Literature DB >> 26594399

Crystal structure of (μ-4-hy-droxy-benzene-thiol-ato-κ(2) S:S)bis-(μ-phenyl-methane-thiol-ato-κ(2) S:S)bis-[(η(6)-1-isopropyl-4-methyl-benzene)-ruthenium(II)] tetra-fluorido-borate.

David Stíbal1, Georg Süss-Fink1, Bruno Therrien1.   

Abstract

The crystal structure of the dinuclear arene ruthenium title complex, [Ru2(C6H5OS)(C7H7S)2(C10H14)2]BF4, shows the two Ru(II) atoms to be bridged by two benzyl-thio-pheno-late units and one 4-hy-droxy-thio-pheno-late unit, with the remaining three coordination sites of each Ru(II) atom being occupied by p-cymene ligands, completing the typical piano-stool coordination geometry. The BF4 (-) counter-anion is surrounded by four cationic dinuclear complexes, showing an O-H⋯F hydrogen bond and several weak C-H⋯F inter-actions. This is the first example of an X-ray analysis of a mixed dinuclear tri-thiol-ate arene ruthenium(II) complex.

Entities:  

Keywords:  crystal structure; piano-stool coordination geometry; ruthenium complex; thiol­ate ligands

Year:  2015        PMID: 26594399      PMCID: PMC4647355          DOI: 10.1107/S2056989015016953

Source DB:  PubMed          Journal:  Acta Crystallogr E Crystallogr Commun


Chemical context

In the search for novel metal-based anti­cancer agents, several series of dinuclear tri­thiol­ate arene ruthenium complexes have been synthesized by our group (Gras et al., 2010 ▸; Giannini et al., 2012 ▸, 2013a ▸). The biological studies in vitro showed the chloride salts of these complexes to have IC50 values regularly in the nanomolar range, making them some of the most active ruthenium complexes found to date. The recent discovery of di­thiol­ate complexes (Ibao et al., 2012 ▸) allowed us to synthesize the so-called mixed tri­thiol­ate complexes of the type [(p-MeC6H4 Pr)2Ru2(SCH2 R 1)2(S-p-C6H4-R 2]+ (R 1 = C6H5, CH2C6H5, p-C6H4 Bu; R 2 = H, OH, F, Br, Pr, Bu). All of the complexes were found to be highly cytotoxic against ovarian cancer cell lines A2780 and A2780cisR as chloride salts, none of them could however be crystallized and analyzed by X-ray crystallography (Giannini et al., 2013b ▸). Herein we report the isolation and the crystal structure of the title compound, [(p-MeC6H4 Pr)2Ru2(SCH2C6H5)2(S-p-C6H4OH)]BF4, (I), the first reported structure of a mixed tri­thiol­ate complex.

Structural commentary

The structures of the mol­ecular components of compound (I) are presented in Fig. 1 ▸. Both RuII atoms adopt the typical piano-stool geometry with the p-cymene ligand being bound facially, formally occupying three coordination sites; the other three positions are occupied by two benzyl­thio­pheno­late units and one 4-hy­droxy­thio­pheno­late unit. In agreement with the electron count, there is no metalmetal bond, the Ru⋯Ru distance being 3.3632 (4) Å. The inter­atomic distances between Ru1 and S1, S2 and S3 are 2.3878 (9), 2.4023 (9) and 2.3813 (8) Å, respectively, and between Ru2 and S1, S2 and S3 2.3992 (9), 2.3991 (8) and 2.3882 (8) Å, respectively, showing that the central diruthenium tri­thiol­ate unit is not symmetric. The presence of the two bent benzyl­thiol­ate ligands forces the dinuclear arene ruthenium unit to adopt a distorted geometry – the angle between the two p-cymene planes (C1–C6 and C11–C16) is 6.2 (2)°. The distances between the RuII atoms and the centroids of the associated rings are 1.708 and 1.709 Å.
Figure 1

The structure of the mol­ecular components of (I). Displacement ellipsoids are drawn at the 50% probability level.

Supra­molecular features

In the crystal packing of (I), the BF4anion inter­acts with the –OH group of the 4-hy­droxy­thio­pheno­late unit. In addition, weak C—H⋯F inter­actions are observed (Table 1 ▸), thus creating around the BF4 anion a densely packed arrangement (Fig. 2 ▸). No significant C—H⋯π or π–π stacking inter­actions are observed in the crystal structure.
Table 1

Hydrogen-bond geometry (, )

DHA DHHA D A DHA
O1H1F10.821.992.773(9)161
C3H3F3i 0.932.523.340(11)148
C30H30F2i 0.932.603.472(9)156
C6H6F4ii 0.932.343.249(10)166

Symmetry codes: (i) ; (ii) .

Figure 2

Surroundings of the BF4 − anion in the crystal packing of (I).

Synthesis and crystallization

Complex (I) was obtained from the reaction of 0.127 mmol (100 mg) of the neutral di­thiol­ate precursor [(p-MeC6H4 Pr)2Ru2(SCH2C6H5)2Cl2] (Ibao et al., 2012 ▸) with three equivalents of 4-hy­droxy­thio­phenol in refluxing ethanol. The product was isolated by column chromatography on silica gel, using the solvent mixture CH2Cl2/EtOH 7:1 (v/v) as eluent. The orange band was collected; the product was stirred overnight with ten equivalents of NaBF4 and isolated by filtration and evaporation of the solvent. X-ray quality crystals were obtained by slow diffusion of diethyl ether vapors into the solution of (I) in di­chloro­methane. Yield: 111 mg (94%). ESI–MS (MeOH/CH2Cl2): m/z = 842.3 [M]+. 1H NMR (400 MHz, CDCl3): δ = 7.41 (m, 10H, SCH2C6H5; 2H, S-p-C6H4OH), 7.00 (d, 3 J = 8 Hz, 2H, S-p-C6H4OH) 5.06 [d, 3 J = 6.0 Hz, 2H, p-CH3C6H4CH(CH3)2], 4.94 [d, 3 J = 6.0 Hz, 2H, p-CH3C6H4CH(CH3)2], 4.71 [m, 4H, p-CH3C6H4CH(CH3)2], 3.62 (s, 2H, SCH2C6H5), 3.45 (s, 2H, SCH2C6H5), 2.04 [sept, 3 J = 6.8 Hz, 2H, p-CH3C6H4CH(CH3)2], 1.73 (s, 6H, p-CH3C6H4CH(CH3)2), 1.05 [d, 3 J = 6.8 Hz, 6H, p-CH3C6H4CH(CH3)2], 0.99 [d, 3 J = 6.8 Hz, 6H, p-CH3C6H4CH(CH3)2] p.p.m. 13C{1H} NMR (100 MHz,CDCl3): δ = 159.9, 139.9, 139.7, 133.3, 129.5, 129.2, 128.8, 128.7, 128.2, 128.1, 124.0, 117.1, 107.5, 99.7, 84.1, 83.7, 83.2, 82.0, 39.9, 39.5, 31.0, 23.1, 22.7, 18.0 p.p.m.

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 2 ▸. All H atoms were included in calculated positions and treated as riding atoms, with C—H = 0.93 Å for Carom and 0.96 Å for CH3, and with U iso(H) = 1.2U eq(C) or 1.5U eq(C) for methyl H atoms.
Table 2

Experimental details

Crystal data
Chemical formula[Ru2(C6H5OS)(C7H7S)2(C10H14)2]BF4
M r 928.91
Crystal system, space groupMonoclinic, C c
Temperature (K)173
a, b, c ()15.4807(10), 14.3435(11), 17.7605(10)
()99.435(5)
V (3)3890.3(4)
Z 4
Radiation typeMo K
(mm1)0.99
Crystal size (mm)0.22 0.20 0.18
 
Data collection
DiffractometerStoe IPDS
No. of measured, independent and observed [I > 2(I)] reflections34511, 10178, 8902
R int 0.060
(sin /)max (1)0.690
 
Refinement
R[F 2 > 2(F 2)], wR(F 2), S 0.032, 0.074, 0.95
No. of reflections10178
No. of parameters466
No. of restraints2
H-atom treatmentH-atom parameters constrained
max, min (e 3)0.52, 0.69
Absolute structureFlack x determined using 3741 quotients [(I +)(I )]/[(I +)+(I )] (Parsons et al., 2013).
Absolute structure parameter0.01(2)

Computer programs: EXPOSE, CELL and INTEGRATE in IPDS Software (Stoe Cie, 2000 ▸), SHELXS97 and SHELXL97 (Sheldrick, 2008 ▸), SHELXL2014 (Sheldrick, 2015 ▸) and ORTEP-32 (Farrugia, 2012 ▸).

Crystal structure: contains datablock(s) I, global. DOI: 10.1107/S2056989015016953/wm5210sup1.cif Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989015016953/wm5210Isup2.hkl CCDC reference: 1423473 Additional supporting information: crystallographic information; 3D view; checkCIF report
[Ru2(C6H5OS)(C7H7S)2(C10H14)2]BF4F(000) = 1888
Mr = 928.91Dx = 1.586 Mg m3
Monoclinic, CcMo Kα radiation, λ = 0.71073 Å
Hall symbol: C -2ycCell parameters from 8000 reflections
a = 15.4807 (10) Åθ = 2.1–28.7°
b = 14.3435 (11) ŵ = 0.99 mm1
c = 17.7605 (10) ÅT = 173 K
β = 99.435 (5)°Block, red
V = 3890.3 (4) Å30.22 × 0.20 × 0.18 mm
Z = 4
Stoe IPDS diffractometer8902 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tubeRint = 0.060
Graphite monochromatorθmax = 29.4°, θmin = 2.0°
Detector resolution: 0.81 pixels mm-1h = −21→21
phi oscillation scansk = −19→19
34511 measured reflectionsl = −24→24
10178 independent reflections
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.032H-atom parameters constrained
wR(F2) = 0.074w = 1/[σ2(Fo2) + (0.0431P)2] where P = (Fo2 + 2Fc2)/3
S = 0.95(Δ/σ)max = 0.001
10178 reflectionsΔρmax = 0.52 e Å3
466 parametersΔρmin = −0.69 e Å3
2 restraintsAbsolute structure: Flack x determined using 3741 quotients [(I+)-(I-)]/[(I+)+(I-)] (Parsons et al., 2013).
Primary atom site location: structure-invariant direct methodsAbsolute structure parameter: −0.01 (2)
Experimental. A crystal was mounted at 173 K on a Stoe Image Plate Diffraction System (Stoe & Cie, 2000) using Mo Kα graphite monochromated radiation. Image plate distance 100 mm, φ oscillation scans 0 - 180°, step Δφ = 1.2°, 5 minutes per frame.
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.
Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.
xyzUiso*/Ueq
C10.3292 (2)0.1913 (3)−0.0509 (2)0.0418 (9)
C20.3924 (2)0.1437 (2)0.0030 (2)0.0331 (8)
H20.42490.0957−0.01360.040*
C30.4066 (2)0.1680 (3)0.0807 (3)0.0374 (8)
H30.44900.13660.11460.045*
C40.3569 (3)0.2402 (3)0.1080 (3)0.0465 (10)
C50.2935 (3)0.2860 (3)0.0556 (3)0.0528 (13)
H50.26010.33300.07250.063*
C60.2797 (3)0.2620 (3)−0.0221 (3)0.0539 (13)
H60.23690.2934−0.05550.065*
C70.3156 (3)0.1726 (5)−0.1358 (3)0.0646 (15)
H70.25310.1806−0.15560.077*
C80.3413 (5)0.0761 (5)−0.1566 (3)0.085 (2)
H8A0.40370.0691−0.14360.128*
H8B0.32380.0665−0.21040.128*
H8C0.31300.0310−0.12900.128*
C90.3654 (6)0.2436 (6)−0.1742 (5)0.110 (3)
H9A0.42710.2323−0.16050.165*
H9B0.35200.3050−0.15810.165*
H9C0.34890.2386−0.22860.165*
C100.3719 (3)0.2648 (4)0.1917 (3)0.0667 (16)
H10A0.42220.30470.20300.100*
H10B0.38170.20880.22150.100*
H10C0.32130.29650.20380.100*
C11−0.0326 (3)−0.0067 (3)0.0892 (3)0.0397 (10)
C120.0199 (3)−0.0321 (3)0.1574 (3)0.0441 (10)
H120.01790.00320.20100.053*
C130.0767 (3)−0.1107 (3)0.1620 (3)0.0466 (10)
H130.1105−0.12680.20840.056*
C140.0818 (3)−0.1643 (3)0.0962 (3)0.0484 (11)
C150.0298 (3)−0.1365 (3)0.0277 (3)0.0472 (10)
H150.0328−0.1701−0.01660.057*
C16−0.0262 (2)−0.0602 (3)0.0242 (3)0.0419 (9)
H16−0.0601−0.0443−0.02220.050*
C17−0.0956 (3)0.0766 (3)0.0801 (3)0.0545 (12)
H17−0.09070.10710.03160.065*
C18−0.0757 (4)0.1487 (4)0.1421 (5)0.082 (2)
H18A−0.07990.12080.19050.123*
H18B−0.11700.19890.13240.123*
H18C−0.01750.17240.14300.123*
C19−0.1899 (3)0.0414 (4)0.0745 (6)0.095 (3)
H19A−0.2025−0.00170.03280.143*
H19B−0.22960.09320.06600.143*
H19C−0.19670.01070.12120.143*
C200.1397 (3)−0.2491 (3)0.0989 (5)0.091 (3)
H20A0.1881−0.24280.13990.137*
H20B0.1613−0.25500.05150.137*
H20C0.1065−0.30370.10710.137*
C210.1759 (2)0.1523 (2)0.2144 (2)0.0318 (7)
C220.1763 (2)0.1270 (3)0.2903 (2)0.0381 (8)
H220.19590.06800.30690.046*
C230.1479 (3)0.1880 (3)0.3412 (2)0.0456 (9)
H230.14760.16980.39140.055*
C240.1202 (2)0.2753 (3)0.3176 (2)0.0431 (9)
C250.1177 (3)0.3026 (3)0.2427 (2)0.0407 (8)
H250.09760.36170.22690.049*
C260.1457 (2)0.2409 (3)0.1908 (2)0.0365 (8)
H260.14400.25890.14030.044*
C270.3138 (2)−0.1002 (3)0.0697 (3)0.0413 (9)
H27A0.3159−0.08590.12340.050*
H27B0.2955−0.16460.06170.050*
C280.4040 (2)−0.0887 (3)0.0494 (3)0.0382 (9)
C290.4732 (3)−0.0540 (3)0.1000 (3)0.0463 (10)
H290.4660−0.04010.14970.056*
C300.5543 (3)−0.0392 (3)0.0774 (3)0.0540 (12)
H300.6005−0.01530.11210.065*
C310.5663 (3)−0.0597 (3)0.0048 (3)0.0536 (11)
H310.6203−0.0487−0.01010.064*
C320.4971 (3)−0.0975 (3)−0.0476 (3)0.0601 (13)
H320.5052−0.1129−0.09680.072*
C330.4171 (3)−0.1112 (3)−0.0250 (3)0.0500 (11)
H330.3710−0.1358−0.05950.060*
C340.0879 (2)0.1145 (3)−0.0955 (2)0.0406 (8)
H34A0.10730.1690−0.12050.049*
H34B0.12090.0612−0.10880.049*
C35−0.0078 (2)0.0988 (3)−0.1235 (2)0.0376 (8)
C36−0.0411 (3)0.0170 (3)−0.1584 (3)0.0511 (10)
H36−0.0032−0.0302−0.16780.061*
C37−0.1319 (4)0.0053 (4)−0.1796 (3)0.0602 (13)
H37−0.1538−0.0494−0.20360.072*
C38−0.1877 (3)0.0729 (4)−0.1652 (3)0.0652 (14)
H38−0.24780.0638−0.17820.078*
C39−0.1565 (3)0.1543 (5)−0.1317 (3)0.0691 (15)
H39−0.19500.2013−0.12290.083*
C40−0.0678 (3)0.1665 (3)−0.1112 (3)0.0494 (10)
H40−0.04720.2222−0.08820.059*
O10.0975 (2)0.3350 (3)0.3719 (2)0.0593 (8)
H10.08200.38520.35190.089*
S10.22003 (5)0.07062 (6)0.15529 (5)0.02976 (16)
S20.23352 (5)−0.02440 (6)0.01262 (5)0.02999 (17)
S30.11024 (5)0.13178 (6)0.00909 (5)0.02880 (17)
Ru10.265363 (15)0.136095 (17)0.044464 (15)0.02751 (6)
Ru20.107114 (15)−0.013494 (17)0.074285 (15)0.02631 (6)
B10.1140 (3)0.5937 (4)0.2810 (3)0.0508 (12)
F10.0880 (5)0.5128 (3)0.3096 (4)0.161 (3)
F20.1726 (2)0.5769 (3)0.23242 (19)0.0842 (11)
F30.0429 (4)0.6320 (7)0.2444 (4)0.196 (4)
F40.1457 (4)0.6454 (6)0.3380 (4)0.212 (5)
U11U22U33U12U13U23
C10.0331 (17)0.046 (2)0.049 (2)−0.0089 (16)0.0128 (17)0.0188 (18)
C20.0272 (16)0.0314 (17)0.043 (2)−0.0065 (13)0.0120 (15)0.0043 (15)
C30.0244 (15)0.0380 (19)0.050 (2)−0.0071 (14)0.0069 (15)0.0017 (18)
C40.0360 (18)0.035 (2)0.070 (3)−0.0164 (16)0.0148 (19)−0.009 (2)
C50.044 (2)0.0277 (19)0.093 (4)−0.0083 (16)0.030 (3)0.002 (2)
C60.037 (2)0.037 (2)0.091 (4)−0.0002 (16)0.020 (2)0.033 (2)
C70.044 (2)0.104 (4)0.048 (3)−0.009 (3)0.015 (2)0.029 (3)
C80.111 (5)0.102 (5)0.041 (3)−0.062 (4)0.011 (3)−0.002 (3)
C90.147 (7)0.088 (4)0.119 (6)0.024 (4)0.089 (5)0.058 (4)
C100.048 (2)0.073 (3)0.082 (4)−0.022 (2)0.021 (2)−0.042 (3)
C110.0280 (17)0.0348 (19)0.060 (3)−0.0046 (14)0.0184 (18)0.0097 (18)
C120.046 (2)0.050 (2)0.044 (2)−0.0096 (18)0.0295 (19)0.0008 (19)
C130.0347 (18)0.058 (2)0.049 (2)−0.0050 (17)0.0108 (17)0.030 (2)
C140.0350 (19)0.0304 (18)0.086 (4)−0.0031 (15)0.029 (2)0.017 (2)
C150.041 (2)0.040 (2)0.066 (3)−0.0169 (17)0.028 (2)−0.014 (2)
C160.0275 (17)0.054 (2)0.045 (2)−0.0154 (17)0.0077 (16)0.0044 (19)
C170.038 (2)0.041 (2)0.088 (4)0.0049 (17)0.020 (2)0.014 (2)
C180.058 (3)0.047 (3)0.147 (6)0.004 (2)0.034 (4)−0.018 (3)
C190.036 (2)0.049 (3)0.205 (8)0.001 (2)0.032 (4)−0.002 (4)
C200.051 (3)0.037 (2)0.197 (8)0.004 (2)0.053 (4)0.031 (4)
C210.0247 (14)0.0372 (18)0.0332 (18)−0.0013 (13)0.0034 (13)0.0016 (14)
C220.0385 (18)0.041 (2)0.0360 (19)0.0022 (15)0.0097 (15)0.0095 (15)
C230.047 (2)0.060 (3)0.033 (2)0.0005 (19)0.0154 (17)0.0044 (18)
C240.0354 (19)0.056 (2)0.041 (2)0.0008 (17)0.0153 (16)−0.0088 (18)
C250.0425 (19)0.0381 (19)0.042 (2)0.0079 (16)0.0078 (17)−0.0012 (16)
C260.0432 (19)0.0360 (18)0.0303 (18)0.0049 (15)0.0062 (15)0.0029 (14)
C270.0338 (18)0.0351 (19)0.058 (3)0.0087 (15)0.0176 (18)0.0067 (18)
C280.0307 (17)0.0327 (19)0.054 (2)0.0045 (14)0.0142 (17)0.0050 (17)
C290.041 (2)0.045 (2)0.054 (3)0.0077 (17)0.0079 (18)0.0115 (19)
C300.0323 (19)0.056 (3)0.070 (3)−0.0020 (18)−0.002 (2)0.014 (2)
C310.034 (2)0.051 (3)0.080 (3)0.0052 (18)0.022 (2)0.006 (2)
C320.054 (3)0.053 (3)0.082 (4)−0.005 (2)0.038 (3)−0.015 (3)
C330.040 (2)0.047 (2)0.067 (3)−0.0054 (17)0.020 (2)−0.014 (2)
C340.0354 (18)0.058 (2)0.0292 (19)0.0035 (16)0.0076 (15)0.0106 (17)
C350.0370 (18)0.043 (2)0.033 (2)−0.0005 (15)0.0069 (15)0.0046 (16)
C360.064 (3)0.050 (2)0.040 (2)0.003 (2)0.008 (2)−0.0050 (19)
C370.067 (3)0.054 (3)0.055 (3)−0.022 (2)−0.004 (2)−0.005 (2)
C380.047 (2)0.079 (4)0.064 (3)−0.006 (3)−0.008 (2)0.008 (3)
C390.039 (2)0.092 (4)0.071 (4)0.010 (2)−0.006 (2)−0.015 (3)
C400.039 (2)0.048 (2)0.057 (3)0.0047 (17)−0.0073 (19)−0.005 (2)
O10.071 (2)0.064 (2)0.0481 (18)0.0128 (17)0.0241 (16)−0.0114 (16)
S10.0282 (4)0.0300 (4)0.0310 (4)0.0016 (3)0.0046 (3)0.0047 (3)
S20.0257 (4)0.0291 (4)0.0370 (5)−0.0027 (3)0.0104 (3)0.0007 (3)
S30.0242 (4)0.0319 (4)0.0307 (4)−0.0001 (3)0.0057 (3)0.0069 (3)
Ru10.02280 (11)0.02572 (12)0.03464 (14)−0.00190 (10)0.00659 (10)0.00523 (11)
Ru20.02355 (11)0.02625 (12)0.03065 (13)−0.00107 (11)0.00895 (9)0.00414 (12)
B10.045 (2)0.054 (3)0.053 (3)0.005 (2)0.008 (2)−0.008 (2)
F10.235 (7)0.072 (3)0.220 (7)0.026 (3)0.171 (6)0.007 (3)
F20.080 (2)0.118 (3)0.060 (2)0.033 (2)0.0282 (17)0.0103 (19)
F30.111 (4)0.341 (11)0.141 (5)0.118 (5)0.035 (4)0.067 (6)
F40.189 (6)0.306 (9)0.170 (6)−0.184 (7)0.113 (5)−0.171 (6)
C1—C61.416 (7)C20—H20A0.9600
C1—C21.425 (6)C20—H20B0.9600
C1—C71.513 (7)C20—H20C0.9600
C1—Ru12.240 (4)C21—C261.395 (5)
C2—C31.406 (6)C21—C221.396 (5)
C2—Ru12.213 (3)C21—S11.782 (4)
C2—H20.9300C22—C231.382 (6)
C3—C41.421 (6)C22—H220.9300
C3—Ru12.224 (4)C23—C241.367 (6)
C3—H30.9300C23—H230.9300
C4—C51.400 (7)C24—O11.376 (5)
C4—C101.508 (7)C24—C251.382 (6)
C4—Ru12.233 (4)C25—C261.396 (5)
C5—C61.404 (8)C25—H250.9300
C5—Ru12.196 (4)C26—H260.9300
C5—H50.9300C27—C281.508 (5)
C6—Ru12.189 (4)C27—S21.828 (4)
C6—H60.9300C27—H27A0.9700
C7—C81.504 (9)C27—H27B0.9700
C7—C91.507 (8)C28—C291.375 (6)
C7—H70.9800C28—C331.406 (6)
C8—H8A0.9600C29—C301.395 (6)
C8—H8B0.9600C29—H290.9300
C8—H8C0.9600C30—C311.364 (8)
C9—H9A0.9600C30—H300.9300
C9—H9B0.9600C31—C321.408 (8)
C9—H9C0.9600C31—H310.9300
C10—H10A0.9600C32—C331.377 (6)
C10—H10B0.9600C32—H320.9300
C10—H10C0.9600C33—H330.9300
C11—C121.392 (7)C34—C351.501 (5)
C11—C161.403 (6)C34—S31.849 (4)
C11—C171.534 (6)C34—H34A0.9700
C11—Ru22.223 (4)C34—H34B0.9700
C12—C131.424 (6)C35—C401.385 (6)
C12—Ru22.174 (4)C35—C361.386 (6)
C12—H120.9300C36—C371.405 (7)
C13—C141.411 (7)C36—H360.9300
C13—Ru22.199 (4)C37—C381.350 (8)
C13—H130.9300C37—H370.9300
C14—C151.402 (7)C38—C391.363 (8)
C14—C201.507 (6)C38—H380.9300
C14—Ru22.244 (4)C39—C401.372 (6)
C15—C161.391 (6)C39—H390.9300
C15—Ru22.215 (4)C40—H400.9300
C15—H150.9300O1—H10.8200
C16—Ru22.213 (4)S1—Ru12.3878 (9)
C16—H160.9300S1—Ru22.3992 (9)
C17—C181.505 (8)S2—Ru22.3991 (8)
C17—C191.532 (6)S2—Ru12.4023 (9)
C17—H170.9800S3—Ru12.3813 (8)
C18—H18A0.9600S3—Ru22.3882 (8)
C18—H18B0.9600B1—F41.286 (7)
C18—H18C0.9600B1—F31.304 (7)
C19—H19A0.9600B1—F11.355 (7)
C19—H19B0.9600B1—F21.372 (6)
C19—H19C0.9600
C6—C1—C2117.0 (4)C25—C26—H26119.8
C6—C1—C7119.4 (4)C28—C27—S2112.0 (3)
C2—C1—C7123.6 (4)C28—C27—H27A109.2
C6—C1—Ru169.4 (2)S2—C27—H27A109.2
C2—C1—Ru170.3 (2)C28—C27—H27B109.2
C7—C1—Ru1133.2 (3)S2—C27—H27B109.2
C3—C2—C1121.4 (4)H27A—C27—H27B107.9
C3—C2—Ru171.9 (2)C29—C28—C33118.7 (4)
C1—C2—Ru172.4 (2)C29—C28—C27122.4 (4)
C3—C2—H2119.3C33—C28—C27118.8 (4)
C1—C2—H2119.3C28—C29—C30120.6 (4)
Ru1—C2—H2128.7C28—C29—H29119.7
C2—C3—C4120.6 (4)C30—C29—H29119.7
C2—C3—Ru171.1 (2)C31—C30—C29120.5 (4)
C4—C3—Ru171.7 (2)C31—C30—H30119.7
C2—C3—H3119.7C29—C30—H30119.7
C4—C3—H3119.7C30—C31—C32120.0 (4)
Ru1—C3—H3130.0C30—C31—H31120.0
C5—C4—C3118.4 (4)C32—C31—H31120.0
C5—C4—C10121.5 (4)C33—C32—C31119.1 (5)
C3—C4—C10120.1 (4)C33—C32—H32120.5
C5—C4—Ru170.2 (2)C31—C32—H32120.5
C3—C4—Ru171.1 (2)C32—C33—C28121.0 (4)
C10—C4—Ru1129.5 (3)C32—C33—H33119.5
C4—C5—C6121.0 (4)C28—C33—H33119.5
C4—C5—Ru173.0 (2)C35—C34—S3111.4 (3)
C6—C5—Ru171.1 (2)C35—C34—H34A109.3
C4—C5—H5119.5S3—C34—H34A109.3
C6—C5—H5119.5C35—C34—H34B109.3
Ru1—C5—H5128.8S3—C34—H34B109.3
C5—C6—C1121.7 (4)H34A—C34—H34B108.0
C5—C6—Ru171.6 (2)C40—C35—C36117.0 (4)
C1—C6—Ru173.3 (2)C40—C35—C34119.6 (4)
C5—C6—H6119.1C36—C35—C34123.4 (4)
C1—C6—H6119.1C35—C36—C37120.3 (4)
Ru1—C6—H6128.2C35—C36—H36119.9
C8—C7—C9109.5 (5)C37—C36—H36119.9
C8—C7—C1114.1 (4)C38—C37—C36120.4 (4)
C9—C7—C1109.5 (6)C38—C37—H37119.8
C8—C7—H7107.8C36—C37—H37119.8
C9—C7—H7107.8C37—C38—C39120.4 (5)
C1—C7—H7107.8C37—C38—H38119.8
C7—C8—H8A109.5C39—C38—H38119.8
C7—C8—H8B109.5C38—C39—C40119.5 (5)
H8A—C8—H8B109.5C38—C39—H39120.3
C7—C8—H8C109.5C40—C39—H39120.3
H8A—C8—H8C109.5C39—C40—C35122.5 (5)
H8B—C8—H8C109.5C39—C40—H40118.8
C7—C9—H9A109.5C35—C40—H40118.8
C7—C9—H9B109.5C24—O1—H1109.5
H9A—C9—H9B109.5C21—S1—Ru1114.81 (12)
C7—C9—H9C109.5C21—S1—Ru2111.85 (11)
H9A—C9—H9C109.5Ru1—S1—Ru289.27 (3)
H9B—C9—H9C109.5C27—S2—Ru2108.48 (13)
C4—C10—H10A109.5C27—S2—Ru1110.18 (15)
C4—C10—H10B109.5Ru2—S2—Ru188.93 (3)
H10A—C10—H10B109.5C34—S3—Ru1106.43 (12)
C4—C10—H10C109.5C34—S3—Ru2110.79 (14)
H10A—C10—H10C109.5Ru1—S3—Ru289.68 (3)
H10B—C10—H10C109.5C6—Ru1—C537.3 (2)
C12—C11—C16117.6 (4)C6—Ru1—C266.74 (14)
C12—C11—C17124.4 (4)C5—Ru1—C278.89 (15)
C16—C11—C17118.0 (4)C6—Ru1—C378.73 (16)
C12—C11—Ru269.6 (2)C5—Ru1—C366.47 (16)
C16—C11—Ru271.2 (2)C2—Ru1—C336.95 (15)
C17—C11—Ru2129.5 (3)C6—Ru1—C466.98 (19)
C11—C12—C13121.6 (4)C5—Ru1—C436.83 (18)
C11—C12—Ru273.5 (2)C2—Ru1—C467.04 (15)
C13—C12—Ru271.9 (2)C3—Ru1—C437.19 (15)
C11—C12—H12119.2C6—Ru1—C137.27 (17)
C13—C12—H12119.2C5—Ru1—C167.45 (18)
Ru2—C12—H12127.5C2—Ru1—C137.31 (14)
C14—C13—C12120.1 (4)C3—Ru1—C167.13 (15)
C14—C13—Ru273.2 (2)C4—Ru1—C179.82 (16)
C12—C13—Ru270.0 (2)C6—Ru1—S393.80 (11)
C14—C13—H13119.9C5—Ru1—S3103.06 (12)
C12—C13—H13119.9C2—Ru1—S3145.72 (11)
Ru2—C13—H13129.1C3—Ru1—S3169.43 (11)
C15—C14—C13117.4 (4)C4—Ru1—S3132.82 (11)
C15—C14—C20120.7 (5)C1—Ru1—S3111.14 (11)
C13—C14—C20121.8 (5)C6—Ru1—S1147.03 (15)
C15—C14—Ru270.5 (2)C5—Ru1—S1113.05 (15)
C13—C14—Ru269.7 (2)C2—Ru1—S1133.72 (11)
C20—C14—Ru2131.6 (3)C3—Ru1—S1104.49 (11)
C16—C15—C14121.9 (4)C4—Ru1—S195.42 (12)
C16—C15—Ru271.6 (2)C1—Ru1—S1170.98 (11)
C14—C15—Ru272.8 (2)S3—Ru1—S177.72 (3)
C16—C15—H15119.1C6—Ru1—S2134.30 (16)
C14—C15—H15119.1C5—Ru1—S2171.64 (15)
Ru2—C15—H15129.0C2—Ru1—S297.38 (10)
C15—C16—C11121.4 (4)C3—Ru1—S2114.82 (11)
C15—C16—Ru271.8 (2)C4—Ru1—S2148.05 (12)
C11—C16—Ru272.0 (2)C1—Ru1—S2105.05 (12)
C15—C16—H16119.3S3—Ru1—S275.75 (3)
C11—C16—H16119.3S1—Ru1—S274.95 (3)
Ru2—C16—H16129.5C12—Ru2—C1338.01 (17)
C18—C17—C19110.6 (5)C12—Ru2—C1666.05 (17)
C18—C17—C11114.1 (5)C13—Ru2—C1678.40 (16)
C19—C17—C11109.4 (4)C12—Ru2—C1578.34 (16)
C18—C17—H17107.5C13—Ru2—C1566.03 (18)
C19—C17—H17107.5C16—Ru2—C1536.62 (17)
C11—C17—H17107.5C12—Ru2—C1136.90 (18)
C17—C18—H18A109.5C13—Ru2—C1167.55 (15)
C17—C18—H18B109.5C16—Ru2—C1136.87 (16)
H18A—C18—H18B109.5C15—Ru2—C1166.59 (15)
C17—C18—H18C109.5C12—Ru2—C1467.56 (16)
H18A—C18—H18C109.5C13—Ru2—C1437.03 (19)
H18B—C18—H18C109.5C16—Ru2—C1466.43 (17)
C17—C19—H19A109.5C15—Ru2—C1436.65 (19)
C17—C19—H19B109.5C11—Ru2—C1479.68 (14)
H19A—C19—H19B109.5C12—Ru2—S3120.02 (12)
C17—C19—H19C109.5C13—Ru2—S3157.02 (13)
H19A—C19—H19C109.5C16—Ru2—S399.26 (12)
H19B—C19—H19C109.5C15—Ru2—S3124.53 (14)
C14—C20—H20A109.5C11—Ru2—S396.70 (10)
C14—C20—H20B109.5C14—Ru2—S3160.63 (15)
H20A—C20—H20B109.5C12—Ru2—S2161.04 (13)
C14—C20—H20C109.5C13—Ru2—S2124.58 (12)
H20A—C20—H20C109.5C16—Ru2—S2124.98 (12)
H20B—C20—H20C109.5C15—Ru2—S2102.07 (11)
C26—C21—C22118.4 (3)C11—Ru2—S2159.91 (13)
C26—C21—S1124.4 (3)C14—Ru2—S2101.26 (10)
C22—C21—S1117.2 (3)S3—Ru2—S275.68 (3)
C23—C22—C21121.1 (4)C12—Ru2—S197.29 (12)
C23—C22—H22119.5C13—Ru2—S196.53 (12)
C21—C22—H22119.5C16—Ru2—S1158.92 (12)
C24—C23—C22119.9 (4)C15—Ru2—S1157.00 (14)
C24—C23—H23120.1C11—Ru2—S1122.26 (13)
C22—C23—H23120.1C14—Ru2—S1120.75 (14)
C23—C24—O1117.3 (4)S3—Ru2—S177.37 (3)
C23—C24—C25120.8 (4)S2—Ru2—S174.81 (3)
O1—C24—C25121.9 (4)F4—B1—F3109.4 (7)
C24—C25—C26119.6 (4)F4—B1—F1107.3 (6)
C24—C25—H25120.2F3—B1—F1105.7 (6)
C26—C25—H25120.2F4—B1—F2113.0 (5)
C21—C26—C25120.3 (4)F3—B1—F2110.6 (5)
C21—C26—H26119.8F1—B1—F2110.6 (5)
C6—C1—C2—C3−1.9 (5)C2—C1—Ru1—S2−82.3 (2)
C7—C1—C2—C3175.7 (4)C7—C1—Ru1—S235.7 (5)
Ru1—C1—C2—C3−54.9 (3)C34—S3—Ru1—C663.2 (2)
C6—C1—C2—Ru153.1 (3)Ru2—S3—Ru1—C6174.80 (16)
C7—C1—C2—Ru1−129.4 (4)C34—S3—Ru1—C599.8 (2)
C1—C2—C3—C41.1 (5)Ru2—S3—Ru1—C5−148.57 (15)
Ru1—C2—C3—C4−54.1 (3)C34—S3—Ru1—C210.4 (2)
C1—C2—C3—Ru155.1 (3)Ru2—S3—Ru1—C2122.06 (17)
C2—C3—C4—C50.2 (5)C34—S3—Ru1—C3107.7 (6)
Ru1—C3—C4—C5−53.6 (3)Ru2—S3—Ru1—C3−140.7 (6)
C2—C3—C4—C10179.2 (4)C34—S3—Ru1—C4125.0 (2)
Ru1—C3—C4—C10125.4 (4)Ru2—S3—Ru1—C4−123.41 (17)
C2—C3—C4—Ru153.8 (3)C34—S3—Ru1—C129.23 (19)
C3—C4—C5—C6−0.5 (6)Ru2—S3—Ru1—C1140.85 (12)
C10—C4—C5—C6−179.5 (4)C34—S3—Ru1—S1−149.03 (15)
Ru1—C4—C5—C6−54.6 (3)Ru2—S3—Ru1—S1−37.41 (3)
C3—C4—C5—Ru154.1 (3)C34—S3—Ru1—S2−71.67 (15)
C10—C4—C5—Ru1−124.9 (4)Ru2—S3—Ru1—S239.95 (3)
C4—C5—C6—C1−0.4 (6)C21—S1—Ru1—C61.2 (3)
Ru1—C5—C6—C1−55.9 (3)Ru2—S1—Ru1—C6115.0 (2)
C4—C5—C6—Ru155.5 (3)C21—S1—Ru1—C522.52 (19)
C2—C1—C6—C51.6 (5)Ru2—S1—Ru1—C5136.35 (13)
C7—C1—C6—C5−176.1 (4)C21—S1—Ru1—C2119.24 (18)
Ru1—C1—C6—C555.1 (3)Ru2—S1—Ru1—C2−126.92 (14)
C2—C1—C6—Ru1−53.5 (3)C21—S1—Ru1—C392.76 (17)
C7—C1—C6—Ru1128.8 (4)Ru2—S1—Ru1—C3−153.41 (11)
C6—C1—C7—C8−156.4 (4)C21—S1—Ru1—C456.07 (17)
C2—C1—C7—C826.1 (6)Ru2—S1—Ru1—C4169.91 (11)
Ru1—C1—C7—C8−67.8 (6)C21—S1—Ru1—S3−76.62 (13)
C6—C1—C7—C980.4 (6)Ru2—S1—Ru1—S337.22 (3)
C2—C1—C7—C9−97.1 (6)C21—S1—Ru1—S2−154.94 (13)
Ru1—C1—C7—C9169.0 (4)Ru2—S1—Ru1—S2−41.11 (3)
C16—C11—C12—C13−1.5 (5)C27—S2—Ru1—C6129.7 (2)
C17—C11—C12—C13179.6 (3)Ru2—S2—Ru1—C6−120.97 (15)
Ru2—C11—C12—C13−55.8 (3)C27—S2—Ru1—C265.17 (18)
C16—C11—C12—Ru254.4 (3)Ru2—S2—Ru1—C2174.49 (11)
C17—C11—C12—Ru2−124.6 (4)C27—S2—Ru1—C331.07 (18)
C11—C12—C13—C141.0 (6)Ru2—S2—Ru1—C3140.39 (12)
Ru2—C12—C13—C14−55.6 (3)C27—S2—Ru1—C47.6 (3)
C11—C12—C13—Ru256.5 (3)Ru2—S2—Ru1—C4116.9 (2)
C12—C13—C14—C150.4 (5)C27—S2—Ru1—C1102.46 (17)
Ru2—C13—C14—C15−53.7 (3)Ru2—S2—Ru1—C1−148.22 (11)
C12—C13—C14—C20−178.8 (4)C27—S2—Ru1—S3−149.06 (14)
Ru2—C13—C14—C20127.1 (3)Ru2—S2—Ru1—S3−39.74 (3)
C12—C13—C14—Ru254.1 (3)C27—S2—Ru1—S1−68.20 (14)
C13—C14—C15—C16−1.1 (5)Ru2—S2—Ru1—S141.11 (3)
C20—C14—C15—C16178.0 (3)C11—C12—Ru2—C13−132.2 (4)
Ru2—C14—C15—C16−54.5 (3)C11—C12—Ru2—C16−30.0 (2)
C13—C14—C15—Ru253.3 (3)C13—C12—Ru2—C16102.2 (3)
C20—C14—C15—Ru2−127.5 (3)C11—C12—Ru2—C15−66.4 (3)
C14—C15—C16—C110.6 (6)C13—C12—Ru2—C1565.8 (3)
Ru2—C15—C16—C11−54.4 (3)C13—C12—Ru2—C11132.2 (4)
C14—C15—C16—Ru255.0 (3)C11—C12—Ru2—C14−103.1 (3)
C12—C11—C16—C150.7 (5)C13—C12—Ru2—C1429.0 (3)
C17—C11—C16—C15179.7 (3)C11—C12—Ru2—S357.0 (3)
Ru2—C11—C16—C1554.3 (3)C13—C12—Ru2—S3−170.9 (2)
C12—C11—C16—Ru2−53.6 (3)C11—C12—Ru2—S2−159.6 (3)
C17—C11—C16—Ru2125.4 (3)C13—C12—Ru2—S2−27.4 (5)
C12—C11—C17—C1820.0 (6)C11—C12—Ru2—S1136.5 (2)
C16—C11—C17—C18−159.0 (4)C13—C12—Ru2—S1−91.3 (3)
Ru2—C11—C17—C18−71.1 (6)C14—C13—Ru2—C12131.8 (4)
C12—C11—C17—C19−104.6 (6)C14—C13—Ru2—C1666.1 (3)
C16—C11—C17—C1976.4 (6)C12—C13—Ru2—C16−65.8 (3)
Ru2—C11—C17—C19164.4 (5)C14—C13—Ru2—C1529.7 (2)
C26—C21—C22—C23−0.4 (6)C12—C13—Ru2—C15−102.1 (3)
S1—C21—C22—C23176.4 (3)C14—C13—Ru2—C11103.0 (3)
C21—C22—C23—C24−1.0 (6)C12—C13—Ru2—C11−28.8 (3)
C22—C23—C24—O1−176.3 (4)C12—C13—Ru2—C14−131.8 (4)
C22—C23—C24—C251.9 (6)C14—C13—Ru2—S3152.4 (3)
C23—C24—C25—C26−1.4 (6)C12—C13—Ru2—S320.6 (5)
O1—C24—C25—C26176.8 (4)C14—C13—Ru2—S2−58.6 (3)
C22—C21—C26—C251.0 (5)C12—C13—Ru2—S2169.5 (2)
S1—C21—C26—C25−175.6 (3)C14—C13—Ru2—S1−134.7 (2)
C24—C25—C26—C21−0.1 (6)C12—C13—Ru2—S193.5 (3)
S2—C27—C28—C29115.2 (4)C15—C16—Ru2—C12−103.1 (3)
S2—C27—C28—C33−62.6 (4)C11—C16—Ru2—C1230.0 (2)
C33—C28—C29—C301.6 (6)C15—C16—Ru2—C13−65.2 (3)
C27—C28—C29—C30−176.2 (4)C11—C16—Ru2—C1367.9 (3)
C28—C29—C30—C31−0.5 (7)C11—C16—Ru2—C15133.1 (4)
C29—C30—C31—C32−1.1 (7)C15—C16—Ru2—C11−133.1 (4)
C30—C31—C32—C331.5 (7)C15—C16—Ru2—C14−28.3 (3)
C31—C32—C33—C28−0.3 (7)C11—C16—Ru2—C14104.8 (3)
C29—C28—C33—C32−1.1 (7)C15—C16—Ru2—S3138.0 (3)
C27—C28—C33—C32176.7 (4)C11—C16—Ru2—S3−88.8 (2)
S3—C34—C35—C4059.4 (5)C15—C16—Ru2—S259.1 (3)
S3—C34—C35—C36−117.3 (4)C11—C16—Ru2—S2−167.78 (19)
C40—C35—C36—C37−0.1 (7)C15—C16—Ru2—S1−143.1 (3)
C34—C35—C36—C37176.6 (4)C11—C16—Ru2—S1−10.0 (5)
C35—C36—C37—C38−0.9 (8)C16—C15—Ru2—C1265.3 (3)
C36—C37—C38—C391.7 (9)C14—C15—Ru2—C12−67.9 (3)
C37—C38—C39—C40−1.3 (9)C16—C15—Ru2—C13103.3 (3)
C38—C39—C40—C350.3 (9)C14—C15—Ru2—C13−30.0 (2)
C36—C35—C40—C390.4 (7)C14—C15—Ru2—C16−133.3 (4)
C34—C35—C40—C39−176.4 (5)C16—C15—Ru2—C1128.5 (3)
C26—C21—S1—Ru117.9 (3)C14—C15—Ru2—C11−104.8 (3)
C22—C21—S1—Ru1−158.7 (2)C16—C15—Ru2—C14133.3 (4)
C26—C21—S1—Ru2−81.9 (3)C16—C15—Ru2—S3−53.2 (3)
C22—C21—S1—Ru2101.5 (3)C14—C15—Ru2—S3173.49 (19)
C28—C27—S2—Ru2−162.8 (3)C16—C15—Ru2—S2−134.0 (2)
C28—C27—S2—Ru1−67.0 (3)C14—C15—Ru2—S292.7 (2)
C35—C34—S3—Ru1173.0 (3)C16—C15—Ru2—S1146.4 (2)
C35—C34—S3—Ru276.9 (3)C14—C15—Ru2—S113.2 (4)
C1—C6—Ru1—C5132.7 (4)C16—C11—Ru2—C12−130.4 (4)
C5—C6—Ru1—C2−102.6 (3)C17—C11—Ru2—C12118.4 (6)
C1—C6—Ru1—C230.1 (2)C12—C11—Ru2—C1329.6 (3)
C5—C6—Ru1—C3−65.8 (3)C16—C11—Ru2—C13−100.9 (3)
C1—C6—Ru1—C366.9 (3)C17—C11—Ru2—C13148.0 (5)
C5—C6—Ru1—C4−28.7 (2)C12—C11—Ru2—C16130.4 (4)
C1—C6—Ru1—C4104.0 (3)C17—C11—Ru2—C16−111.2 (6)
C5—C6—Ru1—C1−132.7 (4)C12—C11—Ru2—C15102.1 (3)
C5—C6—Ru1—S3106.6 (2)C16—C11—Ru2—C15−28.3 (3)
C1—C6—Ru1—S3−120.7 (3)C17—C11—Ru2—C15−139.5 (5)
C5—C6—Ru1—S133.5 (4)C12—C11—Ru2—C1466.2 (3)
C1—C6—Ru1—S1166.17 (19)C16—C11—Ru2—C14−64.2 (3)
C5—C6—Ru1—S2−179.61 (19)C17—C11—Ru2—C14−175.4 (5)
C1—C6—Ru1—S2−46.9 (3)C12—C11—Ru2—S3−133.0 (2)
C4—C5—Ru1—C6−132.4 (4)C16—C11—Ru2—S396.5 (2)
C4—C5—Ru1—C2−66.4 (3)C17—C11—Ru2—S3−14.7 (5)
C6—C5—Ru1—C266.0 (2)C12—C11—Ru2—S2160.8 (3)
C4—C5—Ru1—C3−29.8 (3)C16—C11—Ru2—S230.3 (4)
C6—C5—Ru1—C3102.7 (3)C17—C11—Ru2—S2−80.9 (6)
C6—C5—Ru1—C4132.4 (4)C12—C11—Ru2—S1−53.8 (3)
C4—C5—Ru1—C1−103.6 (3)C16—C11—Ru2—S1175.8 (2)
C6—C5—Ru1—C128.8 (2)C17—C11—Ru2—S164.6 (5)
C4—C5—Ru1—S3148.7 (2)C15—C14—Ru2—C12100.9 (3)
C6—C5—Ru1—S3−78.9 (2)C13—C14—Ru2—C12−29.8 (3)
C4—C5—Ru1—S166.6 (3)C20—C14—Ru2—C12−144.9 (7)
C6—C5—Ru1—S1−161.0 (2)C15—C14—Ru2—C13130.6 (3)
C3—C2—Ru1—C6102.6 (3)C20—C14—Ru2—C13−115.1 (7)
C1—C2—Ru1—C6−30.1 (3)C15—C14—Ru2—C1628.3 (2)
C3—C2—Ru1—C565.4 (3)C13—C14—Ru2—C16−102.4 (3)
C1—C2—Ru1—C5−67.2 (3)C20—C14—Ru2—C16142.5 (7)
C1—C2—Ru1—C3−132.7 (3)C13—C14—Ru2—C15−130.6 (3)
C3—C2—Ru1—C428.8 (2)C20—C14—Ru2—C15114.3 (7)
C1—C2—Ru1—C4−103.8 (3)C15—C14—Ru2—C1164.4 (3)
C3—C2—Ru1—C1132.7 (3)C13—C14—Ru2—C11−66.2 (3)
C3—C2—Ru1—S3162.38 (19)C20—C14—Ru2—C11178.7 (7)
C1—C2—Ru1—S329.7 (3)C15—C14—Ru2—S3−16.3 (5)
C3—C2—Ru1—S1−45.9 (3)C13—C14—Ru2—S3−147.0 (3)
C1—C2—Ru1—S1−178.6 (2)C20—C14—Ru2—S397.9 (7)
C3—C2—Ru1—S2−122.1 (2)C15—C14—Ru2—S2−95.1 (2)
C1—C2—Ru1—S2105.2 (2)C13—C14—Ru2—S2134.2 (2)
C2—C3—Ru1—C6−66.1 (3)C20—C14—Ru2—S219.1 (6)
C4—C3—Ru1—C666.6 (3)C15—C14—Ru2—S1−174.05 (19)
C2—C3—Ru1—C5−103.2 (3)C13—C14—Ru2—S155.3 (3)
C4—C3—Ru1—C529.5 (3)C20—C14—Ru2—S1−59.8 (7)
C4—C3—Ru1—C2132.7 (4)C34—S3—Ru2—C12−124.07 (19)
C2—C3—Ru1—C4−132.7 (4)Ru1—S3—Ru2—C12128.45 (14)
C2—C3—Ru1—C1−28.9 (2)C34—S3—Ru2—C13−138.6 (3)
C4—C3—Ru1—C1103.8 (3)Ru1—S3—Ru2—C13114.0 (3)
C2—C3—Ru1—S3−111.6 (6)C34—S3—Ru2—C16−56.46 (17)
C4—C3—Ru1—S321.1 (8)Ru1—S3—Ru2—C16−163.94 (12)
C2—C3—Ru1—S1147.6 (2)C34—S3—Ru2—C15−27.50 (18)
C4—C3—Ru1—S1−79.7 (3)Ru1—S3—Ru2—C15−134.98 (13)
C2—C3—Ru1—S267.7 (2)C34—S3—Ru2—C11−93.62 (18)
C4—C3—Ru1—S2−159.6 (2)Ru1—S3—Ru2—C11158.90 (13)
C5—C4—Ru1—C629.1 (3)C34—S3—Ru2—C14−15.7 (3)
C3—C4—Ru1—C6−102.0 (3)Ru1—S3—Ru2—C14−123.2 (3)
C10—C4—Ru1—C6144.1 (5)C34—S3—Ru2—S267.45 (13)
C3—C4—Ru1—C5−131.1 (4)Ru1—S3—Ru2—S2−40.03 (3)
C10—C4—Ru1—C5115.0 (5)C34—S3—Ru2—S1144.75 (13)
C5—C4—Ru1—C2102.5 (3)Ru1—S3—Ru2—S137.27 (3)
C3—C4—Ru1—C2−28.6 (2)C27—S2—Ru2—C122.7 (4)
C10—C4—Ru1—C2−142.5 (5)Ru1—S2—Ru2—C12−108.2 (4)
C5—C4—Ru1—C3131.1 (4)C27—S2—Ru2—C13−17.4 (2)
C10—C4—Ru1—C3−113.8 (5)Ru1—S2—Ru2—C13−128.38 (16)
C5—C4—Ru1—C165.8 (3)C27—S2—Ru2—C16−118.1 (2)
C3—C4—Ru1—C1−65.4 (3)Ru1—S2—Ru2—C16130.99 (14)
C10—C4—Ru1—C1−179.2 (5)C27—S2—Ru2—C15−86.5 (2)
C5—C4—Ru1—S3−43.7 (3)Ru1—S2—Ru2—C15162.55 (14)
C3—C4—Ru1—S3−174.84 (19)C27—S2—Ru2—C11−139.8 (3)
C10—C4—Ru1—S371.3 (5)Ru1—S2—Ru2—C11109.3 (3)
C5—C4—Ru1—S1−122.0 (3)C27—S2—Ru2—C14−49.1 (2)
C3—C4—Ru1—S1106.9 (2)Ru1—S2—Ru2—C14−160.00 (15)
C10—C4—Ru1—S1−6.9 (4)C27—S2—Ru2—S3150.56 (16)
C5—C4—Ru1—S2167.9 (2)Ru1—S2—Ru2—S339.61 (3)
C3—C4—Ru1—S236.8 (4)C27—S2—Ru2—S170.03 (15)
C10—C4—Ru1—S2−77.0 (5)Ru1—S2—Ru2—S1−40.91 (3)
C2—C1—Ru1—C6130.4 (4)C21—S1—Ru2—C12−39.83 (18)
C7—C1—Ru1—C6−111.6 (6)Ru1—S1—Ru2—C12−156.38 (13)
C6—C1—Ru1—C5−28.9 (3)C21—S1—Ru2—C13−78.12 (18)
C2—C1—Ru1—C5101.6 (3)Ru1—S1—Ru2—C13165.33 (12)
C7—C1—Ru1—C5−140.4 (5)C21—S1—Ru2—C16−3.5 (3)
C6—C1—Ru1—C2−130.4 (4)Ru1—S1—Ru2—C16−120.1 (3)
C7—C1—Ru1—C2118.0 (6)C21—S1—Ru2—C15−117.1 (3)
C6—C1—Ru1—C3−101.8 (3)Ru1—S1—Ru2—C15126.3 (3)
C2—C1—Ru1—C328.7 (2)C21—S1—Ru2—C11−10.60 (19)
C7—C1—Ru1—C3146.7 (5)Ru1—S1—Ru2—C11−127.14 (13)
C6—C1—Ru1—C4−65.2 (3)C21—S1—Ru2—C14−108.01 (18)
C2—C1—Ru1—C465.3 (2)Ru1—S1—Ru2—C14135.44 (13)
C7—C1—Ru1—C4−176.7 (5)C21—S1—Ru2—S379.40 (13)
C6—C1—Ru1—S367.0 (3)Ru1—S1—Ru2—S3−37.15 (3)
C2—C1—Ru1—S3−162.58 (19)C21—S1—Ru2—S2157.76 (13)
C7—C1—Ru1—S3−44.6 (5)Ru1—S1—Ru2—S241.21 (3)
C6—C1—Ru1—S2147.2 (3)
D—H···AD—HH···AD···AD—H···A
O1—H1···F10.821.992.773 (9)161
C3—H3···F3i0.932.523.340 (11)148
C30—H30···F2i0.932.603.472 (9)156
C6—H6···F4ii0.932.343.249 (10)166
  5 in total

1.  Thiophenolato-bridged dinuclear arene ruthenium complexes: a new family of highly cytotoxic anticancer agents.

Authors:  Michaël Gras; Bruno Therrien; Georg Süss-Fink; Olivier Zava; Paul J Dyson
Journal:  Dalton Trans       Date:  2010-10-04       Impact factor: 4.390

2.  A short history of SHELX.

Authors:  George M Sheldrick
Journal:  Acta Crystallogr A       Date:  2007-12-21       Impact factor: 2.290

3.  Highly cytotoxic trithiophenolatodiruthenium complexes of the type [(η6-p-MeC6H4Pri)2Ru2(SC6H4-p-X)3]+: synthesis, molecular structure, electrochemistry, cytotoxicity, and glutathione oxidation potential.

Authors:  Federico Giannini; Julien Furrer; Anne-Flore Ibao; Georg Süss-Fink; Bruno Therrien; Olivier Zava; Mathurin Baquie; Paul J Dyson; Petr Stěpnička
Journal:  J Biol Inorg Chem       Date:  2012-06-16       Impact factor: 3.358

4.  Crystal structure refinement with SHELXL.

Authors:  George M Sheldrick
Journal:  Acta Crystallogr C Struct Chem       Date:  2015-01-01       Impact factor: 1.172

5.  Use of intensity quotients and differences in absolute structure refinement.

Authors:  Simon Parsons; Howard D Flack; Trixie Wagner
Journal:  Acta Crystallogr B Struct Sci Cryst Eng Mater       Date:  2013-05-17
  5 in total

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