Crystal structure of 2-chloro-1,3-(2,6-diiso-propyl-phen-yl)-4,5-dihydro-1H-imidazol-3-ium tetra-kis-(3,5-tri-fluoro-methyl-phen-yl)borate.

The title compound, C27H38ClN2+·C32H12BF24-, was synthesized by reacting the product formed from a previous reaction between 1,3-bis-(2,6-diiso-propyl-phen-yl)imidazolinium-2-carboxyl-ate (SIPrCO2), and SOCl2, with sodium tetra-kis-[3,5-bis-(tri-fluoro-meth-yl)phen-yl]borate (NaBARF). In the cation, the imidazole ring is in a half-chair conformation and the formerly carbene carbon atom is bonded in a distorted trigonal-planar geometry with N-C-Cl angles of 122.96 (16) and 122.21 (16)° and an N-C-N angle of 114.83 (18)°. In the crystal, weak C-H⋯F hydrogen bonds link the cations and anions, forming a three-dimensional network. In addition, a short Cl⋯F contact of 3.213 Å and several short F⋯F contacts less than the sum of the van der Waals radii [1.47 Å + 1.47 Å = 2.94 Å] are observed. The F atoms of two of the CF3 groups were refined as disordered over four sets of sites.

Chemical context

The use of main group elements as a way to stabilize singlet carbenes was first investigated in-depth by Bertrand & Reed (1994 ▸), leading to the discovery of the first n class="Chemical">phosphino silyl carbenes (Igau et al., 1988 ▸) followed by other novel singlet carbenes (Lavallo et al., 2005 ▸; Frey et al., 2007 ▸; Aldeco-Perez et al., 2009 ▸). However, the report of the first ‘bottleable’ crystalline N-heterocyclic carbene (NHC) (Arduengo et al., 1991 ▸) initiated a new paradigm in synthetic chemistry (Bourissou et al., 2000 ▸). In particular, NHCs are favoured due to their stability and ease of synthesis. The ability of these stable carbenes to activate small mol­ecules and to help stabilize highly reactive inter­mediates makes this an increasingly desirable area of research. The crystal structure of the compound under investigation incorporates a popular five-membered saturated NHC (known as SIPr) coordinated with a Cl atom attached at the formally carbene atom as a borate salt.

Structural commentary

The mol­ecular structure of the title salt compound is shown in Fig. 1 ▸. The formerly n class="Chemical">carbene carbon has a distorted trigonal–planar geometry and is flanked by the two sterically bulky N-diiso­propyl­phenyl groups of the heterocycle. The imidazolidinium ring is in a half-chair conformation having approximate C 2 symmetry. The dihedral angle between the mean planes of the benzene rings is 36.7 (1)°. The isopropyl groups containing C12 and C27 are essentially bis­ected by the plane of the benzene ring to which they are attached, subtending dihedral angles of 116.0 (2)° (C16/C21/C25/C27) and 112.4 (2)° (C4/C9/C10/C12), relative to the ipso carbon atoms C4 and C16 while the isopropyl groups containing C15 and C23 deviate significantly from this bis­ected geometry with dihedral angles of 26.1 (2)° (C4/C5/C13/C15) and 46.7 (2)° (C16/C17/C22/C23) relative to the ipso carbon atoms C4 and C16. The C1—Cl1 bond length of 1.681 (2) Å is slightly less than the average value of 1.73 Å for a Csp 2⋯Cl bond length.

Figure 1

The mol­ecular structure of the title compound showing the atom labelling. Fluorine atom labels and hydrogen atoms have been omitted for clarity. Displacement ellipsoids are drawn at the 50% probability level.

Supra­molecular features

In the crystal, short-contact H⋯F inter­actions between the isopropyl groups of the NHC and the tri­fluoro­methyl groups of the anion are observed. These are due to weak C—H⋯F n class="Chemical">hydrogen bonds (Table 1 ▸), which link the cations and anions, forming a three-dimensional network (Fig. 2 ▸). There is one short Cl1⋯F20( − x, − + y,  − z) contact with a distance of 3.213 (2) Å as well as multiple short F⋯F contacts with lengths less than 2.94 Å.

Table 1

Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C3—H3A⋯F15i	0.99	2.43	3.256 (3)	141
C12—H12A⋯F17C ii	0.98	2.53	3.269 (12)	132
C19—H19⋯F8D iii	0.95	2.48	3.297 (18)	144
C29—H29⋯F9D iii	0.95	2.35	3.180 (14)	146

Symmetry codes: (i) ; (ii) ; (iii) .

Figure 2

Part of the crystal structure with weak C—H⋯F hydrogen bonds shown as dashed lines.

Database survey

A search of the Cambridge Structural Database (CSD; Groom et al., 2016 ▸) revealed two hits for structures which are n class="Chemical">imidazolidinium salts with N-methyl groups in place of the N-diiso­propyl­phenyl groups of the title compound. One of the structures contains a tetra­chloro­nickel counter-anion and the other is that of a chloride [XAMQAE (Kremzow et al., 2005 ▸) and SISVUN (Böttcher et al., 2014 ▸)]. The CSD also contains two structures of unsaturated five-membered NHC compounds that contain C—Cl bonds in the C2 position [NUXPOL (Arduengo et al., 1997 ▸) and XOMMER (Kuhn et al., 2002 ▸)].

Synthesis and crystallization

In a glovebox, prior to the synthesis of the title compound, SIPrCO2 (Zhou et al., 2008 ▸) was reacted with SOCl2 in an attempt to synthesize n class="Chemical">SIPrCOCl2. The exact composition of the product was unconfirmed; however, the decision was made to take a portion of this product and move forward to test its chemistry. This product is the primary reagent for the synthesis of the title salt. In a vial equipped with a magnetic stirring bar was placed the resulting product from the SIPrCO2/SOCl2 reaction (0.0478 g, 9.745 × 10−2 mmol), NaBARF (0.0863 g, 9.738 × 10−2 mmol) and 5 mL of di­chloro­methane. The mixture was left to stir overnight (18 h) after which the insol­uble solids were removed by filtering the solution into a pre-weighed vial. This was done using a glass pipette containing a small layer of diatomaceous earth. Volatiles were removed in vacuo, leaving behind a pale-yellow-coloured solid (0.0596 g, 4.623 × 10−2 mmol). The purity of the sample was confirmed using 1H NMR spectroscopy in deuterated chloro­form (CDCl3). The recrystallization was carried out by evaporation of CDCl3, followed by cooling in the freezer overnight, to afford colourless needle-shaped crystals. 1H NMR (300 MHz, 298 K, C6D6): δ 1.26 (d, CH(CH 3)2, 12H), 1.33 (d, CH(CH 3)2, 12H), 3.84 (sept., CH(CH3)2, 4H), 4.52 (s, CH 2, 4H), 7.34 (d, m-Ar-H, 4H), 7.50 (s, p-Ar-H, 4H), 7.56 (t, p-Ar-H, 2H), 7.68 ppm (t, m-Ar-H, 8H). 19F NMR (282.5 MHz, 298 K, C6D6): δ −63.1 ppm (s). 11B NMR (96.3 MHz, 298 K, C6D6): δ −6.18 ppm (s). Tri­fluoro­toluene was used as an external reference for the 19F NMR spectrum and boron trifluoride diethyl etherate was used as the external reference for the 11B NMR spectrum.

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 2 ▸. Hydrogen atoms were included at geometrically idealized positions and were included in a riding-motion approximation. For the methyl groups, the dihedral angle of the idealized n class="Species">tetra­hedral CH3 fragment was allowed to refine.

Table 2

Experimental details

Crystal data
Chemical formula	C17H38ClN2 +·C32H12BF24
M r	1289.27
Crystal system, space group	Monoclinic, P21/n
Temperature (K)	125
a, b, c (Å)	18.5025 (12), 17.8739 (12), 19.7857 (13)
β (°)	116.428 (1)
V (Å3)	5859.5 (7)
Z	4
Radiation type	Mo Kα
μ (mm−1)	0.18
Crystal size (mm)	0.39 × 0.38 × 0.08
Data collection
Diffractometer	Siemens/Bruker APEXII
Absorption correction	Multi-scan (SADABS; Bruker, 2008 ▸)
T min, T max	0.660, 0.746
No. of measured, independent and observed [I > 2σ(I)] reflections	40063, 10921, 8363
R int	0.033
(sin θ/λ)max (Å−1)	0.606
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S	0.044, 0.113, 1.02
No. of reflections	10921
No. of parameters	830
No. of restraints	38
H-atom treatment	H-atom parameters constrained
Δρmax, Δρmin (e Å−3)	0.52, −0.45

Computer programs: APEX2 and SAINT (Bruker, 2008 ▸), XS in SHELXTL (Sheldrick, 2008 ▸), SHELXL2014/7 (Sheldrick, 2015 ▸), ORTEP-3 for Windows (Farrugia, 2012 ▸), PLATON (Spek, 2009 ▸) and publCIF (Westrip, 2010 ▸).

Prior to final refinement, there was significant disorder associated with one of the CF3 groups attached to each of C34 and C58. After trying to assess whether the groups had two components of a disorder, it became clear that each of these CF3 groups actually had four components of disorder that needed to be resolved. In order to do this, the SUMP command was applied to all of the fluorine atoms involved. This involved grouping the four components into PART 1, PART 2, PART 3, and PART 4, respectively, and assigning a free variable to each of the individual parts, where the weighted sum of the free variables was set to equal 1.0 (C58: 0.5: 0.3: 0.1: 0.1 and C34: 0.4: 0.3: 0.2: 0.1). Following refinement using the SUMP command, the EADP command was applied, which allowed for all of the anisotropic parameters of the n class="Chemical">fluorine ellipsoids to be similar in size. Lastly, the SADI command was applied to each of the affected C—F bonds in the disordered CF3 groups in order to have similar bond lengths for each of the disordered F atoms (i.e. the bond lengths were approximately equal for C58—F16A–D, C58—F17A–D, etc). The combination of these commands allowed for complete refinement of the CF3 disorder.

Crystal structure: contains datablock(s) I. DOI: 10.1107/S2056989016014584/lh5822sup1.cif

Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989016014584/lh5822Isup2.hkl

CCDC reference: 1504219

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

C17H38ClN2+·C32H12BF24	F(000) = 2624
Mr = 1289.27	Dx = 1.461 Mg m−3
Monoclinic, P21/n	Mo Kα radiation, λ = 0.71073 Å
a = 18.5025 (12) Å	Cell parameters from 9997 reflections
b = 17.8739 (12) Å	θ = 2.3–27.8°
c = 19.7857 (13) Å	µ = 0.18 mm−1
β = 116.428 (1)°	T = 125 K
V = 5859.5 (7) Å3	Needle, colourless
Z = 4	0.39 × 0.38 × 0.08 mm

Siemens/Bruker APEXII diffractometer	8363 reflections with I > 2σ(I)
φ and ω scans	Rint = 0.033
Absorption correction: multi-scan (SADABS; Bruker, 2008)	θmax = 25.5°, θmin = 2.0°
Tmin = 0.660, Tmax = 0.746	h = −22→22
40063 measured reflections	k = −21→21
10921 independent reflections	l = −23→23

Refinement on F2	38 restraints
Least-squares matrix: full	Hydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.044	H-atom parameters constrained
wR(F2) = 0.113	w = 1/[σ2(Fo2) + (0.0464P)2 + 4.6564P] where P = (Fo2 + 2Fc2)/3
S = 1.02	(Δ/σ)max < 0.001
10921 reflections	Δρmax = 0.52 e Å−3
830 parameters	Δρmin = −0.45 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.

	x	y	z	Uiso*/Ueq	Occ. (<1)
Cl1	0.57779 (3)	0.07669 (3)	0.80176 (3)	0.03051 (14)
F1	0.71125 (9)	0.20864 (8)	0.39608 (8)	0.0499 (4)
F2	0.76498 (9)	0.31577 (9)	0.43499 (10)	0.0592 (5)
F3	0.71913 (9)	0.25293 (9)	0.49856 (8)	0.0469 (4)
F4	0.38941 (10)	0.28263 (11)	0.39231 (9)	0.0641 (5)
F5	0.41659 (10)	0.18771 (9)	0.34260 (12)	0.0690 (5)
F6	0.34175 (9)	0.27432 (9)	0.27269 (8)	0.0507 (4)
F10	0.33308 (9)	0.78402 (7)	0.23647 (8)	0.0459 (4)
F11	0.26822 (9)	0.70653 (8)	0.14865 (9)	0.0537 (4)
F12	0.38410 (10)	0.74577 (8)	0.16469 (9)	0.0497 (4)
F13	0.25354 (8)	0.41455 (8)	0.01425 (8)	0.0445 (4)
F14	0.27430 (8)	0.52975 (8)	0.00069 (8)	0.0385 (3)
F15	0.28655 (8)	0.44738 (9)	−0.07256 (7)	0.0470 (4)
F19	0.82744 (9)	0.65439 (9)	0.51987 (8)	0.0488 (4)
F20	0.81541 (11)	0.53617 (9)	0.52327 (8)	0.0657 (5)
F21	0.72766 (10)	0.60866 (10)	0.53192 (8)	0.0561 (5)
F22	0.67492 (8)	0.67563 (8)	0.16727 (7)	0.0426 (4)
F23	0.75829 (10)	0.73793 (8)	0.26143 (9)	0.0490 (4)
F24	0.79387 (9)	0.63343 (9)	0.23298 (9)	0.0492 (4)
N1	0.49006 (10)	0.03298 (9)	0.66179 (9)	0.0219 (4)
N2	0.47084 (10)	−0.03195 (9)	0.74765 (9)	0.0225 (4)
C1	0.50909 (12)	0.02306 (11)	0.73361 (11)	0.0219 (4)
C2	0.43398 (13)	−0.02710 (12)	0.61751 (12)	0.0273 (5)
H2A	0.4616	−0.0647	0.6004	0.033*
H2B	0.3871	−0.0066	0.5731	0.033*
C3	0.40817 (13)	−0.06074 (13)	0.67455 (11)	0.0275 (5)
H3A	0.3537	−0.0433	0.6651	0.033*
H3B	0.4085	−0.1161	0.6731	0.033*
C4	0.46845 (12)	−0.04819 (12)	0.81830 (11)	0.0239 (5)
C5	0.50674 (13)	−0.11362 (12)	0.85634 (12)	0.0262 (5)
C6	0.49935 (14)	−0.13078 (13)	0.92158 (12)	0.0308 (5)
H6	0.5246	−0.1745	0.9493	0.037*
C7	0.45600 (14)	−0.08535 (13)	0.94660 (12)	0.0317 (5)
H7	0.4515	−0.0984	0.9911	0.038*
C8	0.41908 (14)	−0.02121 (13)	0.90777 (12)	0.0311 (5)
H8	0.3898	0.0095	0.9261	0.037*
C9	0.42415 (13)	−0.00086 (12)	0.84220 (12)	0.0261 (5)
C10	0.38168 (13)	0.06998 (13)	0.80057 (13)	0.0304 (5)
H10	0.3933	0.0762	0.7561	0.037*
C11	0.41371 (15)	0.13920 (13)	0.85073 (14)	0.0378 (6)
H11A	0.3886	0.1842	0.8213	0.057*
H11B	0.4724	0.1421	0.8695	0.057*
H11C	0.4006	0.1356	0.8935	0.057*
C12	0.29009 (14)	0.06342 (15)	0.77105 (15)	0.0431 (6)
H12A	0.2643	0.1097	0.7450	0.065*
H12B	0.2773	0.0550	0.8135	0.065*
H12C	0.2701	0.0213	0.7358	0.065*
C13	0.55597 (14)	−0.16215 (13)	0.82903 (13)	0.0312 (5)
H13	0.5292	−0.1605	0.7726	0.037*
C14	0.64129 (15)	−0.13026 (15)	0.85628 (15)	0.0419 (6)
H14A	0.6718	−0.1614	0.8372	0.063*
H14B	0.6686	−0.1300	0.9116	0.063*
H14C	0.6380	−0.0790	0.8375	0.063*
C15	0.56033 (19)	−0.24404 (14)	0.85261 (16)	0.0466 (7)
H15A	0.5056	−0.2642	0.8343	0.070*
H15B	0.5883	−0.2477	0.9078	0.070*
H15C	0.5900	−0.2728	0.8309	0.070*
C16	0.52057 (13)	0.08945 (11)	0.62913 (11)	0.0228 (4)
C17	0.47416 (13)	0.15411 (12)	0.60097 (11)	0.0252 (5)
C18	0.50294 (15)	0.20684 (12)	0.56719 (12)	0.0313 (5)
H18	0.4733	0.2516	0.5476	0.038*
C19	0.57381 (15)	0.19514 (13)	0.56161 (13)	0.0335 (5)
H19	0.5922	0.2317	0.5380	0.040*
C20	0.61821 (14)	0.13085 (13)	0.59001 (12)	0.0307 (5)
H20	0.6669	0.1238	0.5858	0.037*
C21	0.59283 (13)	0.07586 (12)	0.62487 (11)	0.0253 (5)
C22	0.39771 (14)	0.16936 (13)	0.60966 (13)	0.0310 (5)
H22	0.3813	0.1213	0.6247	0.037*
C23	0.32750 (15)	0.19532 (16)	0.53670 (14)	0.0439 (6)
H23A	0.3406	0.2439	0.5219	0.066*
H23B	0.2790	0.2002	0.5445	0.066*
H23C	0.3178	0.1586	0.4968	0.066*
C24	0.41498 (16)	0.22592 (16)	0.67338 (14)	0.0432 (6)
H24A	0.4300	0.2742	0.6597	0.065*
H24B	0.4594	0.2075	0.7200	0.065*
H24C	0.3666	0.2322	0.6811	0.065*
C25	0.64282 (14)	0.00569 (13)	0.65617 (13)	0.0318 (5)
H25	0.6175	−0.0237	0.6830	0.038*
C26	0.72921 (16)	0.02464 (17)	0.71340 (17)	0.0543 (8)
H26A	0.7561	0.0522	0.6881	0.081*
H26B	0.7589	−0.0217	0.7349	0.081*
H26C	0.7280	0.0556	0.7538	0.081*
C27	0.64207 (18)	−0.04305 (14)	0.59237 (15)	0.0442 (7)
H27A	0.5862	−0.0555	0.5573	0.066*
H27B	0.6724	−0.0892	0.6135	0.066*
H27C	0.6671	−0.0157	0.5653	0.066*
C28	0.46452 (12)	0.54706 (11)	0.28500 (11)	0.0214 (4)
C29	0.44991 (12)	0.54002 (12)	0.34834 (11)	0.0236 (4)
H29	0.4736	0.4994	0.3819	0.028*
C30	0.40201 (13)	0.59036 (12)	0.36383 (12)	0.0251 (5)
C31	0.36629 (13)	0.65038 (12)	0.31637 (12)	0.0271 (5)
H31	0.3326	0.6843	0.3263	0.033*
C32	0.38103 (12)	0.65968 (12)	0.25381 (12)	0.0240 (5)
C33	0.42937 (12)	0.60951 (11)	0.23918 (12)	0.0228 (4)
H33	0.4391	0.6177	0.1965	0.027*
C34	0.39268 (15)	0.58098 (14)	0.43418 (14)	0.0357 (6)
C35	0.34218 (14)	0.72339 (13)	0.20124 (13)	0.0305 (5)
C36	0.53982 (12)	0.41235 (11)	0.31391 (11)	0.0215 (4)
C37	0.47298 (13)	0.37166 (12)	0.30880 (11)	0.0248 (5)
H37	0.4207	0.3928	0.2823	0.030*
C38	0.48060 (13)	0.30127 (12)	0.34134 (12)	0.0274 (5)
C39	0.55582 (13)	0.26877 (12)	0.38019 (12)	0.0270 (5)
H39	0.5612	0.2208	0.4026	0.032*
C40	0.62297 (13)	0.30745 (12)	0.38578 (11)	0.0243 (5)
C41	0.61488 (13)	0.37765 (12)	0.35287 (11)	0.0230 (4)
H41	0.6619	0.4028	0.3570	0.028*
C42	0.70419 (14)	0.27203 (12)	0.42822 (13)	0.0299 (5)
C43	0.40729 (15)	0.26223 (14)	0.33705 (14)	0.0367 (6)
C44	0.61133 (12)	0.54189 (11)	0.30350 (11)	0.0207 (4)
C45	0.65695 (13)	0.55098 (12)	0.38128 (12)	0.0235 (4)
H45	0.6407	0.5253	0.4143	0.028*
C46	0.72526 (13)	0.59620 (12)	0.41220 (12)	0.0249 (5)
C47	0.75007 (13)	0.63552 (12)	0.36600 (12)	0.0252 (5)
H47	0.7966	0.6665	0.3867	0.030*
C48	0.70505 (12)	0.62841 (11)	0.28859 (12)	0.0226 (4)
C49	0.63740 (12)	0.58233 (11)	0.25804 (11)	0.0220 (4)
H49	0.6081	0.5783	0.2047	0.026*
C50	0.77279 (15)	0.59941 (14)	0.49580 (13)	0.0351 (6)
C51	0.73266 (13)	0.66856 (12)	0.23798 (12)	0.0267 (5)
C52	0.49542 (12)	0.46987 (11)	0.18099 (11)	0.0215 (4)
C53	0.54765 (12)	0.43508 (12)	0.15634 (12)	0.0235 (4)
H53	0.6028	0.4289	0.1912	0.028*
C54	0.52144 (13)	0.40933 (12)	0.08269 (12)	0.0248 (5)
C55	0.44147 (13)	0.41754 (12)	0.03016 (12)	0.0259 (5)
H55	0.4233	0.4004	−0.0202	0.031*
C56	0.38899 (13)	0.45129 (11)	0.05310 (11)	0.0233 (4)
C57	0.41534 (12)	0.47617 (11)	0.12721 (11)	0.0224 (4)
H57	0.3774	0.4981	0.1414	0.027*
C59	0.30216 (14)	0.46077 (13)	−0.00085 (12)	0.0305 (5)
B1	0.52749 (14)	0.49284 (13)	0.27032 (13)	0.0212 (5)
C58	0.57881 (14)	0.36974 (13)	0.06062 (12)	0.0334 (5)
F16A	0.5578 (3)	0.3839 (2)	−0.01354 (12)	0.0362 (4)	0.457 (3)
F17A	0.5790 (3)	0.29508 (11)	0.0682 (3)	0.0362 (4)	0.457 (3)
F18A	0.65707 (14)	0.3914 (3)	0.0972 (3)	0.0362 (4)	0.457 (3)
F16B	0.5558 (5)	0.3618 (4)	−0.01471 (13)	0.0362 (4)	0.315 (3)
F17B	0.5990 (4)	0.30242 (19)	0.0940 (3)	0.0362 (4)	0.315 (3)
F18B	0.6470 (2)	0.4117 (3)	0.0875 (4)	0.0362 (4)	0.315 (3)
F16C	0.5496 (8)	0.2997 (4)	0.0363 (9)	0.0362 (4)	0.118 (3)
F17C	0.6562 (3)	0.3652 (9)	0.1125 (6)	0.0362 (4)	0.118 (3)
F18C	0.5837 (9)	0.3942 (8)	−0.0020 (5)	0.0362 (4)	0.118 (3)
F16D	0.5391 (7)	0.3310 (8)	−0.0051 (6)	0.0362 (4)	0.110 (3)
F17D	0.6205 (9)	0.3188 (6)	0.1136 (6)	0.0362 (4)	0.110 (3)
F18D	0.6404 (6)	0.4108 (7)	0.0606 (9)	0.0362 (4)	0.110 (3)
F7A	0.3939 (5)	0.51089 (14)	0.4606 (3)	0.0351 (5)	0.398 (3)
F8A	0.3370 (4)	0.6223 (4)	0.4436 (4)	0.0351 (5)	0.398 (3)
F9A	0.4609 (2)	0.6116 (3)	0.49079 (19)	0.0351 (5)	0.398 (3)
F7B	0.3620 (4)	0.51232 (18)	0.4344 (3)	0.0351 (5)	0.338 (3)
F8B	0.3334 (5)	0.6281 (5)	0.4284 (4)	0.0351 (5)	0.338 (3)
F9B	0.4625 (2)	0.5889 (3)	0.4999 (2)	0.0351 (5)	0.338 (3)
F7C	0.3999 (9)	0.50701 (19)	0.4506 (7)	0.0351 (5)	0.190 (3)
F8C	0.3188 (3)	0.5964 (6)	0.4282 (5)	0.0351 (5)	0.190 (3)
F9C	0.4455 (4)	0.6156 (6)	0.4995 (4)	0.0351 (5)	0.190 (3)
F7D	0.3279 (8)	0.5350 (9)	0.4112 (10)	0.0351 (5)	0.0734 (19)
F8D	0.3577 (12)	0.6383 (9)	0.4527 (14)	0.0351 (5)	0.0734 (19)
F9D	0.4442 (10)	0.5377 (10)	0.4934 (7)	0.0351 (5)	0.0734 (19)

	U11	U22	U33	U12	U13	U23
Cl1	0.0307 (3)	0.0299 (3)	0.0250 (3)	−0.0082 (2)	0.0070 (2)	−0.0015 (2)
F1	0.0515 (9)	0.0446 (9)	0.0496 (9)	0.0195 (7)	0.0189 (8)	−0.0124 (7)
F2	0.0289 (8)	0.0459 (9)	0.0903 (13)	0.0045 (7)	0.0153 (8)	0.0269 (9)
F3	0.0488 (9)	0.0569 (10)	0.0318 (8)	0.0221 (7)	0.0149 (7)	0.0079 (7)
F4	0.0546 (10)	0.1007 (14)	0.0528 (10)	−0.0322 (10)	0.0381 (9)	−0.0135 (9)
F5	0.0544 (10)	0.0349 (9)	0.1155 (16)	−0.0146 (8)	0.0357 (11)	0.0160 (9)
F6	0.0337 (8)	0.0657 (11)	0.0449 (9)	−0.0190 (7)	0.0105 (7)	0.0062 (8)
F10	0.0632 (10)	0.0234 (7)	0.0480 (9)	0.0094 (7)	0.0220 (8)	0.0000 (6)
F11	0.0391 (9)	0.0390 (9)	0.0491 (9)	0.0009 (7)	−0.0108 (7)	0.0055 (7)
F12	0.0595 (10)	0.0430 (9)	0.0576 (10)	0.0171 (7)	0.0360 (8)	0.0254 (7)
F13	0.0288 (7)	0.0461 (9)	0.0550 (9)	−0.0129 (6)	0.0153 (7)	−0.0047 (7)
F14	0.0290 (7)	0.0378 (8)	0.0402 (8)	0.0058 (6)	0.0077 (6)	−0.0012 (6)
F15	0.0330 (8)	0.0726 (11)	0.0245 (7)	0.0039 (7)	0.0029 (6)	−0.0126 (7)
F19	0.0449 (9)	0.0591 (10)	0.0325 (8)	−0.0212 (8)	0.0082 (7)	−0.0156 (7)
F20	0.0818 (12)	0.0504 (10)	0.0300 (8)	0.0155 (9)	−0.0065 (8)	0.0039 (7)
F21	0.0561 (10)	0.0880 (13)	0.0281 (7)	−0.0215 (9)	0.0221 (7)	−0.0141 (8)
F22	0.0393 (8)	0.0531 (9)	0.0333 (7)	−0.0058 (7)	0.0143 (6)	0.0144 (7)
F23	0.0696 (11)	0.0312 (8)	0.0549 (9)	−0.0185 (7)	0.0354 (8)	−0.0028 (7)
F24	0.0502 (9)	0.0524 (9)	0.0659 (10)	0.0230 (8)	0.0448 (8)	0.0260 (8)
N1	0.0216 (9)	0.0207 (9)	0.0201 (9)	−0.0012 (7)	0.0064 (7)	0.0005 (7)
N2	0.0224 (9)	0.0213 (9)	0.0202 (9)	−0.0041 (7)	0.0061 (7)	0.0003 (7)
C1	0.0210 (10)	0.0185 (10)	0.0231 (11)	0.0029 (8)	0.0070 (9)	0.0003 (8)
C2	0.0288 (12)	0.0262 (12)	0.0228 (11)	−0.0052 (9)	0.0078 (9)	−0.0034 (9)
C3	0.0264 (11)	0.0291 (12)	0.0218 (11)	−0.0070 (9)	0.0061 (9)	−0.0016 (9)
C4	0.0224 (11)	0.0266 (11)	0.0196 (10)	−0.0074 (9)	0.0068 (9)	0.0004 (8)
C5	0.0264 (11)	0.0242 (11)	0.0241 (11)	−0.0069 (9)	0.0077 (9)	−0.0014 (9)
C6	0.0353 (13)	0.0272 (12)	0.0253 (11)	−0.0045 (10)	0.0093 (10)	0.0037 (9)
C7	0.0353 (13)	0.0363 (13)	0.0229 (11)	−0.0113 (10)	0.0126 (10)	0.0006 (10)
C8	0.0296 (12)	0.0358 (13)	0.0286 (12)	−0.0073 (10)	0.0137 (10)	−0.0054 (10)
C9	0.0225 (11)	0.0273 (12)	0.0251 (11)	−0.0069 (9)	0.0074 (9)	−0.0021 (9)
C10	0.0290 (12)	0.0307 (12)	0.0305 (12)	0.0018 (10)	0.0123 (10)	0.0011 (10)
C11	0.0399 (14)	0.0297 (13)	0.0384 (14)	0.0023 (11)	0.0124 (11)	−0.0016 (10)
C12	0.0302 (13)	0.0440 (15)	0.0480 (15)	0.0028 (11)	0.0110 (12)	0.0026 (12)
C13	0.0363 (13)	0.0264 (12)	0.0274 (12)	0.0007 (10)	0.0112 (10)	0.0032 (9)
C14	0.0324 (13)	0.0399 (15)	0.0492 (15)	0.0057 (11)	0.0142 (12)	0.0022 (12)
C15	0.0691 (19)	0.0267 (13)	0.0488 (16)	0.0030 (13)	0.0305 (15)	0.0038 (11)
C16	0.0262 (11)	0.0220 (11)	0.0179 (10)	−0.0025 (9)	0.0077 (9)	0.0009 (8)
C17	0.0287 (12)	0.0231 (11)	0.0194 (10)	0.0014 (9)	0.0067 (9)	−0.0009 (8)
C18	0.0439 (14)	0.0206 (11)	0.0266 (11)	0.0033 (10)	0.0131 (11)	0.0033 (9)
C19	0.0500 (15)	0.0257 (12)	0.0292 (12)	−0.0057 (11)	0.0215 (11)	0.0017 (9)
C20	0.0336 (13)	0.0325 (13)	0.0312 (12)	−0.0034 (10)	0.0191 (10)	−0.0011 (10)
C21	0.0276 (11)	0.0271 (12)	0.0210 (10)	0.0009 (9)	0.0107 (9)	0.0007 (9)
C22	0.0326 (12)	0.0246 (12)	0.0345 (12)	0.0067 (10)	0.0139 (10)	0.0032 (9)
C23	0.0353 (14)	0.0463 (16)	0.0400 (14)	0.0102 (12)	0.0077 (12)	0.0013 (12)
C24	0.0382 (14)	0.0502 (16)	0.0384 (14)	0.0125 (12)	0.0145 (12)	−0.0052 (12)
C25	0.0328 (12)	0.0318 (13)	0.0349 (12)	0.0071 (10)	0.0187 (11)	0.0084 (10)
C26	0.0375 (15)	0.0547 (18)	0.0590 (18)	0.0144 (13)	0.0109 (14)	0.0113 (15)
C27	0.0641 (18)	0.0307 (14)	0.0510 (16)	0.0119 (13)	0.0375 (15)	0.0066 (12)
C28	0.0192 (10)	0.0233 (11)	0.0194 (10)	−0.0035 (8)	0.0066 (8)	−0.0028 (8)
C29	0.0214 (11)	0.0242 (11)	0.0236 (11)	−0.0007 (9)	0.0085 (9)	−0.0014 (9)
C30	0.0232 (11)	0.0271 (12)	0.0244 (11)	−0.0016 (9)	0.0101 (9)	−0.0039 (9)
C31	0.0233 (11)	0.0257 (12)	0.0318 (12)	−0.0004 (9)	0.0119 (10)	−0.0075 (9)
C32	0.0207 (11)	0.0214 (11)	0.0256 (11)	−0.0030 (8)	0.0065 (9)	−0.0024 (8)
C33	0.0219 (10)	0.0232 (11)	0.0231 (10)	−0.0048 (8)	0.0098 (9)	−0.0018 (8)
C34	0.0395 (14)	0.0370 (14)	0.0373 (13)	0.0063 (11)	0.0231 (12)	0.0004 (11)
C35	0.0292 (12)	0.0267 (12)	0.0317 (12)	0.0024 (9)	0.0100 (10)	−0.0010 (10)
C36	0.0253 (11)	0.0221 (11)	0.0191 (10)	−0.0019 (8)	0.0118 (9)	−0.0028 (8)
C37	0.0247 (11)	0.0271 (12)	0.0226 (10)	−0.0011 (9)	0.0105 (9)	−0.0012 (9)
C38	0.0309 (12)	0.0259 (12)	0.0271 (11)	−0.0072 (9)	0.0145 (10)	−0.0025 (9)
C39	0.0373 (13)	0.0209 (11)	0.0251 (11)	−0.0007 (9)	0.0159 (10)	−0.0001 (9)
C40	0.0304 (12)	0.0223 (11)	0.0219 (10)	0.0002 (9)	0.0132 (9)	−0.0023 (8)
C41	0.0247 (11)	0.0231 (11)	0.0242 (10)	−0.0019 (9)	0.0137 (9)	−0.0029 (8)
C42	0.0341 (13)	0.0235 (12)	0.0338 (13)	0.0042 (10)	0.0167 (11)	0.0006 (9)
C43	0.0362 (14)	0.0363 (14)	0.0369 (13)	−0.0082 (11)	0.0157 (12)	0.0017 (11)
C44	0.0225 (10)	0.0192 (10)	0.0222 (10)	0.0037 (8)	0.0115 (9)	0.0001 (8)
C45	0.0263 (11)	0.0214 (11)	0.0256 (11)	0.0013 (9)	0.0140 (9)	0.0008 (8)
C46	0.0249 (11)	0.0233 (11)	0.0244 (11)	0.0026 (9)	0.0092 (9)	−0.0028 (9)
C47	0.0216 (11)	0.0216 (11)	0.0309 (12)	−0.0003 (9)	0.0103 (9)	−0.0027 (9)
C48	0.0229 (11)	0.0177 (10)	0.0290 (11)	0.0035 (8)	0.0131 (9)	0.0009 (8)
C49	0.0224 (10)	0.0220 (11)	0.0213 (10)	0.0038 (8)	0.0096 (9)	−0.0014 (8)
C50	0.0372 (13)	0.0352 (13)	0.0271 (12)	−0.0042 (11)	0.0089 (11)	−0.0037 (10)
C51	0.0259 (12)	0.0230 (11)	0.0334 (12)	0.0007 (9)	0.0152 (10)	0.0015 (9)
C52	0.0248 (11)	0.0172 (10)	0.0228 (10)	−0.0021 (8)	0.0109 (9)	0.0018 (8)
C53	0.0209 (10)	0.0244 (11)	0.0239 (10)	−0.0009 (8)	0.0088 (9)	0.0005 (8)
C54	0.0280 (11)	0.0222 (11)	0.0270 (11)	−0.0015 (9)	0.0148 (9)	−0.0002 (9)
C55	0.0310 (12)	0.0240 (11)	0.0232 (11)	−0.0033 (9)	0.0126 (10)	−0.0038 (9)
C56	0.0250 (11)	0.0200 (11)	0.0244 (11)	−0.0027 (8)	0.0104 (9)	−0.0004 (8)
C57	0.0231 (11)	0.0204 (11)	0.0255 (11)	−0.0019 (8)	0.0125 (9)	0.0007 (8)
C59	0.0274 (12)	0.0338 (13)	0.0284 (12)	−0.0036 (10)	0.0107 (10)	−0.0062 (10)
B1	0.0208 (12)	0.0223 (12)	0.0199 (11)	0.0010 (9)	0.0085 (10)	0.0010 (9)
C58	0.0317 (13)	0.0377 (14)	0.0305 (12)	0.0009 (10)	0.0136 (10)	−0.0048 (10)
F16A	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F17A	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F18A	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F16B	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F17B	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F18B	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F16C	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F17C	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F18C	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F16D	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F17D	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F18D	0.0396 (8)	0.0351 (10)	0.0406 (8)	0.0062 (7)	0.0239 (7)	−0.0056 (7)
F7A	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F8A	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F9A	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F7B	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F8B	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F9B	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F7C	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F8C	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F9C	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F7D	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F8D	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)
F9D	0.0448 (8)	0.0450 (9)	0.0241 (9)	0.0091 (6)	0.0230 (7)	0.0062 (6)

Cl1—C1	1.681 (2)	C30—C34	1.486 (3)
F1—C42	1.334 (3)	C31—C32	1.391 (3)
F2—C42	1.327 (3)	C32—C33	1.385 (3)
F3—C42	1.337 (3)	C32—C35	1.493 (3)
F4—C43	1.327 (3)	C34—F8C	1.346 (3)
F5—C43	1.341 (3)	C34—F8A	1.347 (3)
F6—C43	1.328 (3)	C34—F8D	1.347 (3)
F10—C35	1.339 (3)	C34—F8B	1.347 (3)
F11—C35	1.334 (3)	C34—F7B	1.353 (3)
F12—C35	1.336 (3)	C34—F7A	1.354 (3)
F13—C59	1.349 (3)	C34—F7C	1.354 (3)
F14—C59	1.342 (3)	C34—F7D	1.354 (3)
F15—C59	1.337 (3)	C34—F9B	1.372 (3)
F19—C50	1.337 (3)	C34—F9D	1.373 (3)
F20—C50	1.347 (3)	C34—F9C	1.373 (3)
F21—C50	1.329 (3)	C34—F9A	1.374 (3)
F22—C51	1.336 (3)	C36—C41	1.398 (3)
F23—C51	1.335 (3)	C36—C37	1.399 (3)
F24—C51	1.337 (3)	C36—B1	1.640 (3)
N1—C1	1.315 (3)	C37—C38	1.392 (3)
N1—C16	1.442 (3)	C38—C39	1.383 (3)
N1—C2	1.479 (3)	C38—C43	1.494 (3)
N2—C1	1.311 (3)	C39—C40	1.383 (3)
N2—C4	1.448 (3)	C40—C41	1.391 (3)
N2—C3	1.486 (3)	C40—C42	1.497 (3)
C2—C3	1.531 (3)	C44—C49	1.397 (3)
C4—C9	1.399 (3)	C44—C45	1.397 (3)
C4—C5	1.400 (3)	C44—B1	1.643 (3)
C5—C6	1.391 (3)	C45—C46	1.392 (3)
C5—C13	1.521 (3)	C46—C47	1.383 (3)
C6—C7	1.379 (3)	C46—C50	1.489 (3)
C7—C8	1.380 (3)	C47—C48	1.386 (3)
C8—C9	1.390 (3)	C48—C49	1.392 (3)
C9—C10	1.524 (3)	C48—C51	1.495 (3)
C10—C11	1.531 (3)	C52—C57	1.392 (3)
C10—C12	1.532 (3)	C52—C53	1.406 (3)
C13—C15	1.527 (3)	C52—B1	1.646 (3)
C13—C14	1.533 (3)	C53—C54	1.393 (3)
C16—C21	1.398 (3)	C54—C55	1.386 (3)
C16—C17	1.399 (3)	C54—C58	1.494 (3)
C17—C18	1.391 (3)	C55—C56	1.380 (3)
C17—C22	1.524 (3)	C56—C57	1.396 (3)
C18—C19	1.380 (3)	C56—C59	1.491 (3)
C19—C20	1.378 (3)	C58—F17A	1.343 (3)
C20—C21	1.397 (3)	C58—F17C	1.343 (3)
C21—C25	1.517 (3)	C58—F17B	1.343 (3)
C22—C23	1.522 (3)	C58—F17D	1.343 (3)
C22—C24	1.535 (3)	C58—F18D	1.355 (3)
C25—C27	1.529 (3)	C58—F18A	1.356 (3)
C25—C26	1.530 (4)	C58—F18C	1.356 (3)
C28—C29	1.400 (3)	C58—F18B	1.356 (3)
C28—C33	1.402 (3)	C58—F16B	1.363 (3)
C28—B1	1.638 (3)	C58—F16D	1.363 (3)
C29—C30	1.390 (3)	C58—F16C	1.364 (3)
C30—C31	1.385 (3)	C58—F16A	1.364 (3)
C1—N1—C16	127.50 (17)	C39—C38—C37	120.4 (2)
C1—N1—C2	108.78 (17)	C39—C38—C43	119.9 (2)
C16—N1—C2	123.64 (16)	C37—C38—C43	119.6 (2)
C1—N2—C4	127.33 (17)	C40—C39—C38	118.7 (2)
C1—N2—C3	108.32 (16)	C39—C40—C41	120.5 (2)
C4—N2—C3	121.63 (16)	C39—C40—C42	118.38 (19)
N2—C1—N1	114.83 (18)	C41—C40—C42	121.1 (2)
N2—C1—Cl1	122.96 (16)	C40—C41—C36	122.1 (2)
N1—C1—Cl1	122.21 (16)	F2—C42—F1	106.87 (19)
N1—C2—C3	102.43 (16)	F2—C42—F3	105.79 (19)
N2—C3—C2	102.55 (16)	F1—C42—F3	105.11 (18)
C9—C4—C5	123.8 (2)	F2—C42—C40	113.68 (18)
C9—C4—N2	118.65 (19)	F1—C42—C40	112.25 (19)
C5—C4—N2	117.44 (19)	F3—C42—C40	112.51 (18)
C6—C5—C4	116.6 (2)	F4—C43—F6	106.8 (2)
C6—C5—C13	121.7 (2)	F4—C43—F5	106.0 (2)
C4—C5—C13	121.67 (19)	F6—C43—F5	105.6 (2)
C7—C6—C5	121.1 (2)	F4—C43—C38	112.2 (2)
C6—C7—C8	120.8 (2)	F6—C43—C38	113.39 (19)
C7—C8—C9	121.0 (2)	F5—C43—C38	112.3 (2)
C8—C9—C4	116.8 (2)	C49—C44—C45	115.90 (19)
C8—C9—C10	119.3 (2)	C49—C44—B1	123.66 (17)
C4—C9—C10	123.96 (19)	C45—C44—B1	120.16 (18)
C9—C10—C11	111.30 (18)	C46—C45—C44	122.49 (19)
C9—C10—C12	111.1 (2)	C47—C46—C45	120.54 (19)
C11—C10—C12	110.6 (2)	C47—C46—C50	120.6 (2)
C5—C13—C15	113.4 (2)	C45—C46—C50	118.8 (2)
C5—C13—C14	110.42 (19)	C46—C47—C48	118.09 (19)
C15—C13—C14	110.0 (2)	C47—C48—C49	121.08 (19)
C21—C16—C17	123.61 (19)	C47—C48—C51	118.68 (19)
C21—C16—N1	118.76 (18)	C49—C48—C51	120.18 (18)
C17—C16—N1	117.60 (19)	C48—C49—C44	121.89 (19)
C18—C17—C16	116.9 (2)	F21—C50—F19	105.88 (19)
C18—C17—C22	120.4 (2)	F21—C50—F20	106.4 (2)
C16—C17—C22	122.61 (19)	F19—C50—F20	105.0 (2)
C19—C18—C17	121.1 (2)	F21—C50—C46	113.6 (2)
C20—C19—C18	120.6 (2)	F19—C50—C46	113.8 (2)
C19—C20—C21	121.2 (2)	F20—C50—C46	111.48 (19)
C20—C21—C16	116.6 (2)	F23—C51—F22	105.73 (17)
C20—C21—C25	120.4 (2)	F23—C51—F24	106.28 (18)
C16—C21—C25	123.01 (19)	F22—C51—F24	106.02 (18)
C23—C22—C17	113.0 (2)	F23—C51—C48	112.81 (18)
C23—C22—C24	110.9 (2)	F22—C51—C48	113.24 (17)
C17—C22—C24	110.26 (19)	F24—C51—C48	112.18 (17)
C21—C25—C27	110.75 (19)	C57—C52—C53	115.63 (19)
C21—C25—C26	111.4 (2)	C57—C52—B1	123.57 (18)
C27—C25—C26	111.1 (2)	C53—C52—B1	120.50 (18)
C29—C28—C33	115.55 (19)	C54—C53—C52	122.39 (19)
C29—C28—B1	122.78 (18)	C55—C54—C53	120.5 (2)
C33—C28—B1	121.23 (18)	C55—C54—C58	119.43 (19)
C30—C29—C28	122.4 (2)	C53—C54—C58	120.02 (19)
C31—C30—C29	120.7 (2)	C56—C55—C54	118.17 (19)
C31—C30—C34	120.2 (2)	C55—C56—C57	121.10 (19)
C29—C30—C34	119.0 (2)	C55—C56—C59	120.39 (19)
C30—C31—C32	118.2 (2)	C57—C56—C59	118.50 (19)
C33—C32—C31	120.6 (2)	C52—C57—C56	122.2 (2)
C33—C32—C35	120.2 (2)	F15—C59—F14	106.54 (18)
C31—C32—C35	119.1 (2)	F15—C59—F13	105.96 (18)
C32—C33—C28	122.5 (2)	F14—C59—F13	104.88 (18)
F8B—C34—F7B	103.9 (5)	F15—C59—C56	113.22 (19)
F8A—C34—F7A	109.7 (4)	F14—C59—C56	112.99 (18)
F8C—C34—F7C	102.1 (7)	F13—C59—C56	112.58 (19)
F8D—C34—F7D	95.3 (12)	C28—B1—C36	111.67 (17)
F8B—C34—F9B	113.8 (5)	C28—B1—C44	103.48 (16)
F7B—C34—F9B	108.1 (3)	C36—B1—C44	111.86 (16)
F8D—C34—F9D	115.6 (13)	C28—B1—C52	113.14 (16)
F7D—C34—F9D	96.9 (12)	C36—B1—C52	104.19 (16)
F8C—C34—F9C	105.0 (5)	C44—B1—C52	112.77 (17)
F7C—C34—F9C	105.2 (8)	F17D—C58—F18D	100.2 (9)
F8A—C34—F9A	98.6 (5)	F17A—C58—F18A	106.0 (3)
F7A—C34—F9A	101.7 (4)	F17C—C58—F18C	103.6 (8)
F11—C35—F12	106.67 (19)	F17B—C58—F18B	107.2 (4)
F11—C35—F10	105.42 (18)	F17B—C58—F16B	109.1 (3)
F12—C35—F10	106.10 (19)	F18B—C58—F16B	105.7 (4)
F11—C35—C32	112.32 (19)	F17D—C58—F16D	106.2 (9)
F12—C35—C32	112.96 (19)	F18D—C58—F16D	111.7 (9)
F10—C35—C32	112.80 (18)	F17C—C58—F16C	109.5 (8)
C41—C36—C37	116.00 (19)	F18C—C58—F16C	98.7 (8)
C41—C36—B1	123.41 (18)	F17A—C58—F16A	106.8 (3)
C37—C36—B1	120.42 (18)	F18A—C58—F16A	104.3 (3)
C38—C37—C36	122.2 (2)

D—H···A	D—H	H···A	D···A	D—H···A
C3—H3A···F15i	0.99	2.43	3.256 (3)	141
C12—H12A···F17Cii	0.98	2.53	3.269 (12)	132
C19—H19···F8Diii	0.95	2.48	3.297 (18)	144
C29—H29···F9Diii	0.95	2.35	3.180 (14)	146