Tetra­iodido[methyl­enebis(diphenyl­phosphine oxide)-κ²O:O′]tin(IV) chloro­form solvate

The title compound, [SnI₄(C₂₅H₂₂O₂P₂)]·CHCl₃, crystallized from a chloro­form solution of SnI₄ and the diphosphine CH₂(PPh₂)₂ exposed to air. The monomeric complex displays a distorted octa­hedral coordinaton for the tin(IV) atom with average Sn—I and Sn—O bond lengths of 2.79 (2) and 2.15 (1) Å, respectively.

Key indicators

• Single-crystal X-ray study
• T = 125 K
• Mean [sigma](C-C) = 0.007 Å
• R factor = 0.021
• wR factor = 0.046
• Data-to-parameter ratio = 21.1

checkCIF/PLATON results

No syntax errors found



Alert level B
PLAT232_ALERT_2_B Hirshfeld Test Diff (M-X)  I1     --  Sn      ..      12.39 su

Alert level C
PLAT220_ALERT_2_C Large Non-Solvent    C     Ueq(max)/Ueq(min) ...       2.89 Ratio
PLAT232_ALERT_2_C Hirshfeld Test Diff (M-X)  I3     --  Sn      ..       5.90 su
PLAT244_ALERT_4_C Low   'Solvent' Ueq as Compared to Neighbors for        C26

Alert level G
REFLT03_ALERT_4_G Please check that the estimate of the number of Friedel pairs is
            correct. If it is not, please give the correct count in the
            _publ_section_exptl_refinement section of the submitted CIF.
           From the CIF: _diffrn_reflns_theta_max           26.73
           From the CIF: _reflns_number_total               7254
           Count of symmetry unique reflns         3743
           Completeness (_total/calc)            193.80%
           TEST3: Check Friedels for noncentro structure
           Estimate of Friedel pairs measured      3511
           Fraction of Friedel pairs measured     0.938
           Are heavy atom types Z>Si present        yes

   0 ALERT level A = In general: serious problem
   1 ALERT level B = Potentially serious problem
   3 ALERT level C = Check and explain
   1 ALERT level G = General alerts; check

   0 ALERT type 1 CIF construction/syntax error, inconsistent or missing data
   3 ALERT type 2 Indicator that the structure model may be wrong or deficient
   0 ALERT type 3 Indicator that the structure quality may be low
   2 ALERT type 4 Improvement, methodology, query or suggestion
   0 ALERT type 5 Informative message, check

---

S1. Comment

Tin(IV) iodide may be readily prepared by oxidation of tin metal with iodine (Woollins, 2003). A relatively weak Lewis acid, SnI₄ nevertheless forms complexes with phosphines and phosphine oxides (Genge et al., 1999; Davis et al., 2006a). Similar phosphine and phosphine oxide complexes have been reported of the more Lewis acidic tin(IV) halides, SnX₄ (X = F, Cl, Br; Davis et al., 2006a, 2006b; Genge et al., 1999; Mohamed et al., 2004). The phosphine oxide complexes are chiefly obtained by air oxidation of the phosphine ligands in the presence of the tin(IV) halide (Levason et al., 2003).

Reaction of SnI₄ with CH₂(PPh₂)₂ in CHCl₃ in the presence of air afforded the title complex [{CH₂(P(O)Ph₂)₂}SnI₄]^.CHCl₃, (I).

Complex (I) exhibits a distorted octahedral coordination at tin. The bis(phosphine oxide) results in a cis coordination of the ligand, with Sn—O distances of 2.136 (3) and 2.157 (3) Å, and Sn—I distances of 2.7770 (4), 2.7805 (4), 2.7911 (4) and 2.8199 (4) Å. The smallest bond angle about the pseudooctahedral tin center, 81.1 (1)°, corresponds to the O1—Sn—O2 angle of the chelating bis(phosphine oxide) ligand, with the opposite I2—Sn—I3 angle in the SnO₂I₂ plane being the largest, 100.82 (1)°. These distances and angles are similar to those reported for the related bis(phosphine oxide) complex {o-C₆H₄(P(O)Ph₂)₂}SnI₄ (Genge et al., 1999). The SnO₂P₂C six-membered heterocycle in complex (I) is in a distorted boat conformation.

Related literature

For examples of structurally characterized tin(IV)–halide complexes of phosphine oxide ligands, see: Genge et al. (1999); Davis et al. (2006a,b); Mohamed et al. (2004). For related literature, see: Levason et al. (2003); Woollins (2003).

S2. Experimental

Complex (I) was prepared by treating a chloroform (ca 5 ml) solution of SnI₄ (655 mg, 1.1 mmol) with an excess of CH₂(PPh₂)₂ (922 mg, 2.6 mmol) in the presence of air. Suitable crystals for single crystal X-ray analysis formed within 1 week at room temperature. A small sample of crystals was separated for structural analysis, and the remaining crystals were collected by filtration on a glass frit, washed three times with ca 5 ml of chloroform, and dried briefly under vacuum (yield 659 mg (54%) of a red-orange product). Elemental analysis confirmed that the compound was obtained as the chloroform solvate: anal. calcd. for (I) C, 26.87%; H, 1.99%; N, 0.00%. Found C, 26.97%; H, 1.73%; N, <0.02%. (Elemental analysis performed by Robertson Microlit Laboratories, Madison, NJ, USA.)

S3. Refinement

H atoms on carbon were included in calculated positions and were refined using a riding model with U_iso(H) = 1.2U_eq(C) of the parent atom.

Computing details

Data collection: APEX2 (Bruker, 2007); cell refinement: SAINT (Bruker, 2007); data reduction: SAINT (Bruker, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures

Fig. 1. A view of complex (I) with displacement ellipsoids shown at the 50% probability level. H atoms have been omitted for clarity.

Tetraiodido[methylenebis(diphenylphosphine oxide)-κ²O:O']tin(IV) chloroform solvate

Crystal data

[SnI4(C25H22O2P2)]·CHCl3	F(000) = 1076
Mr = 1162.02	Dx = 2.259 Mg m^−3
Monoclinic, P21	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2yb	Cell parameters from 9838 reflections
a = 9.2639 (5) Å	θ = 2.3–28.3°
b = 19.0609 (11) Å	µ = 4.71 mm^−1
c = 10.1991 (6) Å	T = 125 K
β = 108.479 (1)°	Plate, orange
V = 1708.08 (17) Å^3	0.14 × 0.13 × 0.02 mm
Z = 2

Data collection

Bruker APEXII CCD diffractometer	7254 independent reflections
Radiation source: fine-focus sealed tube	6994 reflections with I > 2σ(I)
Graphite monochromator	Rint = 0.027
ϕ and ω scans	θmax = 26.7°, θmin = 2.1°
Absorption correction: multi-scan (SADABS; Bruker, 2007)	h = −11→11
Tmin = 0.558, Tmax = 0.912	k = −24→24
20220 measured reflections	l = −12→12

Refinement

Refinement on F^2	Secondary atom site location: difference Fourier map
Least-squares matrix: full	Hydrogen site location: inferred from neighbouring sites
R[F^2 > 2σ(F^2)] = 0.021	H-atom parameters constrained
wR(F^2) = 0.046	w = 1/[σ^2(Fo^2) + (0.0195P)^2 + 0.2278P] where P = (Fo^2 + 2Fc^2)/3
S = 1.03	(Δ/σ)max = 0.002
7254 reflections	Δρmax = 0.73 e Å^−3
344 parameters	Δρmin = −0.50 e Å^−3
1 restraint	Absolute structure: Flack (1983), 3512 Friedel pairs
Primary atom site location: structure-invariant direct methods	Absolute structure parameter: 0.004 (14)

Special details

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

Refinement. A suitable crystal was mounted in a nylon loop with Paratone-N cryoprotectant oil and data was collected on a Bruker APEX 2 CCD platform diffractometer. The data was cut off at 0.79 Å because data in the highest resolution range (0.75-0.78 Å) was very incomplete, acting to reduce the overall completeness to 99.4%. The structure was solved using direct methods and standard difference map techniques, and was refined by full-matrix least-squares procedures on F² with SHELXTL Version 6.14 (Sheldrick, 2008). One least squares restraint is required for the floating origin of space group P2₁. All non-hydrogen atoms were refined anisotropically. 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. EXTI refined to zero and was removed from the refinement.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Ų)

	x	y	z	Uiso*/Ueq
Sn	0.83582 (3)	0.791335 (15)	0.25375 (3)	0.01631 (6)
I1	0.75473 (3)	0.673729 (13)	0.38291 (3)	0.02340 (7)
I2	0.98608 (3)	0.706487 (16)	0.11538 (3)	0.02731 (7)
I3	1.07128 (3)	0.821230 (17)	0.49436 (3)	0.02768 (7)
I4	0.89066 (3)	0.910079 (14)	0.11840 (3)	0.02389 (7)
P1	0.54635 (12)	0.85261 (5)	0.35831 (11)	0.0155 (2)
P2	0.45533 (11)	0.79067 (6)	0.06921 (10)	0.0162 (2)
O1	0.6960 (3)	0.85997 (14)	0.3271 (3)	0.0178 (6)
O2	0.6235 (3)	0.77647 (14)	0.0902 (3)	0.0166 (6)
C1	0.3884 (5)	0.8709 (2)	−0.0204 (4)	0.0193 (9)
C2	0.2576 (5)	0.9026 (3)	−0.0116 (5)	0.0329 (11)
H2A	0.2042	0.8827	0.0450	0.039*
C3	0.2044 (6)	0.9636 (3)	−0.0854 (6)	0.0420 (13)
H3A	0.1151	0.9859	−0.0789	0.050*
C4	0.2817 (7)	0.9918 (3)	−0.1683 (6)	0.0487 (15)
H4A	0.2453	1.0336	−0.2187	0.058*
C5	0.4107 (6)	0.9603 (3)	−0.1788 (5)	0.0372 (13)
H5A	0.4625	0.9798	−0.2371	0.045*
C6	0.4650 (5)	0.9000 (3)	−0.1042 (4)	0.0272 (10)
H6A	0.5551	0.8784	−0.1102	0.033*
C7	0.3424 (5)	0.7198 (2)	−0.0266 (4)	0.0187 (9)
C8	0.2165 (5)	0.7324 (3)	−0.1412 (4)	0.0269 (10)
H8A	0.1873	0.7791	−0.1699	0.032*
C9	0.1332 (5)	0.6761 (3)	−0.2139 (4)	0.0316 (11)
H9A	0.0471	0.6843	−0.2929	0.038*
C10	0.1755 (6)	0.6084 (3)	−0.1715 (5)	0.0303 (11)
H10A	0.1178	0.5701	−0.2210	0.036*
C11	0.3025 (6)	0.5957 (3)	−0.0562 (5)	0.0322 (11)
H11A	0.3310	0.5490	−0.0267	0.039*
C12	0.3863 (5)	0.6516 (2)	0.0146 (5)	0.0253 (10)
H12A	0.4744	0.6433	0.0918	0.030*
C13	0.4575 (5)	0.9369 (2)	0.3409 (4)	0.0194 (9)
C14	0.3480 (5)	0.9506 (2)	0.4051 (5)	0.0280 (10)
H14A	0.3271	0.9166	0.4649	0.034*
C15	0.2702 (5)	1.0132 (3)	0.3818 (6)	0.0341 (12)
H15A	0.1950	1.0220	0.4249	0.041*
C16	0.3002 (6)	1.0628 (2)	0.2971 (5)	0.0345 (12)
H16A	0.2462	1.1059	0.2820	0.041*
C17	0.4098 (6)	1.0500 (2)	0.2331 (5)	0.0320 (11)
H17A	0.4297	1.0841	0.1732	0.038*
C18	0.4897 (5)	0.9874 (2)	0.2569 (5)	0.0255 (10)
H18A	0.5667	0.9792	0.2156	0.031*
C19	0.5743 (5)	0.8157 (2)	0.5259 (4)	0.0181 (8)
C20	0.4710 (5)	0.7703 (2)	0.5528 (4)	0.0218 (9)
H20A	0.3760	0.7615	0.4841	0.026*
C21	0.5063 (5)	0.7376 (2)	0.6807 (4)	0.0244 (10)
H21A	0.4348	0.7069	0.6998	0.029*
C22	0.6457 (6)	0.7497 (2)	0.7807 (4)	0.0285 (10)
H22A	0.6704	0.7264	0.8674	0.034*
C23	0.7478 (5)	0.7954 (2)	0.7542 (4)	0.0272 (10)
H23A	0.8426	0.8038	0.8235	0.033*
C24	0.7148 (5)	0.8295 (2)	0.6282 (4)	0.0255 (9)
H24A	0.7853	0.8615	0.6110	0.031*
C25	0.4202 (4)	0.7925 (2)	0.2343 (4)	0.0168 (8)
H25A	0.4335	0.7447	0.2740	0.020*
H25B	0.3133	0.8067	0.2192	0.020*
C26	0.1709 (7)	0.5583 (3)	0.3620 (5)	0.0447 (14)
H26A	0.0865	0.5924	0.3219	0.054*
Cl1	0.3366 (3)	0.60552 (10)	0.4432 (2)	0.1039 (9)
Cl2	0.19826 (17)	0.50905 (9)	0.22600 (15)	0.0518 (4)
Cl3	0.11844 (19)	0.50376 (8)	0.47642 (15)	0.0522 (4)

Atomic displacement parameters (Ų)

	U^11	U^22	U^33	U^12	U^13	U^23
Sn	0.01542 (13)	0.01735 (13)	0.01582 (13)	0.00235 (11)	0.00450 (10)	0.00282 (10)
I1	0.02927 (16)	0.01839 (14)	0.02235 (14)	0.00030 (12)	0.00790 (12)	0.00269 (11)
I2	0.03002 (16)	0.03117 (15)	0.02356 (14)	0.01382 (13)	0.01252 (12)	0.00496 (13)
I3	0.01861 (14)	0.03691 (17)	0.02288 (14)	−0.00201 (13)	0.00001 (11)	0.00444 (13)
I4	0.02432 (14)	0.02220 (14)	0.02621 (15)	−0.00028 (12)	0.00951 (12)	0.00677 (11)
P1	0.0163 (5)	0.0144 (5)	0.0159 (5)	−0.0010 (4)	0.0053 (4)	−0.0008 (4)
P2	0.0160 (5)	0.0178 (5)	0.0132 (5)	0.0002 (5)	0.0027 (4)	0.0005 (4)
O1	0.0178 (14)	0.0193 (15)	0.0154 (14)	−0.0023 (11)	0.0041 (11)	−0.0042 (11)
O2	0.0173 (14)	0.0179 (15)	0.0133 (13)	0.0013 (11)	0.0029 (11)	0.0007 (11)
C1	0.024 (2)	0.015 (2)	0.016 (2)	−0.0008 (17)	0.0017 (17)	0.0056 (16)
C2	0.021 (2)	0.037 (3)	0.038 (3)	0.006 (2)	0.006 (2)	0.009 (2)
C3	0.035 (3)	0.037 (3)	0.050 (3)	0.012 (2)	0.006 (3)	0.019 (3)
C4	0.037 (3)	0.035 (3)	0.060 (4)	0.009 (2)	−0.005 (3)	0.023 (3)
C5	0.034 (3)	0.036 (3)	0.035 (3)	−0.009 (2)	0.003 (2)	0.017 (2)
C6	0.020 (2)	0.034 (3)	0.024 (2)	−0.001 (2)	0.0028 (18)	0.007 (2)
C7	0.018 (2)	0.022 (2)	0.0162 (19)	−0.0016 (17)	0.0069 (16)	−0.0033 (17)
C8	0.029 (3)	0.027 (2)	0.021 (2)	−0.006 (2)	0.0034 (19)	−0.0019 (18)
C9	0.030 (3)	0.040 (3)	0.018 (2)	−0.006 (2)	−0.0014 (19)	0.000 (2)
C10	0.033 (3)	0.033 (3)	0.023 (2)	−0.011 (2)	0.005 (2)	−0.007 (2)
C11	0.038 (3)	0.025 (3)	0.030 (3)	−0.003 (2)	0.006 (2)	−0.002 (2)
C12	0.029 (3)	0.023 (2)	0.019 (2)	−0.0035 (19)	0.0013 (19)	−0.0034 (18)
C13	0.017 (2)	0.0147 (19)	0.023 (2)	0.0010 (16)	0.0021 (17)	−0.0006 (17)
C14	0.026 (2)	0.020 (2)	0.043 (3)	−0.0018 (19)	0.019 (2)	−0.005 (2)
C15	0.026 (3)	0.026 (3)	0.058 (3)	0.000 (2)	0.025 (2)	−0.008 (2)
C16	0.035 (3)	0.016 (2)	0.046 (3)	0.006 (2)	0.004 (2)	−0.002 (2)
C17	0.040 (3)	0.023 (2)	0.033 (3)	0.000 (2)	0.012 (2)	0.004 (2)
C18	0.030 (2)	0.020 (2)	0.026 (2)	−0.0014 (19)	0.010 (2)	−0.0008 (18)
C19	0.025 (2)	0.016 (2)	0.0158 (19)	0.0014 (17)	0.0098 (17)	−0.0028 (16)
C20	0.017 (2)	0.025 (2)	0.024 (2)	−0.0006 (17)	0.0089 (18)	−0.0023 (17)
C21	0.028 (2)	0.027 (2)	0.023 (2)	0.0009 (19)	0.0145 (19)	0.0016 (18)
C22	0.046 (3)	0.027 (2)	0.014 (2)	0.005 (2)	0.011 (2)	0.0030 (18)
C23	0.032 (3)	0.033 (3)	0.015 (2)	0.004 (2)	0.0050 (18)	−0.0048 (19)
C24	0.026 (2)	0.026 (2)	0.022 (2)	−0.0040 (19)	0.0036 (18)	−0.0037 (19)
C25	0.0190 (19)	0.0148 (18)	0.0162 (19)	−0.0010 (18)	0.0048 (15)	0.0025 (17)
C26	0.059 (4)	0.027 (3)	0.036 (3)	−0.003 (3)	−0.002 (3)	0.010 (2)
Cl1	0.1176 (17)	0.0573 (12)	0.0806 (14)	−0.0501 (12)	−0.0484 (12)	0.0197 (10)
Cl2	0.0441 (8)	0.0688 (10)	0.0441 (8)	0.0007 (7)	0.0161 (7)	0.0017 (7)
Cl3	0.0719 (10)	0.0461 (8)	0.0415 (8)	0.0182 (8)	0.0221 (7)	0.0119 (7)

Geometric parameters (Å, º)

Sn—O1	2.136 (3)	C10—H10A	0.9500
Sn—O2	2.157 (3)	C11—C12	1.379 (6)
Sn—I3	2.7770 (4)	C11—H11A	0.9500
Sn—I4	2.7805 (4)	C12—H12A	0.9500
Sn—I2	2.7911 (4)	C13—C18	1.383 (6)
Sn—I1	2.8199 (4)	C13—C14	1.395 (6)
P1—O1	1.524 (3)	C14—C15	1.375 (7)
P1—C13	1.788 (4)	C14—H14A	0.9500
P1—C19	1.790 (4)	C15—C16	1.366 (7)
P1—C25	1.828 (4)	C15—H15A	0.9500
P2—O2	1.527 (3)	C16—C17	1.392 (7)
P2—C1	1.788 (4)	C16—H16A	0.9500
P2—C7	1.795 (4)	C17—C18	1.383 (6)
P2—C25	1.814 (4)	C17—H17A	0.9500
C1—C2	1.383 (6)	C18—H18A	0.9500
C1—C6	1.388 (6)	C19—C20	1.381 (6)
C2—C3	1.389 (7)	C19—C24	1.411 (6)
C2—H2A	0.9500	C20—C21	1.387 (6)
C3—C4	1.378 (8)	C20—H20A	0.9500
C3—H3A	0.9500	C21—C22	1.388 (6)
C4—C5	1.372 (8)	C21—H21A	0.9500
C4—H4A	0.9500	C22—C23	1.375 (7)
C5—C6	1.382 (7)	C22—H22A	0.9500
C5—H5A	0.9500	C23—C24	1.385 (6)
C6—H6A	0.9500	C23—H23A	0.9500
C7—C8	1.386 (6)	C24—H24A	0.9500
C7—C12	1.387 (6)	C25—H25A	0.9900
C8—C9	1.391 (6)	C25—H25B	0.9900
C8—H8A	0.9500	C26—Cl3	1.742 (6)
C9—C10	1.377 (7)	C26—Cl1	1.746 (6)
C9—H9A	0.9500	C26—Cl2	1.758 (6)
C10—C11	1.397 (7)	C26—H26A	1.0000
O1—Sn—O2	81.11 (10)	C9—C10—H10A	119.8
O1—Sn—I3	87.62 (7)	C11—C10—H10A	119.8
O2—Sn—I3	168.16 (7)	C12—C11—C10	119.4 (4)
O1—Sn—I4	84.36 (8)	C12—C11—H11A	120.3
O2—Sn—I4	89.34 (7)	C10—C11—H11A	120.3
I3—Sn—I4	93.196 (12)	C11—C12—C7	120.2 (4)
O1—Sn—I2	170.71 (7)	C11—C12—H12A	119.9
O2—Sn—I2	90.68 (7)	C7—C12—H12A	119.9
I3—Sn—I2	100.824 (13)	C18—C13—C14	119.5 (4)
I4—Sn—I2	91.247 (12)	C18—C13—P1	120.3 (3)
O1—Sn—I1	92.43 (8)	C14—C13—P1	120.1 (3)
O2—Sn—I1	86.79 (7)	C15—C14—C13	120.0 (4)
I3—Sn—I1	90.070 (12)	C15—C14—H14A	120.0
I4—Sn—I1	175.320 (14)	C13—C14—H14A	120.0
I2—Sn—I1	91.431 (12)	C16—C15—C14	120.6 (4)
O1—P1—C13	108.51 (18)	C16—C15—H15A	119.7
O1—P1—C19	111.71 (18)	C14—C15—H15A	119.7
C13—P1—C19	111.74 (19)	C15—C16—C17	120.0 (4)
O1—P1—C25	109.74 (17)	C15—C16—H16A	120.0
C13—P1—C25	108.71 (19)	C17—C16—H16A	120.0
C19—P1—C25	106.37 (19)	C18—C17—C16	119.9 (4)
O2—P2—C1	113.34 (18)	C18—C17—H17A	120.1
O2—P2—C7	109.60 (18)	C16—C17—H17A	120.1
C1—P2—C7	108.48 (19)	C13—C18—C17	120.0 (4)
O2—P2—C25	110.39 (17)	C13—C18—H18A	120.0
C1—P2—C25	108.8 (2)	C17—C18—H18A	120.0
C7—P2—C25	105.94 (19)	C20—C19—C24	120.3 (4)
P1—O1—Sn	135.20 (17)	C20—C19—P1	122.4 (3)
P2—O2—Sn	136.45 (16)	C24—C19—P1	117.0 (3)
C2—C1—C6	119.7 (4)	C19—C20—C21	119.7 (4)
C2—C1—P2	120.7 (3)	C19—C20—H20A	120.1
C6—C1—P2	119.6 (3)	C21—C20—H20A	120.1
C1—C2—C3	119.9 (5)	C20—C21—C22	120.3 (4)
C1—C2—H2A	120.0	C20—C21—H21A	119.8
C3—C2—H2A	120.0	C22—C21—H21A	119.8
C4—C3—C2	119.7 (5)	C23—C22—C21	119.9 (4)
C4—C3—H3A	120.2	C23—C22—H22A	120.1
C2—C3—H3A	120.2	C21—C22—H22A	120.1
C5—C4—C3	120.8 (5)	C22—C23—C24	121.1 (4)
C5—C4—H4A	119.6	C22—C23—H23A	119.5
C3—C4—H4A	119.6	C24—C23—H23A	119.5
C4—C5—C6	119.7 (5)	C23—C24—C19	118.7 (4)
C4—C5—H5A	120.1	C23—C24—H24A	120.7
C6—C5—H5A	120.1	C19—C24—H24A	120.7
C5—C6—C1	120.2 (4)	P2—C25—P1	113.0 (2)
C5—C6—H6A	119.9	P2—C25—H25A	109.0
C1—C6—H6A	119.9	P1—C25—H25A	109.0
C8—C7—C12	120.3 (4)	P2—C25—H25B	109.0
C8—C7—P2	121.2 (3)	P1—C25—H25B	109.0
C12—C7—P2	118.4 (3)	H25A—C25—H25B	107.8
C7—C8—C9	119.5 (4)	Cl3—C26—Cl1	112.4 (3)
C7—C8—H8A	120.2	Cl3—C26—Cl2	110.5 (3)
C9—C8—H8A	120.2	Cl1—C26—Cl2	108.9 (4)
C10—C9—C8	120.0 (4)	Cl3—C26—H26A	108.3
C10—C9—H9A	120.0	Cl1—C26—H26A	108.3
C8—C9—H9A	120.0	Cl2—C26—H26A	108.3
C9—C10—C11	120.4 (4)
C13—P1—O1—Sn	−154.2 (2)	C9—C10—C11—C12	−0.5 (8)
C19—P1—O1—Sn	82.2 (3)	C10—C11—C12—C7	1.6 (7)
C25—P1—O1—Sn	−35.5 (3)	C8—C7—C12—C11	−1.7 (7)
O2—Sn—O1—P1	54.1 (2)	P2—C7—C12—C11	179.9 (4)
I3—Sn—O1—P1	−122.2 (2)	O1—P1—C13—C18	24.9 (4)
I4—Sn—O1—P1	144.3 (2)	C19—P1—C13—C18	148.5 (4)
I1—Sn—O1—P1	−32.3 (2)	C25—P1—C13—C18	−94.4 (4)
C1—P2—O2—Sn	97.2 (3)	O1—P1—C13—C14	−159.1 (3)
C7—P2—O2—Sn	−141.4 (2)	C19—P1—C13—C14	−35.5 (4)
C25—P2—O2—Sn	−25.1 (3)	C25—P1—C13—C14	81.6 (4)
O1—Sn—O2—P2	−16.7 (2)	C18—C13—C14—C15	1.7 (7)
I3—Sn—O2—P2	1.4 (6)	P1—C13—C14—C15	−174.3 (4)
I4—Sn—O2—P2	−101.1 (2)	C13—C14—C15—C16	−0.7 (8)
I2—Sn—O2—P2	167.6 (2)	C14—C15—C16—C17	0.3 (8)
I1—Sn—O2—P2	76.2 (2)	C15—C16—C17—C18	−0.9 (8)
O2—P2—C1—C2	−159.9 (3)	C14—C13—C18—C17	−2.3 (7)
C7—P2—C1—C2	78.1 (4)	P1—C13—C18—C17	173.7 (3)
C25—P2—C1—C2	−36.7 (4)	C16—C17—C18—C13	1.9 (7)
O2—P2—C1—C6	22.7 (4)	O1—P1—C19—C20	−144.0 (3)
C7—P2—C1—C6	−99.3 (4)	C13—P1—C19—C20	94.2 (4)
C25—P2—C1—C6	145.9 (3)	C25—P1—C19—C20	−24.3 (4)
C6—C1—C2—C3	−0.5 (7)	O1—P1—C19—C24	30.0 (4)
P2—C1—C2—C3	−177.9 (4)	C13—P1—C19—C24	−91.8 (4)
C1—C2—C3—C4	0.6 (8)	C25—P1—C19—C24	149.7 (3)
C2—C3—C4—C5	0.1 (9)	C24—C19—C20—C21	−0.6 (6)
C3—C4—C5—C6	−0.8 (9)	P1—C19—C20—C21	173.2 (3)
C4—C5—C6—C1	0.9 (8)	C19—C20—C21—C22	−0.8 (7)
C2—C1—C6—C5	−0.3 (7)	C20—C21—C22—C23	1.5 (7)
P2—C1—C6—C5	177.1 (4)	C21—C22—C23—C24	−0.6 (7)
O2—P2—C7—C8	−130.5 (4)	C22—C23—C24—C19	−0.8 (7)
C1—P2—C7—C8	−6.3 (4)	C20—C19—C24—C23	1.4 (6)
C25—P2—C7—C8	110.4 (4)	P1—C19—C24—C23	−172.7 (3)
O2—P2—C7—C12	47.8 (4)	O2—P2—C25—P1	52.7 (3)
C1—P2—C7—C12	172.0 (3)	C1—P2—C25—P1	−72.2 (3)
C25—P2—C7—C12	−71.3 (4)	C7—P2—C25—P1	171.3 (2)
C12—C7—C8—C9	0.8 (7)	O1—P1—C25—P2	−27.7 (3)
P2—C7—C8—C9	179.1 (3)	C13—P1—C25—P2	90.8 (3)
C7—C8—C9—C10	0.3 (7)	C19—P1—C25—P2	−148.7 (2)
C8—C9—C10—C11	−0.5 (7)