the second N atom of both tetra­zole rings (N2 and N6, Fig. 3 ▸). The dihedral angles between the phenyl group and tetra­zolyl ring are somewhat different in the two phenyl­tetra­zolyl groups. One phenyl­tetra­zolyl group (N1–N4/C1–C7) is almost planar with an angle of 5.32 (6)° between the mean planes of the rings. However, the other phenyl­tetra­zolyl group (N5–N8/C9–C15) is tilted with a dihedral angle of 15.37 (7)°.

Figure 3

A view of the mol­ecular structure of the title compound, with the atom labelling and 30% probability displacement ellipsoids.

Two intra­molecular C—H⋯N hydrogen bonds (Table 1 ▸) occur, which are shown as yellow dashed lines in Fig. 4 ▸. These inter­actions may contribute to the planarity of the phenyl­tetra­zolyl units.

Table 1

Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C7—H7⋯N4	0.95	2.48	2.8371 (16)	102
C15—H15⋯N8	0.95	2.53	2.8586 (17)	101
C17—H17A⋯O1i	0.99	2.58	3.4337 (15)	144

Symmetry code: (i) .

Figure 4

A plot showing the intra­molecular C—H⋯N hydrogen bonding (dashed yellow lines) and short contacts between mol­ecules (dashed pink, sky-blue and blue lines).

Supra­molecular features

The two phenyl­tetra­zolyl fragments exhibit different inter­molecular inter­actions. The tilted fragment (N5–N8/C9–C15) inter­acts with the butyl bridge of a glide-related mol­ecule through C19—H19A⋯C14ii [H⋯A = 2.812 (2) Å; symmetry code: (ii) x, −y + , z + ], C19—H19A⋯C15ii [H⋯A = 2.895 (2) Å] and C17—H17B⋯N8ii [H⋯A = 2.729 (2) Å] contacts (Fig. 4 ▸, pink dashed lines). There is an additional weak C14ii—H14ii⋯O2 inter­action [H⋯A = 2.624 (2) Å] between the same pair of mol­ecules, which is indicated by a sky-blue dashed line in Fig. 4 ▸. The bridging butyl group forms a further C18—H18B⋯C5iii [H⋯C = 2.738 (2) Å; symmetry code: (iii) x, −y + , z − ] close contact (Fig. 4 ▸, red dashed line) with a mol­ecule generated by an adjacent glide plane. The planar fragments of screw-related mol­ecules form C4—H4⋯C1iv [H⋯A = 2.692 (2) Å; symmetry code: (iv) −x + 2, y − , −z + ] and C8—H8C⋯C7iv [H⋯A = 2.828 (2) Å] close contacts, which are indicated by blue dashed lines in the right-hand side of Fig. 4 ▸ (for clarity a different reference mol­ecule was used for the illustration of this contact). It is inter­esting that the C1 atom has another close C—H⋯C contact from the opposite side of the aromatic plane (Fig. 4 ▸, purple dashed lines), C16—H16A⋯C1v [H⋯C = 2.798 (2) Å; symmetry code: (v) −x + 1, y + , −z − ]. There is one notable close contact, C17—H17A⋯O1i that can be considered a weak hydrogen bond, which is indicated by green dashed line in Fig. 5 ▸. This contact forms a dimeric rectangle between two mol­ecules. This rectangle extends in the c-axis direction by the short inter­actions described above.

Figure 5

A plot showing the short contacts between mol­ecules (dashed green and blue lines).

To provide an overall view of the weak inter­actions between the mol­ecules, a Hirshfeld surface analysis (Spackman & Jayatilaka, 2009 ▸) was performed with CrystalExplorer17 (Turner et al., 2017 ▸). The Hirshfeld surface was calculated using a standard (high) surface resolution with the three-dimensional (3D) d norm surface plotted over a fixed colour scale of −0.1339 (red) to 1.4773 a.u. (blue). The 3D d norm surface of the title complex is shown in Fig. 6 ▸ a and 6b. The red spots indicate short contacts, i.e., negative d norm values on the surface, which highlight the most important weak inter­actions: C17—H17A⋯O1i hydrogen bond (green dashed line), C4—H4⋯C1iv contact (blue in Fig. 6 ▸ a), C18—H18B⋯C5iii (pink in Fig. 6 ▸ a, red in Fig. 6 ▸ b) and C16—H16A⋯C1v (blue in Fig. 6 ▸ b).

Figure 6

d norm mapped on the Hirshfeld surface for visualizing the inter­molecular inter­actions.(a) front side, (b) back side.

Database survey

A search of the Cambridge Structural Database (CSD Version 5.40, November 2018; Groom et al., 2016 ▸) for bis­(tetra­zol­yl)alkane fragments provided four hits with a methyl­ene bridge [SAVPAJ, SAVPIR (Freis et al., 2017 ▸), OYIWOK02 (Feng, Qiu et al., 2016 ▸) and UMOJEN (Feng, Bi et al., 2016 ▸)] and two with a propyl­ene bridge (SIBFIV, SIBFUH; Wurzenberger et al., 2018 ▸). The butyl­ene-bridged examples include a bis­tetra­zolyl copper complex (SIBGIW; Wurzenberger et al., 2018 ▸) and three bis­(pyridyl­tetra­zol­yl)silver complexes (QOKBAV, QOKBEZ, QOKBID; Wang et al., 2014 ▸). All of the above bis­(tetra­zol­yl)alkane structures are metal complexes. It is worth noting that inter­esting metal-free cyclic bis­tetra­zolyl compounds have been reported (VELPUZ, VELPOT; Voitekhovich et al., 2012 ▸) in which the bis­(tetra­zol­yl)butane fragment is part of a ring.

Synthesis and crystallization

The synthesis scheme for the title compound is represented in Fig. 1 ▸. The sodium salt of 5-(2-meth­oxy­phen­yl)-1H-tetra­zole (495 mg, 2.5 mmol) and di­bromo­butane (150 µl, 1.25 mmol) were dissolved in aceto­nitrile and refluxed for 2 d. The resulting white solid was filtered and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel using hexa­ne:acetone (1:1) as eluent. Three isomeric compounds were obtained, as shown in Fig. 1 ▸. The major product (I) (yield = 35%) was recrystallized in ethanol by the slow evaporation method and yielded colourless crystals of the title compound.

Spectroscopic data: 1H NMR (DMSO, 400 MHz): δ = 7.62 (t, 2H, Ph), 7.36 (d, 2H, Ph), 7.22 (d, 2H, Ph), 7.12 (t, 2H, Ph), 4.13 (s, 4H, CH2), 3.71 (s, 6H, OCH3), 1.66 (s, 4H, CH2). 13C NMR (125 MHz, DMSO): 156.56, 152.18, 133.10, 131.20, 120.80, 112.26, 111.91, 55.50, 46.63, 25.57 ppm.

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 2 ▸. All H atoms were included in calculated positions using a riding model, with C—H = 0.95–1.00 Å and U iso(H) = 1.5U eq(C) for methyl H atoms and U iso(H) = 1.2U eq(C) for all others. Two reflections (100 and 110) were omitted because of truncation by the beamstop.

Table 2

Experimental details

Crystal data
Chemical formula	C20H22N8O2
M r	406.45
Crystal system, space group	Monoclinic, P21/c
Temperature (K)	100
a, b, c (Å)	13.2904 (2), 10.2785 (2), 14.4968 (3)
β (°)	100.2538 (9)
V (Å3)	1948.71 (6)
Z	4
Radiation type	Mo Kα
μ (mm−1)	0.10
Crystal size (mm)	0.1 × 0.1 × 0.08
Data collection
Diffractometer	Bruker APEXII CCD
Absorption correction	Multi-scan (SADABS; Krause et al., 2015 ▸)
T min, T max	0.706, 0.745
No. of measured, independent and observed [I > 2σ(I)] reflections	26494, 4008, 3516
R int	0.021
(sin θ/λ)max (Å−1)	0.627
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S	0.037, 0.098, 1.05
No. of reflections	4008
No. of parameters	273
H-atom treatment	H-atom parameters constrained
Δρmax, Δρmin (e Å−3)	0.25, −0.37

Computer programs: APEX2 and SAINT (Bruker, 2014 ▸), SHELXS (Sheldrick, 2008 ▸), SHELXL (Sheldrick, 2015 ▸), Mercury (Macrae et al., 2008 ▸) and OLEX2 (Dolomanov et al., 2009 ▸).

Crystal structure: contains datablock(s) I. DOI: 10.1107/S2056989019014877/fy2138sup1.cif

Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989019014877/fy2138Isup2.hkl

Click here for additional data file.

Supporting information file. DOI: 10.1107/S2056989019014877/fy2138Isup3.cdx

Click here for additional data file.

Supporting information file. DOI: 10.1107/S2056989019014877/fy2138Isup4.cml

CCDC references: 1963337, 1963337

Additional supporting information: crystallographic information; 3D view; checkCIF report

C20H22N8O2	F(000) = 856
Mr = 406.45	Dx = 1.385 Mg m−3
Monoclinic, P21/c	Mo Kα radiation, λ = 0.71073 Å
a = 13.2904 (2) Å	Cell parameters from 9933 reflections
b = 10.2785 (2) Å	θ = 2.5–26.4°
c = 14.4968 (3) Å	µ = 0.10 mm−1
β = 100.2538 (9)°	T = 100 K
V = 1948.71 (6) Å3	Block, colorless
Z = 4	0.1 × 0.1 × 0.08 mm

Bruker APEXII CCD diffractometer	3516 reflections with I > 2σ(I)
φ and ω scans	Rint = 0.021
Absorption correction: multi-scan (SADABS; Krause et al., 2015)	θmax = 26.5°, θmin = 2.4°
Tmin = 0.706, Tmax = 0.745	h = −16→16
26494 measured reflections	k = −12→12
4008 independent reflections	l = −18→18

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)] = 0.037	Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.098	H-atom parameters constrained
S = 1.05	w = 1/[σ2(Fo2) + (0.0491P)2 + 0.7236P] where P = (Fo2 + 2Fc2)/3
4008 reflections	(Δ/σ)max = 0.001
273 parameters	Δρmax = 0.25 e Å−3
0 restraints	Δρmin = −0.37 e Å−3

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. 1. Fixed Uiso At 1.2 times of: All C(H) groups, All C(H,H) groups At 1.5 times of: All C(H,H,H) groups 2.a Secondary CH2 refined with riding coordinates: C18(H18A,H18B), C19(H19A,H19B), C17(H17A,H17B), C20(H20A,H20B) 2.b Aromatic/amide H refined with riding coordinates: C7(H7), C13(H13), C15(H15), C4(H4), C6(H6), C12(H12), C5(H5), C14(H14) 2.c Idealised Me refined as rotating group: C8(H8A,H8B,H8C), C16(H16A,H16B,H16C)

	x	y	z	Uiso*/Ueq
O1	0.95431 (7)	0.24652 (8)	0.11811 (6)	0.0258 (2)
N1	0.86468 (7)	0.47789 (10)	0.06134 (7)	0.0217 (2)
N2	0.81869 (8)	0.58734 (10)	0.02753 (7)	0.0217 (2)
N5	0.60298 (7)	0.58496 (10)	−0.44500 (7)	0.0226 (2)
N6	0.68182 (8)	0.51604 (10)	−0.40215 (7)	0.0247 (2)
N4	0.77518 (8)	0.57102 (11)	0.15994 (7)	0.0269 (2)
C3	0.92713 (9)	0.26068 (12)	0.20399 (8)	0.0220 (3)
C1	0.83621 (8)	0.46963 (11)	0.14486 (8)	0.0198 (2)
N3	0.76475 (8)	0.64445 (11)	0.08397 (7)	0.0278 (2)
C9	0.62616 (9)	0.59998 (12)	−0.52995 (8)	0.0220 (2)
O2	0.46627 (8)	0.77149 (12)	−0.51135 (6)	0.0463 (3)
C10	0.56607 (9)	0.67077 (12)	−0.60922 (8)	0.0215 (2)
N8	0.71619 (9)	0.54247 (13)	−0.53723 (8)	0.0348 (3)
C7	0.83412 (9)	0.38359 (12)	0.30302 (8)	0.0238 (3)
H7	0.7911	0.4547	0.3117	0.029*
C2	0.86647 (9)	0.36911 (12)	0.21675 (8)	0.0207 (2)
C13	0.46290 (10)	0.80750 (13)	−0.76430 (9)	0.0284 (3)
H13	0.4280	0.8544	−0.8169	0.034*
C18	0.74738 (9)	0.55296 (12)	−0.13870 (8)	0.0232 (3)
H18A	0.6763	0.5728	−0.1314	0.028*
H18B	0.7596	0.4593	−0.1251	0.028*
C19	0.75877 (9)	0.57977 (12)	−0.23988 (8)	0.0242 (3)
H19A	0.7355	0.6692	−0.2580	0.029*
H19B	0.8314	0.5718	−0.2464	0.029*
C15	0.59024 (9)	0.65380 (12)	−0.69829 (8)	0.0237 (3)
H15	0.6431	0.5947	−0.7061	0.028*
C4	0.95664 (9)	0.17429 (12)	0.27783 (9)	0.0268 (3)
H4	0.9983	0.1016	0.2696	0.032*
C6	0.86318 (10)	0.29699 (13)	0.37594 (9)	0.0282 (3)
H6	0.8405	0.3085	0.4339	0.034*
N7	0.75068 (9)	0.48940 (13)	−0.45441 (8)	0.0366 (3)
C17	0.82070 (9)	0.63252 (12)	−0.06795 (8)	0.0240 (3)
H17A	0.8909	0.6243	−0.0814	0.029*
H17B	0.8010	0.7255	−0.0736	0.029*
C12	0.43688 (10)	0.82663 (13)	−0.67683 (9)	0.0299 (3)
H12	0.3844	0.8866	−0.6698	0.036*
C11	0.48755 (10)	0.75822 (13)	−0.59921 (8)	0.0276 (3)
C8	1.00848 (10)	0.13020 (13)	0.10279 (10)	0.0302 (3)
H8A	1.0215	0.1294	0.0383	0.045*
H8B	0.9673	0.0541	0.1129	0.045*
H8C	1.0737	0.1275	0.1467	0.045*
C5	0.92583 (10)	0.19321 (13)	0.36327 (9)	0.0289 (3)
H5	0.9478	0.1346	0.4135	0.035*
C20	0.69416 (10)	0.48127 (13)	−0.30300 (8)	0.0259 (3)
H20A	0.7268	0.3946	−0.2934	0.031*
H20B	0.6259	0.4753	−0.2849	0.031*
C14	0.53931 (10)	0.72068 (13)	−0.77559 (8)	0.0265 (3)
H14	0.5566	0.7071	−0.8357	0.032*
C16	0.38052 (17)	0.8497 (2)	−0.50095 (12)	0.0780 (8)
H16A	0.3195	0.8174	−0.5428	0.117*
H16B	0.3934	0.9400	−0.5170	0.117*
H16C	0.3697	0.8453	−0.4359	0.117*

	U11	U22	U33	U12	U13	U23
O1	0.0290 (5)	0.0251 (4)	0.0246 (4)	0.0063 (4)	0.0083 (4)	0.0012 (3)
N1	0.0245 (5)	0.0214 (5)	0.0190 (5)	0.0009 (4)	0.0038 (4)	0.0011 (4)
N2	0.0242 (5)	0.0221 (5)	0.0186 (5)	0.0009 (4)	0.0035 (4)	0.0003 (4)
N5	0.0233 (5)	0.0256 (5)	0.0184 (5)	0.0025 (4)	0.0024 (4)	0.0011 (4)
N6	0.0260 (5)	0.0293 (6)	0.0184 (5)	0.0058 (4)	0.0030 (4)	0.0014 (4)
N4	0.0316 (6)	0.0290 (6)	0.0208 (5)	0.0073 (4)	0.0070 (4)	0.0029 (4)
C3	0.0189 (5)	0.0251 (6)	0.0217 (6)	−0.0028 (4)	0.0029 (4)	0.0003 (5)
C1	0.0183 (5)	0.0222 (6)	0.0186 (5)	−0.0020 (4)	0.0024 (4)	−0.0023 (4)
N3	0.0332 (6)	0.0288 (6)	0.0227 (5)	0.0071 (5)	0.0082 (4)	0.0018 (4)
C9	0.0234 (6)	0.0241 (6)	0.0185 (6)	0.0016 (5)	0.0037 (4)	−0.0030 (5)
O2	0.0503 (6)	0.0703 (8)	0.0190 (5)	0.0395 (6)	0.0080 (4)	0.0032 (5)
C10	0.0227 (6)	0.0234 (6)	0.0181 (6)	−0.0002 (5)	0.0024 (4)	−0.0010 (5)
N8	0.0351 (6)	0.0489 (7)	0.0212 (5)	0.0174 (5)	0.0067 (5)	0.0042 (5)
C7	0.0229 (6)	0.0275 (6)	0.0208 (6)	−0.0020 (5)	0.0032 (5)	−0.0014 (5)
C2	0.0192 (5)	0.0233 (6)	0.0188 (6)	−0.0028 (4)	0.0015 (4)	0.0004 (5)
C13	0.0335 (7)	0.0285 (6)	0.0214 (6)	−0.0001 (5)	0.0000 (5)	0.0046 (5)
C18	0.0253 (6)	0.0254 (6)	0.0188 (6)	0.0001 (5)	0.0040 (5)	0.0036 (5)
C19	0.0268 (6)	0.0267 (6)	0.0193 (6)	0.0018 (5)	0.0047 (5)	0.0038 (5)
C15	0.0265 (6)	0.0242 (6)	0.0213 (6)	−0.0004 (5)	0.0067 (5)	−0.0012 (5)
C4	0.0221 (6)	0.0264 (6)	0.0313 (7)	0.0007 (5)	0.0030 (5)	0.0052 (5)
C6	0.0283 (6)	0.0363 (7)	0.0200 (6)	−0.0044 (5)	0.0047 (5)	0.0025 (5)
N7	0.0370 (6)	0.0523 (8)	0.0214 (5)	0.0202 (6)	0.0075 (5)	0.0051 (5)
C17	0.0292 (6)	0.0245 (6)	0.0189 (6)	−0.0004 (5)	0.0062 (5)	0.0041 (5)
C12	0.0311 (7)	0.0320 (7)	0.0254 (6)	0.0100 (5)	0.0019 (5)	0.0018 (5)
C11	0.0293 (6)	0.0345 (7)	0.0187 (6)	0.0067 (5)	0.0035 (5)	−0.0008 (5)
C8	0.0318 (7)	0.0250 (6)	0.0356 (7)	0.0057 (5)	0.0107 (6)	−0.0010 (5)
C5	0.0259 (6)	0.0338 (7)	0.0256 (6)	−0.0028 (5)	0.0008 (5)	0.0098 (5)
C20	0.0304 (6)	0.0292 (7)	0.0174 (6)	0.0015 (5)	0.0026 (5)	0.0046 (5)
C14	0.0335 (7)	0.0288 (6)	0.0177 (6)	−0.0033 (5)	0.0060 (5)	0.0005 (5)
C16	0.0869 (14)	0.1223 (19)	0.0290 (8)	0.0798 (14)	0.0218 (9)	0.0134 (10)

O1—C3	1.3644 (14)	C18—H18A	0.9900
O1—C8	1.4331 (15)	C18—H18B	0.9900
N1—N2	1.3315 (14)	C18—C19	1.5262 (16)
N1—C1	1.3339 (15)	C18—C17	1.5214 (17)
N2—N3	1.3179 (14)	C19—H19A	0.9900
N2—C17	1.4647 (14)	C19—H19B	0.9900
N5—N6	1.3243 (14)	C19—C20	1.5232 (17)
N5—C9	1.3306 (15)	C15—H15	0.9500
N6—N7	1.3166 (15)	C15—C14	1.3843 (17)
N6—C20	1.4618 (15)	C4—H4	0.9500
N4—C1	1.3619 (15)	C4—C5	1.3858 (18)
N4—N3	1.3218 (15)	C6—H6	0.9500
C3—C2	1.4069 (17)	C6—C5	1.3854 (19)
C3—C4	1.3924 (17)	C17—H17A	0.9900
C1—C2	1.4719 (16)	C17—H17B	0.9900
C9—C10	1.4700 (16)	C12—H12	0.9500
C9—N8	1.3555 (16)	C12—C11	1.3945 (18)
O2—C11	1.3597 (15)	C8—H8A	0.9800
O2—C16	1.4242 (18)	C8—H8B	0.9800
C10—C15	1.3959 (16)	C8—H8C	0.9800
C10—C11	1.4043 (17)	C5—H5	0.9500
N8—N7	1.3240 (16)	C20—H20A	0.9900
C7—H7	0.9500	C20—H20B	0.9900
C7—C2	1.4009 (16)	C14—H14	0.9500
C7—C6	1.3833 (18)	C16—H16A	0.9800
C13—H13	0.9500	C16—H16B	0.9800
C13—C12	1.3864 (18)	C16—H16C	0.9800
C13—C14	1.3834 (18)
C3—O1—C8	116.89 (10)	C10—C15—H15	119.1
N2—N1—C1	101.66 (9)	C14—C15—C10	121.79 (11)
N1—N2—C17	122.10 (10)	C14—C15—H15	119.1
N3—N2—N1	114.36 (9)	C3—C4—H4	119.7
N3—N2—C17	123.30 (10)	C5—C4—C3	120.67 (12)
N6—N5—C9	101.65 (9)	C5—C4—H4	119.7
N5—N6—C20	122.20 (10)	C7—C6—H6	120.4
N7—N6—N5	114.48 (10)	C7—C6—C5	119.12 (11)
N7—N6—C20	123.17 (10)	C5—C6—H6	120.4
N3—N4—C1	106.28 (10)	N6—N7—N8	105.79 (10)
O1—C3—C2	117.10 (10)	N2—C17—C18	110.45 (9)
O1—C3—C4	123.32 (11)	N2—C17—H17A	109.6
C4—C3—C2	119.58 (11)	N2—C17—H17B	109.6
N1—C1—N4	111.73 (10)	C18—C17—H17A	109.6
N1—C1—C2	126.98 (10)	C18—C17—H17B	109.6
N4—C1—C2	121.26 (10)	H17A—C17—H17B	108.1
N2—N3—N4	105.96 (10)	C13—C12—H12	119.9
N5—C9—C10	126.72 (10)	C13—C12—C11	120.22 (12)
N5—C9—N8	111.99 (10)	C11—C12—H12	119.9
N8—C9—C10	121.28 (10)	O2—C11—C10	116.32 (11)
C11—O2—C16	117.36 (11)	O2—C11—C12	123.66 (11)
C15—C10—C9	118.61 (11)	C12—C11—C10	120.02 (11)
C15—C10—C11	118.25 (11)	O1—C8—H8A	109.5
C11—C10—C9	123.11 (10)	O1—C8—H8B	109.5
N7—N8—C9	106.08 (10)	O1—C8—H8C	109.5
C2—C7—H7	119.1	H8A—C8—H8B	109.5
C6—C7—H7	119.1	H8A—C8—H8C	109.5
C6—C7—C2	121.70 (12)	H8B—C8—H8C	109.5
C3—C2—C1	123.62 (10)	C4—C5—H5	119.8
C7—C2—C3	118.41 (11)	C6—C5—C4	120.45 (12)
C7—C2—C1	117.97 (11)	C6—C5—H5	119.8
C12—C13—H13	119.7	N6—C20—C19	112.38 (10)
C14—C13—H13	119.7	N6—C20—H20A	109.1
C14—C13—C12	120.50 (12)	N6—C20—H20B	109.1
H18A—C18—H18B	107.8	C19—C20—H20A	109.1
C19—C18—H18A	109.0	C19—C20—H20B	109.1
C19—C18—H18B	109.0	H20A—C20—H20B	107.9
C17—C18—H18A	109.0	C13—C14—C15	119.21 (11)
C17—C18—H18B	109.0	C13—C14—H14	120.4
C17—C18—C19	112.93 (10)	C15—C14—H14	120.4
C18—C19—H19A	110.0	O2—C16—H16A	109.5
C18—C19—H19B	110.0	O2—C16—H16B	109.5
H19A—C19—H19B	108.4	O2—C16—H16C	109.5
C20—C19—C18	108.39 (10)	H16A—C16—H16B	109.5
C20—C19—H19A	110.0	H16A—C16—H16C	109.5
C20—C19—H19B	110.0	H16B—C16—H16C	109.5

D—H···A	D—H	H···A	D···A	D—H···A
C7—H7···N4	0.95	2.48	2.8371 (16)	102
C15—H15···N8	0.95	2.53	2.8586 (17)	101
C17—H17A···O1i	0.99	2.58	3.4337 (15)	144